Item | Value |
---|---|
geneid | 6491 |
ensemblid | ENSG00000123473.17 |
hgncid | 10879 |
symbol | STIL |
name | STIL centriolar assembly protein |
refseq_nuc | NM_001048166.1 |
refseq_prot | NP_001041631.1 |
ensembl_nuc | ENST00000371877.8 |
ensembl_prot | ENSP00000360944.3 |
mane_status | MANE Select |
chr | chr1 |
start | 47250139 |
end | 47314147 |
strand | - |
ver | v1.2 |
region | chr1:47250139-47314147 |
region5000 | chr1:47245139-47319147 |
regionname0 | STIL_chr1_47250139_47314147 |
regionname5000 | STIL_chr1_47245139_47319147 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1288 | 193 | 59 | 22 | 99 | 3 | 10 | 79 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0002 | 1/1 | 1288 | 124 | 4 | 25 | 71 | 7 | 15 | 58 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0003 | 0/0 | 1288 | 57 | 23 | 13 | 2 | 5 | 14 | 0 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0004 | 0/0 | 1288 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0005 | 0/0 | 1288 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0006 | 0/0 | 1288 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0007 | 0/0 | 1288 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0008 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0009 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0010 | 0/0 | 1288 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0011 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0012 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0013 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0014 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
a0015 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | MEPIY others(1283): Show |
chr1 | 47245139 | 47319147 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 3864 | 99 | 33 | 4 | 56 | 0 | 6 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0001c0003 | 0/0 | 3864 | 94 | 26 | 18 | 43 | 3 | 4 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0002c0001 | 0/1 | 3864 | 122 | 4 | 25 | 70 | 7 | 15 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0002c0009 | 1/0 | 3864 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0002c0011 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0003c0004 | 0/0 | 3864 | 56 | 23 | 13 | 2 | 5 | 13 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0003c0015 | 0/0 | 3864 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0004c0005 | 0/0 | 3864 | 4 | 4 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0005c0007 | 0/0 | 3864 | 2 | 2 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0005c0017 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0006c0006 | 0/0 | 3864 | 2 | 0 | 0 | 2 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0007c0010 | 0/0 | 3864 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0008c0016 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0009c0013 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0010c0019 | 0/0 | 3864 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0011c0018 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0012c0012 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0013c0020 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0014c0008 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 | ||
a0015c0014 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | ATGGA others(3859): Show |
chr1 | 47245139 | 47319147 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 5019 | 67 | 3 | 3 | 55 | 0 | 6 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0001c0002t0003 | 0/0 | 5019 | 26 | 25 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0001c0002t0004 | 0/0 | 5019 | 5 | 5 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0001c0002t0012 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0001c0003t0001 | 0/0 | 5019 | 90 | 24 | 17 | 42 | 3 | 4 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0001c0003t0006 | 0/0 | 5019 | 2 | 2 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0001c0003t0007 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0001c0003t0010 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0002c0001t0002 | 0/1 | 5017 | 115 | 3 | 25 | 65 | 6 | 15 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5012): Show |
chr1 | 47245139 | 47319147 |
a0002c0001t0005 | 0/0 | 5017 | 3 | 0 | 0 | 3 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5012): Show |
chr1 | 47245139 | 47319147 |
a0002c0001t0009 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5012): Show |
chr1 | 47245139 | 47319147 |
a0002c0001t0011 | 0/0 | 5017 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5012): Show |
chr1 | 47245139 | 47319147 |
a0002c0001t0013 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5012): Show |
chr1 | 47245139 | 47319147 |
a0002c0001t0015 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5012): Show |
chr1 | 47245139 | 47319147 |
a0002c0009t0001 | 1/0 | 5019 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0002c0011t0002 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5012): Show |
chr1 | 47245139 | 47319147 |
a0003c0004t0001 | 0/0 | 5019 | 55 | 23 | 12 | 2 | 5 | 13 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0003c0004t0014 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0003c0015t0001 | 0/0 | 5019 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0004c0005t0002 | 0/0 | 5017 | 4 | 4 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5012): Show |
chr1 | 47245139 | 47319147 |
a0005c0007t0004 | 0/0 | 5019 | 2 | 2 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0005c0017t0004 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0006c0006t0001 | 0/0 | 5019 | 2 | 0 | 0 | 2 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0007c0010t0002 | 0/0 | 5017 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5012): Show |
chr1 | 47245139 | 47319147 |
a0008c0016t0001 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0009c0013t0001 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0010c0019t0001 | 0/0 | 5019 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0011c0018t0008 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0012c0012t0002 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5012): Show |
chr1 | 47245139 | 47319147 |
a0013c0020t0001 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
a0014c0008t0002 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5012): Show |
chr1 | 47245139 | 47319147 |
a0015c0014t0001 | 0/0 | 5019 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | AGTTC others(5014): Show |
chr1 | 47245139 | 47319147 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0002t0012g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0007g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0001c0003t0010g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0249 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0002g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0009g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0011g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0013g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0001t0015g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0009t0001g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0002c0011t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0001g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0004t0014g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0003c0015t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0004c0005t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0004c0005t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0004c0005t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0004c0005t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0005c0007t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0005c0007t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0005c0017t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0006c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0006c0006t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0007c0010t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0008c0016t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0009c0013t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0010c0019t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0011c0018t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0012c0012t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0013c0020t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0014c0008t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
a0015c0014t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0004 | t0001 | g0340 | EUR | GBR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00099 | hp2 | a0002 | c0001 | t0002 | g0253 | EUR | GBR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00140 | hp1 | a0002 | c0001 | t0002 | g0309 | EUR | GBR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00140 | hp2 | a0002 | c0001 | t0011 | g0306 | EUR | GBR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00280 | hp1 | a0002 | c0001 | t0002 | g0262 | EUR | FIN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00280 | hp2 | a0002 | c0001 | t0002 | g0053 | EUR | FIN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00323 | hp1 | a0007 | c0010 | t0002 | g0301 | EUR | FIN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00323 | hp2 | a0003 | c0004 | t0001 | g0349 | EUR | FIN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00408 | hp1 | a0002 | c0001 | t0002 | g0285 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00544 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00597 | hp1 | a0002 | c0001 | t0002 | g0307 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00597 | hp2 | a0003 | c0004 | t0001 | g0354 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00609 | hp1 | a0002 | c0001 | t0002 | g0056 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00621 | hp1 | a0001 | c0003 | t0001 | g0076 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00621 | hp2 | a0002 | c0001 | t0002 | g0252 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0184 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0219 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00642 | hp1 | a0003 | c0004 | t0001 | g0025 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00642 | hp2 | a0003 | c0004 | t0001 | g0373 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00673 | hp2 | a0002 | c0001 | t0002 | g0040 | EAS | CHS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00735 | hp1 | a0003 | c0004 | t0014 | g0370 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00735 | hp2 | a0003 | c0004 | t0001 | g0346 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00738 | hp1 | a0002 | c0001 | t0002 | g0265 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00738 | hp2 | a0008 | c0016 | t0001 | g0368 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00741 | hp1 | a0002 | c0001 | t0002 | g0310 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG00741 | hp2 | a0003 | c0004 | t0001 | g0347 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01069 | hp1 | a0002 | c0001 | t0002 | g0233 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0016 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01071 | hp1 | a0002 | c0001 | t0002 | g0318 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01071 | hp2 | a0002 | c0001 | t0002 | g0232 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01074 | hp1 | a0002 | c0001 | t0002 | g0235 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01074 | hp2 | a0001 | c0003 | t0001 | g0114 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01081 | hp1 | a0002 | c0001 | t0002 | g0316 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01081 | hp2 | a0003 | c0004 | t0001 | g0345 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0108 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01099 | hp2 | a0002 | c0001 | t0002 | g0308 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01106 | hp1 | a0003 | c0004 | t0001 | g0348 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0077 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01167 | hp1 | a0003 | c0004 | t0001 | g0337 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01167 | hp2 | a0001 | c0003 | t0007 | g0005 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0109 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01168 | hp2 | a0002 | c0001 | t0002 | g0243 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01169 | hp1 | a0003 | c0004 | t0001 | g0332 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01169 | hp2 | a0002 | c0001 | t0002 | g0287 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01175 | hp1 | a0002 | c0001 | t0002 | g0244 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0331 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01192 | hp1 | a0002 | c0001 | t0002 | g0248 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01192 | hp2 | a0003 | c0004 | t0001 | g0334 | AMR | PUR | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01257 | hp1 | a0003 | c0004 | t0001 | g0341 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01257 | hp2 | a0002 | c0001 | t0002 | g0058 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01258 | hp1 | a0003 | c0004 | t0001 | g0004 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01258 | hp2 | a0002 | c0001 | t0002 | g0303 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01346 | hp1 | a0002 | c0001 | t0002 | g0259 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01358 | hp1 | a0003 | c0004 | t0001 | g0333 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0082 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01361 | hp1 | a0002 | c0001 | t0002 | g0315 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01361 | hp2 | a0002 | c0001 | t0002 | g0236 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01433 | hp1 | a0002 | c0001 | t0002 | g0270 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0125 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01496 | hp1 | a0002 | c0001 | t0002 | g0274 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0106 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0189 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01515 | hp2 | a0003 | c0004 | t0001 | g0339 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01516 | hp1 | a0003 | c0004 | t0001 | g0336 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0118 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0100 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01517 | hp2 | a0003 | c0004 | t0001 | g0335 | EUR | IBS | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01884 | hp1 | a0001 | c0002 | t0004 | g0231 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01884 | hp2 | a0005 | c0007 | t0004 | g0214 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0216 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0123 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0079 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01934 | hp2 | a0002 | c0001 | t0002 | g0261 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01975 | hp1 | a0001 | c0003 | t0001 | g0113 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0206 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01978 | hp1 | a0002 | c0001 | t0002 | g0245 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0078 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01993 | hp1 | a0002 | c0001 | t0002 | g0254 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01993 | hp2 | a0009 | c0013 | t0001 | g0207 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02004 | hp1 | a0001 | c0003 | t0001 | g0208 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02004 | hp2 | a0002 | c0001 | t0002 | g0319 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02027 | hp1 | a0001 | c0003 | t0001 | g0099 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0192 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02040 | hp1 | a0002 | c0001 | t0002 | g0050 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0102 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02055 | hp1 | a0003 | c0004 | t0001 | g0365 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02055 | hp2 | a0001 | c0002 | t0003 | g0028 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02056 | hp1 | a0002 | c0001 | t0002 | g0041 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02071 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02071 | hp2 | a0002 | c0001 | t0002 | g0272 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02083 | hp1 | a0002 | c0001 | t0002 | g0321 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0116 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0117 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02132 | hp2 | a0002 | c0001 | t0002 | g0385 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02145 | hp1 | a0001 | c0002 | t0004 | g0229 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02145 | hp2 | a0001 | c0002 | t0003 | g0325 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02148 | hp1 | a0002 | c0001 | t0002 | g0269 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0101 | AMR | PEL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02155 | hp1 | a0002 | c0001 | t0002 | g0045 | EAS | CDX | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | CDX | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02165 | hp1 | a0002 | c0001 | t0002 | g0275 | EAS | CDX | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02165 | hp2 | a0002 | c0001 | t0002 | g0047 | EAS | CDX | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02257 | hp1 | a0001 | c0002 | t0003 | g0019 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0227 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02258 | hp1 | a0002 | c0001 | t0013 | g0062 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02258 | hp2 | a0002 | c0001 | t0002 | g0266 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02280 | hp1 | a0003 | c0004 | t0001 | g0031 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02523 | hp2 | a0001 | c0003 | t0010 | g0199 | EAS | KHV | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02572 | hp1 | a0003 | c0004 | t0001 | g0023 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0217 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02602 | hp1 | a0010 | c0019 | t0001 | g0175 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02602 | hp2 | a0002 | c0001 | t0002 | g0304 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02615 | hp1 | a0004 | c0005 | t0002 | g0065 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02615 | hp2 | a0003 | c0004 | t0001 | g0352 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02622 | hp1 | a0002 | c0001 | t0002 | g0042 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0007 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02630 | hp1 | a0001 | c0002 | t0004 | g0228 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0223 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02647 | hp2 | a0003 | c0004 | t0001 | g0363 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02683 | hp1 | a0002 | c0001 | t0002 | g0267 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02683 | hp2 | a0003 | c0004 | t0001 | g0344 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0126 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02698 | hp2 | a0003 | c0004 | t0001 | g0338 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0327 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02717 | hp2 | a0004 | c0005 | t0002 | g0066 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02735 | hp1 | a0003 | c0004 | t0001 | g0357 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02735 | hp2 | a0003 | c0004 | t0001 | g0369 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02738 | hp1 | a0003 | c0004 | t0001 | g0360 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02738 | hp2 | a0002 | c0001 | t0002 | g0297 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02809 | hp2 | a0003 | c0004 | t0001 | g0366 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02818 | hp1 | a0004 | c0005 | t0002 | g0064 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02818 | hp2 | a0002 | c0001 | t0002 | g0057 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02886 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0226 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0211 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02896 | hp1 | a0001 | c0002 | t0003 | g0328 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02896 | hp2 | a0003 | c0004 | t0001 | g0376 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0330 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02922 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02922 | hp2 | a0003 | c0004 | t0001 | g0380 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02965 | hp1 | a0003 | c0004 | t0001 | g0382 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02970 | hp1 | a0011 | c0018 | t0008 | g0212 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02970 | hp2 | a0003 | c0004 | t0001 | g0362 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0324 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02976 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03017 | hp1 | a0002 | c0001 | t0002 | g0035 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03017 | hp2 | a0003 | c0004 | t0001 | g0356 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03041 | hp1 | a0003 | c0004 | t0001 | g0377 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0218 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03098 | hp1 | a0003 | c0004 | t0001 | g0351 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03098 | hp2 | a0003 | c0004 | t0001 | g0022 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03130 | hp2 | a0001 | c0002 | t0003 | g0021 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03139 | hp1 | a0001 | c0002 | t0003 | g0010 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03139 | hp2 | a0003 | c0004 | t0001 | g0359 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03209 | hp1 | a0003 | c0004 | t0001 | g0024 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0225 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0133 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03225 | hp2 | a0001 | c0003 | t0006 | g0027 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0151 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03239 | hp2 | a0002 | c0001 | t0002 | g0276 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03453 | hp1 | a0001 | c0002 | t0003 | g0020 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03453 | hp2 | a0004 | c0005 | t0002 | g0063 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03486 | hp1 | a0003 | c0004 | t0001 | g0381 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0326 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03491 | hp1 | a0001 | c0003 | t0001 | g0209 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03491 | hp2 | a0002 | c0001 | t0002 | g0260 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03492 | hp1 | a0002 | c0001 | t0002 | g0302 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03492 | hp2 | a0001 | c0003 | t0001 | g0205 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0072 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0224 | AFR | ESN | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03540 | hp1 | a0003 | c0004 | t0001 | g0364 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | GWD | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03579 | hp1 | a0003 | c0004 | t0001 | g0378 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0222 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03654 | hp1 | a0003 | c0004 | t0001 | g0342 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0176 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0174 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0132 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03704 | hp1 | a0002 | c0001 | t0002 | g0034 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03710 | hp1 | a0002 | c0001 | t0002 | g0281 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03710 | hp2 | a0003 | c0004 | t0001 | g0372 | SAS | PJL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03831 | hp1 | a0002 | c0001 | t0002 | g0257 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03834 | hp1 | a0002 | c0001 | t0002 | g0234 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03834 | hp2 | a0003 | c0004 | t0001 | g0004 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03927 | hp1 | a0002 | c0001 | t0002 | g0239 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03927 | hp2 | a0003 | c0004 | t0001 | g0343 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03942 | hp1 | a0002 | c0001 | t0002 | g0237 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03942 | hp2 | a0003 | c0004 | t0001 | g0371 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG04184 | hp2 | a0003 | c0004 | t0001 | g0374 | SAS | BEB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG04199 | hp1 | a0003 | c0004 | t0001 | g0358 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG04199 | hp2 | a0002 | c0001 | t0002 | g0268 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG04204 | hp1 | a0003 | c0015 | t0001 | g0367 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG04204 | hp2 | a0002 | c0001 | t0002 | g0263 | SAS | STU | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18522 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18522 | hp2 | a0001 | c0002 | t0003 | g0018 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18612 | hp1 | a0003 | c0004 | t0001 | g0355 | EAS | CHB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18612 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | CHB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0098 | EAS | CHB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18747 | hp2 | a0012 | c0012 | t0002 | g0298 | EAS | CHB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0124 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18906 | hp2 | a0003 | c0004 | t0001 | g0375 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18939 | hp2 | a0002 | c0001 | t0002 | g0313 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18940 | hp2 | a0002 | c0001 | t0002 | g0032 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18942 | hp1 | a0002 | c0001 | t0002 | g0280 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18942 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18944 | hp2 | a0002 | c0001 | t0002 | g0055 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18945 | hp1 | a0002 | c0001 | t0015 | g0388 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18945 | hp2 | a0002 | c0001 | t0002 | g0383 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18946 | hp1 | a0002 | c0001 | t0002 | g0311 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18946 | hp2 | a0002 | c0001 | t0002 | g0044 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18947 | hp1 | a0002 | c0001 | t0002 | g0033 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18948 | hp2 | a0002 | c0001 | t0005 | g0241 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18949 | hp1 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18949 | hp2 | a0002 | c0001 | t0002 | g0258 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18951 | hp1 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18952 | hp2 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18956 | hp1 | a0006 | c0006 | t0001 | g0084 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18956 | hp2 | a0002 | c0001 | t0002 | g0037 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18959 | hp2 | a0006 | c0006 | t0001 | g0139 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18961 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18961 | hp2 | a0002 | c0001 | t0002 | g0279 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0190 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18963 | hp1 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18964 | hp1 | a0002 | c0001 | t0002 | g0052 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18965 | hp1 | a0013 | c0020 | t0001 | g0149 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18965 | hp2 | a0002 | c0001 | t0002 | g0061 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18966 | hp1 | a0002 | c0001 | t0002 | g0277 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18967 | hp2 | a0002 | c0001 | t0002 | g0320 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18968 | hp2 | a0002 | c0001 | t0002 | g0060 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18969 | hp2 | a0002 | c0001 | t0002 | g0291 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18970 | hp2 | a0002 | c0001 | t0002 | g0242 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18971 | hp2 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18977 | hp1 | a0002 | c0001 | t0002 | g0387 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18977 | hp2 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18979 | hp2 | a0002 | c0001 | t0002 | g0246 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18980 | hp2 | a0002 | c0001 | t0002 | g0288 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18982 | hp1 | a0002 | c0001 | t0002 | g0292 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18985 | hp1 | a0002 | c0001 | t0009 | g0283 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18985 | hp2 | a0001 | c0003 | t0001 | g0131 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18986 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18987 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18988 | hp1 | a0002 | c0001 | t0002 | g0282 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18989 | hp1 | a0002 | c0001 | t0002 | g0305 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18991 | hp2 | a0002 | c0001 | t0002 | g0240 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18992 | hp1 | a0002 | c0001 | t0002 | g0051 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18993 | hp2 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18994 | hp1 | a0002 | c0001 | t0002 | g0299 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18994 | hp2 | a0001 | c0003 | t0001 | g0104 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18995 | hp1 | a0002 | c0001 | t0002 | g0300 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18998 | hp1 | a0002 | c0001 | t0002 | g0286 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18999 | hp1 | a0002 | c0001 | t0002 | g0295 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0103 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19003 | hp2 | a0002 | c0001 | t0002 | g0039 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19004 | hp1 | a0002 | c0001 | t0002 | g0036 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19004 | hp2 | a0001 | c0002 | t0012 | g0153 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19005 | hp1 | a0002 | c0001 | t0002 | g0271 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19007 | hp1 | a0002 | c0001 | t0002 | g0046 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19007 | hp2 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19009 | hp1 | a0002 | c0001 | t0002 | g0293 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19010 | hp2 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19012 | hp2 | a0002 | c0001 | t0002 | g0312 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19030 | hp1 | a0003 | c0004 | t0001 | g0350 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0096 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19043 | hp1 | a0001 | c0002 | t0003 | g0030 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19043 | hp2 | a0005 | c0007 | t0004 | g0213 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19055 | hp1 | a0002 | c0001 | t0002 | g0386 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19055 | hp2 | a0002 | c0001 | t0002 | g0296 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19058 | hp1 | a0002 | c0001 | t0002 | g0054 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19058 | hp2 | a0002 | c0001 | t0005 | g0273 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19062 | hp1 | a0002 | c0001 | t0002 | g0255 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19063 | hp2 | a0014 | c0008 | t0002 | g0251 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19064 | hp1 | a0001 | c0003 | t0001 | g0196 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19064 | hp2 | a0002 | c0001 | t0002 | g0238 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19065 | hp1 | a0002 | c0011 | t0002 | g0290 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19065 | hp2 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19066 | hp2 | a0002 | c0001 | t0002 | g0284 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19072 | hp2 | a0002 | c0001 | t0002 | g0314 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19074 | hp1 | a0002 | c0001 | t0002 | g0384 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19077 | hp1 | a0002 | c0001 | t0002 | g0247 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19078 | hp1 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19078 | hp2 | a0002 | c0001 | t0002 | g0043 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19080 | hp1 | a0002 | c0001 | t0002 | g0059 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19080 | hp2 | a0001 | c0003 | t0001 | g0135 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19082 | hp1 | a0002 | c0001 | t0002 | g0250 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19082 | hp2 | a0015 | c0014 | t0001 | g0191 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19084 | hp1 | a0002 | c0001 | t0002 | g0048 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19085 | hp2 | a0002 | c0001 | t0002 | g0278 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19088 | hp1 | a0002 | c0001 | t0005 | g0294 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19240 | hp1 | a0003 | c0004 | t0001 | g0361 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0080 | AFR | YRI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA20129 | hp1 | a0001 | c0002 | t0004 | g0230 | AFR | ASW | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0323 | AFR | ASW | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA20805 | hp1 | a0002 | c0001 | t0002 | g0264 | EUR | TSI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA20805 | hp2 | a0002 | c0001 | t0002 | g0317 | EUR | TSI | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01123 | hp1 | a0002 | c0001 | t0002 | g0289 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG01123 | hp2 | a0001 | c0003 | t0001 | g0071 | AMR | CLM | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0183 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02109 | hp2 | a0003 | c0004 | t0001 | g0353 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0329 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02486 | hp2 | a0001 | c0003 | t0006 | g0026 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0095 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG02559 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | ACB | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0221 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0134 | AFR | MSL | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG06807 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | USA | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
HG06807 | hp2 | a0005 | c0017 | t0004 | g0215 | AFR | USA | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18955 | hp1 | a0002 | c0001 | t0002 | g0049 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA18955 | hp2 | a0002 | c0001 | t0002 | g0256 | EAS | JPT | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA20300 | hp1 | a0003 | c0004 | t0001 | g0379 | AFR | USA | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | USA | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0322 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | LWK | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
homoSapiens | chm13v2 | a0002 | c0001 | t0002 | g0249 | REF | REF | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
homoSapiens | grch38p0 | a0002 | c0009 | t0001 | g0038 | REF | REF | STIL_chr1_47245139_47319147 | STIL | chr1 | 47245139 | 47319147 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:47251308 | C | T | 1 | a0011 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.3695G>A | p.Arg1232Gln | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3850/5019 | 3695/3867 | 1232/1288 | chr1 | 47251308 | |||
chr1:47251488 | G | A | 1 | a0010 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.3515C>T | p.Ser1172Phe | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3670/5019 | 3515/3867 | 1172/1288 | chr1 | 47251488 | |||
chr1:47251566 | G | A | 1 | a0006 | 2 | NA18956.hp1 NA18959.hp2 |
missense_variant | MODERATE | c.3437C>T | p.Ala1146Val | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3592/5019 | 3437/3867 | 1146/1288 | chr1 | 47251566 | |||
chr1:47251573 | C | T | 1 | a0005 | 3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.3430G>A | p.Asp1144Asn | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3585/5019 | 3430/3867 | 1144/1288 | chr1 | 47251573 | |||
chr1:47251708 | T | C | 1 | a0009 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.3295A>G | p.Ile1099Val | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3450/5019 | 3295/3867 | 1099/1288 | chr1 | 47251708 | |||
chr1:47251746 | G | A | 1 | a0007 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.3257C>T | p.Ser1086Leu | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3412/5019 | 3257/3867 | 1086/1288 | chr1 | 47251746 | |||
chr1:47251833 | T | C | 1 | a0013 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.3170A>G | p.Asn1057Ser | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3325/5019 | 3170/3867 | 1057/1288 | chr1 | 47251833 | |||
chr1:47260308 | G | A | 1 | a0015 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.3061C>T | p.His1021Tyr | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/17 | 3216/5019 | 3061/3867 | 1021/1288 | chr1 | 47260308 | |||
chr1:47260415 | T | C | 2 | a0003 a0008 |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
missense_variant | MODERATE | c.2954A>G | p.His985Arg | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/17 | 3109/5019 | 2954/3867 | 985/1288 | chr1 | 47260415 | |||
chr1:47260463 | T | C | 1 | a0008 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.2906A>G | p.His969Arg | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/17 | 3061/5019 | 2906/3867 | 969/1288 | chr1 | 47260463 | |||
chr1:47280441 | T | C | 1 | a0004 | 4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.2017A>G | p.Ser673Gly | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/17 | 2172/5019 | 2017/3867 | 673/1288 | chr1 | 47280441 | |||
chr1:47289458 | T | C | 1 | a0012 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.1000A>G | p.Lys334Glu | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/17 | 1155/5019 | 1000/3867 | 334/1288 | chr1 | 47289458 | |||
chr1:47301737 | C | T | 1 | a0014 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.277G>A | p.Val93Ile | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/17 | 432/5019 | 277/3867 | 93/1288 | chr1 | 47301737 | |||
chr1:47302242 | G | A | 10 | a0001 a0003 a0005 others(7): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
missense_variant | MODERATE | c.257C>T | p.Ala86Val | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 4/17 | 412/5019 | 257/3867 | 86/1288 | chr1 | 47302242 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:47251217 | C | T | 2 | a0003c0015 a0008c0016 |
2 | HG00738.hp2 HG04204.hp1 |
synonymous_variant | LOW | c.3786G>A | p.Thr1262Thr | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3941/5019 | 3786/3867 | 1262/1288 | chr1 | 47251217 | |||
chr1:47251517 | A | G | 7 | a0002c0001 a0002c0011 a0004c0005 others(4): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
synonymous_variant | LOW | c.3486T>C | p.Pro1162Pro | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 3641/5019 | 3486/3867 | 1162/1288 | chr1 | 47251517 | |||
chr1:47281006 | G | C | 6 | a0001c0002 a0005c0007 a0005c0017 others(3): Show |
105 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(102): Show |
synonymous_variant | LOW | c.1452C>G | p.Ser484Ser | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/17 | 1607/5019 | 1452/3867 | 484/1288 | chr1 | 47281006 | |||
chr1:47282414 | G | A | 1 | a0002c0011 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.1179C>T | p.His393His | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/17 | 1334/5019 | 1179/3867 | 393/1288 | chr1 | 47282414 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:47250144 | T | C | 1 | a0002c0001t0009 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*992A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 992 | chr1 | 47250144 | ||||||
chr1:47250226 | A | G | 1 | a0011c0018t0008 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*910T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 910 | chr1 | 47250226 | ||||||
chr1:47250253 | T | C | 1 | a0002c0001t0005 | 3 | NA18948.hp2 NA19058.hp2 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*883A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 883 | chr1 | 47250253 | ||||||
chr1:47250368 | TAA | T | 11 | a0002c0001t0002 a0002c0001t0005 a0002c0001t0009 others(8): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*766_*767delTT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 766 | chr1 | 47250368 | ||||||
chr1:47250406 | T | C | 1 | a0001c0003t0010 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*730A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 730 | chr1 | 47250406 | ||||||
chr1:47250559 | C | T | 1 | a0001c0002t0003 | 26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*577G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 577 | chr1 | 47250559 | ||||||
chr1:47250591 | G | A | 1 | a0002c0001t0011 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*545C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 545 | chr1 | 47250591 | ||||||
chr1:47250605 | A | C | 1 | a0001c0003t0006 | 2 | HG02486.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*531T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 531 | chr1 | 47250605 | ||||||
chr1:47250609 | C | A | 1 | a0001c0002t0012 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 527 | chr1 | 47250609 | ||||||
chr1:47250820 | A | G | 5 | a0001c0002t0003 a0001c0002t0004 a0005c0007t0004 others(2): Show |
35 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*316T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 316 | chr1 | 47250820 | ||||||
chr1:47250868 | G | C | 1 | a0002c0001t0013 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*268C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 268 | chr1 | 47250868 | ||||||
chr1:47251013 | T | C | 1 | a0003c0004t0014 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*123A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 17/17 | 123 | chr1 | 47251013 | ||||||
chr1:47314094 | G | C | 1 | a0002c0001t0015 | 1 | NA18945.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-102C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/17 | chr1 | 47314094 | |||||||
chr1:47314113 | G | T | 1 | a0001c0003t0007 | 1 | HG01167.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/17 | 3794 | chr1 | 47314113 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:47252110 | G | C | 1 | a0001c0003t0001g0072 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3081-188C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252110 | |||||||
chr1:47252137 | T | C | 1 | a0003c0004t0001g0363 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3081-215A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252137 | |||||||
chr1:47252202 | A | G | 1 | a0001c0002t0001g0097 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3081-280T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252202 | |||||||
chr1:47252333 | G | A | 2 | a0003c0004t0001g0365 a0003c0004t0001g0366 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3081-411C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252333 | |||||||
chr1:47252337 | G | A | 1 | a0002c0001t0002g0032 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3081-415C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252337 | |||||||
chr1:47252346 | C | T | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3081-424G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252346 | |||||||
chr1:47252363 | C | T | 9 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.3081-441G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252363 | |||||||
chr1:47252433 | C | T | 1 | a0003c0004t0001g0346 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3081-511G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252433 | |||||||
chr1:47252463 | A | G | 1 | a0001c0002t0003g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3081-541T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252463 | |||||||
chr1:47252646 | A | G | 129 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3081-724T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252646 | |||||||
chr1:47252686 | G | A | 129 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3081-764C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252686 | |||||||
chr1:47252778 | T | TAC | 45 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0001g0075 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.3081-858_3081-857d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | T | TACAC | 33 | a0001c0002t0001g0170 a0001c0002t0003g0227 a0001c0003t0001g0071 others(30): Show |
33 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3081-860_3081-857d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | T | TACACAC | 10 | a0002c0001t0002g0041 a0002c0001t0002g0383 a0003c0004t0001g0335 others(7): Show |
10 | HG01516.hp1 HG01517.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.3081-862_3081-857d others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | T | TACACACA others(1): Show |
6 | a0003c0004t0001g0333 a0003c0004t0001g0363 a0003c0004t0001g0371 others(3): Show |
6 | HG00738.hp2 HG01358.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3081-864_3081-857d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | TAC | T | 131 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(128): Show |
132 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.3081-858_3081-857d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | TACAC | T | 24 | a0001c0002t0003g0007 a0001c0002t0003g0009 a0001c0002t0003g0012 others(21): Show |
24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.3081-860_3081-857d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | TACACAC | T | 29 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0179 others(26): Show |
31 | HG00639.hp1 HG00639.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.3081-862_3081-857d others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | TACACACA others(1): Show |
T | 12 | a0001c0002t0003g0010 a0001c0002t0003g0011 a0001c0003t0001g0193 others(9): Show |
12 | HG01167.hp2 HG01891.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.3081-864_3081-857d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | TACACACA others(5): Show |
T | 3 | a0005c0007t0004g0213 a0005c0007t0004g0214 a0005c0017t0004g0215 |
3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3081-868_3081-857d others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | TACACACA others(6): Show |
T | 1 | a0001c0003t0001g0206 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3081-869_3081-857d others(15): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | TACACACA others(7): Show |
T | 6 | a0001c0002t0004g0211 a0001c0002t0004g0231 a0001c0003t0001g0133 others(3): Show |
6 | HG01884.hp1 HG01993.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3081-870_3081-857d others(16): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | TACACACA others(9): Show |
T | 3 | a0001c0002t0004g0228 a0001c0002t0004g0229 a0001c0002t0004g0230 |
3 | HG02145.hp1 HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3081-872_3081-857d others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | TACACACA others(17): Show |
T | 2 | a0003c0004t0001g0365 a0003c0004t0001g0366 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3081-880_3081-857d others(26): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252778 | TACACACA others(19): Show |
T | 1 | a0002c0001t0002g0285 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3081-882_3081-857d others(28): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252778 | |||||||
chr1:47252823 | ACG | A | 8 | a0002c0001t0002g0040 a0002c0001t0002g0043 a0002c0001t0002g0046 others(5): Show |
8 | HG00609.hp1 HG00673.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.3081-903_3081-902d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252823 | |||||||
chr1:47252825 | G | A | 3 | a0002c0001t0002g0033 a0002c0001t0002g0044 a0002c0001t0002g0048 |
3 | NA18946.hp2 NA18947.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3081-903C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252825 | |||||||
chr1:47252938 | T | C | 3 | a0005c0007t0004g0213 a0005c0007t0004g0214 a0005c0017t0004g0215 |
3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3081-1016A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47252938 | |||||||
chr1:47253141 | T | C | 1 | a0007c0010t0002g0301 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3081-1219A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253141 | |||||||
chr1:47253339 | C | A | 59 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3081-1417G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253339 | |||||||
chr1:47253436 | C | T | 59 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3081-1514G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253436 | |||||||
chr1:47253445 | G | A | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3081-1523C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253445 | |||||||
chr1:47253684 | T | C | 1 | a0002c0001t0002g0279 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3081-1762A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253684 | |||||||
chr1:47253857 | G | A | 2 | a0001c0003t0001g0120 a0001c0003t0001g0192 |
2 | HG02027.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3081-1935C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47253857 | |||||||
chr1:47254049 | C | T | 1 | a0002c0001t0002g0319 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3081-2127G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254049 | |||||||
chr1:47254050 | G | A | 59 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3081-2128C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254050 | |||||||
chr1:47254150 | C | T | 26 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(23): Show |
26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.3081-2228G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254150 | |||||||
chr1:47254180 | C | CA | 53 | a0001c0002t0001g0002 a0001c0002t0001g0068 a0001c0002t0001g0069 others(50): Show |
54 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.3081-2259dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | |||||||
chr1:47254180 | C | CAA | 47 | a0001c0002t0001g0070 a0001c0002t0001g0085 a0001c0002t0001g0088 others(44): Show |
48 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.3081-2260_3081-225 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | |||||||
chr1:47254180 | C | CAAA | 19 | a0001c0002t0001g0093 a0003c0004t0001g0022 a0003c0004t0001g0023 others(16): Show |
19 | HG01167.hp1 HG02055.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.3081-2261_3081-225 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | |||||||
chr1:47254180 | CA | C | 6 | a0001c0002t0001g0167 a0001c0002t0001g0177 a0001c0002t0001g0187 others(3): Show |
6 | HG03704.hp2 NA18951.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.3081-2259delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | |||||||
chr1:47254180 | CAA | C | 8 | a0002c0001t0002g0041 a0002c0001t0002g0045 a0002c0001t0002g0051 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.3081-2260_3081-225 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | |||||||
chr1:47254180 | CAAA | C | 51 | a0001c0002t0003g0028 a0001c0002t0003g0227 a0001c0002t0003g0325 others(48): Show |
51 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.3081-2261_3081-225 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | |||||||
chr1:47254180 | CAAAA | C | 95 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(92): Show |
95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.3081-2262_3081-225 others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | |||||||
chr1:47254180 | CAAAAA | C | 11 | a0001c0002t0003g0328 a0001c0002t0004g0228 a0001c0003t0001g0140 others(8): Show |
11 | HG00738.hp1 HG01433.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3081-2263_3081-225 others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | |||||||
chr1:47254180 | CAAAAAAA others(3): Show |
C | 1 | a0001c0003t0001g0223 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3081-2268_3081-225 others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | |||||||
chr1:47254180 | CAAAAAAA others(4): Show |
C | 15 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(12): Show |
16 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3081-2269_3081-225 others(15): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254180 | |||||||
chr1:47254529 | G | GT | 26 | a0001c0002t0001g0164 a0001c0002t0003g0006 a0001c0002t0003g0007 others(23): Show |
26 | HG00741.hp1 HG01069.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.3081-2608dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254529 | |||||||
chr1:47254529 | GT | G | 57 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3081-2608delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254529 | |||||||
chr1:47254540 | G | GT | 5 | a0002c0001t0002g0258 a0004c0005t0002g0063 a0004c0005t0002g0064 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.3081-2619dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254540 | |||||||
chr1:47254734 | T | C | 2 | a0003c0004t0001g0335 a0003c0004t0001g0336 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3081-2812A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254734 | |||||||
chr1:47254962 | G | C | 92 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0232 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.3081-3040C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254962 | |||||||
chr1:47254970 | G | C | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3081-3048C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47254970 | |||||||
chr1:47255120 | C | T | 4 | a0004c0005t0002g0063 a0004c0005t0002g0064 a0004c0005t0002g0065 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3081-3198G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255120 | |||||||
chr1:47255186 | G | A | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3081-3264C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255186 | |||||||
chr1:47255283 | G | A | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3081-3361C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255283 | |||||||
chr1:47255310 | G | T | 26 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(23): Show |
26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.3081-3388C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255310 | |||||||
chr1:47255315 | A | T | 2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3081-3393T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255315 | |||||||
chr1:47255464 | C | T | 130 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.3081-3542G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255464 | |||||||
chr1:47255506 | G | A | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3081-3584C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255506 | |||||||
chr1:47255532 | G | A | 1 | a0001c0003t0001g0072 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3081-3610C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255532 | |||||||
chr1:47255550 | C | CA | 70 | a0001c0002t0003g0011 a0001c0002t0003g0021 a0001c0002t0003g0028 others(67): Show |
71 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.3081-3629dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255550 | |||||||
chr1:47255550 | C | CAA | 115 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0035 others(112): Show |
115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.3081-3630_3081-362 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255550 | |||||||
chr1:47255550 | C | CAAA | 7 | a0002c0001t0002g0040 a0002c0001t0002g0237 a0002c0001t0002g0238 others(4): Show |
7 | HG00673.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.3081-3631_3081-362 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255550 | |||||||
chr1:47255550 | CA | C | 143 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(140): Show |
145 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.3081-3629delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255550 | |||||||
chr1:47255582 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3081-3660G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255582 | |||||||
chr1:47255652 | T | C | 59 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3081-3730A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255652 | |||||||
chr1:47255823 | C | A | 1 | a0002c0001t0002g0309 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3081-3901G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255823 | |||||||
chr1:47255839 | C | T | 1 | a0001c0003t0001g0219 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3081-3917G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47255839 | |||||||
chr1:47256184 | T | C | 129 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3080+4105A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256184 | |||||||
chr1:47256369 | T | A | 1 | a0001c0002t0001g0069 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3080+3920A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256369 | |||||||
chr1:47256397 | C | G | 1 | a0004c0005t0002g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3080+3892G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256397 | |||||||
chr1:47256584 | A | G | 239 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.3080+3705T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256584 | |||||||
chr1:47256620 | C | CA | 21 | a0001c0002t0001g0180 a0001c0003t0001g0003 a0001c0003t0001g0096 others(18): Show |
22 | HG00639.hp2 HG01167.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3080+3668dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256620 | |||||||
chr1:47256620 | C | CAA | 53 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(50): Show |
54 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.3080+3667_3080+366 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256620 | |||||||
chr1:47256620 | CA | C | 9 | a0001c0002t0001g0158 a0001c0002t0003g0007 a0001c0002t0003g0008 others(6): Show |
9 | HG01074.hp1 HG02622.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.3080+3668delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256620 | |||||||
