Item | Value |
---|---|
geneid | 26054 |
ensemblid | ENSG00000112701.18 |
hgncid | 20944 |
symbol | SENP6 |
name | SUMO specific peptidase 6 |
refseq_nuc | NM_015571.4 |
refseq_prot | NP_056386.2 |
ensembl_nuc | ENST00000447266.7 |
ensembl_prot | ENSP00000402527.2 |
mane_status | MANE Select |
chr | chr6 |
start | 75601880 |
end | 75718281 |
strand | + |
ver | v1.2 |
region | chr6:75601880-75718281 |
region5000 | chr6:75596880-75723281 |
regionname0 | SENP6_chr6_75601880_75718281 |
regionname5000 | SENP6_chr6_75596880_75723281 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1112 | 321 | 81 | 37 | 163 | 12 | 27 | 127 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
a0002 | 0/1 | 1112 | 26 | 2 | 7 | 7 | 4 | 5 | 5 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
a0003 | 0/0 | 1112 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
a0004 | 0/0 | 1112 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
a0005 | 0/0 | 1112 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
a0006 | 0/0 | 1112 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
a0007 | 0/0 | 1112 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
a0008 | 0/0 | 1112 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
a0009 | 0/0 | 1112 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
a0010 | 0/0 | 1112 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
a0011 | 0/0 | 1112 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
a0012 | 0/0 | 1112 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | MAAGK others(1107): Show |
chr6 | 75596880 | 75723281 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3336 | 257 | 43 | 36 | 140 | 12 | 26 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0001c0002 | 1/0 | 3336 | 45 | 19 | 1 | 23 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0001c0004 | 0/0 | 3336 | 10 | 10 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0001c0005 | 0/0 | 3336 | 5 | 5 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0001c0008 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0001c0016 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0001c0017 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0002c0003 | 0/1 | 3336 | 26 | 2 | 7 | 7 | 4 | 5 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0003c0007 | 0/0 | 3336 | 3 | 3 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0004c0006 | 0/0 | 3336 | 3 | 0 | 0 | 3 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0005c0009 | 0/0 | 3336 | 2 | 0 | 0 | 2 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0006c0015 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0007c0013 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0008c0010 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0009c0018 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0010c0014 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0011c0011 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 | ||
a0012c0012 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | ATGGC others(3331): Show |
chr6 | 75596880 | 75723281 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6669 | 89 | 6 | 19 | 49 | 6 | 9 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6664): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0002 | 0/0 | 6671 | 84 | 22 | 8 | 40 | 2 | 12 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0003 | 0/0 | 6671 | 6 | 5 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0004 | 0/0 | 6671 | 29 | 0 | 2 | 26 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0005 | 0/0 | 6671 | 20 | 4 | 5 | 6 | 3 | 2 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0007 | 0/0 | 6671 | 9 | 0 | 1 | 8 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0008 | 0/0 | 6665 | 8 | 0 | 0 | 8 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6660): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0010 | 0/0 | 6671 | 3 | 3 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0012 | 0/0 | 6671 | 2 | 0 | 0 | 2 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0013 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0015 | 0/0 | 6671 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0016 | 0/0 | 6669 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6664): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0017 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0018 | 0/0 | 6671 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0020 | 0/0 | 6669 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6664): Show |
chr6 | 75596880 | 75723281 |
a0001c0001t0023 | 0/0 | 6669 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6664): Show |
chr6 | 75596880 | 75723281 |
a0001c0002t0002 | 1/0 | 6671 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0002t0003 | 0/0 | 6671 | 35 | 11 | 1 | 22 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0002t0009 | 0/0 | 6671 | 5 | 5 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0002t0011 | 0/0 | 6671 | 2 | 2 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0002t0021 | 0/0 | 6671 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0002t0022 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0004t0003 | 0/0 | 6671 | 9 | 9 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0004t0014 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0005t0006 | 0/0 | 6671 | 5 | 5 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0008t0003 | 0/0 | 6671 | 2 | 2 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0016t0006 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0001c0017t0002 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0002c0003t0003 | 0/0 | 6671 | 25 | 2 | 7 | 7 | 4 | 5 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0002c0003t0019 | 0/1 | 6671 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0003c0007t0006 | 0/0 | 6671 | 3 | 3 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0004c0006t0005 | 0/0 | 6671 | 3 | 0 | 0 | 3 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0005c0009t0001 | 0/0 | 6669 | 2 | 0 | 0 | 2 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6664): Show |
chr6 | 75596880 | 75723281 |
a0006c0015t0001 | 0/0 | 6669 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6664): Show |
chr6 | 75596880 | 75723281 |
a0007c0013t0005 | 0/0 | 6671 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0008c0010t0009 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0009c0018t0001 | 0/0 | 6669 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6664): Show |
chr6 | 75596880 | 75723281 |
a0010c0014t0002 | 0/0 | 6671 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0011c0011t0003 | 0/0 | 6671 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
a0012c0012t0003 | 0/0 | 6671 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | AGCGG others(6666): Show |
chr6 | 75596880 | 75723281 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0007g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0007g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0007g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0007g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0007g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0007g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0007g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0007g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0010g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0012g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0012g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0015g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0016g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0017g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0018g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0020g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0001t0023g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0002g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0009g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0021g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0002t0022g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0004t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0004t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0004t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0004t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0004t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0004t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0004t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0004t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0004t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0004t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0005t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0005t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0005t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0005t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0005t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0008t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0008t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0016t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0001c0017t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0002c0003t0019g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0003c0007t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0003c0007t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0003c0007t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0004c0006t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0004c0006t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0004c0006t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0005c0009t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0005c0009t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0006c0015t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0007c0013t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0008c0010t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0009c0018t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0010c0014t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0011c0011t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
a0012c0012t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | GBR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00099 | hp2 | a0001 | c0001 | t0018 | g0063 | EUR | GBR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | GBR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | GBR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0137 | EUR | FIN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0158 | EUR | FIN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0323 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00423 | hp1 | a0001 | c0002 | t0003 | g0353 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00423 | hp2 | a0001 | c0001 | t0008 | g0260 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0320 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00609 | hp2 | a0001 | c0002 | t0003 | g0343 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0147 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0322 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00738 | hp1 | a0002 | c0003 | t0003 | g0046 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00741 | hp1 | a0002 | c0003 | t0003 | g0029 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0165 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01074 | hp1 | a0006 | c0015 | t0001 | g0287 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01074 | hp2 | a0002 | c0003 | t0003 | g0050 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01081 | hp2 | a0002 | c0003 | t0003 | g0044 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0170 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0163 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01168 | hp1 | a0002 | c0003 | t0003 | g0039 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0162 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01169 | hp2 | a0002 | c0003 | t0003 | g0043 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01243 | hp2 | a0002 | c0003 | t0003 | g0042 | AMR | PUR | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01256 | hp2 | a0001 | c0001 | t0005 | g0153 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01346 | hp1 | a0007 | c0013 | t0005 | g0142 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0157 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01516 | hp1 | a0002 | c0003 | t0003 | g0054 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01517 | hp1 | a0002 | c0003 | t0003 | g0055 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0274 | EUR | IBS | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01891 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0306 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01975 | hp2 | a0001 | c0001 | t0007 | g0308 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0305 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02015 | hp2 | a0005 | c0009 | t0001 | g0192 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02027 | hp1 | a0001 | c0002 | t0003 | g0354 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0318 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02040 | hp2 | a0005 | c0009 | t0001 | g0193 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02055 | hp2 | a0001 | c0004 | t0003 | g0182 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02056 | hp1 | a0002 | c0003 | t0003 | g0034 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02083 | hp2 | a0001 | c0002 | t0003 | g0348 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02132 | hp1 | a0001 | c0001 | t0008 | g0228 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02132 | hp2 | a0002 | c0003 | t0003 | g0031 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02145 | hp1 | a0001 | c0001 | t0017 | g0076 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02145 | hp2 | a0002 | c0003 | t0003 | g0049 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02155 | hp1 | a0001 | c0001 | t0008 | g0243 | EAS | CDX | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | CDX | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CDX | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02257 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02257 | hp2 | a0001 | c0005 | t0006 | g0297 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02280 | hp1 | a0001 | c0004 | t0003 | g0175 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02451 | hp1 | a0002 | c0003 | t0003 | g0047 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02451 | hp2 | a0003 | c0007 | t0006 | g0295 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02572 | hp2 | a0001 | c0004 | t0003 | g0181 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02622 | hp1 | a0001 | c0001 | t0010 | g0183 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02622 | hp2 | a0001 | c0002 | t0009 | g0172 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02630 | hp1 | a0001 | c0002 | t0022 | g0022 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02647 | hp1 | a0003 | c0007 | t0006 | g0291 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02698 | hp1 | a0002 | c0003 | t0003 | g0045 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0314 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02717 | hp1 | a0001 | c0004 | t0003 | g0179 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02717 | hp2 | a0001 | c0017 | t0002 | g0112 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02723 | hp2 | a0001 | c0002 | t0009 | g0171 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02735 | hp1 | a0002 | c0003 | t0003 | g0030 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02735 | hp2 | a0001 | c0001 | t0020 | g0253 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02738 | hp1 | a0002 | c0003 | t0003 | g0048 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02738 | hp2 | a0001 | c0001 | t0015 | g0132 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0299 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02886 | hp2 | a0001 | c0001 | t0016 | g0122 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02895 | hp2 | a0001 | c0004 | t0003 | g0177 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02897 | hp1 | a0001 | c0004 | t0003 | g0176 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02922 | hp1 | a0001 | c0002 | t0003 | g0018 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02965 | hp1 | a0001 | c0002 | t0011 | g0015 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0185 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03041 | hp2 | a0001 | c0002 | t0003 | g0008 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03098 | hp1 | a0001 | c0008 | t0003 | g0186 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03098 | hp2 | a0001 | c0001 | t0010 | g0188 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03130 | hp1 | a0001 | c0002 | t0003 | g0007 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03130 | hp2 | a0001 | c0002 | t0009 | g0013 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03139 | hp2 | a0001 | c0002 | t0003 | g0021 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03195 | hp1 | a0001 | c0001 | t0010 | g0184 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03209 | hp2 | a0008 | c0010 | t0009 | g0011 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03225 | hp1 | a0001 | c0004 | t0014 | g0052 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03225 | hp2 | a0001 | c0002 | t0003 | g0023 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03453 | hp1 | a0001 | c0005 | t0006 | g0292 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03453 | hp2 | a0001 | c0004 | t0003 | g0178 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03516 | hp1 | a0001 | c0004 | t0003 | g0180 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03516 | hp2 | a0001 | c0008 | t0003 | g0187 | AFR | ESN | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03540 | hp1 | a0001 | c0005 | t0006 | g0296 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03579 | hp1 | a0001 | c0002 | t0003 | g0024 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0159 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0154 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03831 | hp1 | a0002 | c0003 | t0003 | g0040 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03831 | hp2 | a0009 | c0018 | t0001 | g0237 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03834 | hp1 | a0010 | c0014 | t0002 | g0088 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03834 | hp2 | a0001 | c0002 | t0003 | g0340 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG04115 | hp1 | a0002 | c0003 | t0003 | g0038 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | BEB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | STU | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18522 | hp1 | a0001 | c0005 | t0006 | g0294 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18522 | hp2 | a0001 | c0002 | t0009 | g0010 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | CHB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18612 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | CHB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CHB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CHB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18906 | hp2 | a0001 | c0004 | t0003 | g0174 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18939 | hp1 | a0001 | c0002 | t0003 | g0347 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18940 | hp1 | a0002 | c0003 | t0003 | g0033 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18940 | hp2 | a0001 | c0002 | t0003 | g0355 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0315 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18941 | hp2 | a0002 | c0003 | t0003 | g0035 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18946 | hp1 | a0001 | c0001 | t0007 | g0330 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0356 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18949 | hp2 | a0002 | c0003 | t0003 | g0037 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18962 | hp1 | a0001 | c0001 | t0007 | g0310 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18962 | hp2 | a0002 | c0003 | t0003 | g0036 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18964 | hp2 | a0001 | c0002 | t0003 | g0357 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18965 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18966 | hp1 | a0001 | c0002 | t0003 | g0345 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18967 | hp1 | a0001 | c0001 | t0007 | g0331 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18968 | hp1 | a0001 | c0002 | t0003 | g0337 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18972 | hp2 | a0001 | c0001 | t0007 | g0304 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18973 | hp1 | a0001 | c0002 | t0003 | g0338 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18975 | hp2 | a0001 | c0002 | t0003 | g0358 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18977 | hp1 | a0001 | c0001 | t0007 | g0316 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18978 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0335 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18980 | hp1 | a0004 | c0006 | t0005 | g0161 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18982 | hp2 | a0001 | c0002 | t0003 | g0349 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18983 | hp1 | a0001 | c0002 | t0003 | g0350 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18984 | hp2 | a0001 | c0001 | t0008 | g0196 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18988 | hp2 | a0001 | c0001 | t0012 | g0150 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18991 | hp1 | a0001 | c0002 | t0021 | g0342 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18993 | hp1 | a0001 | c0002 | t0003 | g0359 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18994 | hp1 | a0001 | c0001 | t0023 | g0143 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18994 | hp2 | a0004 | c0006 | t0005 | g0152 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18995 | hp1 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18995 | hp2 | a0001 | c0002 | t0003 | g0339 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18997 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18998 | hp1 | a0001 | c0001 | t0007 | g0317 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19000 | hp1 | a0001 | c0001 | t0007 | g0327 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19004 | hp2 | a0001 | c0002 | t0003 | g0341 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19005 | hp1 | a0011 | c0011 | t0003 | g0344 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19006 | hp1 | a0001 | c0001 | t0004 | g0307 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19006 | hp2 | a0001 | c0001 | t0008 | g0254 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19054 | hp1 | a0001 | c0001 | t0012 | g0149 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19054 | hp2 | a0001 | c0001 | t0008 | g0210 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0352 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19057 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19062 | hp2 | a0001 | c0002 | t0003 | g0351 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19066 | hp1 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19074 | hp1 | a0001 | c0002 | t0003 | g0346 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19085 | hp1 | a0001 | c0001 | t0007 | g0303 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19087 | hp1 | a0002 | c0003 | t0003 | g0032 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19088 | hp1 | a0004 | c0006 | t0005 | g0151 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19090 | hp2 | a0001 | c0001 | t0008 | g0259 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19240 | hp1 | a0012 | c0012 | t0003 | g0167 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0016 | AFR | YRI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA20129 | hp1 | a0001 | c0005 | t0006 | g0293 | AFR | ASW | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ASW | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA20752 | hp1 | a0002 | c0003 | t0003 | g0041 | EUR | TSI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0155 | EUR | TSI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA20805 | hp2 | a0002 | c0003 | t0003 | g0053 | EUR | TSI | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | GIH | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | GIH | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02109 | hp2 | a0003 | c0007 | t0006 | g0168 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02486 | hp2 | a0001 | c0002 | t0009 | g0012 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG06807 | hp1 | a0001 | c0002 | t0011 | g0020 | AFR | USA | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
HG06807 | hp2 | a0001 | c0016 | t0006 | g0298 | AFR | USA | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | USA | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | USA | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
homoSapiens | chm13v2 | a0002 | c0003 | t0019 | g0051 | REF | REF | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0019 | REF | REF | SENP6_chr6_75596880_75723281 | SENP6 | chr6 | 75596880 | 75723281 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:75621591 | C | T | 1 | a0009 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.112C>T | p.His38Tyr | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/24 | 757/6671 | 112/3339 | 38/1112 | chr6 | 75621591 | |||
chr6:75634715 | C | T | 2 | a0002 a0005 |
27 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(24): Show |
missense_variant | MODERATE | c.362C>T | p.Thr121Met | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/24 | 1007/6671 | 362/3339 | 121/1112 | chr6 | 75634715 | |||
chr6:75659265 | G | A | 1 | a0008 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.554G>A | p.Arg185His | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/24 | 1199/6671 | 554/3339 | 185/1112 | chr6 | 75659265 | |||
chr6:75659328 | A | G | 1 | a0006 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.617A>G | p.Gln206Arg | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/24 | 1262/6671 | 617/3339 | 206/1112 | chr6 | 75659328 | |||
chr6:75670644 | C | T | 1 | a0010 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1316C>T | p.Ser439Phe | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/24 | 1961/6671 | 1316/3339 | 439/1112 | chr6 | 75670644 | |||
chr6:75678608 | T | C | 1 | a0004 | 3 | NA18980.hp1 NA18994.hp2 NA19088.hp1 |
missense_variant | MODERATE | c.1874T>C | p.Leu625Pro | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 15/24 | 2519/6671 | 1874/3339 | 625/1112 | chr6 | 75678608 | |||
chr6:75678611 | G | A | 1 | a0011 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.1877G>A | p.Arg626Lys | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 15/24 | 2522/6671 | 1877/3339 | 626/1112 | chr6 | 75678611 | |||
chr6:75702739 | A | G | 1 | a0007 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2383A>G | p.Lys795Glu | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/24 | 3028/6671 | 2383/3339 | 795/1112 | chr6 | 75702739 | |||
chr6:75702815 | C | T | 1 | a0003 | 3 | HG02109.hp2 HG02451.hp2 HG02647.hp1 |
missense_variant | MODERATE | c.2459C>T | p.Ala820Val | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/24 | 3104/6671 | 2459/3339 | 820/1112 | chr6 | 75702815 | |||
chr6:75715470 | G | A | 1 | a0012 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.3215G>A | p.Arg1072Gln | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 3860/6671 | 3215/3339 | 1072/1112 | chr6 | 75715470 | |||
chr6:75715572 | A | G | 1 | a0002 | 25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
missense_variant | MODERATE | c.3317A>G | p.Tyr1106Cys | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 3962/6671 | 3317/3339 | 1106/1112 | chr6 | 75715572 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:75634788 | A | T | 1 | a0001c0017 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.435A>T | p.Pro145Pro | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/24 | 1080/6671 | 435/3339 | 145/1112 | chr6 | 75634788 | |||
chr6:75647788 | G | T | 3 | a0001c0005 a0001c0016 a0003c0007 |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
synonymous_variant | LOW | c.537G>T | p.Arg179Arg | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/24 | 1182/6671 | 537/3339 | 179/1112 | chr6 | 75647788 | |||
chr6:75659338 | A | G | 15 | a0001c0001 a0001c0004 a0001c0005 others(12): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
synonymous_variant | LOW | c.627A>G | p.Arg209Arg | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/24 | 1272/6671 | 627/3339 | 209/1112 | chr6 | 75659338 | |||
chr6:75663286 | G | A | 2 | a0001c0005 a0003c0007 |
8 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
synonymous_variant | LOW | c.762G>A | p.Thr254Thr | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/24 | 1407/6671 | 762/3339 | 254/1112 | chr6 | 75663286 | |||
chr6:75666836 | G | A | 2 | a0001c0004 a0002c0003 |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
synonymous_variant | LOW | c.1119G>A | p.Ala373Ala | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/24 | 1764/6671 | 1119/3339 | 373/1112 | chr6 | 75666836 | |||
chr6:75678820 | A | G | 1 | a0001c0008 | 2 | HG03098.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1968A>G | p.Val656Val | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/24 | 2613/6671 | 1968/3339 | 656/1112 | chr6 | 75678820 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:75601899 | G | A | 1 | a0001c0001t0013 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-626G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/24 | 626 | chr6 | 75601899 | ||||||
chr6:75602002 | C | T | 5 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0023 others(2): Show |
27 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-523C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/24 | 523 | chr6 | 75602002 | ||||||
chr6:75602033 | G | T | 2 | a0001c0001t0004 a0001c0001t0007 |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-492G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/24 | 492 | chr6 | 75602033 | ||||||
chr6:75602205 | G | C | 1 | a0001c0004t0014 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-320G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/24 | 320 | chr6 | 75602205 | ||||||
chr6:75602443 | C | T | 1 | a0001c0002t0022 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/24 | 82 | chr6 | 75602443 | ||||||
chr6:75715657 | A | T | 2 | a0001c0002t0011 a0001c0002t0022 |
3 | HG02630.hp1 HG02965.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*63A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 63 | chr6 | 75715657 | ||||||
chr6:75715825 | A | G | 1 | a0001c0002t0021 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*231A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 231 | chr6 | 75715825 | ||||||
chr6:75715878 | A | C | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(21): Show |
235 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*284A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 284 | chr6 | 75715878 | ||||||
chr6:75716048 | A | G | 1 | a0001c0001t0018 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 454 | chr6 | 75716048 | ||||||
chr6:75716056 | T | C | 1 | a0001c0001t0007 | 9 | HG01975.hp2 NA18946.hp1 NA18962.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*462T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 462 | chr6 | 75716056 | ||||||
chr6:75716253 | C | A | 1 | a0001c0001t0015 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*659C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 659 | chr6 | 75716253 | ||||||
chr6:75716465 | T | A | 1 | a0001c0001t0012 | 2 | NA18988.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*871T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 871 | chr6 | 75716465 | ||||||
chr6:75716686 | G | A | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(21): Show |
235 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*1092G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 1092 | chr6 | 75716686 | ||||||
chr6:75717088 | C | G | 2 | a0001c0002t0009 a0008c0010t0009 |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1494C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 1494 | chr6 | 75717088 | ||||||
chr6:75717205 | A | T | 1 | a0001c0001t0017 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1611A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 1611 | chr6 | 75717205 | ||||||
chr6:75717349 | A | G | 31 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(28): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*1755A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 1755 | chr6 | 75717349 | ||||||
chr6:75717401 | A | C | 1 | a0001c0001t0020 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1807A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 1807 | chr6 | 75717401 | ||||||
chr6:75717795 | TTAGA | T | 1 | a0001c0001t0008 | 8 | HG00423.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2207_*2210delAGAT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 2207 | INFO_REALIGN_3_PRIME | chr6 | 75717795 | |||||
chr6:75717805 | C | A | 2 | a0001c0001t0010 a0001c0001t0013 |
4 | HG02622.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2211C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 2211 | chr6 | 75717805 | ||||||
chr6:75718107 | CTT | C | 8 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0016 others(5): Show |
104 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2514_*2515delTT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 24/24 | 2514 | chr6 | 75718107 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:75602599 | C | T | 24 | a0001c0002t0003g0003 a0001c0002t0003g0337 a0001c0002t0003g0338 others(21): Show |
25 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.52+23C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75602599 | |||||||
chr6:75602930 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.52+354A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75602930 | |||||||
chr6:75603047 | A | G | 2 | a0001c0001t0005g0299 a0001c0001t0005g0300 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.52+471A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603047 | |||||||
chr6:75603071 | C | T | 8 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(5): Show |
8 | HG02257.hp2 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.52+495C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603071 | |||||||
chr6:75603086 | C | T | 102 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.52+510C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603086 | |||||||
chr6:75603128 | C | T | 6 | a0001c0001t0010g0183 a0001c0001t0010g0184 a0001c0001t0010g0188 others(3): Show |
6 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+552C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603128 | |||||||
chr6:75603194 | C | G | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+618C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603194 | |||||||
chr6:75603208 | T | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0005 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.52+632T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603208 | |||||||
chr6:75603256 | G | A | 1 | a0001c0001t0004g0301 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.52+680G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603256 | |||||||
chr6:75603261 | A | G | 1 | a0001c0001t0004g0336 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.52+685A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603261 | |||||||