chr1:47256639 | AT | A | 7 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3080+3649delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256639 | |||||||
chr1:47256640 | T | A | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3080+3649A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256640 | |||||||
chr1:47256704 | C | G | 1 | a0002c0001t0002g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3080+3585G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256704 | |||||||
chr1:47256723 | G | A | 1 | a0003c0004t0001g0022 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3080+3566C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47256723 | |||||||
chr1:47257390 | A | C | 1 | a0001c0002t0001g0148 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3080+2899T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257390 | |||||||
chr1:47257615 | G | A | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3080+2674C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257615 | |||||||
chr1:47257671 | T | C | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3080+2618A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257671 | |||||||
chr1:47257773 | A | T | 1 | a0001c0002t0001g0161 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3080+2516T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257773 | |||||||
chr1:47257874 | T | C | 1 | a0002c0001t0002g0238 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3080+2415A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257874 | |||||||
chr1:47257902 | T | C | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3080+2387A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47257902 | |||||||
chr1:47258152 | C | G | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.3080+2137G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258152 | |||||||
chr1:47258432 | C | T | 1 | a0001c0002t0003g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3080+1857G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258432 | |||||||
chr1:47258494 | C | T | 26 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(23): Show |
26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.3080+1795G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258494 | |||||||
chr1:47258507 | A | T | 129 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3080+1782T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258507 | |||||||
chr1:47258604 | C | T | 69 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(66): Show |
70 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.3080+1685G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258604 | |||||||
chr1:47258635 | A | G | 3 | a0001c0003t0001g0083 a0001c0003t0001g0131 a0001c0003t0001g0141 |
3 | NA18939.hp1 NA18961.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.3080+1654T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258635 | |||||||
chr1:47258644 | A | C | 4 | a0003c0004t0001g0375 a0003c0004t0001g0376 a0003c0004t0001g0377 others(1): Show |
4 | HG02896.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3080+1645T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258644 | |||||||
chr1:47258728 | T | C | 239 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.3080+1561A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258728 | |||||||
chr1:47258861 | C | T | 129 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3080+1428G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258861 | |||||||
chr1:47258928 | TATACTTG others(3): Show |
T | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3080+1351_3080+136 others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258928 | |||||||
chr1:47258992 | C | CTTTTTTT others(3): Show |
12 | a0001c0002t0004g0231 a0001c0003t0001g0003 a0001c0003t0001g0217 others(9): Show |
13 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.3080+1287_3080+129 others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | |||||||
chr1:47258992 | C | CTTTTTTT others(4): Show |
11 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0003t0001g0322 others(8): Show |
11 | HG01167.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.3080+1286_3080+129 others(15): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | |||||||
chr1:47258992 | C | CTTTTTTT others(5): Show |
116 | a0001c0002t0003g0327 a0001c0002t0003g0328 a0001c0002t0003g0329 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.3080+1285_3080+129 others(16): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | |||||||
chr1:47258992 | C | CTTTTTTT others(6): Show |
66 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0004g0228 others(63): Show |
66 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.3080+1284_3080+129 others(17): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | |||||||
chr1:47258992 | C | CTTTTTTT others(7): Show |
11 | a0001c0002t0003g0010 a0001c0002t0003g0011 a0002c0001t0002g0036 others(8): Show |
11 | HG02056.hp1 HG02615.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.3080+1283_3080+129 others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | |||||||
chr1:47258992 | C | CTTTTTTT others(8): Show |
2 | a0002c0001t0002g0048 a0002c0001t0002g0387 |
2 | NA18977.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3080+1296_3080+129 others(19): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | |||||||
chr1:47258992 | C | CTTTTTTT others(9): Show |
8 | a0001c0002t0003g0007 a0001c0002t0003g0009 a0001c0002t0003g0013 others(5): Show |
8 | HG01069.hp2 HG02622.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.3080+1296_3080+129 others(20): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | |||||||
chr1:47258992 | C | CTTTTTTT others(10): Show |
6 | a0001c0002t0003g0006 a0001c0002t0003g0008 a0001c0002t0003g0012 others(3): Show |
6 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3080+1296_3080+129 others(21): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47258992 | |||||||
chr1:47259011 | C | CAG | 223 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.3080+1276_3080+127 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259011 | |||||||
chr1:47259040 | G | A | 1 | a0001c0003t0001g0185 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3080+1249C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259040 | |||||||
chr1:47259087 | C | T | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3080+1202G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259087 | |||||||
chr1:47259096 | C | T | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3080+1193G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259096 | |||||||
chr1:47259193 | A | G | 94 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(91): Show |
95 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.3080+1096T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259193 | |||||||
chr1:47259196 | C | T | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3080+1093G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259196 | |||||||
chr1:47259259 | T | TACAGGTG others(2): Show |
6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3080+1021_3080+102 others(13): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259259 | |||||||
chr1:47259281 | C | T | 6 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(3): Show |
6 | HG02622.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3080+1008G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259281 | |||||||
chr1:47259285 | C | CT | 88 | a0001c0002t0001g0143 a0001c0002t0001g0148 a0001c0002t0001g0166 others(85): Show |
89 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.3080+1003dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | |||||||
chr1:47259285 | C | CTT | 40 | a0001c0002t0003g0028 a0001c0002t0003g0227 a0001c0002t0004g0228 others(37): Show |
40 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.3080+1002_3080+100 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | |||||||
chr1:47259285 | C | CTTT | 84 | a0001c0002t0004g0211 a0002c0001t0002g0039 a0002c0001t0002g0041 others(81): Show |
84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.3080+1001_3080+100 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | |||||||
chr1:47259285 | C | CTTTT | 15 | a0001c0002t0003g0008 a0001c0002t0004g0229 a0001c0002t0004g0230 others(12): Show |
15 | HG00597.hp1 HG00621.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.3080+1000_3080+100 others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | |||||||
chr1:47259285 | CT | C | 6 | a0001c0002t0001g0070 a0001c0002t0001g0088 a0001c0002t0001g0154 others(3): Show |
6 | HG01517.hp1 HG03688.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.3080+1003delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | |||||||
chr1:47259285 | CTTTTTTT others(3): Show |
C | 2 | a0002c0001t0002g0316 a0002c0001t0002g0317 |
2 | HG01081.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3080+994_3080+1003 others(13): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259285 | |||||||
chr1:47259445 | C | T | 2 | a0001c0002t0001g0165 a0001c0002t0001g0167 |
2 | NA18951.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.3080+844G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259445 | |||||||
chr1:47259479 | C | T | 69 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(66): Show |
70 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.3080+810G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259479 | |||||||
chr1:47259556 | T | C | 1 | a0001c0003t0001g0133 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3080+733A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259556 | |||||||
chr1:47259584 | C | T | 1 | a0001c0002t0001g0086 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3080+705G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259584 | |||||||
chr1:47259585 | G | A | 4 | a0004c0005t0002g0063 a0004c0005t0002g0064 a0004c0005t0002g0065 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3080+704C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259585 | |||||||
chr1:47259705 | A | G | 3 | a0001c0003t0001g0206 a0001c0003t0001g0208 a0009c0013t0001g0207 |
3 | HG01975.hp2 HG01993.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.3080+584T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47259705 | |||||||
chr1:47260099 | T | A | 1 | a0001c0003t0001g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3080+190A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47260099 | |||||||
chr1:47260131 | C | T | 1 | a0003c0004t0001g0350 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3080+158G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47260131 | |||||||
chr1:47260145 | A | G | 2 | a0001c0002t0004g0211 a0011c0018t0008g0212 |
2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3080+144T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47260145 | |||||||
chr1:47260159 | G | A | 1 | a0001c0002t0001g0151 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3080+130C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47260159 | |||||||
chr1:47260206 | C | G | 2 | a0002c0001t0002g0238 a0002c0001t0002g0258 |
2 | NA18949.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3080+83G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 16/16 | chr1 | 47260206 | |||||||
chr1:47260593 | C | T | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2830-54G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260593 | |||||||
chr1:47260635 | A | C | 11 | a0001c0003t0001g0003 a0001c0003t0001g0217 a0001c0003t0001g0218 others(8): Show |
12 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2830-96T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260635 | |||||||
chr1:47260749 | G | C | 1 | a0001c0003t0001g0076 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2830-210C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260749 | |||||||
chr1:47260794 | C | T | 2 | a0001c0002t0001g0146 a0001c0002t0001g0178 |
2 | NA19009.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.2830-255G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260794 | |||||||
chr1:47260878 | T | A | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2830-339A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260878 | |||||||
chr1:47260963 | A | G | 1 | a0013c0020t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2830-424T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260963 | |||||||
chr1:47260996 | T | A | 1 | a0001c0002t0012g0153 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2830-457A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47260996 | |||||||
chr1:47261133 | A | G | 1 | a0002c0001t0002g0265 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2830-594T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261133 | |||||||
chr1:47261245 | G | A | 1 | a0002c0001t0002g0036 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2830-706C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261245 | |||||||
chr1:47261258 | C | G | 2 | a0001c0003t0001g0100 a0001c0003t0001g0189 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2830-719G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261258 | |||||||
chr1:47261261 | A | G | 8 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2830-722T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261261 | |||||||
chr1:47261272 | C | T | 1 | a0001c0003t0001g0192 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2830-733G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261272 | |||||||
chr1:47261343 | G | C | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2830-804C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261343 | |||||||
chr1:47261344 | C | T | 5 | a0001c0002t0004g0211 a0001c0002t0004g0229 a0001c0002t0004g0230 others(2): Show |
5 | HG01884.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2830-805G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261344 | |||||||
chr1:47261466 | C | T | 1 | a0001c0002t0001g0069 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2830-927G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261466 | |||||||
chr1:47261604 | G | A | 8 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2830-1065C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261604 | |||||||
chr1:47261745 | C | CA | 27 | a0001c0002t0001g0146 a0001c0002t0001g0147 a0001c0002t0001g0166 others(24): Show |
28 | HG00639.hp2 HG01934.hp2 HG02572.hp2 others(25): Show |
intron_variant | MODIFIER | c.2829+1157dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261745 | |||||||
chr1:47261745 | CA | C | 94 | a0001c0002t0001g0067 a0001c0002t0003g0006 a0001c0002t0003g0007 others(91): Show |
95 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.2829+1157delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261745 | |||||||
chr1:47261763 | T | A | 128 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(125): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.2829+1140A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261763 | |||||||
chr1:47261882 | A | C | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2829+1021T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261882 | |||||||
chr1:47261907 | C | CA | 15 | a0001c0002t0001g0143 a0001c0002t0001g0168 a0001c0002t0004g0229 others(12): Show |
15 | HG01258.hp2 HG01884.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.2829+995dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261907 | |||||||
chr1:47261907 | CA | C | 6 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0167 others(3): Show |
6 | NA18941.hp1 NA18951.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.2829+995delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261907 | |||||||
chr1:47261962 | T | C | 1 | a0001c0003t0006g0026 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2829+941A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47261962 | |||||||
chr1:47262232 | G | A | 2 | a0002c0001t0002g0041 a0002c0001t0002g0050 |
2 | HG02040.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2829+671C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262232 | |||||||
chr1:47262251 | G | A | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2829+652C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262251 | |||||||
chr1:47262275 | C | G | 56 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2829+628G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262275 | |||||||
chr1:47262385 | A | T | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2829+518T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262385 | |||||||
chr1:47262426 | C | A | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2829+477G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262426 | |||||||
chr1:47262481 | T | G | 1 | a0001c0003t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2829+422A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262481 | |||||||
chr1:47262488 | T | G | 3 | a0001c0003t0001g0095 a0001c0003t0001g0123 a0001c0003t0001g0124 |
3 | HG01891.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2829+415A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262488 | |||||||
chr1:47262506 | C | T | 1 | a0001c0002t0001g0151 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2829+397G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262506 | |||||||
chr1:47262553 | C | A | 13 | a0001c0003t0001g0001 a0001c0003t0001g0076 a0001c0003t0001g0098 others(10): Show |
14 | HG00621.hp1 HG01515.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.2829+350G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262553 | |||||||
chr1:47262766 | A | G | 1 | a0002c0001t0002g0270 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2829+137T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262766 | |||||||
chr1:47262787 | A | G | 1 | a0001c0002t0003g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2829+116T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262787 | |||||||
chr1:47262818 | C | T | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2829+85G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 15/16 | chr1 | 47262818 | |||||||
chr1:47263354 | G | T | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2616-238C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263354 | |||||||
chr1:47263362 | T | A | 32 | a0002c0001t0002g0033 a0002c0001t0002g0034 a0002c0001t0002g0035 others(29): Show |
32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.2616-246A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263362 | |||||||
chr1:47263362 | T | G | 207 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(204): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.2616-246A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263362 | |||||||
chr1:47263626 | A | G | 1 | a0002c0001t0002g0265 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2616-510T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263626 | |||||||
chr1:47263744 | G | GT | 43 | a0001c0002t0001g0070 a0001c0002t0001g0089 a0001c0002t0001g0094 others(40): Show |
44 | HG00639.hp2 HG00673.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.2616-629dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | |||||||
chr1:47263744 | G | GTT | 10 | a0001c0002t0003g0227 a0001c0002t0003g0327 a0001c0002t0003g0330 others(7): Show |
10 | HG01978.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2616-630_2616-629d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | |||||||
chr1:47263744 | G | GTTT | 7 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0328 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2616-631_2616-629d others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | |||||||
chr1:47263744 | G | GTTTTT | 9 | a0003c0004t0001g0023 a0003c0004t0001g0335 a0003c0004t0001g0363 others(6): Show |
9 | HG01517.hp2 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2616-633_2616-629d others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | |||||||
chr1:47263744 | G | GTTTTTT | 22 | a0001c0003t0006g0027 a0003c0004t0001g0004 a0003c0004t0001g0022 others(19): Show |
23 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.2616-634_2616-629d others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | |||||||
chr1:47263744 | G | GTTTTTTT | 19 | a0001c0003t0006g0026 a0003c0004t0001g0332 a0003c0004t0001g0333 others(16): Show |
19 | HG00597.hp2 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2616-635_2616-629d others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | |||||||
chr1:47263744 | G | GTTTTTTT others(1): Show |
7 | a0003c0004t0001g0347 a0003c0004t0001g0353 a0003c0004t0001g0360 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.2616-636_2616-629d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | |||||||
chr1:47263744 | G | GTTTTTTT others(4): Show |
1 | a0003c0004t0001g0350 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2616-639_2616-629d others(13): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | |||||||
chr1:47263744 | G | GTTTTTTT others(5): Show |
1 | a0003c0004t0001g0358 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2616-640_2616-629d others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | |||||||
chr1:47263744 | GTTTTTTT | G | 25 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(22): Show |
25 | HG01069.hp2 HG01175.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.2616-635_2616-629d others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | |||||||
chr1:47263744 | GTTTTTTT others(1): Show |
G | 122 | a0001c0002t0003g0028 a0001c0002t0003g0030 a0002c0001t0002g0032 others(119): Show |
122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.2616-636_2616-629d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263744 | |||||||
chr1:47263814 | G | A | 1 | a0003c0004t0001g0023 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2616-698C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263814 | |||||||
chr1:47263897 | C | T | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2616-781G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263897 | |||||||
chr1:47263965 | C | G | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2616-849G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47263965 | |||||||
chr1:47264000 | G | A | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2616-884C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264000 | |||||||
chr1:47264016 | G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2616-900C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264016 | |||||||
chr1:47264040 | A | C | 1 | a0003c0004t0001g0372 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2616-924T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264040 | |||||||
chr1:47264213 | C | T | 130 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2616-1097G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264213 | |||||||
chr1:47264425 | A | T | 1 | a0003c0004t0001g0359 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2616-1309T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264425 | |||||||
chr1:47264473 | C | T | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2616-1357G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264473 | |||||||
chr1:47264505 | A | T | 1 | a0002c0001t0002g0051 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2616-1389T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264505 | |||||||
chr1:47264512 | A | C | 69 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(66): Show |
70 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.2616-1396T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264512 | |||||||
chr1:47264650 | G | A | 34 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(31): Show |
34 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.2616-1534C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264650 | |||||||
chr1:47264743 | G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2616-1627C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264743 | |||||||
chr1:47264786 | T | C | 1 | a0001c0003t0001g0114 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2616-1670A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264786 | |||||||
chr1:47264786 | T | TAATCCAA others(6): Show |
2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2616-1683_2616-167 others(17): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264786 | |||||||
chr1:47264930 | T | TA | 103 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(100): Show |
104 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.2616-1815dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264930 | |||||||
chr1:47264930 | T | TAA | 116 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.2616-1816_2616-181 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264930 | |||||||
chr1:47264930 | TA | T | 66 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(63): Show |
67 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.2616-1815delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264930 | |||||||
chr1:47264951 | A | G | 4 | a0004c0005t0002g0063 a0004c0005t0002g0064 a0004c0005t0002g0065 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2616-1835T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47264951 | |||||||
chr1:47265002 | G | A | 5 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(2): Show |
5 | HG02622.hp2 HG02922.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2616-1886C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265002 | |||||||
chr1:47265104 | C | T | 34 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(31): Show |
34 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.2616-1988G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265104 | |||||||
chr1:47265158 | C | T | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2616-2042G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265158 | |||||||
chr1:47265237 | C | CA | 45 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(42): Show |
45 | HG00621.hp1 HG00639.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2616-2122dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAA | 11 | a0001c0002t0003g0017 a0001c0002t0003g0227 a0001c0002t0004g0211 others(8): Show |
11 | HG01358.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2616-2123_2616-212 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAA | 25 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0010 others(22): Show |
25 | HG00597.hp2 HG00738.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.2616-2124_2616-212 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAAA | 35 | a0001c0002t0003g0009 a0001c0002t0003g0011 a0001c0002t0003g0013 others(32): Show |
36 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2616-2125_2616-212 others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAAAA | 7 | a0003c0004t0001g0334 a0003c0004t0001g0338 a0003c0004t0001g0343 others(4): Show |
7 | HG00735.hp2 HG01106.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.2616-2126_2616-212 others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAAAAAA | 44 | a0002c0001t0002g0232 a0002c0001t0002g0233 a0002c0001t0002g0235 others(41): Show |
44 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2616-2128_2616-212 others(11): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAAAAAA others(1): Show |
37 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0234 others(34): Show |
37 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.2616-2129_2616-212 others(12): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAAAAAA others(2): Show |
7 | a0002c0001t0002g0236 a0002c0001t0002g0237 a0002c0001t0002g0248 others(4): Show |
7 | HG01192.hp1 HG01346.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.2616-2130_2616-212 others(13): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAAAAAA others(4): Show |
2 | a0004c0005t0002g0063 a0004c0005t0002g0064 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2616-2132_2616-212 others(15): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAAAAAA others(5): Show |
5 | a0002c0001t0002g0035 a0002c0001t0002g0037 a0002c0001t0002g0046 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.2616-2133_2616-212 others(16): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAAAAAA others(6): Show |
10 | a0002c0001t0002g0034 a0002c0001t0002g0036 a0002c0001t0002g0040 others(7): Show |
10 | HG00673.hp2 HG02040.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.2616-2134_2616-212 others(17): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAAAAAA others(7): Show |
7 | a0002c0001t0002g0041 a0002c0001t0002g0043 a0002c0001t0002g0048 others(4): Show |
7 | HG01257.hp2 HG02056.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2616-2135_2616-212 others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAAAAAA others(8): Show |
7 | a0002c0001t0002g0033 a0002c0001t0002g0042 a0002c0001t0002g0049 others(4): Show |
7 | HG00280.hp2 HG00609.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2616-2136_2616-212 others(19): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265237 | C | CAAAAAAA others(9): Show |
1 | a0002c0001t0002g0039 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2616-2137_2616-212 others(20): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265237 | |||||||
chr1:47265250 | A | AC | 5 | a0001c0002t0001g0069 a0001c0002t0001g0092 a0001c0002t0001g0146 others(2): Show |
5 | NA18947.hp2 NA18960.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.2616-2135_2616-213 others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265250 | |||||||
chr1:47265250 | A | C | 63 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(60): Show |
64 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.2616-2134T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265250 | |||||||
chr1:47265252 | A | AAAAAAAA others(3): Show |
1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2616-2137_2616-213 others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265252 | |||||||