chr6:75603297 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.52+721G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603297 | |||||||
chr6:75603322 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.52+746G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603322 | |||||||
chr6:75603334 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.52+758C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603334 | |||||||
chr6:75603342 | A | G | 2 | a0001c0002t0009g0171 a0001c0002t0009g0172 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.52+766A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603342 | |||||||
chr6:75603646 | C | T | 1 | a0001c0002t0003g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.52+1070C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603646 | |||||||
chr6:75603753 | G | T | 1 | a0001c0001t0002g0169 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.52+1177G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603753 | |||||||
chr6:75603843 | C | G | 1 | a0001c0001t0001g0290 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.52+1267C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75603843 | |||||||
chr6:75604058 | A | G | 1 | a0001c0016t0006g0298 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.52+1482A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604058 | |||||||
chr6:75604262 | A | G | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.52+1686A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604262 | |||||||
chr6:75604282 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.52+1706C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604282 | |||||||
chr6:75604379 | C | T | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+1803C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604379 | |||||||
chr6:75604452 | C | T | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+1876C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604452 | |||||||
chr6:75604482 | T | G | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+1906T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604482 | |||||||
chr6:75604625 | C | CA | 42 | a0001c0001t0001g0191 a0001c0001t0001g0194 a0001c0001t0001g0195 others(39): Show |
42 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.52+2060dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75604625 | ||||||
chr6:75604711 | G | C | 1 | a0001c0001t0008g0196 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.52+2135G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604711 | |||||||
chr6:75604804 | G | A | 1 | a0002c0003t0003g0029 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.52+2228G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604804 | |||||||
chr6:75604811 | G | A | 1 | a0001c0001t0003g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.52+2235G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604811 | |||||||
chr6:75604941 | C | T | 3 | a0002c0003t0003g0053 a0002c0003t0003g0054 a0002c0003t0003g0055 |
3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.52+2365C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604941 | |||||||
chr6:75604966 | G | T | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.52+2390G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75604966 | |||||||
chr6:75605126 | T | C | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+2550T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605126 | |||||||
chr6:75605680 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.52+3104T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605680 | |||||||
chr6:75605829 | TAGG | T | 22 | a0001c0001t0005g0144 a0001c0001t0005g0145 a0001c0001t0005g0146 others(19): Show |
22 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.52+3254_52+3256del others(3): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605829 | |||||||
chr6:75605910 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.52+3334G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605910 | |||||||
chr6:75605917 | G | A | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.52+3341G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605917 | |||||||
chr6:75605950 | T | C | 1 | a0002c0003t0003g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.52+3374T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605950 | |||||||
chr6:75605969 | T | A | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.52+3393T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75605969 | |||||||
chr6:75606054 | G | T | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+3478G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606054 | |||||||
chr6:75606156 | C | G | 3 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0006c0015t0001g0287 |
3 | HG01074.hp1 HG01975.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.52+3580C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606156 | |||||||
chr6:75606292 | G | A | 3 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0012c0012t0003g0167 |
3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+3716G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606292 | |||||||
chr6:75606350 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.52+3774A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606350 | |||||||
chr6:75606693 | C | T | 1 | a0001c0001t0004g0335 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.52+4117C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606693 | |||||||
chr6:75606791 | AAAAATCT | A | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.52+4216_52+4222del others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606791 | |||||||
chr6:75606897 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.52+4321G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606897 | |||||||
chr6:75606987 | G | A | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+4411G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75606987 | |||||||
chr6:75607254 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.52+4678G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607254 | |||||||
chr6:75607286 | C | G | 1 | a0001c0001t0005g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.52+4710C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607286 | |||||||
chr6:75607302 | A | C | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+4726A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607302 | |||||||
chr6:75607497 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.52+4921T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607497 | |||||||
chr6:75607529 | A | G | 1 | a0001c0001t0023g0143 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.52+4953A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607529 | |||||||
chr6:75607547 | C | CT | 36 | a0001c0001t0001g0285 a0001c0001t0004g0002 a0001c0001t0004g0301 others(33): Show |
37 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.52+4981dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75607547 | ||||||
chr6:75607580 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.52+5004A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607580 | |||||||
chr6:75607622 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.52+5046C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607622 | |||||||
chr6:75607758 | C | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0283 |
2 | HG02027.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.52+5182C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75607758 | |||||||
chr6:75607912 | C | CA | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.52+5337dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75607912 | ||||||
chr6:75608119 | T | C | 2 | a0001c0001t0004g0305 a0001c0001t0004g0306 |
2 | HG01928.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.52+5543T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608119 | |||||||
chr6:75608276 | C | A | 3 | a0002c0003t0003g0031 a0002c0003t0003g0032 a0002c0003t0003g0033 |
3 | HG02132.hp2 NA18940.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.52+5700C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608276 | |||||||
chr6:75608386 | C | G | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.52+5810C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608386 | |||||||
chr6:75608550 | A | G | 311 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(308): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.52+5974A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608550 | |||||||
chr6:75608679 | TACTTA | T | 90 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(87): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.52+6108_52+6112del others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75608679 | ||||||
chr6:75608837 | A | G | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.52+6261A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608837 | |||||||
chr6:75608916 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.52+6340G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75608916 | |||||||
chr6:75609077 | T | G | 5 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+6501T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609077 | |||||||
chr6:75609126 | T | TG | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.52+6554dupG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75609126 | ||||||
chr6:75609206 | C | G | 8 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(5): Show |
8 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+6630C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609206 | |||||||
chr6:75609207 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.52+6631G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609207 | |||||||
chr6:75609520 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.52+6944G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609520 | |||||||
chr6:75609618 | G | A | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.52+7042G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609618 | |||||||
chr6:75609773 | T | G | 3 | a0002c0003t0003g0053 a0002c0003t0003g0054 a0002c0003t0003g0055 |
3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.52+7197T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609773 | |||||||
chr6:75609791 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0002g0131 |
2 | HG02897.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.52+7215A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609791 | |||||||
chr6:75609816 | G | T | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.52+7240G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609816 | |||||||
chr6:75609932 | C | T | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | HG00741.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.52+7356C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609932 | |||||||
chr6:75609945 | G | A | 1 | a0001c0001t0004g0307 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.52+7369G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75609945 | |||||||
chr6:75610047 | C | T | 1 | a0001c0002t0003g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.52+7471C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610047 | |||||||
chr6:75610071 | A | C | 2 | a0002c0003t0003g0054 a0002c0003t0003g0055 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.52+7495A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610071 | |||||||
chr6:75610141 | C | T | 1 | a0007c0013t0005g0142 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.52+7565C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610141 | |||||||
chr6:75610383 | A | T | 34 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(31): Show |
34 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.52+7807A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610383 | |||||||
chr6:75610671 | C | T | 1 | a0001c0001t0002g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.52+8095C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610671 | |||||||
chr6:75610764 | A | G | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.52+8188A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610764 | |||||||
chr6:75610906 | T | TGAAACAG others(80): Show |
26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.52+8333_52+8419dup others(87): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75610906 | ||||||
chr6:75610917 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.52+8341G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75610917 | |||||||
chr6:75611081 | T | C | 5 | a0001c0001t0002g0062 a0001c0001t0002g0064 a0001c0001t0002g0169 others(2): Show |
5 | HG00099.hp2 HG02486.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+8505T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611081 | |||||||
chr6:75611130 | C | T | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.52+8554C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611130 | |||||||
chr6:75611190 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.52+8614A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611190 | |||||||
chr6:75611383 | G | A | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.52+8807G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611383 | |||||||
chr6:75611666 | T | G | 1 | a0001c0001t0004g0335 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.52+9090T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611666 | |||||||
chr6:75611835 | C | T | 5 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+9259C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75611835 | |||||||
chr6:75612229 | G | A | 4 | a0001c0001t0010g0183 a0001c0001t0010g0184 a0001c0001t0013g0185 others(1): Show |
4 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-9303G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612229 | |||||||
chr6:75612306 | A | G | 3 | a0001c0001t0005g0163 a0001c0001t0005g0164 a0001c0001t0005g0165 |
3 | HG01069.hp1 HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-9226A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612306 | |||||||
chr6:75612378 | C | T | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-9154C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612378 | |||||||
chr6:75612542 | G | T | 1 | a0001c0001t0002g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.53-8990G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612542 | |||||||
chr6:75612584 | C | G | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.53-8948C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612584 | |||||||
chr6:75612597 | T | C | 1 | a0001c0002t0003g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.53-8935T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612597 | |||||||
chr6:75612674 | A | G | 3 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0012c0012t0003g0167 |
3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-8858A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612674 | |||||||
chr6:75612824 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.53-8708A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75612824 | |||||||
chr6:75613114 | T | TA | 122 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(119): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.53-8405dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75613114 | ||||||
chr6:75613459 | T | C | 350 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(347): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.53-8073T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613459 | |||||||
chr6:75613464 | A | C | 1 | a0001c0001t0001g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.53-8068A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613464 | |||||||
chr6:75613651 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.53-7881G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613651 | |||||||
chr6:75613683 | G | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | NA18970.hp1 NA18981.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-7849G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613683 | |||||||
chr6:75613717 | G | A | 7 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 others(4): Show |
7 | HG02056.hp1 HG03139.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-7815G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613717 | |||||||
chr6:75613833 | A | G | 1 | a0002c0003t0003g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.53-7699A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613833 | |||||||
chr6:75613952 | T | A | 1 | a0001c0001t0002g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-7580T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613952 | |||||||
chr6:75613954 | G | T | 1 | a0001c0001t0002g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-7578G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75613954 | |||||||
chr6:75614009 | A | G | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.53-7523A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614009 | |||||||
chr6:75614055 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.53-7477C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614055 | |||||||
chr6:75614056 | G | A | 6 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0013 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-7476G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614056 | |||||||
chr6:75614064 | G | T | 1 | a0001c0002t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53-7468G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614064 | |||||||
chr6:75614089 | G | T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | NA18612.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.53-7443G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614089 | |||||||
chr6:75614102 | T | A | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.53-7430T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614102 | |||||||
chr6:75614208 | G | A | 1 | a0001c0002t0003g0337 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.53-7324G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614208 | |||||||
chr6:75614260 | C | CT | 13 | a0001c0001t0001g0195 a0001c0001t0001g0273 a0001c0001t0001g0274 others(10): Show |
13 | HG01517.hp2 HG02027.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-7253dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75614260 | ||||||
chr6:75614272 | T | G | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.53-7260T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614272 | |||||||
chr6:75614274 | T | G | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.53-7258T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614274 | |||||||
chr6:75614276 | T | G | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.53-7256T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614276 | |||||||
chr6:75614280 | G | T | 1 | a0001c0001t0002g0064 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.53-7252G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614280 | |||||||
chr6:75614353 | C | T | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.53-7179C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614353 | |||||||
chr6:75614682 | A | C | 350 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(347): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.53-6850A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614682 | |||||||
chr6:75614913 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.53-6619T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614913 | |||||||
chr6:75614969 | C | T | 1 | a0001c0008t0003g0186 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.53-6563C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75614969 | |||||||
chr6:75615262 | C | T | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-6270C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615262 | |||||||
chr6:75615328 | C | T | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.53-6204C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615328 | |||||||
chr6:75615380 | G | A | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.53-6152G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615380 | |||||||
chr6:75615417 | T | C | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.53-6115T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615417 | |||||||
chr6:75615528 | T | C | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-6004T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615528 | |||||||
chr6:75615938 | T | G | 6 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(3): Show |
6 | HG00642.hp2 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-5594T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615938 | |||||||
chr6:75615959 | C | G | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.53-5573C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615959 | |||||||
chr6:75615974 | T | C | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.53-5558T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615974 | |||||||
chr6:75615980 | A | G | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG00738.hp2 HG01169.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5552A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615980 | |||||||
chr6:75615984 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.53-5548C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615984 | |||||||
chr6:75615997 | C | T | 1 | a0001c0001t0003g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.53-5535C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75615997 | |||||||
chr6:75616452 | G | A | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.53-5080G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75616452 | |||||||
chr6:75616516 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-5016A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75616516 | |||||||
chr6:75616540 | G | A | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.53-4992G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75616540 | |||||||
chr6:75616745 | C | CA | 48 | a0001c0001t0001g0191 a0001c0001t0001g0203 a0001c0001t0001g0204 others(45): Show |
49 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.53-4768dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75616745 | ||||||
chr6:75616851 | A | C | 2 | a0001c0001t0002g0131 a0001c0001t0016g0122 |
2 | HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.53-4681A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75616851 | |||||||
chr6:75616875 | T | C | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-4657T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75616875 | |||||||
chr6:75617023 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-4509G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617023 | |||||||
chr6:75617223 | T | C | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.53-4309T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617223 | |||||||
chr6:75617236 | A | T | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-4296A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617236 | |||||||
chr6:75617263 | C | CT | 36 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.53-4242dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617263 | ||||||
chr6:75617263 | C | CTT | 8 | a0002c0003t0003g0029 a0002c0003t0003g0033 a0002c0003t0003g0037 others(5): Show |
8 | HG00741.hp1 HG01074.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.53-4243_53-4242dup others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617263 | ||||||
chr6:75617263 | CT | C | 105 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0268 others(102): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.53-4242delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617263 | ||||||
chr6:75617263 | CTT | C | 86 | a0001c0001t0001g0205 a0001c0001t0002g0001 a0001c0001t0002g0057 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.53-4243_53-4242del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617263 | ||||||
chr6:75617263 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0017g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53-4258_53-4242del others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617263 | ||||||
chr6:75617265 | T | TTC | 7 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0069 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-4266_53-4265ins others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75617265 | ||||||
chr6:75617268 | T | C | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.53-4264T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617268 | |||||||
chr6:75617330 | A | G | 1 | a0001c0001t0003g0028 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53-4202A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617330 | |||||||
chr6:75617514 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.53-4018C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617514 | |||||||
chr6:75617553 | C | T | 1 | a0001c0001t0003g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.53-3979C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617553 | |||||||
chr6:75617972 | A | G | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.53-3560A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75617972 | |||||||
chr6:75618070 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-3462G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618070 | |||||||
chr6:75618135 | C | T | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.53-3397C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618135 | |||||||
chr6:75618240 | A | C | 1 | a0001c0001t0002g0128 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.53-3292A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618240 | |||||||
chr6:75618272 | C | T | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-3260C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618272 | |||||||
chr6:75618303 | GTTTAT | G | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.53-3221_53-3217del others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75618303 | ||||||
chr6:75618377 | T | C | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.53-3155T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618377 | |||||||
chr6:75618733 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-2799T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618733 | |||||||
chr6:75618787 | C | G | 1 | a0001c0004t0003g0182 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-2745C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618787 | |||||||
chr6:75618819 | C | T | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.53-2713C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618819 | |||||||
chr6:75618824 | TCTA | T | 4 | a0001c0002t0003g0339 a0001c0002t0003g0350 a0001c0002t0003g0351 others(1): Show |
4 | NA18983.hp1 NA18995.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2704_53-2702del others(3): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75618824 | ||||||
chr6:75618879 | T | C | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-2653T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618879 | |||||||
chr6:75618904 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.53-2628G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75618904 | |||||||
chr6:75619018 | C | CT | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.53-2502dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619018 | ||||||
chr6:75619018 | CT | C | 102 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.53-2502delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619018 | ||||||
chr6:75619239 | C | T | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.53-2293C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75619239 | |||||||
chr6:75619392 | A | G | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2140A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75619392 | |||||||
chr6:75619443 | CTA | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.53-2087_53-2086del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619443 | ||||||
chr6:75619445 | A | ATG | 31 | a0001c0001t0001g0201 a0001c0001t0003g0056 a0001c0002t0003g0016 others(28): Show |
31 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.53-2059_53-2058dup others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619445 | ||||||
chr6:75619445 | A | ATGTGTGT others(5): Show |
3 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0024 |
3 | HG03041.hp2 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.53-2069_53-2058dup others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619445 | ||||||
chr6:75619445 | A | ATGTGTGT others(7): Show |
2 | a0001c0002t0003g0006 a0001c0002t0003g0009 |
2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.53-2071_53-2058dup others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619445 | ||||||
chr6:75619445 | ATG | A | 165 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(162): Show |
166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.53-2059_53-2058del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619445 | ||||||
chr6:75619445 | ATGTG | A | 88 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(85): Show |
89 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.53-2061_53-2058del others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75619445 | ||||||
chr6:75619582 | A | T | 1 | a0001c0002t0009g0013 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.53-1950A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75619582 | |||||||
chr6:75619650 | G | T | 3 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0012c0012t0003g0167 |
3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-1882G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75619650 | |||||||
chr6:75619747 | C | G | 1 | a0001c0001t0003g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.53-1785C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75619747 | |||||||
chr6:75620007 | C | A | 1 | a0001c0001t0003g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.53-1525C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620007 | |||||||
chr6:75620007 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.53-1525C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620007 | |||||||
chr6:75620082 | C | CA | 26 | a0001c0004t0014g0052 a0001c0008t0003g0187 a0002c0003t0003g0029 others(23): Show |
26 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.53-1429dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | ||||||
chr6:75620082 | C | CAA | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-1430_53-1429dup others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | ||||||
chr6:75620082 | CA | C | 133 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(130): Show |
134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.53-1429delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | ||||||
chr6:75620082 | CAA | C | 6 | a0001c0001t0001g0252 a0001c0001t0001g0266 a0001c0001t0001g0267 others(3): Show |
6 | HG01928.hp1 HG02735.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-1430_53-1429del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | ||||||
chr6:75620082 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0017g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53-1438_53-1429del others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | ||||||
chr6:75620082 | CAAAAAAA others(4): Show |
C | 123 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(120): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.53-1439_53-1429del others(11): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr6 | 75620082 | ||||||
chr6:75620267 | A | C | 1 | a0001c0001t0003g0028 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53-1265A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620267 | |||||||
chr6:75620635 | G | T | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.53-897G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620635 | |||||||
chr6:75620718 | G | C | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.53-814G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620718 | |||||||
chr6:75620768 | C | T | 2 | a0002c0003t0003g0047 a0002c0003t0003g0050 |
2 | HG01074.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.53-764C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75620768 | |||||||
chr6:75621032 | T | C | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.53-500T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75621032 | |||||||
chr6:75621123 | T | G | 1 | a0001c0001t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.53-409T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75621123 | |||||||
chr6:75621126 | C | T | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-406C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75621126 | |||||||
chr6:75621155 | T | C | 1 | a0001c0002t0009g0171 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.53-377T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 1/23 | chr6 | 75621155 | |||||||
chr6:75621741 | ACT | A | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.146+119_146+120del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr6 | 75621741 | ||||||
chr6:75622268 | A | G | 1 | a0001c0002t0009g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146+643A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622268 | |||||||
chr6:75622329 | A | G | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.146+704A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622329 | |||||||
chr6:75622429 | T | C | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.146+804T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622429 | |||||||
chr6:75622483 | C | T | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.146+858C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622483 | |||||||
chr6:75622500 | A | G | 1 | a0001c0001t0002g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.146+875A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622500 | |||||||
chr6:75622662 | A | G | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.146+1037A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622662 | |||||||
chr6:75622664 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.146+1039A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622664 | |||||||
chr6:75622716 | G | T | 1 | a0001c0001t0004g0328 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.146+1091G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622716 | |||||||
chr6:75622863 | G | A | 1 | a0005c0009t0001g0192 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.147-1037G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622863 | |||||||
chr6:75622947 | A | C | 3 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 |
3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.147-953A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75622947 | |||||||
chr6:75623087 | A | G | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.147-813A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75623087 | |||||||
chr6:75623166 | CGTT | C | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.147-731_147-729del others(3): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr6 | 75623166 | ||||||
chr6:75623218 | A | G | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.147-682A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75623218 | |||||||
chr6:75623546 | A | G | 1 | a0007c0013t0005g0142 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.147-354A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75623546 | |||||||
chr6:75623770 | G | A | 344 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(341): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.147-130G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 2/23 | chr6 | 75623770 | |||||||
chr6:75623999 | A | G | 1 | a0001c0001t0002g0075 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.207+39A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75623999 | |||||||
chr6:75624078 | G | T | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.207+118G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624078 | |||||||
chr6:75624220 | T | G | 1 | a0002c0003t0003g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.207+260T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624220 | |||||||
chr6:75624227 | G | A | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.207+267G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624227 | |||||||
chr6:75624319 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.207+359C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624319 | |||||||
chr6:75624425 | G | C | 1 | a0001c0001t0001g0209 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.207+465G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624425 | |||||||
chr6:75624515 | T | C | 10 | a0001c0001t0002g0001 a0001c0001t0002g0058 a0001c0001t0002g0081 others(7): Show |
11 | HG01123.hp2 HG01192.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+555T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624515 | |||||||
chr6:75624705 | A | G | 1 | a0001c0001t0005g0165 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.207+745A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75624705 | |||||||
chr6:75625060 | T | C | 1 | a0001c0001t0008g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.207+1100T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625060 | |||||||
chr6:75625112 | C | CT | 171 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(168): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.207+1171dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75625112 | ||||||
chr6:75625112 | C | CTT | 79 | a0001c0001t0001g0265 a0001c0001t0002g0078 a0001c0001t0002g0079 others(76): Show |
80 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.207+1170_207+1171d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75625112 | ||||||
chr6:75625112 | C | CTTT | 20 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0001c0001t0004g0302 others(17): Show |
20 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.207+1169_207+1171d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75625112 | ||||||
chr6:75625112 | CT | C | 8 | a0001c0001t0002g0064 a0001c0002t0003g0006 a0001c0002t0003g0007 others(5): Show |
8 | HG02257.hp1 HG02280.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+1171delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75625112 | ||||||
chr6:75625136 | C | T | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.207+1176C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625136 | |||||||
chr6:75625172 | C | T | 1 | a0001c0001t0017g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.207+1212C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625172 | |||||||
chr6:75625216 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.207+1256A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625216 | |||||||
chr6:75625532 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.207+1572G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625532 | |||||||
chr6:75625566 | T | G | 1 | a0001c0001t0002g0127 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.207+1606T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625566 | |||||||
chr6:75625617 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.207+1657C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625617 | |||||||
chr6:75625636 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.207+1676A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625636 | |||||||
chr6:75625693 | A | G | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.207+1733A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625693 | |||||||
chr6:75625825 | C | T | 1 | a0008c0010t0009g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.207+1865C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625825 | |||||||
chr6:75625855 | C | A | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+1895C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625855 | |||||||
chr6:75625856 | G | A | 1 | a0001c0002t0003g0016 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.207+1896G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625856 | |||||||
chr6:75625997 | G | C | 1 | a0001c0001t0001g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.207+2037G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75625997 | |||||||
chr6:75626025 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.207+2065A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626025 | |||||||
chr6:75626125 | T | G | 26 | a0001c0001t0005g0158 a0002c0003t0003g0029 a0002c0003t0003g0030 others(23): Show |
26 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.207+2165T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626125 | |||||||
chr6:75626125 | T | TTTG | 276 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(273): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.207+2183_207+2185d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75626125 | ||||||
chr6:75626143 | G | T | 1 | a0002c0003t0003g0046 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.207+2183G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626143 | |||||||
chr6:75626188 | C | A | 1 | a0001c0001t0002g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.207+2228C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626188 | |||||||
chr6:75626189 | A | G | 3 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0012c0012t0003g0167 |
3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.207+2229A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626189 | |||||||
chr6:75626339 | T | TTA | 17 | a0001c0001t0001g0213 a0001c0001t0001g0251 a0001c0001t0001g0266 others(14): Show |
17 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.207+2395_207+2396d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75626339 | ||||||
chr6:75626339 | T | TTATA | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.207+2393_207+2396d others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75626339 | ||||||
chr6:75626673 | T | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0214 |
2 | HG01081.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.207+2713T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626673 | |||||||
chr6:75626719 | C | T | 2 | a0001c0001t0005g0157 a0001c0001t0005g0162 |
2 | HG01168.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.207+2759C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626719 | |||||||
chr6:75626796 | G | A | 1 | a0001c0001t0003g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.207+2836G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626796 | |||||||
chr6:75626841 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.207+2881A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75626841 | |||||||
chr6:75627543 | C | T | 3 | a0001c0001t0010g0183 a0001c0001t0010g0184 a0001c0001t0013g0185 |
3 | HG02622.hp1 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.207+3583C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75627543 | |||||||
chr6:75627783 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.207+3823C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75627783 | |||||||
chr6:75627859 | G | T | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.207+3899G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75627859 | |||||||
chr6:75627920 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.207+3960C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75627920 | |||||||
chr6:75627952 | G | A | 6 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0013 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+3992G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75627952 | |||||||
chr6:75628161 | A | G | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.207+4201A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75628161 | |||||||
chr6:75628526 | T | G | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+4566T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75628526 | |||||||
chr6:75628795 | C | G | 1 | a0001c0001t0001g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.208-4786C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75628795 | |||||||
chr6:75628829 | A | C | 344 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(341): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.208-4752A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75628829 | |||||||
chr6:75628832 | G | A | 16 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(13): Show |
16 | HG02293.hp2 HG02486.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.208-4749G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75628832 | |||||||
chr6:75629060 | A | G | 3 | a0003c0007t0006g0168 a0003c0007t0006g0291 a0003c0007t0006g0295 |
3 | HG02109.hp2 HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.208-4521A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629060 | |||||||
chr6:75629154 | T | G | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.208-4427T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629154 | |||||||
chr6:75629326 | G | T | 1 | a0001c0001t0001g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-4255G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629326 | |||||||
chr6:75629437 | C | A | 1 | a0001c0001t0001g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-4144C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629437 | |||||||
chr6:75629728 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.208-3853G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629728 | |||||||
chr6:75629894 | A | T | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.208-3687A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75629894 | |||||||
chr6:75630068 | CT | C | 33 | a0001c0001t0002g0004 a0001c0001t0002g0081 a0001c0001t0004g0309 others(30): Show |
33 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.208-3495delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75630068 | ||||||
chr6:75630111 | C | G | 102 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.208-3470C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630111 | |||||||
chr6:75630244 | A | T | 1 | a0001c0001t0001g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-3337A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630244 | |||||||
chr6:75630245 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-3336T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630245 | |||||||
chr6:75630250 | A | T | 1 | a0001c0001t0001g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-3331A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630250 | |||||||
chr6:75630350 | T | G | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.208-3231T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630350 | |||||||
chr6:75630576 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-3005T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630576 | |||||||
chr6:75630580 | A | G | 1 | a0001c0001t0015g0132 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.208-3001A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630580 | |||||||
chr6:75630730 | T | G | 1 | a0001c0002t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-2851T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630730 | |||||||
chr6:75630848 | T | TA | 8 | a0001c0002t0003g0014 a0001c0002t0009g0010 a0001c0002t0009g0012 others(5): Show |
8 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-2722dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75630848 | ||||||
chr6:75630848 | TA | T | 102 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.208-2722delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75630848 | ||||||
chr6:75630928 | ATC | A | 22 | a0001c0001t0005g0144 a0001c0001t0005g0145 a0001c0001t0005g0146 others(19): Show |
22 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.208-2649_208-2648d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75630928 | ||||||
chr6:75630946 | G | T | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.208-2635G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75630946 | |||||||
chr6:75631206 | C | G | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.208-2375C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631206 | |||||||
chr6:75631222 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208-2359T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631222 | |||||||
chr6:75631584 | CAT | C | 3 | a0001c0001t0010g0183 a0001c0001t0010g0184 a0001c0001t0013g0185 |
3 | HG02622.hp1 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.208-1996_208-1995d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631584 | |||||||
chr6:75631755 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.208-1826A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631755 | |||||||
chr6:75631787 | G | A | 2 | a0001c0001t0002g0134 a0001c0001t0002g0135 |
2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.208-1794G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631787 | |||||||
chr6:75631942 | A | G | 1 | a0001c0002t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-1639A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75631942 | |||||||
chr6:75632010 | C | G | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.208-1571C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632010 | |||||||
chr6:75632122 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.208-1459C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632122 | |||||||
chr6:75632144 | G | C | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.208-1437G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632144 | |||||||
chr6:75632381 | A | G | 1 | a0001c0002t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-1200A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632381 | |||||||
chr6:75632415 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0265 |
2 | NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.208-1166G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632415 | |||||||
chr6:75632456 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.208-1125G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632456 | |||||||
chr6:75632653 | G | A | 1 | a0001c0002t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-928G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632653 | |||||||
chr6:75632673 | C | CT | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.208-906dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr6 | 75632673 | ||||||
chr6:75632730 | A | G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG00609.hp1 NA19058.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.208-851A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75632730 | |||||||
chr6:75633346 | A | G | 10 | a0001c0001t0002g0001 a0001c0001t0002g0058 a0001c0001t0002g0081 others(7): Show |
11 | HG01123.hp2 HG01192.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-235A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75633346 | |||||||
chr6:75633374 | A | T | 1 | a0001c0002t0003g0357 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.208-207A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75633374 | |||||||
chr6:75633456 | A | G | 1 | a0001c0002t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208-125A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 3/23 | chr6 | 75633456 | |||||||
chr6:75633930 | A | G | 1 | a0001c0002t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.353+204A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75633930 | |||||||
chr6:75634067 | A | G | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.353+341A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634067 | |||||||
chr6:75634200 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.353+474A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634200 | |||||||
chr6:75634488 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.354-219T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634488 | |||||||
chr6:75634551 | G | A | 24 | a0001c0002t0003g0003 a0001c0002t0003g0337 a0001c0002t0003g0338 others(21): Show |
25 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.354-156G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634551 | |||||||
chr6:75634639 | G | T | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.354-68G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634639 | |||||||
chr6:75634690 | G | A | 1 | a0001c0002t0022g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.354-17G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 4/23 | chr6 | 75634690 | |||||||
chr6:75634827 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+16G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75634827 | |||||||
chr6:75634968 | T | C | 1 | a0001c0001t0005g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.458+157T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75634968 | |||||||
chr6:75635078 | T | G | 1 | a0001c0002t0003g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.458+267T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75635078 | |||||||
chr6:75635159 | C | T | 5 | a0001c0001t0002g0077 a0001c0001t0002g0116 a0001c0001t0002g0117 others(2): Show |
5 | HG00544.hp1 HG00558.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+348C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75635159 | |||||||
chr6:75635160 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.458+349C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75635160 | |||||||
chr6:75635282 | A | C | 1 | a0001c0001t0002g0118 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.458+471A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75635282 | |||||||
chr6:75635374 | C | G | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.458+563C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75635374 | |||||||
chr6:75636046 | T | TA | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+1244dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75636046 | ||||||
chr6:75636058 | A | G | 3 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0162 |
3 | HG00280.hp2 HG01168.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.458+1247A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636058 | |||||||
chr6:75636062 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.458+1251G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636062 | |||||||
chr6:75636245 | T | A | 1 | a0001c0001t0002g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.458+1434T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636245 | |||||||
chr6:75636296 | T | A | 4 | a0001c0001t0005g0144 a0001c0001t0005g0145 a0001c0001t0005g0146 others(1): Show |
4 | NA18995.hp1 NA19057.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+1485T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636296 | |||||||
chr6:75636323 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.458+1512C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636323 | |||||||
chr6:75636378 | C | T | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.458+1567C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636378 | |||||||
chr6:75636430 | C | T | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.458+1619C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636430 | |||||||
chr6:75636434 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.458+1623G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75636434 | |||||||
chr6:75636875 | A | AT | 142 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(139): Show |
142 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.458+2080dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75636875 | ||||||
chr6:75637140 | T | G | 1 | a0007c0013t0005g0142 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.458+2329T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637140 | |||||||
chr6:75637184 | T | C | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.458+2373T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637184 | |||||||
chr6:75637232 | T | C | 1 | a0001c0002t0003g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.458+2421T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637232 | |||||||
chr6:75637304 | G | A | 37 | a0001c0001t0003g0056 a0001c0004t0003g0174 a0001c0004t0003g0175 others(34): Show |
37 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.458+2493G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637304 | |||||||
chr6:75637307 | G | A | 1 | a0001c0002t0003g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.458+2496G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637307 | |||||||
chr6:75637904 | A | G | 5 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-2780A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637904 | |||||||
chr6:75637910 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.459-2774G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75637910 | |||||||
chr6:75638242 | G | GT | 102 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.459-2428dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638242 | ||||||
chr6:75638242 | G | T | 1 | a0001c0002t0003g0356 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.459-2442G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638242 | |||||||
chr6:75638242 | GT | G | 12 | a0001c0001t0002g0098 a0001c0001t0002g0117 a0001c0001t0004g0311 others(9): Show |
12 | HG00544.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.459-2428delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638242 | ||||||
chr6:75638242 | GTT | G | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
97 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.459-2429_459-2428d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638242 | ||||||
chr6:75638242 | GTTT | G | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.459-2430_459-2428d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638242 | ||||||
chr6:75638385 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0268 |
2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.459-2299C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638385 | |||||||
chr6:75638488 | A | G | 1 | a0002c0003t0003g0045 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.459-2196A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638488 | |||||||
chr6:75638555 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0221 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.459-2102_459-2093d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638555 | ||||||
chr6:75638576 | GTGTGTGT others(19): Show |
G | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.459-2106_459-2081d others(28): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638576 | ||||||
chr6:75638578 | GTGTGTGT others(15): Show |
G | 2 | a0001c0001t0001g0209 a0001c0001t0003g0056 |
2 | NA18955.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.459-2104_459-2083d others(24): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638578 | ||||||
chr6:75638578 | GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0004g0312 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.459-2104_459-2081d others(26): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638578 | ||||||
chr6:75638580 | GTGTGTGT others(5): Show |
G | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.459-2102_459-2091d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638580 | ||||||
chr6:75638580 | GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0001g0214 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.459-2102_459-2087d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638580 | ||||||
chr6:75638580 | GTGTGTGT others(11): Show |
G | 20 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0206 others(17): Show |
20 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.459-2102_459-2085d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638580 | ||||||
chr6:75638580 | GTGTGTGT others(13): Show |
G | 47 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0197 others(44): Show |
47 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.459-2102_459-2083d others(22): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638580 | ||||||
chr6:75638580 | GTGTGTGT others(15): Show |
G | 27 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(24): Show |
27 | HG00642.hp2 HG01070.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.459-2102_459-2081d others(24): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638580 | ||||||
chr6:75638582 | GTGTGTGT others(7): Show |
G | 2 | a0001c0001t0004g0329 a0001c0001t0007g0308 |
2 | HG01975.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.459-2100_459-2087d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638582 | ||||||
chr6:75638582 | GTGTGTGT others(9): Show |
G | 12 | a0001c0001t0002g0075 a0001c0001t0004g0002 a0001c0001t0004g0301 others(9): Show |
13 | HG00673.hp1 HG01928.hp2 NA18906.hp1 others(10): Show |
intron_variant | MODIFIER | c.459-2100_459-2085d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638582 | ||||||
chr6:75638582 | GTGTGTGT others(11): Show |
G | 2 | a0001c0001t0004g0305 a0001c0001t0007g0327 |
2 | HG02004.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.459-2100_459-2083d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638582 | ||||||
chr6:75638582 | GTGTGTGT others(13): Show |
G | 7 | a0001c0001t0001g0189 a0001c0001t0001g0208 a0001c0001t0001g0239 others(4): Show |
7 | HG02027.hp2 HG02602.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2100_459-2081d others(22): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638582 | ||||||
chr6:75638582 | GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0001g0222 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.459-2100_459-2079d others(24): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638582 | ||||||
chr6:75638584 | GTGTGTGT others(3): Show |
G | 6 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 others(3): Show |
6 | HG02040.hp1 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-2098_459-2089d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | ||||||
chr6:75638584 | GTGTGTGT others(5): Show |
G | 8 | a0001c0001t0002g0118 a0001c0001t0002g0140 a0001c0001t0004g0302 others(5): Show |
8 | HG02109.hp1 NA18941.hp1 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-2098_459-2087d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | ||||||
chr6:75638584 | GTGTGTGT others(7): Show |
G | 7 | a0001c0001t0004g0323 a0001c0001t0004g0324 a0001c0001t0004g0333 others(4): Show |
7 | HG00408.hp2 HG00438.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-2098_459-2085d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | ||||||
chr6:75638584 | GTGTGTGT others(9): Show |
G | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.459-2098_459-2083d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | ||||||
chr6:75638584 | GTGTGTGT others(11): Show |
G | 2 | a0001c0001t0004g0313 a0001c0001t0004g0326 |
2 | NA18966.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.459-2098_459-2081d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | ||||||
chr6:75638584 | GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0005g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.459-2098_459-2075d others(26): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638584 | ||||||
chr6:75638586 | G | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG01106.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.459-2098G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638586 | |||||||
chr6:75638586 | GTGTGTAT others(1): Show |
G | 6 | a0001c0002t0003g0003 a0001c0002t0003g0337 a0001c0002t0003g0346 others(3): Show |
6 | NA18612.hp2 NA18940.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-2096_459-2089d others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638586 | ||||||
chr6:75638586 | GTGTGTAT others(3): Show |
G | 13 | a0001c0002t0003g0338 a0001c0002t0003g0340 a0001c0002t0003g0341 others(10): Show |
13 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.459-2096_459-2087d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638586 | ||||||
chr6:75638586 | GTGTGTAT others(5): Show |
G | 8 | a0001c0001t0004g0309 a0001c0001t0004g0320 a0001c0001t0004g0332 others(5): Show |
8 | HG00597.hp1 HG02723.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-2096_459-2085d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638586 | ||||||
chr6:75638586 | GTGTGTAT others(7): Show |
G | 2 | a0001c0001t0002g0123 a0001c0001t0004g0311 |
2 | HG02129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.459-2096_459-2083d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638586 | ||||||
chr6:75638586 | GTGTGTAT others(11): Show |
G | 1 | a0001c0001t0002g0095 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.459-2096_459-2079d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638586 | ||||||
chr6:75638588 | G | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG01106.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.459-2096G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638588 | |||||||
chr6:75638588 | GTGTATAT others(1): Show |
G | 3 | a0001c0001t0002g0001 a0001c0002t0003g0003 a0001c0002t0003g0014 |
3 | HG01192.hp1 HG01891.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.459-2094_459-2087d others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638588 | ||||||
chr6:75638588 | GTGTATAT others(3): Show |
G | 1 | a0001c0001t0002g0089 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.459-2094_459-2085d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638588 | ||||||
chr6:75638588 | GTGTATAT others(5): Show |
G | 18 | a0001c0001t0002g0001 a0001c0001t0002g0058 a0001c0001t0002g0059 others(15): Show |
18 | HG00099.hp2 HG01123.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.459-2094_459-2083d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638588 | ||||||
chr6:75638588 | GTGTATAT others(7): Show |
G | 4 | a0001c0001t0002g0061 a0001c0001t0002g0111 a0001c0001t0002g0121 others(1): Show |
4 | HG01261.hp1 HG02145.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-2094_459-2081d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638588 | ||||||
chr6:75638588 | GTGTATAT others(9): Show |
G | 5 | a0001c0001t0002g0074 a0001c0001t0002g0090 a0001c0001t0002g0097 others(2): Show |
5 | HG02004.hp1 HG03579.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.459-2094_459-2079d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638588 | ||||||
chr6:75638590 | G | A | 19 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0057 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.459-2094G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638590 | |||||||
chr6:75638590 | GTATATAT others(3): Show |
G | 7 | a0001c0001t0002g0064 a0001c0001t0002g0084 a0001c0001t0002g0135 others(4): Show |
7 | HG00741.hp2 HG02602.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2070_459-2061d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638590 | ||||||
chr6:75638590 | GTATATAT others(5): Show |
G | 2 | a0001c0001t0002g0071 a0001c0001t0002g0098 |
2 | HG02055.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.459-2072_459-2061d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638590 | ||||||
chr6:75638590 | GTATATAT others(7): Show |
G | 1 | a0001c0001t0002g0114 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.459-2074_459-2061d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638590 | ||||||
chr6:75638592 | A | G | 90 | a0001c0001t0002g0077 a0001c0001t0002g0102 a0001c0001t0002g0104 others(87): Show |
90 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.459-2092A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638592 | |||||||
chr6:75638594 | A | G | 67 | a0001c0001t0002g0105 a0001c0001t0003g0025 a0001c0001t0003g0026 others(64): Show |
67 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.459-2090A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638594 | |||||||
chr6:75638596 | A | G | 53 | a0001c0001t0005g0144 a0001c0001t0005g0145 a0001c0001t0005g0146 others(50): Show |
53 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.459-2088A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638596 | |||||||
chr6:75638598 | A | G | 34 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0153 others(31): Show |
34 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.459-2086A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638598 | |||||||
chr6:75638600 | A | G | 23 | a0001c0001t0002g0134 a0001c0001t0005g0157 a0001c0001t0005g0158 others(20): Show |
23 | HG00280.hp2 HG00738.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.459-2084A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638600 | |||||||
chr6:75638602 | A | G | 7 | a0002c0003t0003g0034 a0002c0003t0003g0035 a0002c0003t0003g0036 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.459-2082A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638602 | |||||||
chr6:75638604 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.459-2080A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638604 | |||||||
chr6:75638606 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0060 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.459-2076_459-2060d others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638606 | ||||||
chr6:75638608 | ATATATAT others(10): Show |
A | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.459-2074_459-2058d others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638608 | ||||||
chr6:75638608 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0005g0156 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.459-2074_459-2053d others(24): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638608 | ||||||
chr6:75638608 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0005g0148 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.459-2074_459-2051d others(26): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638608 | ||||||
chr6:75638609 | TATATATA others(6): Show |
T | 1 | a0001c0017t0002g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459-2074_459-2062d others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638609 | |||||||
chr6:75638610 | ATATATAT others(6): Show |
A | 5 | a0001c0001t0002g0086 a0001c0001t0002g0099 a0001c0001t0002g0101 others(2): Show |
5 | HG02165.hp2 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-2072_459-2060d others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | ||||||
chr6:75638610 | ATATATAT others(7): Show |
A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0108 |
2 | HG02523.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.459-2072_459-2059d others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | ||||||
chr6:75638610 | ATATATAT others(9): Show |
A | 2 | a0001c0001t0002g0005 a0001c0001t0002g0073 |
2 | HG01071.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.459-2072_459-2057d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | ||||||
chr6:75638610 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0004 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.459-2072_459-2056d others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | ||||||
chr6:75638610 | ATATATAT others(11): Show |
A | 3 | a0001c0005t0006g0296 a0004c0006t0005g0151 a0004c0006t0005g0161 |
3 | HG03540.hp1 NA18980.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.459-2072_459-2055d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | ||||||
chr6:75638610 | ATATATAT others(12): Show |
A | 1 | a0004c0006t0005g0152 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.459-2072_459-2054d others(21): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | ||||||
chr6:75638610 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0012g0149 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.459-2072_459-2052d others(23): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638610 | ||||||
chr6:75638611 | TATATATA others(4): Show |