chr1:47265257 | A | AAAAAAAA others(6): Show |
2 | a0002c0001t0002g0052 a0002c0001t0002g0055 |
2 | NA18944.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2616-2142_2616-214 others(17): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265257 | |||||||
chr1:47265261 | C | A | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2616-2145G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265261 | |||||||
chr1:47265263 | C | A | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2616-2147G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265263 | |||||||
chr1:47265264 | A | AAAAAAAA others(8): Show |
1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2616-2149_2616-214 others(19): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265264 | |||||||
chr1:47265427 | G | A | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2616-2311C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265427 | |||||||
chr1:47265466 | G | GT | 6 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2616-2351dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265466 | |||||||
chr1:47265481 | T | C | 1 | a0001c0002t0001g0163 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2616-2365A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265481 | |||||||
chr1:47265637 | C | T | 1 | a0001c0002t0001g0169 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2616-2521G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265637 | |||||||
chr1:47265655 | C | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0093 |
2 | NA18992.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2616-2539G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265655 | |||||||
chr1:47265716 | G | T | 1 | a0002c0001t0002g0281 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2616-2600C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265716 | |||||||
chr1:47265717 | G | A | 1 | a0001c0002t0001g0170 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2616-2601C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265717 | |||||||
chr1:47265783 | C | CA | 38 | a0001c0002t0001g0067 a0001c0002t0001g0075 a0001c0002t0003g0013 others(35): Show |
39 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2616-2668dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265783 | |||||||
chr1:47265783 | C | CAA | 122 | a0001c0002t0001g0002 a0001c0002t0001g0068 a0001c0002t0001g0069 others(119): Show |
124 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.2616-2669_2616-266 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265783 | |||||||
chr1:47265783 | C | CAAA | 26 | a0001c0002t0001g0085 a0001c0002t0001g0087 a0001c0002t0001g0088 others(23): Show |
26 | HG01109.hp2 HG02027.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.2616-2670_2616-266 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265783 | |||||||
chr1:47265783 | CA | C | 55 | a0001c0002t0003g0007 a0001c0002t0004g0211 a0001c0003t0006g0026 others(52): Show |
56 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2616-2668delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265783 | |||||||
chr1:47265786 | A | G | 2 | a0003c0004t0001g0365 a0003c0004t0001g0366 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2616-2670T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265786 | |||||||
chr1:47265815 | C | T | 4 | a0003c0004t0001g0375 a0003c0004t0001g0376 a0003c0004t0001g0377 others(1): Show |
4 | HG02896.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2616-2699G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265815 | |||||||
chr1:47265829 | C | T | 3 | a0001c0003t0001g0322 a0001c0003t0001g0323 a0001c0003t0001g0324 |
3 | HG02976.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2616-2713G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265829 | |||||||
chr1:47265881 | G | A | 3 | a0003c0004t0001g0353 a0003c0004t0001g0356 a0003c0004t0001g0358 |
3 | HG02109.hp2 HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2616-2765C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265881 | |||||||
chr1:47265882 | G | C | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2616-2766C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47265882 | |||||||
chr1:47266004 | G | A | 129 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.2616-2888C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266004 | |||||||
chr1:47266010 | G | A | 19 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(16): Show |
19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2616-2894C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266010 | |||||||
chr1:47266025 | C | T | 2 | a0003c0004t0001g0024 a0003c0004t0001g0025 |
2 | HG00642.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2616-2909G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266025 | |||||||
chr1:47266462 | G | C | 33 | a0002c0001t0002g0033 a0002c0001t0002g0034 a0002c0001t0002g0035 others(30): Show |
33 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.2615+3173C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266462 | |||||||
chr1:47266495 | A | G | 1 | a0001c0002t0001g0187 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2615+3140T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266495 | |||||||
chr1:47266512 | C | A | 11 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(8): Show |
11 | HG02257.hp1 HG02622.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.2615+3123G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266512 | |||||||
chr1:47266529 | G | A | 1 | a0001c0002t0003g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2615+3106C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266529 | |||||||
chr1:47266590 | C | G | 1 | a0001c0003t0001g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2615+3045G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266590 | |||||||
chr1:47266617 | G | T | 4 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2615+3018C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266617 | |||||||
chr1:47266706 | G | T | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2615+2929C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266706 | |||||||
chr1:47266717 | C | A | 1 | a0003c0004t0001g0356 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2615+2918G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266717 | |||||||
chr1:47266753 | A | T | 2 | a0001c0003t0001g0322 a0001c0003t0001g0323 |
2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2615+2882T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266753 | |||||||
chr1:47266886 | A | G | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2615+2749T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47266886 | |||||||
chr1:47267064 | T | A | 11 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(8): Show |
11 | HG02257.hp1 HG02622.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.2615+2571A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267064 | |||||||
chr1:47267116 | G | T | 1 | a0001c0003t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2615+2519C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267116 | |||||||
chr1:47267266 | T | C | 26 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(23): Show |
26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.2615+2369A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267266 | |||||||
chr1:47267358 | C | T | 2 | a0001c0003t0001g0205 a0001c0003t0001g0209 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2615+2277G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267358 | |||||||
chr1:47267489 | G | A | 1 | a0002c0001t0002g0286 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2615+2146C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267489 | |||||||
chr1:47267522 | T | G | 3 | a0001c0003t0001g0083 a0001c0003t0001g0131 a0001c0003t0001g0141 |
3 | NA18939.hp1 NA18961.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2615+2113A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267522 | |||||||
chr1:47267565 | T | A | 3 | a0001c0003t0001g0119 a0001c0003t0001g0129 a0001c0003t0001g0140 |
3 | NA18963.hp1 NA18977.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2615+2070A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267565 | |||||||
chr1:47267583 | T | G | 1 | a0001c0003t0001g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2615+2052A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267583 | |||||||
chr1:47267617 | G | A | 1 | a0001c0003t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2615+2018C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267617 | |||||||
chr1:47267630 | G | A | 63 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0235 others(60): Show |
63 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2615+2005C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267630 | |||||||
chr1:47267667 | T | TA | 9 | a0001c0002t0001g0067 a0001c0002t0001g0145 a0001c0002t0001g0148 others(6): Show |
9 | HG03516.hp1 HG03704.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.2615+1967dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267667 | |||||||
chr1:47267667 | T | TAA | 58 | a0001c0002t0001g0002 a0001c0002t0001g0068 a0001c0002t0001g0069 others(55): Show |
59 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.2615+1966_2615+196 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267667 | |||||||
chr1:47267667 | TA | T | 205 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.2615+1967delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267667 | |||||||
chr1:47267667 | TAA | T | 14 | a0001c0002t0003g0006 a0001c0002t0003g0014 a0001c0002t0003g0015 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2615+1966_2615+196 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267667 | |||||||
chr1:47267702 | A | G | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2615+1933T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267702 | |||||||
chr1:47267706 | G | T | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2615+1929C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267706 | |||||||
chr1:47267708 | T | TTTTTG | 238 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.2615+1922_2615+192 others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267708 | |||||||
chr1:47267779 | G | A | 129 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.2615+1856C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267779 | |||||||
chr1:47267823 | C | A | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2615+1812G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267823 | |||||||
chr1:47267891 | G | A | 32 | a0002c0001t0002g0033 a0002c0001t0002g0034 a0002c0001t0002g0035 others(29): Show |
32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.2615+1744C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267891 | |||||||
chr1:47267919 | G | GAAAATTT others(3): Show |
1 | a0002c0001t0002g0314 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2615+1706_2615+171 others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47267919 | |||||||
chr1:47268218 | A | G | 1 | a0001c0002t0001g0177 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2615+1417T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268218 | |||||||
chr1:47268267 | G | A | 1 | a0001c0003t0001g0125 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2615+1368C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268267 | |||||||
chr1:47268476 | T | C | 130 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2615+1159A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268476 | |||||||
chr1:47268502 | T | C | 223 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2615+1133A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268502 | |||||||
chr1:47268512 | T | C | 1 | a0001c0002t0001g0155 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2615+1123A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268512 | |||||||
chr1:47268534 | C | T | 1 | a0001c0002t0004g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2615+1101G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268534 | |||||||
chr1:47268554 | C | T | 4 | a0004c0005t0002g0063 a0004c0005t0002g0064 a0004c0005t0002g0065 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2615+1081G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268554 | |||||||
chr1:47268572 | C | T | 223 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2615+1063G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268572 | |||||||
chr1:47268713 | G | A | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2615+922C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268713 | |||||||
chr1:47268740 | AAGAG | A | 5 | a0002c0001t0013g0062 a0004c0005t0002g0063 a0004c0005t0002g0064 others(2): Show |
5 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2615+891_2615+894d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268740 | |||||||
chr1:47268755 | T | C | 8 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2615+880A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268755 | |||||||
chr1:47268758 | C | CATAA | 12 | a0001c0002t0001g0069 a0001c0002t0001g0087 a0001c0002t0001g0147 others(9): Show |
12 | HG01891.hp2 HG02040.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.2615+873_2615+876d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268758 | |||||||
chr1:47268758 | CATAA | C | 218 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2615+873_2615+876d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268758 | |||||||
chr1:47268758 | CATAAATA others(1): Show |
C | 5 | a0001c0003t0001g0193 a0001c0003t0001g0194 a0001c0003t0001g0195 others(2): Show |
5 | NA18942.hp2 NA18949.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.2615+869_2615+876d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268758 | |||||||
chr1:47268758 | CATAAATA others(9): Show |
C | 1 | a0002c0001t0002g0242 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2615+861_2615+876d others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268758 | |||||||
chr1:47268773 | A | T | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2615+862T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268773 | |||||||
chr1:47268777 | A | T | 7 | a0001c0002t0003g0006 a0001c0002t0003g0014 a0001c0002t0003g0015 others(4): Show |
7 | HG01069.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2615+858T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268777 | |||||||
chr1:47268781 | A | T | 32 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(29): Show |
32 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.2615+854T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268781 | |||||||
chr1:47268782 | A | G | 12 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0112 others(9): Show |
12 | HG03491.hp1 HG03492.hp2 NA18941.hp1 others(9): Show |
intron_variant | MODIFIER | c.2615+853T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268782 | |||||||
chr1:47268785 | A | T | 70 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(67): Show |
70 | HG00597.hp2 HG00735.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.2615+850T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268785 | |||||||
chr1:47268789 | A | T | 94 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(91): Show |
95 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.2615+846T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268789 | |||||||
chr1:47268890 | G | A | 1 | a0002c0001t0002g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2615+745C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268890 | |||||||
chr1:47268991 | G | GGAGGCT | 130 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2615+643_2615+644i others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47268991 | |||||||
chr1:47269013 | C | T | 2 | a0002c0001t0002g0040 a0002c0001t0002g0046 |
2 | HG00673.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2615+622G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269013 | |||||||
chr1:47269078 | G | A | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2615+557C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269078 | |||||||
chr1:47269088 | C | CA | 29 | a0001c0002t0001g0088 a0001c0002t0001g0156 a0001c0002t0001g0157 others(26): Show |
29 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.2615+546dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269088 | |||||||
chr1:47269088 | CA | C | 16 | a0001c0002t0001g0067 a0001c0002t0001g0188 a0001c0003t0001g0003 others(13): Show |
17 | HG00597.hp1 HG00639.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.2615+546delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269088 | |||||||
chr1:47269111 | C | T | 1 | a0002c0001t0002g0235 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2615+524G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269111 | |||||||
chr1:47269175 | T | G | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2615+460A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269175 | |||||||
chr1:47269183 | T | A | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2615+452A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269183 | |||||||
chr1:47269370 | C | CA | 6 | a0001c0002t0001g0070 a0003c0004t0001g0353 a0003c0004t0001g0354 others(3): Show |
6 | HG00597.hp2 HG02109.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.2615+264dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269370 | |||||||
chr1:47269589 | A | T | 1 | a0001c0003t0001g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2615+46T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269589 | |||||||
chr1:47269590 | T | A | 1 | a0003c0004t0001g0373 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2615+45A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269590 | |||||||
chr1:47269608 | T | C | 130 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2615+27A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 14/16 | chr1 | 47269608 | |||||||
chr1:47269879 | T | C | 7 | a0002c0001t0002g0053 a0002c0001t0002g0060 a0002c0001t0002g0383 others(4): Show |
7 | HG00280.hp2 HG02132.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.2384-13A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47269879 | |||||||
chr1:47270062 | T | A | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2384-196A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270062 | |||||||
chr1:47270063 | C | T | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2384-197G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270063 | |||||||
chr1:47270101 | T | G | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2384-235A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270101 | |||||||
chr1:47270102 | G | T | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2384-236C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270102 | |||||||
chr1:47270227 | CA | C | 60 | a0001c0002t0003g0016 a0002c0001t0002g0033 a0002c0001t0002g0034 others(57): Show |
60 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.2384-362delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270227 | |||||||
chr1:47270227 | CAA | C | 36 | a0003c0004t0001g0004 a0003c0004t0001g0023 a0003c0004t0001g0024 others(33): Show |
37 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.2384-363_2384-362d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270227 | |||||||
chr1:47270227 | CAAA | C | 11 | a0001c0002t0003g0021 a0002c0001t0002g0032 a0002c0001t0002g0060 others(8): Show |
11 | HG00099.hp2 HG03130.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.2384-364_2384-362d others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270227 | |||||||
chr1:47270233 | A | AAT | 8 | a0001c0003t0001g0003 a0001c0003t0001g0217 a0001c0003t0001g0219 others(5): Show |
9 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2384-368_2384-367i others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270233 | |||||||
chr1:47270235 | A | T | 13 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(10): Show |
14 | HG00639.hp2 HG01891.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2384-369T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270235 | |||||||
chr1:47270237 | A | T | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2384-371T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270237 | |||||||
chr1:47270239 | A | AT | 33 | a0002c0001t0002g0237 a0002c0001t0002g0238 a0002c0001t0002g0243 others(30): Show |
33 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.2384-374_2384-373i others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270239 | |||||||
chr1:47270239 | A | ATAT | 13 | a0002c0001t0002g0235 a0002c0001t0002g0239 a0002c0001t0002g0246 others(10): Show |
13 | HG00597.hp1 HG01074.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.2384-374_2384-373i others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270239 | |||||||
chr1:47270239 | A | T | 25 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(22): Show |
26 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.2384-373T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270239 | |||||||
chr1:47270240 | AAATAT | A | 11 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2384-379_2384-375d others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270240 | |||||||
chr1:47270241 | A | AT | 8 | a0001c0002t0001g0147 a0001c0002t0001g0178 a0001c0002t0003g0014 others(5): Show |
8 | HG02083.hp2 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2384-376_2384-375i others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270241 | |||||||
chr1:47270241 | A | ATAT | 4 | a0001c0002t0001g0091 a0001c0003t0001g0189 a0001c0003t0001g0197 others(1): Show |
4 | HG01346.hp2 HG01515.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2384-376_2384-375i others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270241 | |||||||
chr1:47270241 | A | T | 130 | a0001c0002t0001g0097 a0001c0002t0001g0164 a0001c0002t0001g0177 others(127): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2384-375T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270241 | |||||||
chr1:47270243 | T | A | 3 | a0001c0002t0001g0089 a0005c0007t0004g0213 a0005c0007t0004g0214 |
3 | HG00673.hp1 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2384-377A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270243 | |||||||
chr1:47270247 | T | C | 14 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0002c0001t0002g0235 others(11): Show |
14 | HG00597.hp1 HG01074.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2384-381A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270247 | |||||||
chr1:47270247 | T | TACAC | 3 | a0002c0001t0002g0274 a0002c0001t0002g0281 a0002c0001t0002g0305 |
3 | HG01496.hp1 HG03710.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.2384-382_2384-381i others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270247 | |||||||
chr1:47270247 | TATATATA others(9): Show |
T | 4 | a0004c0005t0002g0063 a0004c0005t0002g0064 a0004c0005t0002g0065 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2384-397_2384-382d others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270247 | |||||||
chr1:47270249 | T | C | 53 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(50): Show |
53 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.2384-383A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270249 | |||||||
chr1:47270249 | T | TACACAC | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2384-384_2384-383i others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270249 | |||||||
chr1:47270251 | T | C | 107 | a0001c0002t0001g0073 a0001c0002t0003g0007 a0001c0002t0003g0008 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.2384-385A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270251 | |||||||
chr1:47270251 | TATATACA others(5): Show |
T | 1 | a0001c0003t0001g0107 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2384-397_2384-386d others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270251 | |||||||
chr1:47270253 | T | C | 157 | a0001c0002t0001g0070 a0001c0002t0001g0073 a0001c0002t0001g0087 others(154): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.2384-387A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270253 | |||||||
chr1:47270253 | T | TAC | 41 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(38): Show |
42 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.2384-388_2384-387i others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270253 | |||||||
chr1:47270253 | T | TACAC | 7 | a0001c0002t0001g0085 a0001c0002t0001g0148 a0001c0002t0001g0164 others(4): Show |
7 | HG01109.hp2 HG02004.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.2384-388_2384-387i others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270253 | |||||||
chr1:47270253 | TATACACA others(5): Show |
T | 3 | a0001c0003t0001g0077 a0001c0003t0001g0078 a0001c0003t0001g0079 |
3 | HG01109.hp1 HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2384-399_2384-388d others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270253 | |||||||
chr1:47270255 | T | C | 218 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(215): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.2384-389A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | |||||||
chr1:47270255 | T | TAC | 15 | a0001c0002t0001g0150 a0001c0003t0001g0103 a0001c0003t0001g0110 others(12): Show |
15 | HG00735.hp1 HG01167.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2384-391_2384-390d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | |||||||
chr1:47270255 | T | TACAC | 46 | a0001c0003t0001g0071 a0001c0003t0001g0076 a0001c0003t0001g0081 others(43): Show |
46 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.2384-393_2384-390d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | |||||||
chr1:47270255 | T | TACACAC | 10 | a0001c0002t0004g0228 a0001c0003t0001g0001 a0001c0003t0001g0083 others(7): Show |
11 | HG02027.hp1 HG02055.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2384-395_2384-390d others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | |||||||
chr1:47270255 | T | TACACACA others(1): Show |
6 | a0001c0003t0001g0137 a0001c0003t0001g0138 a0001c0003t0001g0322 others(3): Show |
6 | HG02735.hp2 HG02976.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384-397_2384-390d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | |||||||
chr1:47270255 | TAC | T | 7 | a0001c0003t0001g0331 a0003c0004t0001g0022 a0003c0004t0001g0031 others(4): Show |
7 | HG00597.hp2 HG01175.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2384-391_2384-390d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | |||||||
chr1:47270255 | TACAC | T | 6 | a0003c0004t0001g0332 a0003c0004t0001g0335 a0003c0004t0001g0337 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384-393_2384-390d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | |||||||
chr1:47270255 | TACACACA others(3): Show |
T | 1 | a0002c0001t0002g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2384-399_2384-390d others(12): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | |||||||
chr1:47270255 | TACACACA others(5): Show |
T | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2384-401_2384-390d others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270255 | |||||||
chr1:47270257 | C | T | 43 | a0001c0002t0004g0211 a0001c0002t0004g0229 a0001c0002t0004g0230 others(40): Show |
44 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2384-391G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270257 | |||||||
chr1:47270259 | C | T | 3 | a0003c0004t0001g0336 a0003c0004t0001g0343 a0003c0004t0001g0372 |
3 | HG01516.hp1 HG03710.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2384-393G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270259 | |||||||
chr1:47270263 | C | T | 2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2384-397G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270263 | |||||||
chr1:47270388 | C | A | 9 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(6): Show |
9 | NA18960.hp1 NA18964.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2384-522G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270388 | |||||||
chr1:47270389 | G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2384-523C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270389 | |||||||
chr1:47270478 | C | T | 1 | a0002c0001t0015g0388 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2384-612G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270478 | |||||||
chr1:47270644 | T | C | 2 | a0001c0002t0001g0002 a0001c0002t0001g0092 |
3 | NA18950.hp1 NA19010.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2384-778A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270644 | |||||||
chr1:47270668 | A | C | 1 | a0002c0001t0002g0314 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2384-802T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270668 | |||||||
chr1:47270670 | C | CT | 44 | a0001c0002t0001g0087 a0001c0002t0001g0089 a0001c0002t0001g0091 others(41): Show |
44 | HG00280.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.2384-805dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | |||||||
chr1:47270670 | C | CTT | 80 | a0002c0001t0002g0032 a0002c0001t0002g0051 a0002c0001t0002g0061 others(77): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.2384-806_2384-805d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | |||||||
chr1:47270670 | C | CTTT | 13 | a0001c0003t0001g0117 a0001c0003t0001g0121 a0001c0003t0001g0122 others(10): Show |
13 | HG00621.hp2 HG01175.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.2384-807_2384-805d others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | |||||||
chr1:47270670 | C | T | 1 | a0002c0001t0002g0314 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2384-804G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | |||||||