T | 1 | a0001c0001t0002g0137 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.459-2072_459-2062d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638611 | |||||||
chr6:75638612 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0002g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.459-2070_459-2060d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | ||||||
chr6:75638612 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0002g0072 a0001c0001t0002g0169 |
2 | HG03927.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.459-2070_459-2059d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | ||||||
chr6:75638612 | ATATATAT others(6): Show |
A | 3 | a0001c0001t0002g0104 a0001c0001t0002g0107 a0001c0001t0002g0109 |
3 | NA18955.hp1 NA18983.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.459-2070_459-2058d others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | ||||||
chr6:75638612 | ATATATAT others(8): Show |
A | 1 | a0002c0003t0003g0031 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.459-2070_459-2056d others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | ||||||
chr6:75638612 | ATATATAT others(9): Show |
A | 2 | a0001c0005t0006g0293 a0001c0005t0006g0294 |
2 | NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.459-2070_459-2055d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | ||||||
chr6:75638612 | ATATATAT others(11): Show |
A | 9 | a0001c0001t0005g0144 a0001c0001t0005g0145 a0001c0001t0005g0160 others(6): Show |
9 | HG01109.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.459-2070_459-2053d others(20): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | ||||||
chr6:75638612 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0005g0165 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.459-2070_459-2052d others(21): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | ||||||
chr6:75638612 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0221 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.459-2070_459-2050d others(23): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638612 | ||||||
chr6:75638614 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0002g0105 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.459-2068_459-2059d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | ||||||
chr6:75638614 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0002g0129 a0001c0002t0003g0349 |
2 | HG03195.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.459-2068_459-2058d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | ||||||
chr6:75638614 | ATATATAT others(5): Show |
A | 3 | a0001c0001t0002g0106 a0001c0001t0002g0120 a0001c0001t0002g0124 |
3 | HG02015.hp1 NA18974.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.459-2068_459-2057d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | ||||||
chr6:75638614 | ATATATAT others(9): Show |
A | 5 | a0001c0001t0005g0146 a0001c0001t0005g0299 a0001c0001t0005g0300 others(2): Show |
5 | HG02257.hp2 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-2068_459-2053d others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | ||||||
chr6:75638614 | ATATATAT others(10): Show |
A | 6 | a0001c0001t0005g0147 a0001c0001t0005g0153 a0001c0001t0005g0154 others(3): Show |
6 | HG00280.hp2 HG00642.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-2068_459-2052d others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | ||||||
chr6:75638614 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0002g0126 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.459-2068_459-2046d others(25): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638614 | ||||||
chr6:75638615 | TATATATA | T | 3 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0102 |
3 | HG04115.hp2 NA18981.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.459-2068_459-2062d others(9): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638615 | |||||||
chr6:75638616 | A | T | 1 | a0001c0002t0003g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.459-2068A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638616 | |||||||
chr6:75638616 | ATATATAT others(3): Show |
A | 3 | a0001c0001t0002g0116 a0001c0002t0003g0348 a0001c0004t0014g0052 |
3 | HG00558.hp2 HG02083.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.459-2066_459-2057d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | ||||||
chr6:75638616 | ATATATAT others(4): Show |
A | 1 | a0002c0003t0003g0032 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.459-2066_459-2056d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | ||||||
chr6:75638616 | ATATATAT others(5): Show |
A | 1 | a0001c0016t0006g0298 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.459-2066_459-2055d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | ||||||
chr6:75638616 | ATATATAT others(8): Show |
A | 2 | a0001c0001t0005g0157 a0001c0001t0005g0162 |
2 | HG01168.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.459-2066_459-2052d others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | ||||||
chr6:75638616 | ATATATAT others(10): Show |
A | 1 | a0007c0013t0005g0142 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.459-2066_459-2050d others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | ||||||
chr6:75638616 | ATATATAT others(14): Show |
A | 1 | a0001c0002t0003g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459-2066_459-2046d others(23): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638616 | ||||||
chr6:75638618 | A | T | 4 | a0001c0002t0003g0006 a0001c0002t0003g0009 a0001c0002t0003g0024 others(1): Show |
4 | HG02257.hp1 HG02280.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-2066A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638618 | |||||||
chr6:75638618 | ATATATTT others(5): Show |
A | 2 | a0001c0001t0010g0183 a0001c0001t0010g0184 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.459-2064_459-2053d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638618 | ||||||
chr6:75638618 | ATATATTT others(6): Show |
A | 1 | a0001c0001t0003g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.459-2064_459-2052d others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638618 | ||||||
chr6:75638620 | A | T | 6 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(3): Show |
6 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-2064A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638620 | |||||||
chr6:75638620 | ATATTTTT others(3): Show |
A | 1 | a0001c0001t0010g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.459-2062_459-2053d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638620 | ||||||
chr6:75638620 | ATATTTTT others(4): Show |
A | 4 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0013g0185 others(1): Show |
4 | HG02145.hp2 HG02293.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-2062_459-2052d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638620 | ||||||
chr6:75638620 | ATATTTTT others(5): Show |
A | 1 | a0001c0001t0003g0026 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459-2062_459-2051d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638620 | ||||||
chr6:75638621 | TA | T | 4 | a0001c0001t0001g0195 a0001c0001t0001g0213 a0001c0001t0001g0267 others(1): Show |
4 | HG02523.hp2 NA18997.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-2062delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638621 | |||||||
chr6:75638622 | A | T | 25 | a0001c0001t0001g0286 a0001c0001t0002g0059 a0001c0001t0002g0068 others(22): Show |
25 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.459-2062A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638622 | |||||||
chr6:75638622 | AT | A | 48 | a0001c0001t0001g0190 a0001c0001t0001g0197 a0001c0001t0001g0203 others(45): Show |
48 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.459-2034delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638622 | ||||||
chr6:75638622 | ATTT | A | 31 | a0001c0001t0001g0194 a0001c0001t0001g0219 a0001c0001t0001g0233 others(28): Show |
31 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.459-2036_459-2034d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638622 | ||||||
chr6:75638622 | ATTTT | A | 23 | a0001c0001t0001g0206 a0001c0001t0001g0217 a0001c0001t0002g0065 others(20): Show |
23 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.459-2037_459-2034d others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638622 | ||||||
chr6:75638622 | ATTTTT | A | 17 | a0001c0001t0001g0214 a0001c0001t0002g0067 a0001c0001t0002g0118 others(14): Show |
17 | HG00408.hp2 HG00738.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.459-2038_459-2034d others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638622 | ||||||
chr6:75638622 | ATTTTTT | A | 8 | a0001c0001t0002g0075 a0001c0001t0004g0302 a0001c0001t0004g0307 others(5): Show |
8 | HG01516.hp1 HG02040.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-2039_459-2034d others(8): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr6 | 75638622 | ||||||
chr6:75638624 | T | A | 47 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(44): Show |
47 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.459-2060T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638624 | |||||||
chr6:75638626 | T | A | 3 | a0001c0001t0002g0078 a0001c0001t0003g0166 a0001c0001t0004g0312 |
3 | HG02559.hp1 HG02683.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.459-2058T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638626 | |||||||
chr6:75638627 | T | A | 8 | a0002c0003t0003g0034 a0002c0003t0003g0035 a0002c0003t0003g0037 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-2057T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638627 | |||||||
chr6:75638628 | T | A | 2 | a0001c0001t0002g0078 a0002c0003t0003g0048 |
2 | HG02683.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.459-2056T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638628 | |||||||
chr6:75638630 | T | A | 1 | a0001c0001t0002g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.459-2054T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638630 | |||||||
chr6:75638631 | T | A | 1 | a0001c0008t0003g0187 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459-2053T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638631 | |||||||
chr6:75638632 | T | A | 1 | a0001c0001t0002g0079 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.459-2052T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638632 | |||||||
chr6:75638893 | A | T | 6 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0013 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-1791A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638893 | |||||||
chr6:75638947 | G | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-1737G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75638947 | |||||||
chr6:75639031 | A | G | 1 | a0001c0001t0020g0253 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.459-1653A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639031 | |||||||
chr6:75639134 | A | G | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.459-1550A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639134 | |||||||
chr6:75639207 | T | C | 1 | a0001c0001t0002g0087 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.459-1477T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639207 | |||||||
chr6:75639389 | T | A | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.459-1295T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639389 | |||||||
chr6:75639390 | A | C | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.459-1294A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639390 | |||||||
chr6:75639452 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.459-1232G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639452 | |||||||
chr6:75639546 | C | T | 4 | a0001c0001t0010g0183 a0001c0001t0010g0184 a0001c0001t0010g0188 others(1): Show |
4 | HG02622.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-1138C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639546 | |||||||
chr6:75639640 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.459-1044A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639640 | |||||||
chr6:75639733 | A | G | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.459-951A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639733 | |||||||
chr6:75639754 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.459-930T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639754 | |||||||
chr6:75639831 | T | A | 1 | a0010c0014t0002g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.459-853T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639831 | |||||||
chr6:75639840 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-844T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639840 | |||||||
chr6:75639998 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.459-686G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75639998 | |||||||
chr6:75640277 | C | T | 6 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0013 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.459-407C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640277 | |||||||
chr6:75640305 | A | G | 1 | a0001c0004t0003g0179 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.459-379A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640305 | |||||||
chr6:75640322 | A | G | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.459-362A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640322 | |||||||
chr6:75640415 | T | C | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.459-269T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640415 | |||||||
chr6:75640478 | CCTGTT | C | 102 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.459-205_459-201del others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640478 | |||||||
chr6:75640561 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.459-123T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640561 | |||||||
chr6:75640597 | C | G | 2 | a0001c0001t0002g0131 a0001c0001t0016g0122 |
2 | HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.459-87C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 5/23 | chr6 | 75640597 | |||||||
chr6:75640924 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.479+220A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75640924 | |||||||
chr6:75641002 | T | A | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.479+298T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641002 | |||||||
chr6:75641014 | T | C | 1 | a0002c0003t0003g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.479+310T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641014 | |||||||
chr6:75641241 | A | C | 1 | a0001c0001t0005g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.479+537A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641241 | |||||||
chr6:75641258 | A | G | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.479+554A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641258 | |||||||
chr6:75641259 | T | C | 1 | a0002c0003t0003g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.479+555T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641259 | |||||||
chr6:75641345 | T | C | 4 | a0001c0001t0005g0141 a0001c0001t0005g0299 a0001c0001t0005g0300 others(1): Show |
4 | HG01346.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+641T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641345 | |||||||
chr6:75641456 | T | G | 1 | a0006c0015t0001g0287 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.479+752T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641456 | |||||||
chr6:75641484 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.479+780T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641484 | |||||||
chr6:75641694 | T | G | 1 | a0001c0002t0022g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.479+990T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641694 | |||||||
chr6:75641745 | A | G | 1 | a0002c0003t0003g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.479+1041A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641745 | |||||||
chr6:75641904 | G | C | 1 | a0001c0002t0009g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.479+1200G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641904 | |||||||
chr6:75641924 | C | T | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.479+1220C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75641924 | |||||||
chr6:75642162 | G | A | 1 | a0001c0001t0017g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.479+1458G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642162 | |||||||
chr6:75642266 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.479+1562T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642266 | |||||||
chr6:75642283 | C | G | 152 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(149): Show |
152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.479+1579C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642283 | |||||||
chr6:75642314 | C | T | 3 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 |
3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.479+1610C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642314 | |||||||
chr6:75642333 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.479+1629G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642333 | |||||||
chr6:75642342 | G | A | 3 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0012c0012t0003g0167 |
3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.479+1638G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642342 | |||||||
chr6:75642794 | A | G | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.479+2090A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75642794 | |||||||
chr6:75643264 | T | A | 2 | a0001c0002t0003g0016 a0001c0002t0003g0018 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.479+2560T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643264 | |||||||
chr6:75643336 | A | G | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.479+2632A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643336 | |||||||
chr6:75643367 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.479+2663G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643367 | |||||||
chr6:75643605 | C | G | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.479+2901C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643605 | |||||||
chr6:75643649 | G | A | 1 | a0001c0002t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.479+2945G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643649 | |||||||
chr6:75643765 | A | G | 2 | a0001c0001t0004g0311 a0001c0001t0004g0324 |
2 | HG00438.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.479+3061A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643765 | |||||||
chr6:75643876 | A | G | 1 | a0001c0002t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.479+3172A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75643876 | |||||||
chr6:75644001 | A | G | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.479+3297A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644001 | |||||||
chr6:75644081 | A | G | 1 | a0002c0003t0003g0047 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.479+3377A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644081 | |||||||
chr6:75644154 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.479+3450A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644154 | |||||||
chr6:75644210 | G | T | 1 | a0001c0001t0001g0247 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.479+3506G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644210 | |||||||
chr6:75644227 | A | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.480-3504A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644227 | |||||||
chr6:75644253 | C | T | 1 | a0001c0001t0017g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.480-3478C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644253 | |||||||
chr6:75644291 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.480-3440A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644291 | |||||||
chr6:75644317 | G | A | 19 | a0001c0001t0005g0144 a0001c0001t0005g0145 a0001c0001t0005g0146 others(16): Show |
19 | HG00280.hp2 HG00642.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.480-3414G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644317 | |||||||
chr6:75644475 | C | CT | 154 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(151): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.480-3242dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 75644475 | ||||||
chr6:75644559 | A | C | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.480-3172A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644559 | |||||||
chr6:75644682 | G | T | 1 | a0001c0001t0002g0126 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.480-3049G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644682 | |||||||
chr6:75644728 | G | T | 1 | a0001c0001t0002g0075 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.480-3003G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644728 | |||||||
chr6:75644738 | G | A | 6 | a0001c0001t0001g0209 a0001c0001t0001g0229 a0001c0001t0001g0230 others(3): Show |
6 | HG02027.hp2 NA18944.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.480-2993G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644738 | |||||||
chr6:75644913 | C | T | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.480-2818C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75644913 | |||||||
chr6:75645381 | C | T | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.480-2350C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75645381 | |||||||
chr6:75645573 | C | T | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.480-2158C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75645573 | |||||||
chr6:75645766 | ACT | A | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.480-1962_480-1961d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr6 | 75645766 | ||||||
chr6:75645802 | C | A | 2 | a0001c0002t0003g0337 a0001c0002t0003g0341 |
2 | NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.480-1929C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75645802 | |||||||
chr6:75645980 | C | T | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.480-1751C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75645980 | |||||||
chr6:75646013 | A | G | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.480-1718A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646013 | |||||||
chr6:75646034 | A | G | 1 | a0001c0002t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.480-1697A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646034 | |||||||
chr6:75646042 | A | T | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.480-1689A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646042 | |||||||
chr6:75646215 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.480-1516C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646215 | |||||||
chr6:75646427 | A | G | 2 | a0001c0001t0001g0205 a0001c0002t0003g0014 |
2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.480-1304A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646427 | |||||||
chr6:75646466 | T | G | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.480-1265T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646466 | |||||||
chr6:75646497 | A | C | 24 | a0001c0002t0003g0003 a0001c0002t0003g0337 a0001c0002t0003g0338 others(21): Show |
25 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.480-1234A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646497 | |||||||
chr6:75646565 | G | A | 2 | a0001c0002t0003g0016 a0001c0002t0003g0018 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.480-1166G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646565 | |||||||
chr6:75646619 | G | A | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.480-1112G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646619 | |||||||
chr6:75646708 | C | T | 37 | a0001c0001t0003g0056 a0001c0004t0003g0174 a0001c0004t0003g0175 others(34): Show |
37 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.480-1023C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646708 | |||||||
chr6:75646729 | G | T | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.480-1002G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646729 | |||||||
chr6:75646814 | C | T | 1 | a0002c0003t0003g0033 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.480-917C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75646814 | |||||||
chr6:75647130 | C | G | 85 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(82): Show |
86 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.480-601C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647130 | |||||||
chr6:75647145 | T | C | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.480-586T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647145 | |||||||
chr6:75647167 | T | G | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.480-564T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647167 | |||||||
chr6:75647176 | A | G | 1 | a0001c0002t0009g0010 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.480-555A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647176 | |||||||
chr6:75647204 | C | T | 1 | a0001c0004t0003g0178 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.480-527C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647204 | |||||||
chr6:75647320 | A | G | 1 | a0001c0001t0004g0323 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.480-411A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647320 | |||||||
chr6:75647463 | T | C | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.480-268T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647463 | |||||||
chr6:75647652 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.480-79T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647652 | |||||||
chr6:75647710 | C | T | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.480-21C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 6/23 | chr6 | 75647710 | |||||||
chr6:75647877 | G | A | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.550+76G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75647877 | |||||||
chr6:75647911 | A | G | 1 | a0001c0001t0010g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.550+110A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75647911 | |||||||
chr6:75647941 | T | A | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.550+140T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75647941 | |||||||
chr6:75647984 | C | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.550+183C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75647984 | |||||||
chr6:75648119 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.550+318T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648119 | |||||||
chr6:75648142 | G | A | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+341G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648142 | |||||||
chr6:75648196 | C | G | 1 | a0001c0005t0006g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.550+395C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648196 | |||||||
chr6:75648204 | C | G | 1 | a0001c0001t0001g0251 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.550+403C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648204 | |||||||
chr6:75648513 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.550+712C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648513 | |||||||
chr6:75648572 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.550+771T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648572 | |||||||
chr6:75648597 | T | G | 1 | a0001c0001t0002g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.550+796T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648597 | |||||||
chr6:75648657 | T | C | 38 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0001c0004t0003g0174 others(35): Show |
38 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.550+856T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75648657 | |||||||
chr6:75649049 | A | C | 1 | a0001c0002t0009g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.550+1248A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649049 | |||||||
chr6:75649085 | C | T | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.550+1284C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649085 | |||||||
chr6:75649137 | C | T | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.550+1336C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649137 | |||||||
chr6:75649172 | G | C | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.550+1371G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649172 | |||||||
chr6:75649307 | T | A | 2 | a0002c0003t0003g0047 a0002c0003t0003g0050 |
2 | HG01074.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.550+1506T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649307 | |||||||
chr6:75649598 | A | G | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+1797A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649598 | |||||||
chr6:75649674 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.550+1873G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649674 | |||||||
chr6:75649706 | G | T | 1 | a0001c0002t0003g0016 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.550+1905G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649706 | |||||||
chr6:75649732 | G | C | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.550+1931G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649732 | |||||||
chr6:75649767 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.550+1966G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649767 | |||||||
chr6:75649797 | C | T | 2 | a0001c0002t0011g0015 a0001c0002t0011g0020 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.550+1996C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649797 | |||||||
chr6:75649816 | T | C | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.550+2015T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649816 | |||||||
chr6:75649925 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.550+2124A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75649925 | |||||||
chr6:75650146 | T | C | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+2345T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75650146 | |||||||
chr6:75650327 | G | A | 1 | a0002c0003t0003g0036 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.550+2526G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75650327 | |||||||
chr6:75650541 | C | T | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+2740C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75650541 | |||||||
chr6:75650962 | G | C | 1 | a0001c0001t0002g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.550+3161G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75650962 | |||||||
chr6:75651343 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.550+3542A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75651343 | |||||||
chr6:75651380 | G | T | 1 | a0001c0016t0006g0298 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.550+3579G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75651380 | |||||||
chr6:75651431 | T | C | 1 | a0001c0001t0004g0301 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.550+3630T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75651431 | |||||||
chr6:75651447 | T | G | 38 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0001c0004t0003g0174 others(35): Show |
38 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.550+3646T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75651447 | |||||||
chr6:75651450 | T | G | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.550+3649T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75651450 | |||||||
chr6:75652134 | G | A | 4 | a0001c0001t0001g0216 a0001c0001t0001g0225 a0001c0001t0001g0232 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+4333G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652134 | |||||||
chr6:75652140 | G | C | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.550+4339G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652140 | |||||||
chr6:75652158 | C | T | 1 | a0001c0001t0005g0144 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.550+4357C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652158 | |||||||
chr6:75652162 | G | A | 2 | a0002c0003t0003g0054 a0002c0003t0003g0055 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.550+4361G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652162 | |||||||
chr6:75652253 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.550+4452C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652253 | |||||||
chr6:75652254 | G | T | 1 | a0001c0001t0001g0276 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.550+4453G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652254 | |||||||
chr6:75652302 | C | T | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.550+4501C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652302 | |||||||
chr6:75652330 | T | C | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.550+4529T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652330 | |||||||
chr6:75652487 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.550+4686A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652487 | |||||||
chr6:75652600 | G | C | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.550+4799G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652600 | |||||||
chr6:75652683 | C | CAAAA | 17 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0013 others(14): Show |
17 | HG01081.hp2 HG02055.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.550+4899_550+4902d others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | ||||||
chr6:75652683 | C | CAAAAA | 23 | a0001c0004t0003g0178 a0002c0003t0003g0029 a0002c0003t0003g0030 others(20): Show |
23 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.550+4898_550+4902d others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | ||||||
chr6:75652683 | C | CAAAAAAA others(1): Show |
25 | a0001c0001t0002g0096 a0001c0001t0002g0128 a0001c0001t0002g0169 others(22): Show |
25 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.550+4895_550+4902d others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | ||||||
chr6:75652683 | C | CAAAAAAA others(2): Show |
82 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
83 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.550+4894_550+4902d others(11): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | ||||||
chr6:75652683 | C | CAAAAAAA others(3): Show |
13 | a0001c0001t0002g0059 a0001c0001t0002g0074 a0001c0001t0002g0083 others(10): Show |
13 | HG00140.hp1 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.550+4893_550+4902d others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | ||||||
chr6:75652683 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.550+4892_550+4902d others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | ||||||
chr6:75652683 | C | CAAGAAAA others(3): Show |
1 | a0001c0001t0002g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.550+4884_550+4885i others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | ||||||
chr6:75652683 | CA | C | 101 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(98): Show |
101 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.550+4902delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652683 | ||||||
chr6:75652696 | A | AAAAAAAA others(4): Show |
3 | a0001c0001t0004g0315 a0001c0001t0004g0335 a0001c0001t0007g0316 |
3 | NA18941.hp1 NA18977.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.550+4902_550+4903i others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652696 | ||||||
chr6:75652696 | A | AAAAAAAA others(3): Show |
34 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(31): Show |
35 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.550+4902_550+4903i others(12): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652696 | ||||||
chr6:75652698 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0003g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.550+4902_550+4903i others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652698 | ||||||
chr6:75652698 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.550+4902_550+4903i others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652698 | ||||||
chr6:75652698 | A | G | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.550+4897A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652698 | |||||||
chr6:75652700 | A | AAG | 9 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(6): Show |
9 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+4900_550+4901i others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75652700 | ||||||
chr6:75652709 | A | G | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.550+4908A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652709 | |||||||
chr6:75652827 | G | C | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0096 |
3 | NA18747.hp2 NA18945.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.550+5026G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75652827 | |||||||
chr6:75653025 | TTTTCTTT others(2): Show |
T | 25 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(22): Show |
25 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.550+5228_550+5236d others(11): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75653025 | ||||||
chr6:75653092 | G | T | 2 | a0002c0003t0003g0039 a0002c0003t0003g0043 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.550+5291G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653092 | |||||||
chr6:75653139 | T | C | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.550+5338T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653139 | |||||||
chr6:75653433 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0268 |
2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.550+5632A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653433 | |||||||
chr6:75653549 | T | G | 1 | a0001c0001t0005g0299 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.551-5713T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653549 | |||||||
chr6:75653653 | A | G | 1 | a0001c0002t0003g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.551-5609A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653653 | |||||||
chr6:75653660 | G | GT | 187 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.551-5590dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75653660 | ||||||
chr6:75653660 | GT | G | 43 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(40): Show |
44 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.551-5590delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75653660 | ||||||
chr6:75653675 | CTA | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0217 a0001c0001t0001g0234 |
3 | HG01884.hp2 HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.551-5586_551-5585d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653675 | |||||||
chr6:75653822 | A | G | 38 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0001c0004t0003g0174 others(35): Show |
38 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.551-5440A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75653822 | |||||||
chr6:75654038 | G | A | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.551-5224G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654038 | |||||||
chr6:75654053 | G | A | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.551-5209G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654053 | |||||||
chr6:75654148 | C | T | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.551-5114C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654148 | |||||||
chr6:75654472 | C | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0263 a0001c0001t0001g0265 |
3 | NA18947.hp1 NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.551-4790C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654472 | |||||||
chr6:75654556 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.551-4706T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654556 | |||||||
chr6:75654604 | A | G | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.551-4658A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654604 | |||||||
chr6:75654708 | G | A | 2 | a0001c0004t0003g0174 a0001c0004t0003g0180 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.551-4554G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654708 | |||||||
chr6:75654884 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.551-4378T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75654884 | |||||||
chr6:75655034 | C | G | 1 | a0001c0001t0017g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.551-4228C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655034 | |||||||
chr6:75655040 | T | G | 4 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0073 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-4222T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655040 | |||||||
chr6:75655187 | C | T | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.551-4075C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655187 | |||||||
chr6:75655509 | T | C | 1 | a0006c0015t0001g0287 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.551-3753T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655509 | |||||||
chr6:75655523 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.551-3739C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655523 | |||||||
chr6:75655526 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.551-3736T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655526 | |||||||
chr6:75655690 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.551-3572C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655690 | |||||||
chr6:75655779 | C | G | 35 | a0001c0001t0002g0001 a0001c0001t0002g0058 a0001c0001t0002g0059 others(32): Show |
36 | HG00099.hp2 HG01123.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.551-3483C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655779 | |||||||
chr6:75655834 | C | G | 5 | a0001c0001t0001g0216 a0001c0001t0001g0225 a0001c0001t0001g0232 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.551-3428C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655834 | |||||||
chr6:75655899 | T | C | 2 | a0001c0001t0010g0183 a0001c0001t0013g0185 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.551-3363T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75655899 | |||||||
chr6:75656053 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0268 |
2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.551-3209A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656053 | |||||||
chr6:75656104 | A | T | 1 | a0001c0002t0011g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.551-3158A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656104 | |||||||
chr6:75656193 | G | A | 6 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0013 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.551-3069G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656193 | |||||||
chr6:75656208 | C | T | 1 | a0002c0003t0003g0040 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.551-3054C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656208 | |||||||
chr6:75656213 | CA | C | 52 | a0001c0001t0001g0204 a0001c0001t0002g0077 a0001c0001t0002g0103 others(49): Show |
53 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.551-3030delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75656213 | ||||||
chr6:75656213 | CAA | C | 284 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(281): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.551-3031_551-3030d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75656213 | ||||||
chr6:75656295 | G | A | 4 | a0001c0001t0010g0183 a0001c0001t0010g0184 a0001c0001t0010g0188 others(1): Show |
4 | HG02622.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-2967G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656295 | |||||||
chr6:75656308 | T | A | 4 | a0001c0001t0002g0057 a0001c0001t0002g0101 a0001c0001t0002g0110 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-2954T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656308 | |||||||
chr6:75656441 | G | C | 1 | a0001c0001t0001g0226 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.551-2821G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656441 | |||||||
chr6:75656531 | G | A | 4 | a0001c0001t0002g0087 a0001c0001t0002g0089 a0001c0001t0002g0093 others(1): Show |
4 | NA18981.hp2 NA19056.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.551-2731G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656531 | |||||||
chr6:75656540 | G | A | 1 | a0007c0013t0005g0142 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.551-2722G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656540 | |||||||
chr6:75656550 | A | G | 5 | a0002c0003t0003g0038 a0002c0003t0003g0042 a0002c0003t0003g0053 others(2): Show |
5 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.551-2712A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75656550 | |||||||
chr6:75657008 | T | C | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.551-2254T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657008 | |||||||
chr6:75657140 | C | G | 1 | a0008c0010t0009g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.551-2122C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657140 | |||||||
chr6:75657342 | A | T | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.551-1920A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657342 | |||||||
chr6:75657482 | A | G | 3 | a0001c0001t0002g0072 a0001c0001t0002g0099 a0001c0001t0002g0113 |
3 | HG02165.hp2 NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.551-1780A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657482 | |||||||
chr6:75657485 | A | G | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.551-1777A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657485 | |||||||
chr6:75657708 | A | G | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.551-1554A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657708 | |||||||
chr6:75657801 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.551-1461A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75657801 | |||||||
chr6:75658124 | G | C | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.551-1138G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658124 | |||||||
chr6:75658179 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.551-1083G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658179 | |||||||
chr6:75658219 | C | T | 1 | a0001c0001t0018g0063 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.551-1043C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658219 | |||||||
chr6:75658225 | A | G | 2 | a0001c0001t0002g0131 a0001c0001t0016g0122 |
2 | HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.551-1037A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658225 | |||||||
chr6:75658405 | A | G | 2 | a0001c0002t0009g0171 a0001c0002t0009g0172 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.551-857A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658405 | |||||||
chr6:75658417 | C | T | 1 | a0001c0001t0008g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.551-845C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658417 | |||||||
chr6:75658614 | A | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0263 a0001c0001t0001g0265 |
3 | NA18947.hp1 NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.551-648A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658614 | |||||||
chr6:75658689 | G | A | 3 | a0001c0001t0002g0111 a0001c0001t0003g0056 a0012c0012t0003g0167 |
3 | HG02809.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.551-573G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658689 | |||||||
chr6:75658721 | G | A | 312 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.551-541G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658721 | |||||||
chr6:75658801 | G | A | 2 | a0001c0001t0005g0299 a0001c0001t0005g0300 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.551-461G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658801 | |||||||
chr6:75658947 | A | G | 1 | a0001c0001t0005g0159 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.551-315A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658947 | |||||||
chr6:75658970 | TC | T | 20 | a0001c0001t0002g0059 a0001c0001t0002g0068 a0001c0001t0002g0071 others(17): Show |
20 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.551-288delC | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658970 | ||||||
chr6:75658973 | C | CA | 3 | a0001c0001t0005g0148 a0001c0001t0005g0299 a0007c0013t0005g0142 |
3 | HG01346.hp1 HG02809.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.551-289_551-288ins others(1): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658973 | |||||||
chr6:75658973 | CCA | C | 76 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(73): Show |
77 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.551-288_551-287del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658973 | |||||||
chr6:75658974 | C | A | 24 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(21): Show |
24 | HG00280.hp2 HG00642.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.551-288C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658974 | |||||||
chr6:75658974 | C | CA | 33 | a0001c0001t0003g0025 a0001c0001t0003g0027 a0001c0001t0003g0028 others(30): Show |
33 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.551-262dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658974 | ||||||
chr6:75658974 | C | CAA | 6 | a0001c0001t0003g0026 a0001c0001t0010g0188 a0001c0008t0003g0186 others(3): Show |
6 | HG02145.hp2 HG02723.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-263_551-262dup others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658974 | ||||||
chr6:75658974 | CA | C | 15 | a0001c0001t0001g0200 a0001c0001t0001g0231 a0001c0001t0001g0240 others(12): Show |
15 | HG00423.hp1 HG00597.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.551-262delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658974 | ||||||
chr6:75658974 | CAA | C | 115 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(112): Show |
116 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.551-263_551-262del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658974 | ||||||
chr6:75658974 | CAAA | C | 6 | a0001c0001t0001g0218 a0001c0001t0001g0225 a0001c0001t0001g0229 others(3): Show |
6 | HG01515.hp2 NA18522.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.551-264_551-262del others(3): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75658974 | ||||||
chr6:75658977 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.551-285A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658977 | |||||||
chr6:75658999 | AAG | A | 33 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(30): Show |
34 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.551-262_551-261del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75658999 | |||||||
chr6:75659000 | A | G | 2 | a0001c0002t0003g0355 a0001c0002t0011g0015 |
2 | HG02965.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.551-262A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75659000 | |||||||
chr6:75659000 | AG | A | 4 | a0001c0001t0003g0166 a0001c0001t0007g0327 a0001c0001t0007g0331 others(1): Show |
4 | HG02559.hp1 HG03225.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.551-258delG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75659000 | ||||||
chr6:75659001 | G | A | 170 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(167): Show |
171 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.551-261G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75659001 | |||||||
chr6:75659034 | G | C | 6 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0013 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.551-228G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75659034 | |||||||
chr6:75659141 | TAAGAG | T | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.551-115_551-111del others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr6 | 75659141 | ||||||
chr6:75659173 | G | A | 2 | a0001c0001t0002g0134 a0001c0001t0002g0135 |
2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.551-89G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 7/23 | chr6 | 75659173 | |||||||
chr6:75659476 | T | C | 11 | a0001c0001t0005g0144 a0001c0001t0005g0145 a0001c0001t0005g0146 others(8): Show |
11 | NA18960.hp1 NA18980.hp1 NA18988.hp2 others(8): Show |
intron_variant | MODIFIER | c.696+69T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75659476 | |||||||
chr6:75659784 | C | T | 1 | a0001c0002t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.696+377C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75659784 | |||||||
chr6:75659842 | G | T | 1 | a0001c0001t0003g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.696+435G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75659842 | |||||||
chr6:75660057 | G | A | 1 | a0001c0002t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.696+650G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660057 | |||||||
chr6:75660057 | G | C | 1 | a0001c0001t0004g0002 | 2 | NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.696+650G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660057 | |||||||
chr6:75660269 | A | G | 343 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(340): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.696+862A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660269 | |||||||
chr6:75660414 | G | T | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.696+1007G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660414 | |||||||
chr6:75660504 | G | C | 32 | a0001c0002t0003g0003 a0001c0002t0003g0023 a0001c0002t0003g0170 others(29): Show |
33 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.696+1097G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660504 | |||||||
chr6:75660679 | C | G | 3 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0012c0012t0003g0167 |
3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.696+1272C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660679 | |||||||
chr6:75660695 | C | T | 6 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0013 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.696+1288C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660695 | |||||||
chr6:75660696 | G | C | 2 | a0001c0001t0002g0061 a0001c0017t0002g0112 |
2 | HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.696+1289G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660696 | |||||||
chr6:75660751 | C | T | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.696+1344C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660751 | |||||||
chr6:75660782 | C | A | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.696+1375C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660782 | |||||||
chr6:75660790 | C | T | 1 | a0001c0001t0005g0146 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.696+1383C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660790 | |||||||
chr6:75660853 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.696+1446A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660853 | |||||||
chr6:75660870 | G | A | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.696+1463G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660870 | |||||||
chr6:75660910 | C | T | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.696+1503C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660910 | |||||||
chr6:75660997 | G | A | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+1590G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75660997 | |||||||
chr6:75661070 | T | C | 1 | a0001c0001t0007g0317 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.696+1663T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661070 | |||||||
chr6:75661076 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.696+1669C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661076 | |||||||
chr6:75661204 | C | A | 5 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.696+1797C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661204 | |||||||
chr6:75661230 | C | T | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.696+1823C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661230 | |||||||
chr6:75661295 | T | C | 1 | a0001c0002t0003g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.696+1888T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661295 | |||||||
chr6:75661405 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.697-1816A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661405 | |||||||
chr6:75661666 | T | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0236 |
2 | NA18939.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.697-1555T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661666 | |||||||
chr6:75661697 | G | C | 1 | a0002c0003t0003g0042 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.697-1524G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75661697 | |||||||
chr6:75662053 | A | AAAAT | 8 | a0001c0001t0001g0272 a0001c0002t0009g0010 a0001c0002t0009g0012 others(5): Show |
8 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.697-1144_697-1141d others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr6 | 75662053 | ||||||
chr6:75662053 | AAAATAAA others(5): Show |
A | 5 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0217 others(2): Show |
5 | HG01070.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-1152_697-1141d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr6 | 75662053 | ||||||
chr6:75662265 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.697-956A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662265 | |||||||
chr6:75662466 | CA | C | 4 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0073 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.697-754delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662466 | |||||||
chr6:75662782 | G | A | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.697-439G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662782 | |||||||
chr6:75662839 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.697-382T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662839 | |||||||
chr6:75662964 | A | G | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.697-257A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662964 | |||||||
chr6:75662985 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.697-236G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75662985 | |||||||
chr6:75663064 | T | G | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.697-157T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75663064 | |||||||
chr6:75663216 | C | T | 1 | a0002c0003t0003g0042 | 1 | HG01243.hp2 | splice_region_variant&intron_variant | LOW | c.697-5C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 8/23 | chr6 | 75663216 | |||||||
chr6:75663558 | C | T | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.994+40C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663558 | |||||||
chr6:75663727 | G | GT | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.994+211dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75663727 | ||||||
chr6:75663797 | G | A | 4 | a0001c0001t0002g0087 a0001c0001t0002g0089 a0001c0001t0002g0093 others(1): Show |
4 | NA18981.hp2 NA19056.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+279G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663797 | |||||||
chr6:75663805 | TG | T | 211 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(208): Show |
213 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.994+290delG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75663805 | ||||||
chr6:75663807 | G | GTT | 9 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(6): Show |
9 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.994+289_994+290ins others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663807 | |||||||
chr6:75663808 | G | T | 57 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0276 others(54): Show |
57 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.994+290G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663808 | |||||||
chr6:75663820 | G | T | 2 | a0001c0008t0003g0187 a0004c0006t0005g0152 |
2 | HG03516.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.994+302G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663820 | |||||||
chr6:75663820 | GT | G | 13 | a0001c0001t0005g0144 a0001c0001t0005g0145 a0001c0001t0005g0148 others(10): Show |
13 | HG00280.hp2 HG01168.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.994+303delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663820 | |||||||
chr6:75663821 | T | G | 18 | a0001c0001t0003g0166 a0001c0001t0005g0141 a0001c0001t0005g0146 others(15): Show |
18 | HG00642.hp1 HG01069.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.994+303T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663821 | |||||||
chr6:75663821 | T | TG | 37 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0272 others(34): Show |
38 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.994+314dupG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75663821 | ||||||
chr6:75663821 | TG | T | 149 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0194 others(146): Show |
150 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.994+314delG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75663821 | ||||||
chr6:75663821 | TGG | T | 32 | a0001c0002t0003g0003 a0001c0002t0003g0023 a0001c0002t0003g0170 others(29): Show |
33 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.994+313_994+314del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75663821 | ||||||
chr6:75663827 | G | C | 1 | a0001c0001t0001g0235 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.994+309G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663827 | |||||||
chr6:75663830 | G | T | 1 | a0001c0001t0005g0162 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.994+312G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663830 | |||||||
chr6:75663851 | G | A | 268 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(265): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.994+333G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663851 | |||||||
chr6:75663884 | A | G | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.994+366A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75663884 | |||||||
chr6:75664023 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.994+505G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664023 | |||||||
chr6:75664115 | A | G | 5 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0217 others(2): Show |
5 | HG01070.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.994+597A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664115 | |||||||
chr6:75664155 | A | G | 13 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(10): Show |
13 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.994+637A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664155 | |||||||
chr6:75664215 | C | T | 37 | a0001c0001t0003g0056 a0001c0004t0003g0174 a0001c0004t0003g0175 others(34): Show |
37 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.994+697C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664215 | |||||||
chr6:75664260 | T | TG | 24 | a0001c0002t0003g0003 a0001c0002t0003g0337 a0001c0002t0003g0338 others(21): Show |
25 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.994+742_994+743ins others(1): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664260 | |||||||
chr6:75664261 | A | G | 21 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(18): Show |
21 | HG01109.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.994+743A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664261 | |||||||
chr6:75664375 | TATAC | T | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.994+860_994+863del others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75664375 | ||||||
chr6:75664482 | AAT | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.994+966_994+967del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75664482 | ||||||
chr6:75664805 | T | A | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.994+1287T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664805 | |||||||
chr6:75664921 | C | T | 1 | a0002c0003t0003g0046 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.994+1403C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664921 | |||||||
chr6:75664998 | A | G | 1 | a0001c0001t0002g0086 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.994+1480A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75664998 | |||||||
chr6:75665057 | C | T | 5 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 others(2): Show |
5 | NA18955.hp1 NA18974.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.994+1539C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665057 | |||||||
chr6:75665069 | G | A | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.994+1551G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665069 | |||||||
chr6:75665280 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.995-1432C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665280 | |||||||
chr6:75665285 | C | CA | 44 | a0001c0001t0001g0231 a0001c0001t0001g0247 a0001c0001t0001g0258 others(41): Show |
45 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.995-1411dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75665285 | ||||||
chr6:75665285 | CA | C | 38 | a0001c0001t0001g0216 a0001c0001t0005g0141 a0001c0001t0005g0144 others(35): Show |
38 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.995-1411delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75665285 | ||||||
chr6:75665448 | G | C | 6 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0013 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-1264G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665448 | |||||||
chr6:75665523 | A | G | 13 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(10): Show |
13 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.995-1189A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665523 | |||||||
chr6:75665605 | A | G | 148 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(145): Show |
149 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.995-1107A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665605 | |||||||
chr6:75665820 | A | G | 1 | a0001c0001t0004g0322 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.995-892A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665820 | |||||||
chr6:75665824 | C | T | 149 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(146): Show |
150 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.995-888C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665824 | |||||||
chr6:75665902 | A | G | 3 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 |
3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.995-810A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665902 | |||||||
chr6:75665914 | G | A | 5 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-798G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665914 | |||||||
chr6:75665930 | G | A | 2 | a0001c0001t0005g0299 a0001c0001t0005g0300 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.995-782G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665930 | |||||||
chr6:75665950 | C | T | 4 | a0001c0001t0002g0061 a0001c0001t0002g0068 a0001c0001t0002g0121 others(1): Show |
4 | HG01261.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-762C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665950 | |||||||
chr6:75665967 | A | G | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.995-745A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75665967 | |||||||
chr6:75666053 | G | GATATATA others(15): Show |
1 | a0001c0001t0002g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.995-626_995-605dup others(22): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666053 | ||||||
chr6:75666073 | GAT | G | 11 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(8): Show |
11 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.995-631_995-630del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666073 | ||||||
chr6:75666086 | CGT | C | 145 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(142): Show |
146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.995-625_995-624del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666086 | |||||||
chr6:75666086 | CGTAT | C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0221 a0001c0001t0001g0267 |
3 | NA18998.hp2 NA19065.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.995-625_995-622del others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666086 | |||||||
chr6:75666108 | T | C | 3 | a0001c0001t0005g0157 a0001c0001t0005g0158 a0001c0001t0005g0162 |
3 | HG00280.hp2 HG01168.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.995-604T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666108 | |||||||
chr6:75666126 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.995-586A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666126 | |||||||
chr6:75666152 | CAT | C | 148 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(145): Show |
149 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.995-555_995-554del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666152 | ||||||
chr6:75666159 | GAT | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.995-543_995-542del others(2): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666159 | ||||||
chr6:75666161 | TATATATA others(15): Show |
T | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.995-518_995-497del others(22): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666161 | ||||||
chr6:75666197 | G | A | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.995-515G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666197 | |||||||
chr6:75666233 | TATG | T | 64 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(61): Show |
65 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.995-476_995-474del others(3): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr6 | 75666233 | ||||||
chr6:75666255 | C | T | 1 | a0001c0002t0009g0013 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.995-457C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666255 | |||||||
chr6:75666320 | A | G | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.995-392A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666320 | |||||||
chr6:75666398 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.995-314A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666398 | |||||||
chr6:75666413 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.995-299A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 9/23 | chr6 | 75666413 | |||||||
chr6:75667116 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1224+175T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667116 | |||||||
chr6:75667262 | A | G | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1224+321A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667262 | |||||||
chr6:75667317 | A | G | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1224+376A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667317 | |||||||
chr6:75667340 | T | C | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1224+399T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667340 | |||||||