chr1:47270670 | CT | C | 36 | a0001c0002t0001g0069 a0001c0002t0001g0073 a0001c0002t0001g0074 others(33): Show |
36 | HG01069.hp2 HG01167.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.2384-805delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | |||||||
chr1:47270670 | CTT | C | 7 | a0001c0002t0003g0227 a0001c0002t0003g0325 a0001c0002t0003g0326 others(4): Show |
7 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2384-806_2384-805d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | |||||||
chr1:47270670 | CTTTTT | C | 57 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(54): Show |
58 | HG00099.hp1 HG00597.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.2384-809_2384-805d others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270670 | |||||||
chr1:47270747 | A | G | 239 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2384-881T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270747 | |||||||
chr1:47270775 | C | T | 19 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(16): Show |
19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2384-909G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270775 | |||||||
chr1:47270816 | C | T | 69 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(66): Show |
70 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.2384-950G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270816 | |||||||
chr1:47270823 | T | A | 1 | a0002c0001t0002g0313 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2384-957A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270823 | |||||||
chr1:47270827 | C | G | 1 | a0002c0001t0002g0314 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2384-961G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270827 | |||||||
chr1:47270828 | G | C | 1 | a0002c0001t0002g0314 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2384-962C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270828 | |||||||
chr1:47270898 | C | T | 3 | a0001c0002t0003g0011 a0001c0003t0006g0026 a0001c0003t0006g0027 |
3 | HG02486.hp2 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2384-1032G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47270898 | |||||||
chr1:47271060 | A | T | 9 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(6): Show |
9 | NA18960.hp1 NA18964.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2383+1016T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271060 | |||||||
chr1:47271141 | T | C | 1 | a0003c0004t0001g0350 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2383+935A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271141 | |||||||
chr1:47271290 | T | G | 1 | a0002c0001t0002g0314 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2383+786A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271290 | |||||||
chr1:47271311 | G | A | 67 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(64): Show |
68 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.2383+765C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271311 | |||||||
chr1:47271317 | C | T | 223 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2383+759G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271317 | |||||||
chr1:47271432 | T | G | 1 | a0002c0001t0002g0314 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2383+644A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271432 | |||||||
chr1:47271434 | T | A | 1 | a0002c0001t0002g0314 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2383+642A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271434 | |||||||
chr1:47271490 | C | T | 1 | a0001c0002t0003g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2383+586G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271490 | |||||||
chr1:47271541 | G | A | 1 | a0002c0001t0002g0037 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2383+535C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271541 | |||||||
chr1:47271546 | G | A | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2383+530C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271546 | |||||||
chr1:47271558 | C | CA | 10 | a0001c0002t0001g0070 a0001c0002t0001g0204 a0001c0002t0003g0013 others(7): Show |
10 | HG00738.hp2 HG02486.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2383+517dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271558 | |||||||
chr1:47271558 | CA | C | 133 | a0001c0002t0001g0203 a0001c0003t0001g0109 a0001c0003t0001g0113 others(130): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.2383+517delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271558 | |||||||
chr1:47271574 | A | G | 1 | a0002c0001t0002g0314 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2383+502T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271574 | |||||||
chr1:47271701 | G | C | 1 | a0003c0004t0001g0345 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2383+375C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271701 | |||||||
chr1:47271802 | C | T | 19 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(16): Show |
19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2383+274G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271802 | |||||||
chr1:47271813 | A | C | 64 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0002c0001t0013g0062 others(61): Show |
65 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.2383+263T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271813 | |||||||
chr1:47271819 | A | C | 3 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 |
3 | HG01069.hp2 HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2383+257T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271819 | |||||||
chr1:47271820 | C | A | 1 | a0002c0001t0002g0260 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2383+256G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271820 | |||||||
chr1:47271821 | A | C | 1 | a0002c0001t0002g0260 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2383+255T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271821 | |||||||
chr1:47271838 | C | A | 4 | a0001c0002t0003g0017 a0001c0002t0004g0229 a0001c0002t0004g0230 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2383+238G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271838 | |||||||
chr1:47271965 | T | C | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2383+111A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 13/16 | chr1 | 47271965 | |||||||
chr1:47272258 | C | T | 32 | a0002c0001t0002g0033 a0002c0001t0002g0034 a0002c0001t0002g0035 others(29): Show |
32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.2218-17G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272258 | |||||||
chr1:47272390 | A | G | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2218-149T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272390 | |||||||
chr1:47272448 | AT | A | 165 | a0001c0002t0003g0227 a0002c0001t0002g0032 a0002c0001t0002g0033 others(162): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2218-208delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272448 | |||||||
chr1:47272448 | ATT | A | 21 | a0003c0004t0001g0004 a0003c0004t0001g0031 a0003c0004t0001g0332 others(18): Show |
22 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.2218-209_2218-208d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272448 | |||||||
chr1:47272524 | T | C | 1 | a0001c0003t0001g0190 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2218-283A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272524 | |||||||
chr1:47272551 | C | T | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2218-310G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272551 | |||||||
chr1:47272598 | C | CACCACCA others(48): Show |
1 | a0002c0001t0002g0043 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2218-412_2218-358d others(57): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272598 | |||||||
chr1:47272978 | C | T | 4 | a0003c0004t0001g0375 a0003c0004t0001g0376 a0003c0004t0001g0377 others(1): Show |
4 | HG02896.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2218-737G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272978 | |||||||
chr1:47272979 | A | G | 56 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2218-738T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47272979 | |||||||
chr1:47273025 | T | C | 1 | a0001c0003t0010g0199 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2218-784A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273025 | |||||||
chr1:47273102 | G | A | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2218-861C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273102 | |||||||
chr1:47273269 | G | A | 1 | a0001c0003t0001g0190 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2218-1028C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273269 | |||||||
chr1:47273285 | T | C | 59 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2218-1044A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273285 | |||||||
chr1:47273408 | C | T | 1 | a0001c0003t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2218-1167G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273408 | |||||||
chr1:47273569 | G | T | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2218-1328C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273569 | |||||||
chr1:47273640 | G | A | 2 | a0003c0004t0001g0347 a0003c0004t0001g0348 |
2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2218-1399C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273640 | |||||||
chr1:47273705 | G | A | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2218-1464C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273705 | |||||||
chr1:47273761 | C | T | 19 | a0001c0003t0001g0081 a0001c0003t0001g0082 a0001c0003t0001g0106 others(16): Show |
19 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.2218-1520G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273761 | |||||||
chr1:47273789 | A | G | 2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2218-1548T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273789 | |||||||
chr1:47273793 | T | A | 1 | a0001c0003t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2218-1552A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273793 | |||||||
chr1:47273989 | T | C | 6 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2218-1748A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47273989 | |||||||
chr1:47274030 | T | C | 1 | a0001c0002t0001g0164 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2218-1789A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274030 | |||||||
chr1:47274095 | TAC | T | 239 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2218-1856_2218-185 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274095 | |||||||
chr1:47274105 | C | G | 2 | a0001c0002t0001g0088 a0001c0002t0001g0171 |
2 | NA18974.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2218-1864G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274105 | |||||||
chr1:47274120 | T | C | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2218-1879A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274120 | |||||||
chr1:47274220 | A | G | 1 | a0003c0004t0001g0350 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2218-1979T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274220 | |||||||
chr1:47274371 | G | A | 1 | a0002c0001t0002g0049 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2218-2130C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274371 | |||||||
chr1:47274455 | C | T | 35 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(32): Show |
35 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.2218-2214G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274455 | |||||||
chr1:47274471 | C | T | 1 | a0001c0003t0001g0142 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2218-2230G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274471 | |||||||
chr1:47274613 | A | G | 227 | a0001c0002t0001g0067 a0001c0002t0001g0165 a0001c0002t0001g0166 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.2218-2372T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274613 | |||||||
chr1:47274730 | A | C | 1 | a0011c0018t0008g0212 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2218-2489T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274730 | |||||||
chr1:47274766 | T | C | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2218-2525A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274766 | |||||||
chr1:47274777 | G | C | 2 | a0001c0002t0001g0200 a0001c0002t0001g0201 |
2 | NA18995.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2218-2536C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274777 | |||||||
chr1:47274807 | CT | C | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2218-2567delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274807 | |||||||
chr1:47274851 | C | T | 4 | a0004c0005t0002g0063 a0004c0005t0002g0064 a0004c0005t0002g0065 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2218-2610G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274851 | |||||||
chr1:47274975 | A | C | 1 | a0002c0001t0002g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2218-2734T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47274975 | |||||||
chr1:47275009 | G | A | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2218-2768C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275009 | |||||||
chr1:47275076 | T | C | 309 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.2218-2835A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275076 | |||||||
chr1:47275147 | T | TCAA | 237 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2218-2909_2218-290 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275147 | |||||||
chr1:47275189 | G | A | 2 | a0001c0002t0004g0228 a0003c0004t0001g0357 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2218-2948C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275189 | |||||||
chr1:47275201 | G | A | 92 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0232 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.2218-2960C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275201 | |||||||
chr1:47275240 | T | A | 4 | a0004c0005t0002g0063 a0004c0005t0002g0064 a0004c0005t0002g0065 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2218-2999A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275240 | |||||||
chr1:47275292 | G | A | 8 | a0003c0004t0001g0022 a0003c0004t0001g0023 a0003c0004t0001g0024 others(5): Show |
8 | HG00642.hp1 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2218-3051C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275292 | |||||||
chr1:47275292 | G | T | 1 | a0001c0003t0001g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2218-3051C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275292 | |||||||
chr1:47275351 | G | C | 1 | a0003c0004t0001g0022 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2218-3110C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275351 | |||||||
chr1:47275400 | A | T | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2218-3159T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275400 | |||||||
chr1:47275466 | G | A | 1 | a0002c0001t0002g0387 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2218-3225C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275466 | |||||||
chr1:47275485 | G | A | 35 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(32): Show |
35 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.2218-3244C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275485 | |||||||
chr1:47275630 | A | AT | 17 | a0001c0003t0001g0003 a0001c0003t0001g0129 a0001c0003t0001g0216 others(14): Show |
18 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2218-3390dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275630 | |||||||
chr1:47275661 | G | C | 7 | a0001c0002t0003g0227 a0001c0002t0003g0325 a0001c0002t0003g0326 others(4): Show |
7 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2218-3420C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275661 | |||||||
chr1:47275664 | G | A | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2218-3423C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275664 | |||||||
chr1:47275676 | G | C | 56 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2218-3435C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275676 | |||||||
chr1:47275687 | C | T | 1 | a0001c0002t0003g0016 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2218-3446G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275687 | |||||||
chr1:47275760 | G | A | 1 | a0001c0003t0010g0199 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2218-3519C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275760 | |||||||
chr1:47275848 | T | A | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2218-3607A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275848 | |||||||
chr1:47275920 | C | A | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2218-3679G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47275920 | |||||||
chr1:47276001 | A | G | 8 | a0003c0004t0001g0369 a0003c0004t0001g0371 a0003c0004t0001g0372 others(5): Show |
8 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.2218-3760T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276001 | |||||||
chr1:47276002 | C | CT | 214 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.2218-3762dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276002 | |||||||
chr1:47276027 | G | A | 35 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(32): Show |
35 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.2218-3786C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276027 | |||||||
chr1:47276051 | G | A | 1 | a0001c0002t0001g0094 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3810C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276051 | |||||||
chr1:47276052 | G | C | 1 | a0001c0002t0001g0094 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3811C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276052 | |||||||
chr1:47276054 | G | C | 1 | a0001c0002t0001g0094 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3813C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276054 | |||||||
chr1:47276056 | G | A | 1 | a0001c0002t0001g0094 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3815C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276056 | |||||||
chr1:47276057 | C | G | 1 | a0001c0002t0001g0094 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3816G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276057 | |||||||
chr1:47276061 | G | C | 1 | a0001c0002t0001g0094 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3820C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276061 | |||||||
chr1:47276063 | T | C | 1 | a0001c0002t0001g0094 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3822A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276063 | |||||||
chr1:47276066 | G | T | 1 | a0001c0003t0001g0192 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2218-3825C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276066 | |||||||
chr1:47276067 | A | T | 1 | a0001c0002t0001g0094 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2218-3826T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276067 | |||||||
chr1:47276097 | G | A | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2218-3856C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276097 | |||||||
chr1:47276183 | G | A | 1 | a0002c0001t0002g0033 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2218-3942C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276183 | |||||||
chr1:47276249 | G | A | 92 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0232 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.2217+3992C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276249 | |||||||
chr1:47276307 | T | G | 129 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.2217+3934A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276307 | |||||||
chr1:47276396 | G | A | 1 | a0003c0004t0001g0374 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2217+3845C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276396 | |||||||
chr1:47276415 | C | CAT | 3 | a0001c0002t0001g0177 a0001c0003t0001g0126 a0010c0019t0001g0175 |
3 | HG02602.hp1 HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2217+3824_2217+382 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276415 | |||||||
chr1:47276415 | CAT | C | 3 | a0003c0004t0001g0380 a0003c0004t0001g0381 a0003c0004t0001g0382 |
3 | HG02922.hp2 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2217+3824_2217+382 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276415 | |||||||
chr1:47276431 | A | C | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2217+3810T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276431 | |||||||
chr1:47276584 | G | T | 2 | a0002c0001t0002g0237 a0002c0001t0002g0281 |
2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2217+3657C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276584 | |||||||
chr1:47276589 | C | T | 56 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2217+3652G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276589 | |||||||
chr1:47276600 | G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2217+3641C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276600 | |||||||
chr1:47276735 | G | A | 1 | a0012c0012t0002g0298 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2217+3506C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276735 | |||||||
chr1:47276744 | A | G | 309 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.2217+3497T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276744 | |||||||
chr1:47276812 | T | TA | 54 | a0001c0002t0001g0068 a0001c0002t0001g0073 a0001c0002t0001g0075 others(51): Show |
54 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.2217+3428dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276812 | |||||||
chr1:47276812 | TA | T | 45 | a0001c0002t0001g0074 a0001c0002t0001g0146 a0001c0002t0004g0231 others(42): Show |
45 | HG00408.hp1 HG00738.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2217+3428delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276812 | |||||||
chr1:47276812 | TAA | T | 73 | a0001c0002t0004g0211 a0001c0002t0004g0229 a0001c0003t0001g0216 others(70): Show |
73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.2217+3427_2217+342 others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276812 | |||||||
chr1:47276812 | TAAA | T | 64 | a0001c0002t0003g0010 a0001c0002t0003g0015 a0001c0002t0003g0019 others(61): Show |
65 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2217+3426_2217+342 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276812 | |||||||
chr1:47276812 | TAAAA | T | 59 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2217+3425_2217+342 others(8): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276812 | |||||||
chr1:47276814 | A | T | 2 | a0002c0001t0002g0239 a0002c0001t0002g0257 |
2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2217+3427T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276814 | |||||||
chr1:47276828 | A | C | 1 | a0001c0003t0001g0112 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2217+3413T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47276828 | |||||||
chr1:47277036 | T | C | 3 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 |
3 | HG02055.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2217+3205A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277036 | |||||||
chr1:47277054 | T | C | 129 | a0002c0001t0002g0032 a0002c0001t0002g0033 a0002c0001t0002g0034 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.2217+3187A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277054 | |||||||
chr1:47277241 | G | C | 3 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 |
3 | HG02055.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2217+3000C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277241 | |||||||
chr1:47277480 | C | T | 4 | a0002c0001t0002g0264 a0002c0001t0002g0265 a0002c0001t0002g0266 others(1): Show |
4 | HG00738.hp1 HG01433.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2217+2761G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277480 | |||||||
chr1:47277491 | G | A | 9 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2217+2750C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277491 | |||||||
chr1:47277506 | A | C | 2 | a0003c0004t0001g0354 a0003c0004t0001g0355 |
2 | HG00597.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2217+2735T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277506 | |||||||
chr1:47277517 | C | A | 32 | a0002c0001t0002g0033 a0002c0001t0002g0034 a0002c0001t0002g0035 others(29): Show |
32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.2217+2724G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277517 | |||||||
chr1:47277712 | A | C | 1 | a0001c0002t0001g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2217+2529T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277712 | |||||||
chr1:47277818 | C | T | 29 | a0002c0001t0002g0232 a0002c0001t0002g0233 a0002c0001t0002g0234 others(26): Show |
29 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.2217+2423G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277818 | |||||||
chr1:47277987 | C | T | 3 | a0005c0007t0004g0213 a0005c0007t0004g0214 a0005c0017t0004g0215 |
3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2217+2254G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47277987 | |||||||
chr1:47278153 | T | C | 147 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(144): Show |
149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.2217+2088A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278153 | |||||||
chr1:47278222 | T | C | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2217+2019A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278222 | |||||||
chr1:47278247 | T | C | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.2217+1994A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278247 | |||||||
chr1:47278286 | C | A | 1 | a0002c0001t0002g0254 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2217+1955G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278286 | |||||||
chr1:47278375 | T | C | 1 | a0001c0002t0003g0014 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2217+1866A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278375 | |||||||
chr1:47278541 | G | A | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.2217+1700C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278541 | |||||||
chr1:47278645 | A | T | 1 | a0002c0001t0002g0043 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2217+1596T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278645 | |||||||
chr1:47278648 | G | A | 4 | a0003c0004t0001g0371 a0003c0004t0001g0372 a0003c0015t0001g0367 others(1): Show |
4 | HG00738.hp2 HG03710.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.2217+1593C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278648 | |||||||
chr1:47278742 | G | A | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.2217+1499C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278742 | |||||||
chr1:47278752 | G | A | 1 | a0002c0001t0002g0386 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2217+1489C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278752 | |||||||
chr1:47278785 | G | A | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.2217+1456C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278785 | |||||||
chr1:47278821 | T | A | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2217+1420A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278821 | |||||||
chr1:47278822 | A | T | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.2217+1419T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278822 | |||||||
chr1:47278881 | CTAAATTT others(128): Show |
C | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1225_2217+135 others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278881 | |||||||
chr1:47278991 | A | G | 2 | a0001c0003t0001g0109 a0001c0003t0001g0118 |
2 | HG01168.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2217+1250T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47278991 | |||||||
chr1:47279028 | A | T | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1213T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279028 | |||||||
chr1:47279049 | A | G | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1192T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279049 | |||||||
chr1:47279060 | G | A | 5 | a0002c0001t0013g0062 a0004c0005t0002g0063 a0004c0005t0002g0064 others(2): Show |
5 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2217+1181C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279060 | |||||||
chr1:47279068 | T | C | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1173A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279068 | |||||||
chr1:47279072 | A | T | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1169T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279072 | |||||||
chr1:47279079 | C | T | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1162G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279079 | |||||||
chr1:47279080 | A | G | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2217+1161T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279080 | |||||||
chr1:47279093 | C | G | 4 | a0004c0005t0002g0063 a0004c0005t0002g0064 a0004c0005t0002g0065 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2217+1148G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279093 | |||||||
chr1:47279118 | A | C | 26 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(23): Show |