chr6:75667386 | C | A | 1 | a0001c0001t0002g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1224+445C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667386 | |||||||
chr6:75667434 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1224+493G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667434 | |||||||
chr6:75667500 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1224+559A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667500 | |||||||
chr6:75667510 | C | A | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1224+569C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667510 | |||||||
chr6:75667591 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1224+650A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667591 | |||||||
chr6:75667633 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1224+692A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667633 | |||||||
chr6:75667789 | G | A | 148 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(145): Show |
149 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1224+848G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75667789 | |||||||
chr6:75668055 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1224+1114T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668055 | |||||||
chr6:75668282 | G | A | 268 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(265): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1224+1341G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668282 | |||||||
chr6:75668307 | T | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1224+1366T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668307 | |||||||
chr6:75668345 | C | T | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1224+1404C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668345 | |||||||
chr6:75668420 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1224+1479A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668420 | |||||||
chr6:75668449 | T | C | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1224+1508T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668449 | |||||||
chr6:75668671 | A | G | 1 | a0001c0001t0007g0316 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1224+1730A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668671 | |||||||
chr6:75668727 | C | T | 5 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0217 others(2): Show |
5 | HG01070.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1224+1786C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668727 | |||||||
chr6:75668816 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1225-1737C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668816 | |||||||
chr6:75668898 | A | T | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225-1655A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75668898 | |||||||
chr6:75669023 | C | T | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1225-1530C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669023 | |||||||
chr6:75669148 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1225-1405G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669148 | |||||||
chr6:75669526 | C | T | 2 | a0001c0001t0004g0315 a0001c0001t0004g0321 |
2 | NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1225-1027C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669526 | |||||||
chr6:75669570 | A | G | 1 | a0010c0014t0002g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1225-983A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669570 | |||||||
chr6:75669938 | A | T | 1 | a0001c0001t0002g0089 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1225-615A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669938 | |||||||
chr6:75669938 | AT | A | 268 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(265): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1225-603delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 75669938 | ||||||
chr6:75669973 | G | A | 1 | a0009c0018t0001g0237 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1225-580G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669973 | |||||||
chr6:75669989 | G | A | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1225-564G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75669989 | |||||||
chr6:75670050 | CAGCCTCC others(5): Show |
C | 1 | a0001c0001t0017g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1225-486_1225-475d others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr6 | 75670050 | ||||||
chr6:75670166 | C | T | 1 | a0001c0002t0003g0355 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1225-387C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75670166 | |||||||
chr6:75670287 | A | T | 32 | a0001c0002t0003g0003 a0001c0002t0003g0023 a0001c0002t0003g0170 others(29): Show |
33 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1225-266A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75670287 | |||||||
chr6:75670319 | A | C | 268 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(265): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1225-234A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75670319 | |||||||
chr6:75670373 | A | G | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1225-180A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 10/23 | chr6 | 75670373 | |||||||
chr6:75670752 | A | G | 3 | a0001c0001t0001g0211 a0001c0001t0001g0224 a0001c0001t0001g0227 |
3 | HG02129.hp2 HG02165.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1392+32A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75670752 | |||||||
chr6:75670850 | C | T | 1 | a0010c0014t0002g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1392+130C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75670850 | |||||||
chr6:75670874 | G | A | 1 | a0001c0002t0003g0355 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1392+154G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75670874 | |||||||
chr6:75670891 | AAATGAGT others(60): Show |
A | 1 | a0001c0001t0001g0238 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1392+201_1392+267d others(69): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75670891 | ||||||
chr6:75670960 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1392+240A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75670960 | |||||||
chr6:75670961 | T | A | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1392+241T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75670961 | |||||||
chr6:75671014 | A | G | 1 | a0001c0001t0002g0173 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1392+294A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671014 | |||||||
chr6:75671152 | G | A | 2 | a0001c0001t0002g0101 a0001c0001t0002g0123 |
2 | HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1392+432G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671152 | |||||||
chr6:75671168 | A | G | 1 | a0001c0008t0003g0186 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1392+448A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671168 | |||||||
chr6:75671172 | T | TA | 3 | a0001c0001t0001g0255 a0001c0001t0001g0263 a0001c0001t0001g0265 |
3 | NA18947.hp1 NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1392+453dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75671172 | ||||||
chr6:75671317 | C | T | 2 | a0001c0002t0003g0016 a0001c0002t0003g0018 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1392+597C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671317 | |||||||
chr6:75671330 | G | T | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1392+610G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671330 | |||||||
chr6:75671449 | C | T | 1 | a0001c0001t0003g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1392+729C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671449 | |||||||
chr6:75671451 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1392+731C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671451 | |||||||
chr6:75671578 | C | T | 4 | a0001c0001t0005g0156 a0004c0006t0005g0151 a0004c0006t0005g0152 others(1): Show |
4 | NA18960.hp1 NA18980.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+858C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671578 | |||||||
chr6:75671614 | C | T | 1 | a0001c0002t0009g0171 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1392+894C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75671614 | |||||||
chr6:75672029 | G | T | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1392+1309G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672029 | |||||||
chr6:75672349 | T | C | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1392+1629T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672349 | |||||||
chr6:75672357 | T | C | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1392+1637T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672357 | |||||||
chr6:75672399 | T | G | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1392+1679T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672399 | |||||||
chr6:75672418 | AT | A | 3 | a0001c0001t0013g0185 a0001c0008t0003g0186 a0001c0008t0003g0187 |
3 | HG03041.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1392+1699delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672418 | |||||||
chr6:75672419 | T | A | 7 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(4): Show |
7 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1392+1699T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672419 | |||||||
chr6:75672444 | A | G | 1 | a0001c0002t0011g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1392+1724A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672444 | |||||||
chr6:75672532 | C | A | 3 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0012c0012t0003g0167 |
3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1392+1812C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672532 | |||||||
chr6:75672824 | G | T | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1392+2104G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672824 | |||||||
chr6:75672852 | G | T | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1392+2132G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75672852 | |||||||
chr6:75673028 | T | C | 8 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(5): Show |
8 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1392+2308T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673028 | |||||||
chr6:75673123 | G | C | 6 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0013 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1393-2312G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673123 | |||||||
chr6:75673146 | C | T | 25 | a0001c0001t0002g0104 a0001c0002t0003g0003 a0001c0002t0003g0337 others(22): Show |
26 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.1393-2289C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673146 | |||||||
chr6:75673147 | G | A | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1393-2288G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673147 | |||||||
chr6:75673171 | C | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1393-2264C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673171 | |||||||
chr6:75673280 | A | G | 7 | a0001c0002t0003g0016 a0001c0002t0003g0017 a0001c0002t0003g0018 others(4): Show |
7 | HG02630.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1393-2155A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673280 | |||||||
chr6:75673319 | C | CT | 45 | a0001c0001t0001g0214 a0001c0001t0001g0265 a0001c0001t0001g0277 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.1393-2096dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75673319 | ||||||
chr6:75673319 | C | CTT | 159 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(156): Show |
160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1393-2097_1393-209 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75673319 | ||||||
chr6:75673319 | C | CTTT | 22 | a0001c0001t0001g0201 a0001c0001t0001g0245 a0001c0001t0001g0286 others(19): Show |
22 | HG00423.hp2 HG01346.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1393-2098_1393-209 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75673319 | ||||||
chr6:75673339 | T | G | 1 | a0001c0002t0022g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1393-2096T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673339 | |||||||
chr6:75673339 | T | TG | 6 | a0001c0002t0003g0016 a0001c0002t0003g0017 a0001c0002t0003g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1393-2095dupG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75673339 | ||||||
chr6:75673418 | G | C | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1393-2017G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673418 | |||||||
chr6:75673460 | A | T | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.1393-1975A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673460 | |||||||
chr6:75673600 | A | G | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1393-1835A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673600 | |||||||
chr6:75673678 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1393-1757A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673678 | |||||||
chr6:75673726 | T | G | 1 | a0001c0001t0007g0303 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1393-1709T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75673726 | |||||||
chr6:75674107 | T | C | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1393-1328T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674107 | |||||||
chr6:75674108 | C | G | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1393-1327C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674108 | |||||||
chr6:75674146 | CT | C | 24 | a0001c0001t0001g0195 a0001c0001t0001g0229 a0001c0001t0001g0239 others(21): Show |
24 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1393-1265delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75674146 | ||||||
chr6:75674167 | T | A | 5 | a0001c0001t0001g0206 a0001c0001t0001g0217 a0001c0001t0001g0234 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1393-1268T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674167 | |||||||
chr6:75674167 | T | TA | 32 | a0001c0001t0001g0212 a0001c0001t0004g0002 a0001c0001t0004g0301 others(29): Show |
33 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.1393-1268_1393-126 others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674167 | |||||||
chr6:75674168 | T | A | 145 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(142): Show |
146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1393-1267T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674168 | |||||||
chr6:75674168 | T | TA | 11 | a0001c0001t0001g0225 a0001c0001t0001g0232 a0001c0001t0001g0233 others(8): Show |
11 | HG01071.hp1 HG01256.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1393-1267_1393-126 others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674168 | |||||||
chr6:75674168 | T | TAA | 5 | a0001c0001t0004g0302 a0001c0001t0004g0320 a0001c0001t0004g0333 others(2): Show |
5 | HG00597.hp1 HG02083.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1393-1267_1393-126 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674168 | |||||||
chr6:75674169 | T | A | 196 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(193): Show |
198 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1393-1266T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674169 | |||||||
chr6:75674170 | T | A | 223 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(220): Show |
225 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1393-1265T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674170 | |||||||
chr6:75674170 | T | TA | 10 | a0001c0001t0003g0056 a0001c0004t0003g0174 a0001c0004t0003g0177 others(7): Show |
10 | HG02055.hp2 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1393-1260dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr6 | 75674170 | ||||||
chr6:75674171 | A | T | 1 | a0001c0001t0002g0127 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1393-1264A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674171 | |||||||
chr6:75674208 | G | C | 102 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1393-1227G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674208 | |||||||
chr6:75674255 | C | G | 2 | a0001c0001t0002g0131 a0001c0001t0016g0122 |
2 | HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1393-1180C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674255 | |||||||
chr6:75674261 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1393-1174A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674261 | |||||||
chr6:75674447 | G | C | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1393-988G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674447 | |||||||
chr6:75674570 | A | C | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1393-865A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674570 | |||||||
chr6:75674695 | A | G | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1393-740A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674695 | |||||||
chr6:75674762 | T | C | 6 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(3): Show |
6 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1393-673T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75674762 | |||||||
chr6:75675076 | G | T | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1393-359G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75675076 | |||||||
chr6:75675196 | A | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0263 a0001c0001t0001g0265 |
3 | NA18947.hp1 NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1393-239A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 11/23 | chr6 | 75675196 | |||||||
chr6:75675614 | G | C | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1426+146G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 12/23 | chr6 | 75675614 | |||||||
chr6:75675795 | A | G | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1427-65A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 12/23 | chr6 | 75675795 | |||||||
chr6:75676157 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1621+103G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676157 | |||||||
chr6:75676168 | A | G | 3 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 |
3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1621+114A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676168 | |||||||
chr6:75676336 | A | G | 1 | a0001c0001t0005g0148 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1621+282A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676336 | |||||||
chr6:75676558 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1622-472T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676558 | |||||||
chr6:75676758 | A | G | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1622-272A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676758 | |||||||
chr6:75676940 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1622-90C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | chr6 | 75676940 | |||||||
chr6:75676996 | GT | G | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1622-25delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr6 | 75676996 | ||||||
chr6:75677282 | T | C | 1 | a0002c0003t0003g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1848+26T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75677282 | |||||||
chr6:75677321 | T | G | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1848+65T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75677321 | |||||||
chr6:75677386 | A | T | 38 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0001c0004t0003g0174 others(35): Show |
38 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.1848+130A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75677386 | |||||||
chr6:75677786 | A | G | 1 | a0001c0001t0004g0312 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1848+530A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75677786 | |||||||
chr6:75677894 | A | G | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1848+638A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75677894 | |||||||
chr6:75678154 | CCT | C | 5 | a0001c0001t0001g0290 a0001c0001t0010g0183 a0001c0001t0010g0184 others(2): Show |
5 | HG02622.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1849-428_1849-427d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678154 | |||||||
chr6:75678220 | A | G | 2 | a0001c0001t0001g0276 a0001c0002t0003g0357 |
2 | NA18964.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1849-363A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678220 | |||||||
chr6:75678221 | C | T | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1849-362C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678221 | |||||||
chr6:75678227 | A | C | 1 | a0001c0001t0001g0219 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1849-356A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678227 | |||||||
chr6:75678265 | C | G | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1849-318C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678265 | |||||||
chr6:75678325 | G | C | 1 | a0001c0001t0007g0331 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1849-258G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678325 | |||||||
chr6:75678328 | G | C | 1 | a0001c0001t0001g0276 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1849-255G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678328 | |||||||
chr6:75678333 | A | T | 1 | a0001c0001t0007g0331 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1849-250A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678333 | |||||||
chr6:75678384 | A | G | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1849-199A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678384 | |||||||
chr6:75678409 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1849-174A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 14/23 | chr6 | 75678409 | |||||||
chr6:75678807 | A | T | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.1959-4A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 15/23 | chr6 | 75678807 | |||||||
chr6:75679186 | G | A | 1 | a0001c0001t0003g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2075+259G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679186 | |||||||
chr6:75679273 | T | G | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2075+346T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679273 | |||||||
chr6:75679316 | A | C | 24 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(21): Show |
24 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.2075+389A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679316 | |||||||
chr6:75679355 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2075+428A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679355 | |||||||
chr6:75679693 | A | G | 1 | a0001c0002t0003g0354 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2075+766A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679693 | |||||||
chr6:75679974 | T | C | 1 | a0001c0002t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2075+1047T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75679974 | |||||||
chr6:75680060 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2075+1133A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680060 | |||||||
chr6:75680182 | G | C | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2075+1255G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680182 | |||||||
chr6:75680290 | G | A | 1 | a0001c0001t0017g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2075+1363G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680290 | |||||||
chr6:75680361 | C | T | 254 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(251): Show |
257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.2075+1434C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680361 | |||||||
chr6:75680372 | G | C | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+1445G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680372 | |||||||
chr6:75680399 | A | G | 5 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2075+1472A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680399 | |||||||
chr6:75680525 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2075+1598A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680525 | |||||||
chr6:75680763 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0268 |
2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.2075+1836C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680763 | |||||||
chr6:75680869 | C | T | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2075+1942C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680869 | |||||||
chr6:75680872 | C | T | 2 | a0001c0001t0007g0303 a0001c0001t0007g0304 |
2 | NA18972.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2075+1945C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680872 | |||||||
chr6:75680968 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2075+2041C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75680968 | |||||||
chr6:75681043 | A | G | 1 | a0001c0001t0004g0322 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2075+2116A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681043 | |||||||
chr6:75681129 | C | T | 1 | a0001c0002t0009g0013 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2075+2202C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681129 | |||||||
chr6:75681221 | C | T | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2075+2294C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681221 | |||||||
chr6:75681446 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0268 |
2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.2075+2519C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681446 | |||||||
chr6:75681462 | CT | C | 28 | a0001c0001t0002g0060 a0001c0001t0004g0325 a0001c0001t0005g0141 others(25): Show |
28 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.2075+2548delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75681462 | ||||||
chr6:75681519 | C | G | 1 | a0001c0001t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2075+2592C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681519 | |||||||
chr6:75681521 | C | T | 1 | a0001c0002t0003g0348 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2075+2594C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681521 | |||||||
chr6:75681532 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2075+2605C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681532 | |||||||
chr6:75681652 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2075+2725A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681652 | |||||||
chr6:75681663 | T | G | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2075+2736T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681663 | |||||||
chr6:75681679 | A | C | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2075+2752A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681679 | |||||||
chr6:75681856 | C | G | 6 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(3): Show |
6 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2075+2929C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681856 | |||||||
chr6:75681978 | G | A | 3 | a0004c0006t0005g0151 a0004c0006t0005g0152 a0004c0006t0005g0161 |
3 | NA18980.hp1 NA18994.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2075+3051G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681978 | |||||||
chr6:75681985 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2075+3058G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75681985 | |||||||
chr6:75682114 | C | G | 3 | a0001c0001t0001g0211 a0001c0001t0001g0224 a0001c0001t0001g0227 |
3 | HG02129.hp2 HG02165.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2075+3187C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682114 | |||||||
chr6:75682140 | A | T | 3 | a0001c0001t0001g0211 a0001c0001t0001g0224 a0001c0001t0001g0227 |
3 | HG02129.hp2 HG02165.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2075+3213A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682140 | |||||||
chr6:75682154 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2075+3227G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682154 | |||||||
chr6:75682199 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2075+3272G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682199 | |||||||
chr6:75682391 | A | G | 6 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0013 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2075+3464A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682391 | |||||||
chr6:75682405 | C | CT | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2075+3490dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75682405 | ||||||
chr6:75682602 | G | A | 2 | a0002c0003t0003g0054 a0002c0003t0003g0055 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2075+3675G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682602 | |||||||
chr6:75682626 | G | A | 252 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0217 others(249): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.2075+3699G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682626 | |||||||
chr6:75682626 | G | C | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2075+3699G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682626 | |||||||
chr6:75682634 | C | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2075+3707C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682634 | |||||||
chr6:75682854 | C | T | 1 | a0001c0005t0006g0294 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2075+3927C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682854 | |||||||
chr6:75682857 | A | C | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.2075+3930A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682857 | |||||||
chr6:75682888 | T | C | 1 | a0002c0003t0003g0046 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2075+3961T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682888 | |||||||
chr6:75682916 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2075+3989T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682916 | |||||||
chr6:75682920 | A | C | 1 | a0001c0001t0001g0262 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2075+3993A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682920 | |||||||
chr6:75682921 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2075+3994G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682921 | |||||||
chr6:75682929 | G | C | 1 | a0001c0001t0001g0262 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2075+4002G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75682929 | |||||||
chr6:75683067 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2075+4140G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683067 | |||||||
chr6:75683106 | C | T | 2 | a0001c0001t0004g0315 a0001c0001t0004g0321 |
2 | NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2075+4179C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683106 | |||||||
chr6:75683114 | G | A | 1 | a0002c0003t0003g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2075+4187G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683114 | |||||||
chr6:75683123 | A | C | 3 | a0001c0002t0009g0012 a0001c0002t0009g0171 a0001c0002t0009g0172 |
3 | HG02486.hp2 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2075+4196A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683123 | |||||||
chr6:75683246 | G | C | 1 | a0001c0001t0002g0086 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2075+4319G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683246 | |||||||
chr6:75683545 | C | T | 1 | a0001c0001t0008g0254 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2075+4618C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683545 | |||||||
chr6:75683569 | T | C | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2075+4642T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683569 | |||||||
chr6:75683666 | TTTC | T | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2075+4742_2075+474 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75683666 | ||||||
chr6:75683741 | G | A | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+4814G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683741 | |||||||
chr6:75683795 | T | C | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2075+4868T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683795 | |||||||
chr6:75683878 | G | A | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2075+4951G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75683878 | |||||||
chr6:75684029 | G | T | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2075+5102G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684029 | |||||||
chr6:75684113 | A | G | 3 | a0001c0001t0005g0163 a0001c0001t0005g0164 a0001c0001t0005g0165 |
3 | HG01069.hp1 HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2075+5186A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684113 | |||||||
chr6:75684143 | T | G | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.2075+5216T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684143 | |||||||
chr6:75684148 | T | C | 1 | a0001c0001t0005g0165 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2075+5221T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684148 | |||||||
chr6:75684365 | A | G | 4 | a0001c0001t0002g0061 a0001c0001t0002g0068 a0001c0001t0002g0121 others(1): Show |
4 | HG01261.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2075+5438A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684365 | |||||||
chr6:75684438 | A | C | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.2075+5511A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684438 | |||||||
chr6:75684612 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2075+5685T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684612 | |||||||
chr6:75684626 | A | C | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.2075+5699A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684626 | |||||||
chr6:75684656 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0268 |
2 | HG01070.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.2075+5729C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75684656 | |||||||
chr6:75685003 | A | G | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.2075+6076A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685003 | |||||||
chr6:75685013 | G | A | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+6086G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685013 | |||||||
chr6:75685062 | A | G | 1 | a0001c0004t0003g0179 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2075+6135A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685062 | |||||||
chr6:75685074 | G | A | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+6147G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685074 | |||||||
chr6:75685301 | A | T | 1 | a0001c0001t0001g0249 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2075+6374A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685301 | |||||||
chr6:75685302 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2075+6375G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685302 | |||||||
chr6:75685348 | A | AT | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+6429dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75685348 | ||||||
chr6:75685362 | G | GT | 7 | a0001c0001t0002g0087 a0001c0001t0002g0169 a0001c0001t0003g0056 others(4): Show |
7 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2075+6443dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75685362 | ||||||