26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.2217+1123T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279118 | |||||||
chr1:47279199 | C | T | 4 | a0002c0001t0002g0236 a0002c0001t0002g0260 a0002c0001t0002g0267 others(1): Show |
4 | HG01361.hp2 HG02683.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2217+1042G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279199 | |||||||
chr1:47279278 | G | A | 1 | a0001c0002t0003g0011 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2217+963C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279278 | |||||||
chr1:47279282 | C | CA | 8 | a0001c0002t0001g0164 a0001c0003t0001g0104 a0001c0003t0001g0133 others(5): Show |
8 | HG01081.hp2 HG02055.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.2217+958dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279282 | |||||||
chr1:47279282 | CA | C | 119 | a0001c0002t0001g0097 a0001c0002t0001g0177 a0001c0003t0001g0003 others(116): Show |
120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.2217+958delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279282 | |||||||
chr1:47279299 | AAT | A | 32 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(29): Show |
32 | HG01069.hp2 HG01884.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.2217+940_2217+941d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279299 | |||||||
chr1:47279301 | T | A | 2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2217+940A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279301 | |||||||
chr1:47279418 | T | C | 1 | a0001c0002t0003g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2217+823A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279418 | |||||||
chr1:47279706 | G | A | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2217+535C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279706 | |||||||
chr1:47279726 | T | A | 1 | a0001c0002t0004g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2217+515A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279726 | |||||||
chr1:47279727 | C | A | 1 | a0001c0002t0004g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2217+514G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279727 | |||||||
chr1:47279727 | C | CA | 102 | a0001c0002t0001g0069 a0001c0002t0001g0086 a0001c0002t0001g0177 others(99): Show |
103 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.2217+513dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279727 | |||||||
chr1:47279727 | C | CAA | 28 | a0001c0002t0003g0006 a0001c0002t0003g0013 a0001c0002t0003g0015 others(25): Show |
29 | HG00639.hp2 HG01891.hp1 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.2217+512_2217+513d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279727 | |||||||
chr1:47279727 | CA | C | 6 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0170 others(3): Show |
6 | HG01168.hp1 NA18947.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2217+513delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279727 | |||||||
chr1:47279740 | A | C | 1 | a0002c0001t0002g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2217+501T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279740 | |||||||
chr1:47279746 | C | A | 11 | a0001c0002t0003g0012 a0001c0002t0003g0013 a0001c0002t0004g0211 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2217+495G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279746 | |||||||
chr1:47279749 | C | A | 1 | a0001c0002t0004g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2217+492G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279749 | |||||||
chr1:47279834 | T | C | 147 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(144): Show |
149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.2217+407A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279834 | |||||||
chr1:47279836 | C | T | 1 | a0002c0001t0005g0273 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2217+405G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279836 | |||||||
chr1:47279972 | A | C | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.2217+269T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47279972 | |||||||
chr1:47280088 | G | A | 1 | a0001c0002t0003g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2217+153C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 12/16 | chr1 | 47280088 | |||||||
chr1:47281321 | G | A | 59 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1249-112C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/16 | chr1 | 47281321 | |||||||
chr1:47281418 | T | C | 59 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1249-209A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/16 | chr1 | 47281418 | |||||||
chr1:47281483 | A | G | 1 | a0002c0001t0002g0305 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1249-274T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/16 | chr1 | 47281483 | |||||||
chr1:47281773 | G | A | 256 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(253): Show |
260 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.1249-564C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/16 | chr1 | 47281773 | |||||||
chr1:47282239 | T | C | 1 | a0001c0003t0010g0199 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1248+106A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 11/16 | chr1 | 47282239 | |||||||
chr1:47282480 | C | G | 1 | a0001c0003t0001g0076 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1134-21G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47282480 | |||||||
chr1:47282571 | T | A | 7 | a0002c0001t0002g0256 a0002c0001t0002g0271 a0002c0001t0002g0291 others(4): Show |
7 | NA18939.hp2 NA18955.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134-112A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47282571 | |||||||
chr1:47282892 | A | G | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134-433T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47282892 | |||||||
chr1:47282958 | A | G | 1 | a0002c0001t0002g0248 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1134-499T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47282958 | |||||||
chr1:47283180 | G | C | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1134-721C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283180 | |||||||
chr1:47283279 | T | C | 59 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1134-820A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283279 | |||||||
chr1:47283581 | T | C | 1 | a0002c0001t0002g0272 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1134-1122A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283581 | |||||||
chr1:47283729 | C | T | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.1134-1270G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283729 | |||||||
chr1:47283921 | T | C | 2 | a0001c0002t0001g0074 a0001c0002t0001g0075 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1134-1462A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283921 | |||||||
chr1:47283922 | A | G | 26 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(23): Show |
26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.1134-1463T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283922 | |||||||
chr1:47283972 | C | T | 1 | a0001c0003t0001g0108 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1134-1513G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283972 | |||||||
chr1:47283981 | C | T | 1 | a0001c0002t0001g0169 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1134-1522G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283981 | |||||||
chr1:47283985 | G | A | 1 | a0002c0001t0002g0297 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1134-1526C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47283985 | |||||||
chr1:47284061 | C | A | 1 | a0001c0002t0003g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1134-1602G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284061 | |||||||
chr1:47284259 | T | C | 147 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(144): Show |
149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1134-1800A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284259 | |||||||
chr1:47284514 | T | C | 2 | a0001c0002t0004g0229 a0001c0002t0004g0230 |
2 | HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1134-2055A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284514 | |||||||
chr1:47284596 | A | G | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.1134-2137T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284596 | |||||||
chr1:47284608 | G | C | 16 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(13): Show |
16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1134-2149C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284608 | |||||||
chr1:47284640 | A | T | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1134-2181T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284640 | |||||||
chr1:47284713 | A | G | 4 | a0004c0005t0002g0063 a0004c0005t0002g0064 a0004c0005t0002g0065 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134-2254T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284713 | |||||||
chr1:47284879 | G | GA | 19 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(16): Show |
19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1134-2421dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284879 | |||||||
chr1:47284889 | C | CA | 32 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(29): Show |
32 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.1134-2431dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47284889 | |||||||
chr1:47285020 | C | CT | 98 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(95): Show |
100 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1133+2530dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285020 | |||||||
chr1:47285020 | C | CTTT | 147 | a0001c0002t0001g0002 a0001c0002t0001g0068 a0001c0002t0001g0069 others(144): Show |
149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1133+2528_1133+253 others(7): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285020 | |||||||
chr1:47285087 | G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1133+2464C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285087 | |||||||
chr1:47285256 | T | G | 1 | a0003c0004t0001g0362 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1133+2295A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285256 | |||||||
chr1:47285340 | T | A | 21 | a0003c0004t0001g0004 a0003c0004t0001g0031 a0003c0004t0001g0332 others(18): Show |
22 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1133+2211A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285340 | |||||||
chr1:47285448 | A | T | 11 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(8): Show |
11 | HG02257.hp1 HG02622.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.1133+2103T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285448 | |||||||
chr1:47285618 | C | T | 5 | a0002c0001t0013g0062 a0004c0005t0002g0063 a0004c0005t0002g0064 others(2): Show |
5 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1133+1933G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285618 | |||||||
chr1:47285647 | G | A | 3 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 |
3 | HG02055.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1133+1904C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285647 | |||||||
chr1:47285919 | G | A | 19 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(16): Show |
19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1133+1632C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47285919 | |||||||
chr1:47286143 | A | G | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.1133+1408T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286143 | |||||||
chr1:47286277 | C | T | 2 | a0001c0003t0001g0080 a0001c0003t0001g0183 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1133+1274G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286277 | |||||||
chr1:47286278 | G | A | 28 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(25): Show |
28 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1133+1273C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286278 | |||||||
chr1:47286292 | C | T | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1133+1259G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286292 | |||||||
chr1:47286323 | C | T | 37 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(34): Show |
37 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1133+1228G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286323 | |||||||
chr1:47286396 | G | A | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1133+1155C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286396 | |||||||
chr1:47286407 | C | T | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1133+1144G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286407 | |||||||
chr1:47286428 | G | A | 44 | a0003c0004t0001g0004 a0003c0004t0001g0031 a0003c0004t0001g0332 others(41): Show |
45 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1133+1123C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286428 | |||||||
chr1:47286447 | G | A | 1 | a0001c0003t0001g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1133+1104C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286447 | |||||||
chr1:47286572 | G | A | 1 | a0002c0001t0002g0297 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1133+979C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286572 | |||||||
chr1:47286588 | G | A | 35 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(32): Show |
35 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1133+963C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286588 | |||||||
chr1:47286648 | T | C | 1 | a0002c0001t0002g0053 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1133+903A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286648 | |||||||
chr1:47286651 | G | A | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1133+900C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286651 | |||||||
chr1:47286660 | C | T | 3 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 |
3 | HG01069.hp2 HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1133+891G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286660 | |||||||
chr1:47286794 | G | A | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1133+757C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286794 | |||||||
chr1:47286829 | C | T | 2 | a0001c0002t0001g0074 a0001c0002t0001g0075 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1133+722G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286829 | |||||||
chr1:47286835 | C | T | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.1133+716G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286835 | |||||||
chr1:47286924 | T | A | 2 | a0001c0002t0004g0211 a0011c0018t0008g0212 |
2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1133+627A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286924 | |||||||
chr1:47286928 | G | C | 59 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1133+623C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286928 | |||||||
chr1:47286963 | T | C | 4 | a0002c0001t0002g0264 a0002c0001t0002g0265 a0002c0001t0002g0266 others(1): Show |
4 | HG00738.hp1 HG01433.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133+588A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286963 | |||||||
chr1:47286964 | C | T | 1 | a0002c0001t0002g0292 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1133+587G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47286964 | |||||||
chr1:47287060 | A | C | 59 | a0001c0003t0006g0026 a0001c0003t0006g0027 a0003c0004t0001g0004 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1133+491T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287060 | |||||||
chr1:47287085 | G | A | 56 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1133+466C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287085 | |||||||
chr1:47287275 | T | G | 1 | a0002c0001t0002g0304 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1133+276A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287275 | |||||||
chr1:47287293 | T | C | 1 | a0008c0016t0001g0368 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1133+258A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287293 | |||||||
chr1:47287324 | T | C | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.1133+227A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287324 | |||||||
chr1:47287379 | A | C | 1 | a0002c0001t0002g0056 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1133+172T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287379 | |||||||
chr1:47287407 | G | C | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1133+144C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287407 | |||||||
chr1:47287489 | C | T | 3 | a0001c0002t0001g0147 a0001c0002t0001g0148 a0001c0002t0001g0179 |
3 | NA18959.hp1 NA18989.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1133+62G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 10/16 | chr1 | 47287489 | |||||||
chr1:47287733 | G | A | 92 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0232 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.1024-73C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47287733 | |||||||
chr1:47287752 | T | A | 19 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(16): Show |
19 | HG01069.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1024-92A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47287752 | |||||||
chr1:47287885 | C | T | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-225G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47287885 | |||||||
chr1:47287993 | A | G | 1 | a0001c0003t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1024-333T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47287993 | |||||||
chr1:47287997 | T | C | 6 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-337A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47287997 | |||||||
chr1:47288074 | A | T | 1 | a0001c0002t0003g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1024-414T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288074 | |||||||
chr1:47288104 | G | A | 5 | a0001c0002t0001g0146 a0001c0002t0001g0160 a0001c0002t0001g0161 others(2): Show |
5 | HG00408.hp2 HG02056.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024-444C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288104 | |||||||
chr1:47288152 | G | C | 34 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(31): Show |
34 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1024-492C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288152 | |||||||
chr1:47288278 | C | A | 26 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(23): Show |
26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.1024-618G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288278 | |||||||
chr1:47288312 | T | C | 1 | a0002c0001t0002g0316 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1024-652A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288312 | |||||||
chr1:47288405 | T | G | 1 | a0002c0001t0002g0040 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1024-745A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288405 | |||||||
chr1:47288423 | A | G | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-763T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288423 | |||||||
chr1:47288548 | C | T | 1 | a0001c0003t0001g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1023+887G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288548 | |||||||
chr1:47288572 | G | A | 1 | a0001c0003t0001g0226 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1023+863C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288572 | |||||||
chr1:47288597 | T | A | 1 | a0001c0002t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1023+838A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288597 | |||||||
chr1:47288792 | A | C | 1 | a0003c0004t0001g0373 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1023+643T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288792 | |||||||
chr1:47288892 | C | CA | 8 | a0002c0001t0002g0036 a0002c0001t0002g0043 a0002c0001t0002g0245 others(5): Show |
8 | HG01433.hp1 HG01978.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+542dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288892 | |||||||
chr1:47288892 | CA | C | 81 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(78): Show |
83 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1023+542delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288892 | |||||||
chr1:47288892 | CAA | C | 144 | a0001c0002t0001g0085 a0001c0002t0001g0145 a0001c0002t0001g0146 others(141): Show |
146 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.1023+541_1023+542d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288892 | |||||||
chr1:47288912 | A | G | 1 | a0001c0002t0001g0145 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1023+523T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288912 | |||||||
chr1:47288913 | A | T | 253 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(250): Show |
257 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.1023+522T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288913 | |||||||
chr1:47288927 | T | C | 7 | a0002c0001t0002g0053 a0002c0001t0002g0060 a0002c0001t0002g0383 others(4): Show |
7 | HG00280.hp2 HG02132.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023+508A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288927 | |||||||
chr1:47288957 | G | T | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1023+478C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288957 | |||||||
chr1:47288958 | A | C | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1023+477T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47288958 | |||||||
chr1:47289028 | C | G | 32 | a0002c0001t0002g0033 a0002c0001t0002g0034 a0002c0001t0002g0035 others(29): Show |
32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1023+407G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289028 | |||||||
chr1:47289049 | G | A | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1023+386C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289049 | |||||||
chr1:47289061 | C | CAA | 71 | a0001c0002t0001g0186 a0001c0002t0001g0187 a0001c0002t0001g0188 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.1023+372_1023+373d others(4): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289061 | |||||||
chr1:47289061 | C | CAAA | 19 | a0002c0001t0002g0032 a0002c0001t0002g0236 a0002c0001t0002g0237 others(16): Show |
19 | HG00621.hp2 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1023+371_1023+373d others(5): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289061 | |||||||
chr1:47289061 | CA | C | 101 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(98): Show |
102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1023+373delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289061 | |||||||
chr1:47289073 | A | AC | 4 | a0001c0002t0001g0070 a0001c0002t0001g0093 a0001c0002t0001g0180 others(1): Show |
4 | HG02056.hp2 NA18985.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+361_1023+362i others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289073 | |||||||
chr1:47289073 | A | C | 140 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(137): Show |
142 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.1023+362T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289073 | |||||||
chr1:47289078 | A | C | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1023+357T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289078 | |||||||
chr1:47289080 | A | AC | 12 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(9): Show |
13 | HG00639.hp2 HG01891.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1023+354_1023+355i others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289080 | |||||||
chr1:47289080 | A | C | 226 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(223): Show |
229 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.1023+355T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289080 | |||||||
chr1:47289318 | TAAAC | T | 34 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(31): Show |
34 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1023+113_1023+116d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289318 | |||||||
chr1:47289362 | G | A | 1 | a0002c0001t0002g0056 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1023+73C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 9/16 | chr1 | 47289362 | |||||||
chr1:47289644 | T | C | 32 | a0002c0001t0002g0033 a0002c0001t0002g0034 a0002c0001t0002g0035 others(29): Show |
32 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.873-59A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289644 | |||||||
chr1:47289653 | G | A | 3 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 |
3 | HG02257.hp1 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.873-68C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289653 | |||||||
chr1:47289749 | C | T | 1 | a0002c0001t0002g0045 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.873-164G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289749 | |||||||
chr1:47289787 | T | C | 1 | a0001c0003t0001g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.873-202A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289787 | |||||||
chr1:47289803 | C | T | 1 | a0003c0004t0001g0382 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.873-218G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289803 | |||||||
chr1:47289916 | C | T | 2 | a0002c0001t0002g0037 a0002c0001t0002g0045 |
2 | HG02155.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.873-331G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289916 | |||||||
chr1:47289938 | C | CA | 9 | a0002c0001t0002g0043 a0002c0001t0002g0246 a0002c0001t0002g0299 others(6): Show |
9 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.873-354dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289938 | |||||||
chr1:47289938 | CA | C | 169 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(166): Show |
172 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.873-354delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289938 | |||||||
chr1:47289938 | CAA | C | 66 | a0001c0002t0001g0144 a0001c0002t0003g0007 a0001c0002t0003g0008 others(63): Show |
67 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.873-355_873-354del others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289938 | |||||||
chr1:47289955 | A | C | 24 | a0001c0002t0001g0186 a0001c0002t0001g0187 a0001c0002t0001g0188 others(21): Show |
24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.873-370T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289955 | |||||||
chr1:47289995 | G | A | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.873-410C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47289995 | |||||||
chr1:47290068 | A | G | 26 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(23): Show |
26 | HG01069.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.873-483T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290068 | |||||||
chr1:47290161 | G | C | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.873-576C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290161 | |||||||
chr1:47290378 | T | G | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.873-793A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290378 | |||||||
chr1:47290380 | T | G | 253 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(250): Show |
257 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.873-795A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290380 | |||||||
chr1:47290576 | A | ACCTGTAG others(10): Show |
1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.873-1008_873-992du others(18): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290576 | |||||||
chr1:47290596 | GGGAGGCT others(651): Show |
G | 1 | a0004c0005t0002g0063 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.873-1669_873-1012d others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290596 | |||||||
chr1:47290604 | G | A | 1 | a0002c0001t0002g0058 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.873-1019C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290604 | |||||||
chr1:47290654 | G | A | 1 | a0002c0001t0002g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.873-1069C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290654 | |||||||
chr1:47290791 | T | G | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.873-1206A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47290791 | |||||||
chr1:47291083 | G | A | 1 | a0002c0001t0002g0258 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.873-1498C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291083 | |||||||
chr1:47291222 | A | G | 259 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(256): Show |
263 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.873-1637T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291222 | |||||||
chr1:47291246 | A | G | 50 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(47): Show |
51 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.873-1661T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291246 | |||||||
chr1:47291263 | A | G | 1 | a0002c0001t0002g0044 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.873-1678T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291263 | |||||||
chr1:47291276 | G | A | 1 | a0002c0001t0015g0388 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.873-1691C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291276 | |||||||
chr1:47291412 | TTAAA | T | 10 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(7): Show |
10 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.873-1831_873-1828d others(6): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291412 | |||||||
chr1:47291537 | A | G | 1 | a0001c0002t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.872+1921T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291537 | |||||||
chr1:47291579 | T | A | 4 | a0001c0002t0001g0067 a0001c0002t0001g0165 a0001c0002t0001g0166 others(1): Show |
4 | NA18948.hp1 NA18951.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+1879A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291579 | |||||||
chr1:47291579 | T | TA | 4 | a0003c0004t0001g0375 a0003c0004t0001g0376 a0003c0004t0001g0377 others(1): Show |
4 | HG02896.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+1878_872+1879i others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291579 | |||||||
chr1:47291679 | C | T | 2 | a0002c0001t0002g0238 a0002c0001t0002g0258 |
2 | NA18949.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.872+1779G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291679 | |||||||
chr1:47291812 | C | T | 31 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(28): Show |
31 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.872+1646G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291812 | |||||||
chr1:47291899 | T | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1559A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291899 | |||||||
chr1:47291905 | T | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1553A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291905 | |||||||
chr1:47291906 | G | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1552C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291906 | |||||||
chr1:47291907 | G | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1551C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291907 | |||||||
chr1:47291908 | A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1550T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291908 | |||||||
chr1:47291923 | T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1535A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291923 | |||||||
chr1:47291933 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1525G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291933 | |||||||
chr1:47291934 | T | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1524A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291934 | |||||||
chr1:47291935 | G | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1523C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291935 | |||||||
chr1:47291939 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1519G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291939 | |||||||
chr1:47291944 | A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1514T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291944 | |||||||
chr1:47291947 | C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1511G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291947 | |||||||
chr1:47291955 | C | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1503G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291955 | |||||||
chr1:47291956 | A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1502T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291956 | |||||||
chr1:47291957 | A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1501T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291957 | |||||||
chr1:47291959 | C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1499G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291959 | |||||||
chr1:47291960 | G | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1498C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291960 | |||||||
chr1:47291963 | C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1495G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47291963 | |||||||
chr1:47292029 | G | GT | 19 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(16): Show |
19 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.872+1428dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292029 | |||||||
chr1:47292093 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1365G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292093 | |||||||
chr1:47292095 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1363G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292095 | |||||||
chr1:47292096 | A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1362T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292096 | |||||||
chr1:47292099 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1359G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292099 | |||||||
chr1:47292100 | G | T | 1 | a0001c0002t0001g0073 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.872+1358C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292100 | |||||||
chr1:47292103 | C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1355G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292103 | |||||||
chr1:47292104 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1354G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292104 | |||||||
chr1:47292105 | T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1353A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292105 | |||||||
chr1:47292106 | C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1352G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292106 | |||||||
chr1:47292107 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1351G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292107 | |||||||
chr1:47292110 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1348G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292110 | |||||||
chr1:47292111 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1347G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292111 | |||||||
chr1:47292113 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1345G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292113 | |||||||
chr1:47292114 | A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1344T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292114 | |||||||
chr1:47292116 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1342G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292116 | |||||||
chr1:47292117 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1341G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292117 | |||||||
chr1:47292119 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1339G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292119 | |||||||
chr1:47292120 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1338G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292120 | |||||||
chr1:47292121 | C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1337G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292121 | |||||||
chr1:47292122 | A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1336T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292122 | |||||||
chr1:47292123 | A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1335T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292123 | |||||||
chr1:47292129 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1329G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292129 | |||||||
chr1:47292130 | A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1328T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292130 | |||||||
chr1:47292136 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1322G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292136 | |||||||
chr1:47292138 | G | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1320C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292138 | |||||||
chr1:47292149 | C | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1309G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292149 | |||||||
chr1:47292150 | A | C | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1308T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292150 | |||||||
chr1:47292152 | A | G | 353 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(350): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.872+1306T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292152 | |||||||
chr1:47292152 | A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1306T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292152 | |||||||
chr1:47292164 | C | G | 5 | a0003c0004t0001g0022 a0003c0004t0001g0023 a0003c0004t0001g0024 others(2): Show |
5 | HG00642.hp1 HG02572.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+1294G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292164 | |||||||
chr1:47292194 | T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1264A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292194 | |||||||
chr1:47292200 | C | CAGGGGGG others(3): Show |
1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1257_872+1258i others(12): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292200 | |||||||
chr1:47292201 | C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1257G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292201 | |||||||
chr1:47292202 | A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1256T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292202 | |||||||
chr1:47292204 | T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1254A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292204 | |||||||
chr1:47292205 | A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1253T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292205 | |||||||
chr1:47292206 | C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1252G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292206 | |||||||
chr1:47292207 | T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1251A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292207 | |||||||
chr1:47292209 | T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1249A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292209 | |||||||
chr1:47292211 | A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1247T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292211 | |||||||
chr1:47292212 | A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1246T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292212 | |||||||
chr1:47292213 | C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1245G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292213 | |||||||
chr1:47292214 | A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1244T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292214 | |||||||
chr1:47292217 | A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1241T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292217 | |||||||
chr1:47292299 | G | A | 30 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(27): Show |
30 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.872+1159C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292299 | |||||||
chr1:47292311 | A | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1147T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292311 | |||||||
chr1:47292320 | A | AATTGAGT others(6): Show |
1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1137_872+1138i others(15): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292320 | |||||||
chr1:47292347 | A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1111T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292347 | |||||||
chr1:47292426 | T | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1032A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292426 | |||||||
chr1:47292442 | C | G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+1016G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292442 | |||||||
chr1:47292486 | A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+972T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292486 | |||||||
chr1:47292512 | CAG | C | 17 | a0001c0002t0001g0068 a0001c0002t0001g0070 a0001c0002t0001g0088 others(14): Show |
17 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.872+944_872+945del others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292512 | |||||||
chr1:47292513 | A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+945T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292513 | |||||||
chr1:47292519 | T | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+939A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292519 | |||||||
chr1:47292542 | A | T | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+916T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292542 | |||||||
chr1:47292558 | C | A | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+900G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292558 | |||||||
chr1:47292571 | GAGGTAAT others(36): Show |
G | 1 | a0002c0001t0002g0256 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.872+844_872+886del others(43): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292571 | |||||||
chr1:47292589 | G | A | 1 | a0003c0004t0001g0357 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.872+869C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292589 | |||||||
chr1:47292614 | C | A | 1 | a0001c0002t0001g0182 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.872+844G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292614 | |||||||
chr1:47292709 | G | A | 1 | a0001c0002t0004g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.872+749C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47292709 | |||||||
chr1:47293206 | T | C | 4 | a0001c0002t0001g0174 a0001c0002t0001g0176 a0001c0002t0001g0177 others(1): Show |
4 | HG02602.hp1 HG03654.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+252A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47293206 | |||||||
chr1:47293276 | C | A | 1 | a0002c0001t0002g0383 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.872+182G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 8/16 | chr1 | 47293276 | |||||||
chr1:47293560 | A | T | 1 | a0002c0001t0002g0237 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.786-16T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47293560 | |||||||
chr1:47294224 | A | G | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.786-680T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294224 | |||||||
chr1:47294347 | C | A | 2 | a0001c0003t0001g0133 a0001c0003t0001g0134 |
2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.786-803G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294347 | |||||||
chr1:47294387 | C | T | 62 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.786-843G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294387 | |||||||
chr1:47294554 | C | T | 11 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(8): Show |
11 | HG02257.hp1 HG02622.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.786-1010G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294554 | |||||||
chr1:47294591 | G | A | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.786-1047C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294591 | |||||||
chr1:47294699 | T | A | 56 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.785+1066A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294699 | |||||||
chr1:47294864 | G | A | 5 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(2): Show |
5 | HG02055.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+901C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294864 | |||||||
chr1:47294929 | A | AT | 7 | a0001c0002t0004g0228 a0001c0002t0004g0229 a0001c0002t0004g0230 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.785+835dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294929 | |||||||
chr1:47294954 | T | C | 1 | a0001c0002t0001g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.785+811A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294954 | |||||||
chr1:47294986 | A | G | 3 | a0002c0001t0002g0253 a0002c0001t0002g0254 a0002c0001t0011g0306 |
3 | HG00099.hp2 HG00140.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.785+779T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47294986 | |||||||
chr1:47295112 | G | A | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.785+653C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295112 | |||||||
chr1:47295116 | T | C | 1 | a0001c0002t0001g0178 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.785+649A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295116 | |||||||
chr1:47295120 | A | G | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.785+645T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295120 | |||||||
chr1:47295142 | T | TGAACTCC others(7): Show |
1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.785+609_785+622dup others(14): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295142 | |||||||
chr1:47295143 | G | C | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.785+622C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295143 | |||||||
chr1:47295230 | C | A | 3 | a0002c0001t0002g0247 a0002c0001t0002g0300 a0002c0001t0002g0321 |
3 | HG02083.hp1 NA18995.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.785+535G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295230 | |||||||
chr1:47295297 | T | C | 147 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(144): Show |
149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.785+468A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 7/16 | chr1 | 47295297 | |||||||
chr1:47295984 | CAG | C | 4 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(1): Show |
4 | HG00323.hp1 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.702-138_702-137del others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47295984 | |||||||
chr1:47296050 | C | A | 2 | a0001c0002t0003g0012 a0001c0002t0003g0013 |
2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.702-202G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296050 | |||||||
chr1:47296137 | C | T | 1 | a0002c0001t0002g0043 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.702-289G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296137 | |||||||
chr1:47296219 | A | G | 256 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(253): Show |
260 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.702-371T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296219 | |||||||
chr1:47296303 | T | G | 2 | a0003c0004t0001g0365 a0003c0004t0001g0366 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.702-455A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296303 | |||||||
chr1:47296421 | A | T | 7 | a0001c0003t0001g0218 a0001c0003t0001g0219 a0001c0003t0001g0220 others(4): Show |
7 | HG00639.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.702-573T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296421 | |||||||
chr1:47296703 | G | A | 1 | a0001c0003t0001g0135 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.702-855C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296703 | |||||||
chr1:47296836 | G | A | 1 | a0003c0004t0001g0381 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.702-988C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296836 | |||||||
chr1:47296922 | G | T | 1 | a0002c0001t0002g0060 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.702-1074C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47296922 | |||||||
chr1:47297219 | G | A | 2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.702-1371C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297219 | |||||||
chr1:47297231 | A | C | 5 | a0002c0001t0013g0062 a0004c0005t0002g0063 a0004c0005t0002g0064 others(2): Show |
5 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.702-1383T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297231 | |||||||
chr1:47297304 | C | G | 62 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.702-1456G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297304 | |||||||
chr1:47297343 | C | CA | 155 | a0002c0001t0002g0032 a0002c0001t0002g0042 a0002c0001t0002g0057 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.702-1496dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297343 | |||||||
chr1:47297343 | CA | C | 6 | a0001c0003t0001g0077 a0001c0003t0001g0078 a0001c0003t0001g0079 others(3): Show |
6 | HG01109.hp1 HG01496.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.702-1496delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297343 | |||||||
chr1:47297480 | A | T | 13 | a0001c0003t0001g0001 a0001c0003t0001g0076 a0001c0003t0001g0098 others(10): Show |
14 | HG00621.hp1 HG01515.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.702-1632T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297480 | |||||||
chr1:47297535 | C | T | 62 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.702-1687G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297535 | |||||||
chr1:47297602 | G | C | 62 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.702-1754C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297602 | |||||||
chr1:47297661 | T | C | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.702-1813A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297661 | |||||||
chr1:47297829 | A | G | 1 | a0001c0002t0001g0143 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.702-1981T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297829 | |||||||
chr1:47297922 | G | A | 1 | a0001c0003t0001g0076 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.701+1983C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297922 | |||||||
chr1:47297985 | G | A | 4 | a0004c0005t0002g0063 a0004c0005t0002g0064 a0004c0005t0002g0065 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.701+1920C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297985 | |||||||
chr1:47297986 | AAGTACTT others(1): Show |
A | 3 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 |
3 | HG01069.hp2 HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.701+1911_701+1918d others(10): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47297986 | |||||||
chr1:47298027 | T | C | 2 | a0001c0002t0004g0211 a0011c0018t0008g0212 |
2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.701+1878A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298027 | |||||||
chr1:47298041 | C | T | 62 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.701+1864G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298041 | |||||||
chr1:47298299 | T | C | 2 | a0001c0002t0001g0002 a0001c0002t0001g0092 |
3 | NA18950.hp1 NA19010.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.701+1606A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298299 | |||||||
chr1:47298471 | C | T | 147 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(144): Show |
149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.701+1434G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298471 | |||||||
chr1:47298626 | G | GA | 7 | a0001c0002t0001g0070 a0001c0002t0003g0325 a0001c0002t0003g0326 others(4): Show |
7 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.701+1278dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298626 | |||||||
chr1:47298636 | A | G | 1 | a0001c0002t0001g0188 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.701+1269T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298636 | |||||||
chr1:47298736 | G | GT | 15 | a0001c0003t0001g0001 a0001c0003t0001g0076 a0001c0003t0001g0098 others(12): Show |
16 | HG00621.hp1 HG01515.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.701+1168dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298736 | |||||||
chr1:47298783 | G | A | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.701+1122C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298783 | |||||||
chr1:47298815 | C | T | 11 | a0001c0003t0001g0003 a0001c0003t0001g0217 a0001c0003t0001g0218 others(8): Show |
12 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.701+1090G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298815 | |||||||
chr1:47298978 | T | A | 4 | a0001c0003t0001g0136 a0001c0003t0001g0137 a0001c0003t0001g0138 others(1): Show |
4 | NA18951.hp1 NA18960.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+927A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47298978 | |||||||
chr1:47299033 | C | CT | 245 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(242): Show |
249 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.701+871dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299033 | |||||||
chr1:47299116 | G | A | 8 | a0002c0001t0002g0234 a0002c0001t0002g0248 a0002c0001t0002g0302 others(5): Show |
8 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.701+789C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299116 | |||||||
chr1:47299134 | A | G | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.701+771T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299134 | |||||||
chr1:47299305 | C | A | 1 | a0002c0001t0002g0305 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.701+600G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299305 | |||||||
chr1:47299396 | T | G | 1 | a0001c0003t0001g0141 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.701+509A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299396 | |||||||
chr1:47299400 | C | CT | 256 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(253): Show |
260 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.701+504dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299400 | |||||||
chr1:47299455 | C | T | 2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.701+450G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299455 | |||||||
chr1:47299466 | C | T | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.701+439G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299466 | |||||||
chr1:47299509 | C | T | 1 | a0002c0001t0013g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.701+396G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299509 | |||||||
chr1:47299550 | G | A | 1 | a0002c0001t0002g0034 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.701+355C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299550 | |||||||
chr1:47299717 | T | C | 77 | a0001c0003t0001g0001 a0001c0003t0001g0071 a0001c0003t0001g0072 others(74): Show |
78 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.701+188A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299717 | |||||||
chr1:47299758 | C | A | 4 | a0001c0002t0003g0017 a0001c0002t0003g0018 a0001c0002t0003g0019 others(1): Show |
4 | HG02257.hp1 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+147G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299758 | |||||||
chr1:47299818 | T | C | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.701+87A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 6/16 | chr1 | 47299818 | |||||||
chr1:47300383 | C | A | 4 | a0003c0004t0001g0369 a0003c0004t0001g0373 a0003c0004t0001g0374 others(1): Show |
4 | HG00642.hp2 HG00735.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-231G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300383 | |||||||
chr1:47300440 | T | A | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.454-288A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300440 | |||||||
chr1:47300473 | T | TTC | 240 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(237): Show |
243 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.454-322_454-321ins others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300473 | |||||||
chr1:47300475 | T | C | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.454-323A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300475 | |||||||
chr1:47300543 | A | T | 3 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 |
3 | HG02055.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.454-391T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300543 | |||||||
chr1:47300562 | G | A | 56 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.454-410C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300562 | |||||||
chr1:47300932 | A | G | 354 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(351): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.453+629T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300932 | |||||||
chr1:47300975 | C | T | 92 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0232 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.453+586G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47300975 | |||||||
chr1:47301171 | G | A | 1 | a0002c0001t0002g0036 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.453+390C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47301171 | |||||||
chr1:47301198 | T | C | 62 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.453+363A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47301198 | |||||||
chr1:47301271 | T | C | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.453+290A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47301271 | |||||||
chr1:47301469 | C | A | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.453+92G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47301469 | |||||||
chr1:47301543 | G | A | 1 | a0001c0002t0004g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.453+18C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 5/16 | chr1 | 47301543 | |||||||
chr1:47301929 | G | A | 1 | a0001c0003t0001g0142 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.266-181C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 4/16 | chr1 | 47301929 | |||||||
chr1:47302182 | A | G | 1 | a0002c0001t0002g0236 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.265+52T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 4/16 | chr1 | 47302182 | |||||||