chr6:75685377 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2075+6450A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685377 | |||||||
chr6:75685382 | C | T | 4 | a0001c0002t0003g0339 a0001c0002t0003g0350 a0001c0002t0003g0351 others(1): Show |
4 | NA18983.hp1 NA18995.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.2075+6455C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685382 | |||||||
chr6:75685404 | G | A | 1 | a0001c0001t0018g0063 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2075+6477G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685404 | |||||||
chr6:75685507 | T | C | 1 | a0001c0001t0004g0319 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2075+6580T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685507 | |||||||
chr6:75685636 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2075+6709C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685636 | |||||||
chr6:75685648 | C | T | 1 | a0002c0003t0003g0040 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2075+6721C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685648 | |||||||
chr6:75685667 | A | G | 2 | a0002c0003t0003g0054 a0002c0003t0003g0055 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2075+6740A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685667 | |||||||
chr6:75685846 | T | C | 1 | a0001c0001t0002g0113 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2075+6919T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685846 | |||||||
chr6:75685951 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2075+7024C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685951 | |||||||
chr6:75685954 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2075+7027C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75685954 | |||||||
chr6:75686476 | G | C | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2075+7549G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75686476 | |||||||
chr6:75686491 | C | T | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2075+7564C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75686491 | |||||||
chr6:75686653 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2075+7726T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75686653 | |||||||
chr6:75686729 | C | A | 1 | a0001c0001t0005g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2075+7802C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75686729 | |||||||
chr6:75687155 | A | G | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2075+8228A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687155 | |||||||
chr6:75687184 | G | T | 1 | a0001c0001t0001g0281 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2075+8257G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687184 | |||||||
chr6:75687236 | A | G | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2075+8309A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687236 | |||||||
chr6:75687343 | A | G | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2075+8416A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687343 | |||||||
chr6:75687360 | A | G | 8 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(5): Show |
8 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2075+8433A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687360 | |||||||
chr6:75687372 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2076-8432T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687372 | |||||||
chr6:75687436 | C | T | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-8368C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687436 | |||||||
chr6:75687457 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2076-8347A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687457 | |||||||
chr6:75687540 | C | A | 1 | a0001c0001t0002g0169 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2076-8264C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687540 | |||||||
chr6:75687554 | T | C | 6 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(3): Show |
6 | HG00642.hp2 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.2076-8250T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687554 | |||||||
chr6:75687770 | C | T | 3 | a0002c0003t0003g0040 a0002c0003t0003g0044 a0002c0003t0003g0048 |
3 | HG01081.hp2 HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2076-8034C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75687770 | |||||||
chr6:75687960 | C | CAGA | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-7842_2076-784 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75687960 | ||||||
chr6:75688125 | G | T | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.2076-7679G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688125 | |||||||
chr6:75688427 | T | C | 72 | a0001c0001t0002g0001 a0001c0001t0002g0057 a0001c0001t0002g0058 others(69): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.2076-7377T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688427 | |||||||
chr6:75688477 | G | A | 3 | a0003c0007t0006g0168 a0003c0007t0006g0291 a0003c0007t0006g0295 |
3 | HG02109.hp2 HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2076-7327G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688477 | |||||||
chr6:75688493 | G | A | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2076-7311G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688493 | |||||||
chr6:75688507 | T | A | 1 | a0001c0001t0007g0330 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2076-7297T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688507 | |||||||
chr6:75688509 | C | T | 1 | a0001c0001t0007g0330 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2076-7295C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688509 | |||||||
chr6:75688538 | C | A | 1 | a0001c0001t0007g0330 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2076-7266C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688538 | |||||||
chr6:75688539 | A | C | 1 | a0001c0001t0007g0330 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2076-7265A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688539 | |||||||
chr6:75688656 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0242 |
2 | HG02293.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2076-7148A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688656 | |||||||
chr6:75688757 | C | T | 1 | a0001c0001t0013g0185 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2076-7047C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688757 | |||||||
chr6:75688806 | G | A | 2 | a0001c0002t0011g0015 a0001c0002t0011g0020 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2076-6998G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75688806 | |||||||
chr6:75689079 | C | T | 1 | a0001c0001t0005g0162 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2076-6725C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689079 | |||||||
chr6:75689085 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2076-6719G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689085 | |||||||
chr6:75689149 | C | G | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2076-6655C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689149 | |||||||
chr6:75689215 | CAG | C | 8 | a0001c0001t0008g0196 a0001c0001t0008g0210 a0001c0001t0008g0228 others(5): Show |
8 | HG00423.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.2076-6586_2076-658 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75689215 | ||||||
chr6:75689323 | G | T | 1 | a0001c0002t0003g0355 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2076-6481G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689323 | |||||||
chr6:75689423 | A | C | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-6381A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689423 | |||||||
chr6:75689439 | T | C | 1 | a0001c0001t0002g0097 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2076-6365T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689439 | |||||||
chr6:75689448 | A | G | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.2076-6356A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689448 | |||||||
chr6:75689581 | G | A | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-6223G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689581 | |||||||
chr6:75689613 | A | G | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2076-6191A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689613 | |||||||
chr6:75689722 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0265 |
2 | NA18954.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.2076-6082G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689722 | |||||||
chr6:75689733 | A | G | 1 | a0002c0003t0003g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2076-6071A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689733 | |||||||
chr6:75689823 | G | T | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2076-5981G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689823 | |||||||
chr6:75689830 | C | CACAACTT others(21): Show |
1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2076-5973_2076-594 others(32): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75689830 | ||||||
chr6:75689872 | C | A | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2076-5932C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75689872 | |||||||
chr6:75690005 | G | A | 1 | a0001c0001t0002g0114 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2076-5799G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690005 | |||||||
chr6:75690172 | A | G | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-5632A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690172 | |||||||
chr6:75690218 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2076-5586A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690218 | |||||||
chr6:75690683 | G | T | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.2076-5121G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690683 | |||||||
chr6:75690699 | G | GT | 85 | a0001c0001t0001g0242 a0001c0001t0002g0113 a0001c0001t0003g0025 others(82): Show |
86 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.2076-5094dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75690699 | ||||||
chr6:75690729 | T | TGTCACCC others(10): Show |
4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2076-5072_2076-505 others(21): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75690729 | ||||||
chr6:75690730 | G | GT | 44 | a0001c0001t0005g0141 a0001c0002t0003g0003 a0001c0002t0003g0006 others(41): Show |
45 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.2076-5073dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75690730 | ||||||
chr6:75690843 | T | C | 3 | a0001c0001t0001g0275 a0001c0001t0002g0136 a0001c0001t0004g0322 |
3 | HG00673.hp1 HG03017.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.2076-4961T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690843 | |||||||
chr6:75690845 | A | G | 2 | a0001c0001t0002g0136 a0001c0001t0004g0322 |
2 | HG00673.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2076-4959A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690845 | |||||||
chr6:75690851 | A | G | 1 | a0001c0001t0002g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2076-4953A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690851 | |||||||
chr6:75690853 | A | G | 1 | a0001c0001t0002g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2076-4951A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690853 | |||||||
chr6:75690865 | G | T | 1 | a0001c0001t0002g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2076-4939G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75690865 | |||||||
chr6:75691006 | A | AT | 50 | a0001c0001t0001g0244 a0001c0001t0001g0256 a0001c0001t0001g0263 others(47): Show |
51 | HG00423.hp1 HG00609.hp2 HG01891.hp2 others(48): Show |
intron_variant | MODIFIER | c.2076-4780dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75691006 | ||||||
chr6:75691081 | C | T | 1 | a0001c0002t0003g0349 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2076-4723C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691081 | |||||||
chr6:75691143 | A | AT | 8 | a0001c0001t0001g0245 a0001c0001t0001g0280 a0001c0002t0003g0346 others(5): Show |
8 | HG02622.hp2 HG02723.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.2076-4646dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75691143 | ||||||
chr6:75691143 | A | ATT | 28 | a0001c0001t0001g0263 a0001c0002t0003g0003 a0001c0002t0003g0007 others(25): Show |
29 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2076-4647_2076-464 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75691143 | ||||||
chr6:75691143 | A | ATTT | 11 | a0001c0002t0003g0006 a0001c0002t0003g0008 a0001c0002t0003g0009 others(8): Show |
11 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2076-4648_2076-464 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75691143 | ||||||
chr6:75691144 | T | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(118): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2076-4660T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691144 | |||||||
chr6:75691145 | T | A | 3 | a0001c0001t0002g0104 a0001c0001t0002g0107 a0001c0001t0002g0115 |
3 | HG02004.hp1 NA18983.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2076-4659T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691145 | |||||||
chr6:75691158 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2076-4646T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691158 | |||||||
chr6:75691163 | G | A | 1 | a0001c0005t0006g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2076-4641G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691163 | |||||||
chr6:75691494 | A | G | 38 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0001c0004t0003g0174 others(35): Show |
38 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.2076-4310A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691494 | |||||||
chr6:75691559 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2076-4245T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691559 | |||||||
chr6:75691607 | GT | G | 27 | a0001c0001t0004g0311 a0001c0001t0004g0313 a0001c0001t0004g0324 others(24): Show |
27 | HG00438.hp1 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2076-4187delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75691607 | ||||||
chr6:75691610 | T | C | 1 | a0001c0002t0003g0339 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2076-4194T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691610 | |||||||
chr6:75691627 | C | T | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2076-4177C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691627 | |||||||
chr6:75691660 | C | T | 1 | a0001c0001t0023g0143 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2076-4144C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691660 | |||||||
chr6:75691744 | G | A | 1 | a0008c0010t0009g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2076-4060G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691744 | |||||||
chr6:75691796 | G | A | 90 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(87): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2076-4008G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691796 | |||||||
chr6:75691837 | G | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0136 |
2 | HG00140.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2076-3967G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75691837 | |||||||
chr6:75692006 | G | A | 3 | a0003c0007t0006g0168 a0003c0007t0006g0291 a0003c0007t0006g0295 |
3 | HG02109.hp2 HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2076-3798G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692006 | |||||||
chr6:75692145 | C | T | 1 | a0001c0001t0007g0330 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2076-3659C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692145 | |||||||
chr6:75692385 | C | T | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.2076-3419C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692385 | |||||||
chr6:75692467 | C | CA | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-3327dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75692467 | ||||||
chr6:75692508 | T | C | 1 | a0001c0005t0006g0294 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2076-3296T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692508 | |||||||
chr6:75692510 | C | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2076-3294C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692510 | |||||||
chr6:75692516 | A | G | 1 | a0001c0002t0011g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2076-3288A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692516 | |||||||
chr6:75692561 | G | C | 1 | a0001c0004t0003g0179 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2076-3243G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692561 | |||||||
chr6:75692617 | CT | C | 3 | a0001c0001t0002g0072 a0001c0001t0002g0099 a0001c0001t0002g0113 |
3 | HG02165.hp2 NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2076-3184delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75692617 | ||||||
chr6:75692625 | C | T | 1 | a0001c0001t0005g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2076-3179C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692625 | |||||||
chr6:75692717 | G | A | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.2076-3087G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692717 | |||||||
chr6:75692723 | C | T | 3 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0012c0012t0003g0167 |
3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2076-3081C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692723 | |||||||
chr6:75692746 | C | A | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.2076-3058C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692746 | |||||||
chr6:75692791 | C | CA | 20 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(17): Show |
20 | HG02055.hp2 HG02280.hp1 HG02293.hp2 others(17): Show |
intron_variant | MODIFIER | c.2076-3001dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75692791 | ||||||
chr6:75692791 | CA | C | 9 | a0001c0001t0002g0140 a0001c0005t0006g0292 a0001c0005t0006g0293 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-3001delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75692791 | ||||||
chr6:75692812 | C | G | 1 | a0001c0001t0008g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2076-2992C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692812 | |||||||
chr6:75692880 | A | G | 38 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0001c0004t0003g0174 others(35): Show |
38 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.2076-2924A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75692880 | |||||||
chr6:75693044 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2076-2760T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693044 | |||||||
chr6:75693060 | C | A | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2076-2744C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693060 | |||||||
chr6:75693130 | T | G | 3 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 |
3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2076-2674T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693130 | |||||||
chr6:75693189 | A | G | 48 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(45): Show |
48 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.2076-2615A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693189 | |||||||
chr6:75693398 | A | G | 87 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2076-2406A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693398 | |||||||
chr6:75693409 | T | A | 1 | a0008c0010t0009g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2076-2395T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693409 | |||||||
chr6:75693409 | T | TA | 30 | a0001c0001t0001g0191 a0001c0001t0002g0069 a0001c0001t0002g0095 others(27): Show |
30 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.2076-2375dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75693409 | ||||||
chr6:75693409 | T | TAA | 43 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(40): Show |
44 | HG00423.hp1 HG00609.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.2076-2376_2076-237 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75693409 | ||||||
chr6:75693409 | TA | T | 9 | a0001c0001t0001g0218 a0001c0001t0001g0256 a0001c0001t0001g0280 others(6): Show |
9 | HG01069.hp1 HG01109.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-2375delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75693409 | ||||||
chr6:75693426 | A | G | 1 | a0001c0001t0002g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2076-2378A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693426 | |||||||
chr6:75693428 | A | AC | 8 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2076-2376_2076-237 others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693428 | |||||||
chr6:75693429 | A | C | 1 | a0001c0001t0020g0253 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2076-2375A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693429 | |||||||
chr6:75693541 | A | G | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2076-2263A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693541 | |||||||
chr6:75693568 | CTG | C | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2076-2232_2076-223 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr6 | 75693568 | ||||||
chr6:75693592 | C | T | 1 | a0001c0001t0002g0071 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2076-2212C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693592 | |||||||
chr6:75693838 | A | G | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2076-1966A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693838 | |||||||
chr6:75693946 | AT | A | 4 | a0001c0001t0008g0196 a0001c0001t0008g0243 a0001c0001t0008g0259 others(1): Show |
4 | HG00423.hp2 HG02155.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.2076-1857delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693946 | |||||||
chr6:75693958 | A | G | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2076-1846A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693958 | |||||||
chr6:75693965 | C | A | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2076-1839C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693965 | |||||||
chr6:75693994 | C | T | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2076-1810C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75693994 | |||||||
chr6:75694040 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2076-1764T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694040 | |||||||
chr6:75694074 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2076-1730T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694074 | |||||||
chr6:75694171 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0274 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2076-1633G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694171 | |||||||
chr6:75694314 | T | C | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-1490T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694314 | |||||||
chr6:75694344 | T | G | 1 | a0001c0001t0004g0312 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2076-1460T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694344 | |||||||
chr6:75694486 | T | G | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2076-1318T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694486 | |||||||
chr6:75694987 | A | G | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-817A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694987 | |||||||
chr6:75694989 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0217 a0001c0001t0001g0234 |
3 | HG01884.hp2 HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2076-815C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75694989 | |||||||
chr6:75695032 | A | G | 254 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(251): Show |
257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.2076-772A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695032 | |||||||
chr6:75695095 | T | C | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2076-709T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695095 | |||||||
chr6:75695125 | C | T | 2 | a0001c0001t0004g0305 a0001c0001t0004g0306 |
2 | HG01928.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2076-679C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695125 | |||||||
chr6:75695231 | C | T | 1 | a0001c0001t0003g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2076-573C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695231 | |||||||
chr6:75695238 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2076-566G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695238 | |||||||
chr6:75695512 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2076-292G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695512 | |||||||
chr6:75695589 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0202 |
2 | HG00642.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2076-215T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695589 | |||||||
chr6:75695644 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2076-160G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 16/23 | chr6 | 75695644 | |||||||
chr6:75695984 | A | G | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2195+61A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75695984 | |||||||
chr6:75696098 | G | C | 1 | a0001c0001t0023g0143 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2195+175G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696098 | |||||||
chr6:75696284 | G | A | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2195+361G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696284 | |||||||
chr6:75696285 | T | G | 1 | a0001c0001t0001g0235 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2195+362T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696285 | |||||||
chr6:75696315 | T | A | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2195+392T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696315 | |||||||
chr6:75696316 | A | T | 3 | a0001c0001t0002g0123 a0001c0002t0003g0349 a0001c0002t0003g0356 |
3 | NA18947.hp2 NA18982.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2195+393A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696316 | |||||||
chr6:75696370 | C | T | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2195+447C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696370 | |||||||
chr6:75696626 | G | A | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG00738.hp2 HG01169.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.2195+703G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696626 | |||||||
chr6:75696835 | T | A | 1 | a0001c0001t0001g0276 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2196-590T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696835 | |||||||
chr6:75696836 | A | C | 1 | a0001c0001t0001g0276 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2196-589A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696836 | |||||||
chr6:75696837 | A | ACTAGATC others(5): Show |
1 | a0001c0001t0001g0276 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2196-588_2196-587i others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75696837 | |||||||
chr6:75697041 | C | T | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2196-384C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75697041 | |||||||
chr6:75697375 | T | G | 1 | a0001c0001t0010g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2196-50T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 17/23 | chr6 | 75697375 | |||||||
chr6:75697566 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2288+49T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75697566 | |||||||
chr6:75697641 | C | T | 7 | a0001c0002t0003g0016 a0001c0002t0003g0017 a0001c0002t0003g0018 others(4): Show |
7 | HG02630.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2288+124C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75697641 | |||||||
chr6:75697808 | C | T | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2288+291C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75697808 | |||||||
chr6:75697897 | G | A | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2288+380G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75697897 | |||||||
chr6:75697904 | A | G | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.2288+387A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75697904 | |||||||
chr6:75698341 | A | G | 1 | a0002c0003t0003g0046 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2288+824A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698341 | |||||||
chr6:75698407 | C | T | 4 | a0001c0002t0003g0337 a0001c0002t0003g0341 a0001c0002t0003g0349 others(1): Show |
4 | NA18947.hp2 NA18968.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2288+890C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698407 | |||||||
chr6:75698452 | T | G | 1 | a0001c0001t0001g0281 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2288+935T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698452 | |||||||
chr6:75698473 | G | A | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2288+956G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698473 | |||||||
chr6:75698485 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+968T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698485 | |||||||
chr6:75698495 | A | AT | 27 | a0001c0001t0001g0275 a0001c0001t0005g0141 a0001c0001t0005g0144 others(24): Show |
27 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.2288+990dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75698495 | ||||||
chr6:75698529 | C | T | 25 | a0001c0002t0003g0003 a0001c0002t0003g0170 a0001c0002t0003g0337 others(22): Show |
26 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2288+1012C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698529 | |||||||
chr6:75698581 | A | C | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2288+1064A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698581 | |||||||
chr6:75698767 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2288+1250T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698767 | |||||||
chr6:75698785 | C | T | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2288+1268C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75698785 | |||||||
chr6:75699006 | A | G | 1 | a0001c0001t0002g0119 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2288+1489A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699006 | |||||||
chr6:75699010 | C | CA | 11 | a0001c0001t0001g0242 a0001c0001t0004g0332 a0001c0004t0003g0174 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.2288+1506dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699010 | ||||||
chr6:75699072 | A | G | 1 | a0001c0001t0004g0313 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2288+1555A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699072 | |||||||
chr6:75699095 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+1578G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699095 | |||||||
chr6:75699212 | G | C | 3 | a0001c0001t0003g0056 a0001c0001t0003g0166 a0012c0012t0003g0167 |
3 | HG02559.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2288+1695G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699212 | |||||||
chr6:75699221 | C | CTAAGTGA others(7): Show |
37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+1704_2288+170 others(18): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699221 | |||||||
chr6:75699222 | C | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+1705C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699222 | |||||||
chr6:75699224 | C | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+1707C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699224 | |||||||
chr6:75699234 | G | A | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2288+1717G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699234 | |||||||
chr6:75699259 | T | C | 1 | a0001c0001t0004g0313 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2288+1742T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699259 | |||||||
chr6:75699269 | G | A | 24 | a0001c0002t0003g0003 a0001c0002t0003g0337 a0001c0002t0003g0338 others(21): Show |
25 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.2288+1752G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699269 | |||||||
chr6:75699354 | C | CT | 14 | a0001c0001t0001g0257 a0001c0001t0001g0273 a0001c0001t0008g0254 others(11): Show |
14 | HG00741.hp1 HG01106.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2288+1857dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | ||||||
chr6:75699354 | C | CTT | 42 | a0001c0001t0002g0004 a0001c0001t0002g0062 a0001c0001t0002g0091 others(39): Show |
42 | HG00738.hp1 HG01069.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.2288+1856_2288+185 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | ||||||
chr6:75699354 | C | CTTT | 88 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0057 others(85): Show |
89 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.2288+1855_2288+185 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | ||||||
chr6:75699354 | C | CTTTT | 32 | a0001c0001t0002g0069 a0001c0001t0002g0086 a0001c0001t0002g0093 others(29): Show |
33 | HG00609.hp2 HG00741.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.2288+1854_2288+185 others(8): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | ||||||
chr6:75699354 | CT | C | 6 | a0001c0001t0001g0209 a0001c0001t0001g0211 a0001c0001t0001g0219 others(3): Show |
6 | HG00438.hp2 HG01070.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2288+1857delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | ||||||
chr6:75699354 | CTTT | C | 37 | a0001c0001t0002g0139 a0001c0001t0004g0002 a0001c0001t0004g0301 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2288+1855_2288+185 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | ||||||
chr6:75699354 | CTTTTT | C | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2288+1853_2288+185 others(9): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | ||||||
chr6:75699354 | CTTTTTT | C | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2288+1852_2288+185 others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75699354 | ||||||
chr6:75699396 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2288+1879C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699396 | |||||||
chr6:75699645 | G | A | 1 | a0001c0002t0003g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2288+2128G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699645 | |||||||
chr6:75699660 | G | A | 10 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2288+2143G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75699660 | |||||||
chr6:75700082 | T | A | 15 | a0001c0001t0004g0302 a0001c0001t0004g0307 a0001c0001t0004g0309 others(12): Show |
15 | HG00408.hp2 HG00597.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.2289-2563T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700082 | |||||||
chr6:75700099 | T | C | 1 | a0001c0001t0002g0113 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2289-2546T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700099 | |||||||
chr6:75700171 | A | AT | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2289-2473dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75700171 | ||||||
chr6:75700203 | G | A | 1 | a0011c0011t0003g0344 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2289-2442G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700203 | |||||||