chr1:47302401 | C | A | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.153-55G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302401 | |||||||
chr1:47302498 | C | G | 1 | a0003c0004t0001g0362 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.153-152G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302498 | |||||||
chr1:47302512 | G | A | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-166C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302512 | |||||||
chr1:47302541 | A | C | 1 | a0002c0001t0002g0037 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.153-195T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302541 | |||||||
chr1:47302563 | A | G | 2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153-217T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302563 | |||||||
chr1:47302611 | A | G | 2 | a0001c0002t0004g0211 a0011c0018t0008g0212 |
2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.153-265T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302611 | |||||||
chr1:47302729 | G | T | 1 | a0001c0003t0006g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153-383C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302729 | |||||||
chr1:47302894 | G | A | 1 | a0001c0002t0001g0182 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.153-548C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47302894 | |||||||
chr1:47303023 | G | T | 23 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(20): Show |
23 | HG01069.hp2 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.153-677C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303023 | |||||||
chr1:47303071 | T | C | 92 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0232 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.153-725A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303071 | |||||||
chr1:47303248 | T | C | 16 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(13): Show |
16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.153-902A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303248 | |||||||
chr1:47303256 | C | T | 11 | a0001c0003t0001g0003 a0001c0003t0001g0217 a0001c0003t0001g0218 others(8): Show |
12 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.153-910G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303256 | |||||||
chr1:47303755 | T | C | 1 | a0002c0001t0002g0305 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.152+1134A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303755 | |||||||
chr1:47303805 | T | C | 66 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(63): Show |
67 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.152+1084A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303805 | |||||||
chr1:47303928 | T | C | 2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+961A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47303928 | |||||||
chr1:47304149 | G | GT | 9 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(6): Show |
9 | HG01167.hp2 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+739dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304149 | |||||||
chr1:47304351 | A | T | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.152+538T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304351 | |||||||
chr1:47304454 | T | C | 1 | a0001c0002t0003g0013 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.152+435A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304454 | |||||||
chr1:47304591 | G | A | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.152+298C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304591 | |||||||
chr1:47304724 | G | A | 3 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 |
3 | HG02055.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.152+165C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304724 | |||||||
chr1:47304741 | G | C | 1 | a0001c0003t0006g0026 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.152+148C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304741 | |||||||
chr1:47304744 | G | A | 6 | a0001c0002t0004g0211 a0001c0002t0004g0228 a0001c0002t0004g0229 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+145C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304744 | |||||||
chr1:47304769 | A | C | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.152+120T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304769 | |||||||
chr1:47304794 | T | C | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.152+95A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 3/16 | chr1 | 47304794 | |||||||
chr1:47305114 | T | A | 92 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0232 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.45-118A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305114 | |||||||
chr1:47305134 | T | C | 57 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(54): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.45-138A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305134 | |||||||
chr1:47305137 | T | A | 9 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(6): Show |
9 | HG02109.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-141A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305137 | |||||||
chr1:47305237 | T | C | 1 | a0001c0003t0001g0184 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.45-241A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305237 | |||||||
chr1:47305315 | G | A | 62 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.45-319C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305315 | |||||||
chr1:47305369 | C | G | 1 | a0003c0004t0001g0361 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45-373G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305369 | |||||||
chr1:47305548 | C | A | 1 | a0001c0002t0003g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45-552G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305548 | |||||||
chr1:47305642 | G | A | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.45-646C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305642 | |||||||
chr1:47305711 | C | G | 1 | a0001c0002t0003g0021 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45-715G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305711 | |||||||
chr1:47305717 | C | T | 1 | a0003c0004t0001g0361 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45-721G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305717 | |||||||
chr1:47305725 | C | CT | 105 | a0001c0002t0003g0028 a0001c0002t0004g0229 a0001c0002t0004g0231 others(102): Show |
105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.45-730dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | |||||||
chr1:47305725 | C | CTT | 58 | a0002c0001t0002g0033 a0002c0001t0002g0037 a0002c0001t0002g0039 others(55): Show |
59 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.45-731_45-730dupAA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | |||||||
chr1:47305725 | C | CTTT | 19 | a0003c0004t0001g0022 a0003c0004t0001g0024 a0003c0004t0001g0333 others(16): Show |
19 | HG00735.hp1 HG00738.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-732_45-730dupAA others(1): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | |||||||
chr1:47305725 | CT | C | 139 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(136): Show |
142 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.45-730delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | |||||||
chr1:47305725 | CTT | C | 18 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(15): Show |
18 | HG01069.hp2 HG02257.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-731_45-730delAA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | |||||||
chr1:47305725 | CTTTTTTT others(4): Show |
C | 2 | a0003c0004t0001g0347 a0003c0004t0001g0348 |
2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.45-740_45-730delAA others(9): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305725 | |||||||
chr1:47305819 | G | A | 4 | a0001c0003t0001g0322 a0001c0003t0001g0323 a0001c0003t0001g0324 others(1): Show |
4 | HG01167.hp2 HG02976.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-823C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305819 | |||||||
chr1:47305881 | G | A | 1 | a0002c0001t0002g0058 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.45-885C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305881 | |||||||
chr1:47305893 | A | G | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-897T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305893 | |||||||
chr1:47305921 | C | T | 1 | a0002c0001t0002g0037 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.45-925G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47305921 | |||||||
chr1:47306010 | C | T | 2 | a0001c0002t0004g0211 a0011c0018t0008g0212 |
2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.45-1014G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306010 | |||||||
chr1:47306125 | T | C | 3 | a0001c0002t0001g0186 a0001c0002t0001g0187 a0001c0002t0001g0188 |
3 | NA18979.hp1 NA18982.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.45-1129A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306125 | |||||||
chr1:47306190 | T | C | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.45-1194A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306190 | |||||||
chr1:47306264 | CT | C | 131 | a0001c0002t0001g0073 a0001c0002t0004g0231 a0001c0003t0001g0072 others(128): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.45-1269delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306264 | |||||||
chr1:47306264 | CTT | C | 246 | a0001c0002t0001g0002 a0001c0002t0001g0068 a0001c0002t0001g0069 others(243): Show |
250 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.45-1270_45-1269del others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306264 | |||||||
chr1:47306264 | CTTT | C | 8 | a0001c0002t0001g0067 a0001c0002t0003g0021 a0001c0002t0003g0330 others(5): Show |
8 | HG01515.hp1 HG02055.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.45-1271_45-1269del others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306264 | |||||||
chr1:47306282 | T | A | 1 | a0001c0002t0004g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.45-1286A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306282 | |||||||
chr1:47306408 | C | T | 1 | a0001c0003t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.45-1412G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306408 | |||||||
chr1:47306416 | A | G | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.45-1420T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306416 | |||||||
chr1:47306435 | G | A | 3 | a0005c0007t0004g0213 a0005c0007t0004g0214 a0005c0017t0004g0215 |
3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.45-1439C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306435 | |||||||
chr1:47306550 | G | A | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.45-1554C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306550 | |||||||
chr1:47306562 | G | A | 2 | a0002c0001t0002g0033 a0002c0001t0002g0059 |
2 | NA18947.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.45-1566C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306562 | |||||||
chr1:47306794 | T | C | 1 | a0002c0001t0002g0319 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.45-1798A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306794 | |||||||
chr1:47306950 | G | A | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-1954C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306950 | |||||||
chr1:47306981 | A | G | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.45-1985T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47306981 | |||||||
chr1:47307001 | A | G | 1 | a0001c0003t0001g0072 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.45-2005T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307001 | |||||||
chr1:47307044 | C | G | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.45-2048G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307044 | |||||||
chr1:47307130 | G | A | 1 | a0015c0014t0001g0191 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.45-2134C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307130 | |||||||
chr1:47307354 | C | T | 2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.45-2358G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307354 | |||||||
chr1:47307514 | C | T | 1 | a0001c0003t0001g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.45-2518G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307514 | |||||||
chr1:47307660 | C | T | 1 | a0002c0001t0002g0235 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.44+2616G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307660 | |||||||
chr1:47307828 | G | A | 4 | a0002c0001t0002g0315 a0002c0001t0002g0316 a0002c0001t0002g0317 others(1): Show |
4 | HG01071.hp1 HG01081.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+2448C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307828 | |||||||
chr1:47307868 | C | T | 6 | a0003c0004t0001g0353 a0003c0004t0001g0354 a0003c0004t0001g0355 others(3): Show |
6 | HG00597.hp2 HG02109.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+2408G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47307868 | |||||||
chr1:47308039 | G | A | 2 | a0003c0004t0001g0024 a0003c0004t0001g0025 |
2 | HG00642.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.44+2237C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308039 | |||||||
chr1:47308162 | C | T | 1 | a0002c0001t0002g0234 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.44+2114G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308162 | |||||||
chr1:47308356 | C | T | 2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.44+1920G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308356 | |||||||
chr1:47308376 | C | T | 147 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(144): Show |
149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.44+1900G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308376 | |||||||
chr1:47308380 | G | A | 16 | a0001c0003t0001g0003 a0001c0003t0001g0216 a0001c0003t0001g0217 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.44+1896C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308380 | |||||||
chr1:47308427 | G | GA | 353 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(350): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.44+1848dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308427 | |||||||
chr1:47308594 | G | A | 147 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(144): Show |
149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.44+1682C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308594 | |||||||
chr1:47308753 | T | A | 1 | a0001c0003t0001g0192 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.44+1523A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308753 | |||||||
chr1:47308764 | A | G | 1 | a0001c0002t0001g0070 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.44+1512T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308764 | |||||||
chr1:47308902 | G | A | 1 | a0002c0001t0002g0319 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.44+1374C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308902 | |||||||
chr1:47308920 | C | T | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.44+1356G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47308920 | |||||||
chr1:47309000 | C | T | 1 | a0003c0004t0001g0332 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.44+1276G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309000 | |||||||
chr1:47309016 | C | A | 5 | a0001c0003t0001g0193 a0001c0003t0001g0194 a0001c0003t0001g0195 others(2): Show |
5 | NA18942.hp2 NA18949.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.44+1260G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309016 | |||||||
chr1:47309052 | C | CA | 7 | a0001c0002t0001g0198 a0001c0002t0003g0325 a0001c0002t0003g0326 others(4): Show |
7 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+1223dupT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309052 | |||||||
chr1:47309062 | A | T | 1 | a0001c0002t0003g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.44+1214T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309062 | |||||||
chr1:47309065 | A | T | 103 | a0001c0002t0001g0069 a0001c0002t0003g0006 a0001c0002t0003g0227 others(100): Show |
103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.44+1211T>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309065 | |||||||
chr1:47309067 | AT | A | 3 | a0001c0002t0004g0229 a0001c0002t0004g0230 a0001c0002t0004g0231 |
3 | HG01884.hp1 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.44+1208delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309067 | |||||||
chr1:47309068 | T | A | 4 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(1): Show |
4 | HG02055.hp2 HG03540.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+1208A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309068 | |||||||
chr1:47309172 | G | A | 1 | a0001c0003t0010g0199 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.44+1104C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309172 | |||||||
chr1:47309233 | A | G | 2 | a0002c0001t0002g0232 a0002c0001t0002g0233 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.44+1043T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309233 | |||||||
chr1:47309241 | T | A | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.44+1035A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309241 | |||||||
chr1:47309350 | T | C | 3 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0202 |
3 | NA18971.hp1 NA18995.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.44+926A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309350 | |||||||
chr1:47309445 | T | C | 1 | a0001c0002t0001g0203 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.44+831A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309445 | |||||||
chr1:47309482 | T | C | 1 | a0011c0018t0008g0212 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44+794A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309482 | |||||||
chr1:47309505 | C | T | 44 | a0003c0004t0001g0004 a0003c0004t0001g0031 a0003c0004t0001g0332 others(41): Show |
45 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.44+771G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309505 | |||||||
chr1:47309655 | A | G | 1 | a0003c0004t0001g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.44+621T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309655 | |||||||
chr1:47309679 | G | A | 8 | a0003c0004t0001g0369 a0003c0004t0001g0371 a0003c0004t0001g0372 others(5): Show |
8 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.44+597C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309679 | |||||||
chr1:47309818 | A | G | 7 | a0001c0002t0003g0007 a0001c0002t0003g0008 a0001c0002t0003g0009 others(4): Show |
7 | HG02622.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.44+458T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309818 | |||||||
chr1:47309975 | G | T | 62 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.44+301C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309975 | |||||||
chr1:47309980 | G | A | 1 | a0003c0004t0001g0382 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44+296C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 2/16 | chr1 | 47309980 | |||||||
chr1:47310470 | T | G | 1 | a0001c0002t0001g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-43-108A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47310470 | |||||||
chr1:47310524 | T | C | 1 | a0002c0001t0002g0321 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-43-162A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47310524 | |||||||
chr1:47310673 | A | C | 56 | a0003c0004t0001g0004 a0003c0004t0001g0022 a0003c0004t0001g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.-43-311T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47310673 | |||||||
chr1:47310933 | C | T | 1 | a0002c0001t0002g0034 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-43-571G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47310933 | |||||||
chr1:47311095 | C | A | 5 | a0001c0003t0001g0205 a0001c0003t0001g0206 a0001c0003t0001g0208 others(2): Show |
5 | HG01975.hp2 HG01993.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-733G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311095 | |||||||
chr1:47311188 | C | T | 16 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(13): Show |
16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-43-826G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311188 | |||||||
chr1:47311200 | T | C | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-43-838A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311200 | |||||||
chr1:47311271 | TTTTCTTT others(5): Show |
T | 1 | a0005c0017t0004g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-43-921_-43-910del others(12): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311271 | |||||||
chr1:47311275 | CT | C | 60 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(57): Show |
61 | HG00099.hp1 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-43-914delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311275 | |||||||
chr1:47311282 | T | C | 1 | a0003c0004t0001g0362 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-43-920A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311282 | |||||||
chr1:47311283 | C | CT | 11 | a0001c0002t0001g0088 a0001c0002t0001g0186 a0001c0002t0001g0200 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-43-922dupA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311283 | |||||||
chr1:47311283 | C | CTT | 16 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(13): Show |
16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-43-923_-43-922dup others(2): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311283 | |||||||
chr1:47311283 | C | T | 2 | a0001c0002t0003g0227 a0003c0004t0001g0362 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-43-921G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311283 | |||||||
chr1:47311283 | CT | C | 10 | a0001c0002t0001g0179 a0001c0003t0001g0209 a0002c0001t0002g0052 others(7): Show |
10 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-922delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311283 | |||||||
chr1:47311284 | T | C | 1 | a0003c0004t0001g0349 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-43-922A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311284 | |||||||
chr1:47311370 | C | T | 62 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-43-1008G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311370 | |||||||
chr1:47311602 | T | G | 5 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(2): Show |
5 | HG02055.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-1240A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311602 | |||||||
chr1:47311646 | T | A | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.-43-1284A>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311646 | |||||||
chr1:47311654 | G | A | 1 | a0001c0002t0001g0210 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-43-1292C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311654 | |||||||
chr1:47311747 | G | A | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-1385C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311747 | |||||||
chr1:47311803 | T | C | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-43-1441A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311803 | |||||||
chr1:47311840 | A | G | 163 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(160): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.-43-1478T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311840 | |||||||
chr1:47311874 | C | T | 2 | a0001c0003t0006g0026 a0001c0003t0006g0027 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-43-1512G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47311874 | |||||||
chr1:47312180 | GA | G | 3 | a0005c0007t0004g0213 a0005c0007t0004g0214 a0005c0017t0004g0215 |
3 | HG01884.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-43-1819delT | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312180 | |||||||
chr1:47312193 | C | G | 2 | a0005c0007t0004g0213 a0005c0007t0004g0214 |
2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-43-1831G>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312193 | |||||||
chr1:47312196 | A | G | 1 | a0001c0002t0001g0068 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-43-1834T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312196 | |||||||
chr1:47312212 | C | T | 44 | a0003c0004t0001g0004 a0003c0004t0001g0031 a0003c0004t0001g0332 others(41): Show |
45 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.-44+1824G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312212 | |||||||
chr1:47312358 | C | T | 2 | a0001c0002t0004g0211 a0011c0018t0008g0212 |
2 | HG02895.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-44+1678G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312358 | |||||||
chr1:47312403 | A | C | 1 | a0001c0002t0001g0067 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-44+1633T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312403 | |||||||
chr1:47312459 | A | C | 147 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(144): Show |
149 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.-44+1577T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312459 | |||||||
chr1:47312561 | G | A | 92 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0232 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.-44+1475C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312561 | |||||||
chr1:47312562 | T | G | 92 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0232 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.-44+1474A>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312562 | |||||||
chr1:47312594 | G | A | 16 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(13): Show |
16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-44+1442C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312594 | |||||||
chr1:47312807 | A | G | 1 | a0002c0001t0002g0033 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-44+1229T>C | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312807 | |||||||
chr1:47312848 | T | C | 257 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(254): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.-44+1188A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312848 | |||||||
chr1:47312905 | C | A | 1 | a0002c0001t0002g0060 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-44+1131G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47312905 | |||||||
chr1:47313161 | T | C | 92 | a0002c0001t0002g0032 a0002c0001t0002g0061 a0002c0001t0002g0232 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.-44+875A>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313161 | |||||||
chr1:47313239 | G | C | 4 | a0001c0003t0001g0322 a0001c0003t0001g0323 a0001c0003t0001g0324 others(1): Show |
4 | HG01167.hp2 HG02976.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+797C>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313239 | |||||||
chr1:47313260 | G | A | 6 | a0001c0002t0003g0325 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+776C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313260 | |||||||
chr1:47313344 | AT | A | 353 | a0001c0002t0001g0002 a0001c0002t0001g0067 a0001c0002t0001g0068 others(350): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.-44+691delA | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313344 | |||||||
chr1:47313430 | A | AC | 21 | a0003c0004t0001g0004 a0003c0004t0001g0031 a0003c0004t0001g0332 others(18): Show |
22 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-44+605dupG | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313430 | |||||||
chr1:47313545 | C | A | 1 | a0001c0003t0001g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-44+491G>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313545 | |||||||
chr1:47313587 | CCTT | C | 62 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-44+446_-44+448del others(3): Show |
STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313587 | |||||||
chr1:47313692 | C | T | 1 | a0002c0001t0002g0032 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-44+344G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313692 | |||||||
chr1:47313720 | G | A | 5 | a0002c0001t0002g0383 a0002c0001t0002g0384 a0002c0001t0002g0385 others(2): Show |
5 | HG02132.hp2 NA18945.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+316C>T | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313720 | |||||||
chr1:47313750 | G | T | 1 | a0001c0002t0003g0006 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-44+286C>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313750 | |||||||
chr1:47313784 | A | C | 1 | a0003c0004t0001g0031 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-44+252T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313784 | |||||||
chr1:47313951 | A | C | 5 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(2): Show |
5 | HG02055.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+85T>G | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47313951 | |||||||
chr1:47314012 | C | T | 4 | a0003c0004t0001g0022 a0003c0004t0001g0023 a0003c0004t0001g0024 others(1): Show |
4 | HG00642.hp1 HG02572.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+24G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47314012 | |||||||
chr1:47314021 | C | T | 16 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0008 others(13): Show |
16 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-44+15G>A | STIL | ENSG00000123473.17 | transcript | ENST00000371877.8 | protein_coding | 1/16 | chr1 | 47314021 |