chr6:75700525 | C | T | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2289-2120C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700525 | |||||||
chr6:75700546 | G | A | 3 | a0001c0001t0005g0163 a0001c0001t0005g0164 a0001c0001t0005g0165 |
3 | HG01069.hp1 HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2289-2099G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700546 | |||||||
chr6:75700611 | A | C | 1 | a0001c0001t0002g0111 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2289-2034A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700611 | |||||||
chr6:75700637 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2289-2008C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75700637 | |||||||
chr6:75701217 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2289-1428C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701217 | |||||||
chr6:75701232 | A | G | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2289-1413A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701232 | |||||||
chr6:75701259 | A | G | 1 | a0001c0001t0010g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2289-1386A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701259 | |||||||
chr6:75701315 | G | A | 3 | a0001c0001t0002g0072 a0001c0001t0002g0099 a0001c0001t0002g0113 |
3 | HG02165.hp2 NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2289-1330G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701315 | |||||||
chr6:75701362 | G | T | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2289-1283G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701362 | |||||||
chr6:75701589 | GA | G | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2289-1050delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701589 | ||||||
chr6:75701633 | C | CT | 161 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0194 others(158): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.2289-989dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | ||||||
chr6:75701633 | C | CTT | 33 | a0001c0001t0001g0191 a0001c0001t0001g0203 a0001c0001t0001g0220 others(30): Show |
33 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.2289-990_2289-989d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | ||||||
chr6:75701633 | C | CTTT | 79 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(76): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.2289-991_2289-989d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | ||||||
chr6:75701633 | C | CTTTT | 29 | a0001c0001t0002g0066 a0001c0001t0002g0071 a0001c0001t0002g0085 others(26): Show |
30 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.2289-992_2289-989d others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | ||||||
chr6:75701633 | C | CTTTTT | 11 | a0001c0001t0004g0309 a0001c0001t0004g0313 a0001c0001t0004g0318 others(8): Show |
11 | HG00597.hp1 HG02040.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.2289-993_2289-989d others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | ||||||
chr6:75701633 | C | CTTTTTT | 9 | a0001c0001t0004g0302 a0001c0001t0004g0307 a0001c0001t0004g0315 others(6): Show |
9 | HG00408.hp2 NA18941.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.2289-994_2289-989d others(8): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | ||||||
chr6:75701633 | CT | C | 7 | a0001c0002t0003g0016 a0001c0002t0003g0017 a0001c0002t0003g0018 others(4): Show |
7 | HG02630.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2289-989delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75701633 | ||||||
chr6:75701660 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2289-985G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701660 | |||||||
chr6:75701670 | C | T | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2289-975C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701670 | |||||||
chr6:75701678 | C | T | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2289-967C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701678 | |||||||
chr6:75701733 | G | A | 14 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(11): Show |
14 | HG01243.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2289-912G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701733 | |||||||
chr6:75701765 | A | G | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2289-880A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701765 | |||||||
chr6:75701929 | C | T | 27 | a0001c0001t0002g0062 a0001c0001t0005g0141 a0001c0001t0005g0144 others(24): Show |
27 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.2289-716C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75701929 | |||||||
chr6:75702007 | C | T | 5 | a0001c0001t0005g0147 a0001c0001t0005g0153 a0001c0001t0005g0154 others(2): Show |
5 | HG00642.hp1 HG01256.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.2289-638C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702007 | |||||||
chr6:75702064 | CAAG | C | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2289-578_2289-576d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75702064 | ||||||
chr6:75702084 | G | A | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2289-561G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702084 | |||||||
chr6:75702127 | G | A | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2289-518G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702127 | |||||||
chr6:75702218 | C | CT | 103 | a0001c0001t0001g0276 a0001c0001t0001g0285 a0001c0001t0002g0001 others(100): Show |
104 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.2289-412dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75702218 | ||||||
chr6:75702218 | CT | C | 49 | a0001c0001t0001g0195 a0001c0001t0004g0002 a0001c0001t0004g0301 others(46): Show |
50 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.2289-412delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr6 | 75702218 | ||||||
chr6:75702359 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2289-286G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702359 | |||||||
chr6:75702456 | G | A | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2289-189G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702456 | |||||||
chr6:75702513 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2289-132C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 18/23 | chr6 | 75702513 | |||||||
chr6:75703122 | A | AT | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2716+56dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75703122 | ||||||
chr6:75703180 | G | A | 3 | a0001c0001t0001g0206 a0001c0001t0001g0217 a0001c0001t0001g0234 |
3 | HG01884.hp2 HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2716+108G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703180 | |||||||
chr6:75703182 | G | A | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2716+110G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703182 | |||||||
chr6:75703226 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2716+154C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703226 | |||||||
chr6:75703243 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2716+171G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703243 | |||||||
chr6:75703263 | G | A | 1 | a0001c0001t0013g0185 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2716+191G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703263 | |||||||
chr6:75703276 | C | G | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2716+204C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703276 | |||||||
chr6:75703276 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2716+204C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703276 | |||||||
chr6:75703293 | C | CA | 38 | a0001c0001t0002g0128 a0001c0001t0004g0002 a0001c0001t0004g0301 others(35): Show |
39 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2716+230dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75703293 | ||||||
chr6:75703362 | A | G | 22 | a0001c0001t0002g0077 a0001c0001t0002g0103 a0001c0001t0002g0104 others(19): Show |
22 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.2716+290A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703362 | |||||||
chr6:75703638 | G | T | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2716+566G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703638 | |||||||
chr6:75703738 | G | A | 3 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0024 |
3 | HG03041.hp2 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2716+666G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703738 | |||||||
chr6:75703781 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2716+709A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703781 | |||||||
chr6:75703962 | T | A | 1 | a0001c0001t0002g0124 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2716+890T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703962 | |||||||
chr6:75703993 | A | G | 36 | a0001c0001t0001g0275 a0001c0004t0003g0174 a0001c0004t0003g0175 others(33): Show |
36 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.2716+921A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75703993 | |||||||
chr6:75704101 | A | G | 1 | a0009c0018t0001g0237 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2716+1029A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704101 | |||||||
chr6:75704115 | G | A | 254 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(251): Show |
257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.2716+1043G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704115 | |||||||
chr6:75704407 | G | A | 3 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 |
3 | HG03139.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2716+1335G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704407 | |||||||
chr6:75704434 | A | G | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2716+1362A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704434 | |||||||
chr6:75704465 | A | G | 1 | a0001c0001t0002g0138 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2716+1393A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704465 | |||||||
chr6:75704543 | G | A | 25 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2716+1471G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704543 | |||||||
chr6:75704617 | G | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2716+1545G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704617 | |||||||
chr6:75704787 | C | T | 1 | a0001c0002t0003g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2716+1715C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704787 | |||||||
chr6:75704939 | G | T | 1 | a0001c0001t0002g0083 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2716+1867G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704939 | |||||||
chr6:75704950 | A | G | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2716+1878A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75704950 | |||||||
chr6:75705027 | G | A | 1 | a0001c0002t0003g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2716+1955G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705027 | |||||||
chr6:75705232 | C | G | 1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2716+2160C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705232 | |||||||
chr6:75705279 | G | A | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2716+2207G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705279 | |||||||
chr6:75705285 | G | A | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2716+2213G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705285 | |||||||
chr6:75705416 | C | A | 1 | a0001c0001t0002g0128 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2716+2344C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705416 | |||||||
chr6:75705440 | G | A | 8 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(5): Show |
8 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2716+2368G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705440 | |||||||
chr6:75705492 | T | C | 254 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(251): Show |
257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.2716+2420T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705492 | |||||||
chr6:75705530 | C | T | 38 | a0001c0001t0001g0199 a0001c0001t0004g0002 a0001c0001t0004g0301 others(35): Show |
39 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2716+2458C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705530 | |||||||
chr6:75705554 | A | T | 3 | a0001c0002t0003g0014 a0001c0002t0003g0337 a0001c0002t0003g0341 |
3 | HG01891.hp2 NA18968.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2716+2482A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705554 | |||||||
chr6:75705558 | A | T | 91 | a0001c0001t0001g0251 a0001c0001t0001g0276 a0001c0001t0002g0001 others(88): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.2716+2486A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705558 | |||||||
chr6:75705562 | T | A | 31 | a0001c0001t0001g0214 a0001c0001t0002g0118 a0001c0004t0014g0052 others(28): Show |
31 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2716+2490T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705562 | |||||||
chr6:75705566 | T | A | 2 | a0001c0004t0014g0052 a0012c0012t0003g0167 |
2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2716+2494T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705566 | |||||||
chr6:75705652 | A | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2716+2580A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705652 | |||||||
chr6:75705731 | ATTTTTC | A | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2716+2662_2716+266 others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75705731 | ||||||
chr6:75705923 | GC | G | 35 | a0001c0001t0010g0183 a0001c0001t0010g0184 a0001c0001t0013g0185 others(32): Show |
36 | HG00609.hp2 HG01891.hp2 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.2716+2853delC | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75705923 | ||||||
chr6:75705924 | C | CT | 12 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0002t0003g0016 others(9): Show |
12 | HG02056.hp1 HG02132.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | C | CTT | 5 | a0001c0002t0003g0017 a0001c0002t0009g0171 a0001c0002t0011g0020 others(2): Show |
5 | HG02630.hp1 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | C | CTTT | 3 | a0001c0002t0009g0010 a0001c0002t0009g0012 a0001c0002t0009g0172 |
3 | HG02486.hp2 HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | C | CTTTTTTT others(5): Show |
1 | a0002c0003t0003g0053 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | C | CTTTTTTT others(6): Show |
2 | a0002c0003t0003g0039 a0002c0003t0003g0043 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0003g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(19): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | C | CTTTTTTT others(10): Show |
1 | a0002c0003t0003g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(21): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | C | CTTTTTTT others(12): Show |
4 | a0002c0003t0003g0029 a0002c0003t0003g0045 a0002c0003t0003g0048 others(1): Show |
4 | HG00741.hp1 HG01074.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(23): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | C | CTTTTTTT others(13): Show |
1 | a0002c0003t0003g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(24): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | C | CTTTTTTT others(14): Show |
1 | a0001c0004t0003g0179 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(25): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | C | CTTTTTTT others(16): Show |
3 | a0002c0003t0003g0042 a0002c0003t0003g0054 a0002c0003t0003g0055 |
3 | HG01243.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2716+2852_2716+285 others(27): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | C | CTTTTTTT others(22): Show |
1 | a0002c0003t0003g0046 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2716+2852_2716+285 others(33): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | CCT | C | 13 | a0001c0001t0005g0148 a0001c0001t0005g0158 a0001c0001t0005g0159 others(10): Show |
13 | HG00280.hp2 HG01109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2716+2853_2716+285 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | CCTT | C | 19 | a0001c0001t0003g0056 a0001c0001t0005g0141 a0001c0001t0005g0144 others(16): Show |
19 | HG00642.hp1 HG01069.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.2716+2853_2716+285 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | CCTTTTTT others(2): Show |
C | 11 | a0001c0001t0002g0001 a0001c0001t0002g0069 a0001c0001t0002g0102 others(8): Show |
11 | HG02572.hp1 HG02738.hp2 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.2716+2853_2716+286 others(13): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | CCTTTTTT others(3): Show |
C | 114 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(111): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2716+2853_2716+286 others(14): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | CCTTTTTT others(4): Show |
C | 2 | a0001c0001t0002g0060 a0001c0001t0002g0128 |
2 | NA18954.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2716+2853_2716+286 others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | CCTTTTTT others(5): Show |
C | 2 | a0001c0008t0003g0186 a0001c0008t0003g0187 |
2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2716+2853_2716+286 others(16): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705924 | CCTTTTTT others(11): Show |
C | 2 | a0001c0002t0003g0345 a0001c0002t0021g0342 |
2 | NA18966.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.2716+2853_2716+287 others(22): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705924 | |||||||
chr6:75705925 | C | CT | 25 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0198 others(22): Show |
25 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.2716+2882dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75705925 | ||||||
chr6:75705925 | C | T | 52 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(49): Show |
52 | HG00423.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.2716+2853C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705925 | |||||||
chr6:75705925 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0219 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2716+2870_2716+288 others(17): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75705925 | ||||||
chr6:75705933 | T | G | 1 | a0001c0004t0014g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2716+2861T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705933 | |||||||
chr6:75705957 | G | A | 89 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2716+2885G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705957 | |||||||
chr6:75705958 | A | G | 1 | a0001c0002t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2716+2886A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705958 | |||||||
chr6:75705961 | G | A | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2716+2889G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705961 | |||||||
chr6:75705967 | C | T | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2716+2895C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75705967 | |||||||
chr6:75706019 | C | T | 1 | a0001c0004t0003g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2716+2947C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706019 | |||||||
chr6:75706099 | A | C | 4 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0109 others(1): Show |
4 | NA18955.hp1 NA18974.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2716+3027A>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706099 | |||||||
chr6:75706256 | G | C | 1 | a0001c0001t0001g0213 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2716+3184G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706256 | |||||||
chr6:75706419 | T | C | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2717-3108T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706419 | |||||||
chr6:75706570 | A | G | 3 | a0001c0001t0002g0072 a0001c0001t0002g0099 a0001c0001t0002g0113 |
3 | HG02165.hp2 NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2717-2957A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706570 | |||||||
chr6:75706600 | T | C | 9 | a0001c0001t0001g0190 a0001c0001t0001g0205 a0001c0001t0001g0216 others(6): Show |
9 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.2717-2927T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706600 | |||||||
chr6:75706678 | T | TAA | 19 | a0001c0001t0005g0144 a0001c0001t0005g0145 a0001c0001t0005g0146 others(16): Show |
19 | HG00280.hp2 HG00642.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.2717-2849_2717-284 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706678 | |||||||
chr6:75706939 | G | A | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2717-2588G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75706939 | |||||||
chr6:75707023 | C | A | 9 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2717-2504C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707023 | |||||||
chr6:75707027 | TG | T | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2717-2499delG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707027 | |||||||
chr6:75707355 | C | CT | 56 | a0001c0001t0001g0197 a0001c0001t0001g0219 a0001c0001t0001g0236 others(53): Show |
57 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.2717-2146dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | ||||||
chr6:75707355 | C | CTT | 10 | a0001c0001t0001g0218 a0001c0001t0001g0264 a0001c0001t0003g0056 others(7): Show |
10 | HG02056.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2717-2147_2717-214 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | ||||||
chr6:75707355 | C | CTTT | 8 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(5): Show |
8 | HG02293.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2717-2148_2717-214 others(7): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | ||||||
chr6:75707355 | CT | C | 67 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0268 others(64): Show |
67 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.2717-2146delT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | ||||||
chr6:75707355 | CTT | C | 22 | a0001c0002t0003g0003 a0001c0002t0003g0337 a0001c0002t0003g0338 others(19): Show |
23 | HG00423.hp1 HG00609.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.2717-2147_2717-214 others(6): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | ||||||
chr6:75707355 | CTTTTTT | C | 83 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2717-2151_2717-214 others(10): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707355 | ||||||
chr6:75707597 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG01106.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2717-1930A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707597 | |||||||
chr6:75707677 | T | G | 1 | a0001c0001t0020g0253 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2717-1850T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707677 | |||||||
chr6:75707724 | GAAGTT | G | 3 | a0001c0001t0002g0072 a0001c0001t0002g0099 a0001c0001t0002g0113 |
3 | HG02165.hp2 NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2717-1799_2717-179 others(9): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr6 | 75707724 | ||||||
chr6:75707924 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2717-1603C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707924 | |||||||
chr6:75707988 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2717-1539A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75707988 | |||||||
chr6:75708029 | T | G | 37 | a0001c0001t0004g0002 a0001c0001t0004g0301 a0001c0001t0004g0302 others(34): Show |
38 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.2717-1498T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708029 | |||||||
chr6:75708070 | C | A | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2717-1457C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708070 | |||||||
chr6:75708101 | C | T | 1 | a0001c0002t0003g0347 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2717-1426C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708101 | |||||||
chr6:75708270 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2717-1257C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708270 | |||||||
chr6:75708333 | A | G | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2717-1194A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708333 | |||||||
chr6:75708350 | TATTAACT others(4): Show |
T | 9 | a0001c0001t0007g0303 a0001c0001t0007g0304 a0001c0001t0007g0308 others(6): Show |
9 | HG01975.hp2 NA18946.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.2717-1176_2717-116 others(15): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708350 | |||||||
chr6:75708362 | C | G | 9 | a0001c0001t0007g0303 a0001c0001t0007g0304 a0001c0001t0007g0308 others(6): Show |
9 | HG01975.hp2 NA18946.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.2717-1165C>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708362 | |||||||
chr6:75708630 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2717-897C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708630 | |||||||
chr6:75708812 | C | T | 1 | a0001c0001t0004g0312 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2717-715C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708812 | |||||||
chr6:75708872 | C | T | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2717-655C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75708872 | |||||||
chr6:75709061 | A | G | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2717-466A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709061 | |||||||
chr6:75709073 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2717-454A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709073 | |||||||
chr6:75709123 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2717-404G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709123 | |||||||
chr6:75709245 | T | C | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2717-282T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709245 | |||||||
chr6:75709283 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2717-244G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709283 | |||||||
chr6:75709337 | A | T | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2717-190A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709337 | |||||||
chr6:75709471 | T | G | 4 | a0002c0003t0003g0034 a0002c0003t0003g0035 a0002c0003t0003g0036 others(1): Show |
4 | HG02056.hp1 NA18941.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.2717-56T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 19/23 | chr6 | 75709471 | |||||||
chr6:75709873 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2820+243G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75709873 | |||||||
chr6:75709932 | G | T | 1 | a0001c0016t0006g0298 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2820+302G>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75709932 | |||||||
chr6:75710008 | C | T | 356 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(353): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.2820+378C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710008 | |||||||
chr6:75710020 | C | T | 35 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(32): Show |
35 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2820+390C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710020 | |||||||
chr6:75710196 | T | TC | 45 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0007 others(42): Show |
46 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.2820+567dupC | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr6 | 75710196 | ||||||
chr6:75710256 | T | A | 10 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG02293.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2820+626T>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710256 | |||||||
chr6:75710563 | T | C | 1 | a0001c0001t0002g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2821-765T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710563 | |||||||
chr6:75710702 | A | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0245 |
2 | NA18975.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2821-626A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710702 | |||||||
chr6:75710721 | A | G | 1 | a0002c0003t0003g0033 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2821-607A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710721 | |||||||
chr6:75710895 | C | T | 1 | a0001c0002t0003g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2821-433C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75710895 | |||||||
chr6:75711187 | T | C | 2 | a0001c0001t0004g0313 a0001c0001t0004g0326 |
2 | NA18966.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2821-141T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75711187 | |||||||
chr6:75711192 | AGT | A | 4 | a0001c0001t0010g0183 a0001c0001t0010g0184 a0001c0001t0010g0188 others(1): Show |
4 | HG02622.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2821-133_2821-132d others(4): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr6 | 75711192 | ||||||
chr6:75711287 | A | G | 35 | a0001c0004t0003g0174 a0001c0004t0003g0175 a0001c0004t0003g0176 others(32): Show |
35 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.2821-41A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 20/23 | chr6 | 75711287 | |||||||
chr6:75711496 | A | T | 1 | a0001c0002t0009g0010 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2909+80A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75711496 | |||||||
chr6:75711819 | C | T | 26 | a0001c0001t0005g0141 a0001c0001t0005g0144 a0001c0001t0005g0145 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2909+403C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75711819 | |||||||
chr6:75711924 | G | C | 209 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(206): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2909+508G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75711924 | |||||||
chr6:75712094 | A | G | 1 | a0003c0007t0006g0295 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2909+678A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712094 | |||||||
chr6:75712102 | G | GAGT | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2909+688_2909+690d others(5): Show |
SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr6 | 75712102 | ||||||
chr6:75712140 | G | A | 1 | a0001c0001t0004g0335 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2909+724G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712140 | |||||||
chr6:75712327 | T | C | 1 | a0001c0001t0004g0312 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2909+911T>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712327 | |||||||
chr6:75712521 | T | TA | 12 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(9): Show |
12 | HG02293.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2910-980dupA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr6 | 75712521 | ||||||
chr6:75712531 | A | T | 9 | a0001c0005t0006g0292 a0001c0005t0006g0293 a0001c0005t0006g0294 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2910-982A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712531 | |||||||
chr6:75712569 | A | AT | 5 | a0002c0003t0003g0029 a0002c0003t0003g0039 a0002c0003t0003g0041 others(2): Show |
5 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2910-936dupT | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr6 | 75712569 | ||||||
chr6:75712678 | A | G | 1 | a0001c0004t0003g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2910-835A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712678 | |||||||
chr6:75712700 | G | C | 1 | a0001c0001t0004g0324 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2910-813G>C | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712700 | |||||||
chr6:75712735 | GA | G | 8 | a0001c0001t0004g0309 a0001c0001t0004g0320 a0001c0001t0004g0323 others(5): Show |
8 | HG00408.hp2 HG00597.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.2910-768delA | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr6 | 75712735 | ||||||
chr6:75712756 | A | G | 1 | a0001c0017t0002g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2910-757A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712756 | |||||||
chr6:75712952 | C | A | 24 | a0002c0003t0003g0029 a0002c0003t0003g0030 a0002c0003t0003g0031 others(21): Show |
24 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.2910-561C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75712952 | |||||||
chr6:75713028 | G | A | 8 | a0001c0001t0001g0190 a0001c0001t0001g0205 a0001c0001t0001g0216 others(5): Show |
8 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2910-485G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75713028 | |||||||
chr6:75713348 | C | T | 2 | a0001c0001t0003g0056 a0012c0012t0003g0167 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2910-165C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75713348 | |||||||
chr6:75713349 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2910-164G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75713349 | |||||||
chr6:75713487 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0221 |
2 | NA19065.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2910-26G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 21/23 | chr6 | 75713487 | |||||||
chr6:75713638 | A | G | 2 | a0001c0001t0004g0305 a0001c0001t0004g0306 |
2 | HG01928.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2979-37A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 22/23 | chr6 | 75713638 | |||||||
chr6:75713878 | G | A | 2 | a0001c0008t0003g0186 a0001c0008t0003g0187 |
2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3129+53G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75713878 | |||||||
chr6:75714585 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3129+760A>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714585 | |||||||
chr6:75714658 | A | T | 103 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.3130-727A>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714658 | |||||||
chr6:75714802 | TG | T | 26 | a0001c0002t0003g0003 a0001c0002t0003g0023 a0001c0002t0003g0170 others(23): Show |
27 | HG00423.hp1 HG00609.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.3130-582delG | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714802 | |||||||
chr6:75714803 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3130-582G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714803 | |||||||
chr6:75714809 | T | G | 1 | a0001c0001t0002g0169 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3130-576T>G | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714809 | |||||||
chr6:75714818 | C | A | 1 | a0012c0012t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3130-567C>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714818 | |||||||
chr6:75714847 | C | T | 1 | a0001c0016t0006g0298 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3130-538C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714847 | |||||||
chr6:75714972 | G | A | 1 | a0001c0001t0003g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3130-413G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75714972 | |||||||
chr6:75715141 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3130-244G>A | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75715141 | |||||||
chr6:75715312 | C | T | 2 | a0002c0003t0003g0047 a0002c0003t0003g0050 |
2 | HG01074.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3130-73C>T | SENP6 | ENSG00000112701.18 | transcript | ENST00000447266.7 | protein_coding | 23/23 | chr6 | 75715312 |