Item | Value |
---|---|
geneid | 6936 |
ensemblid | ENSG00000005436.14 |
hgncid | 1317 |
symbol | GCFC2 |
name | GC-rich sequence DNA-binding factor 2 |
refseq_nuc | NM_003203.5 |
refseq_prot | NP_003194.3 |
ensembl_nuc | ENST00000321027.8 |
ensembl_prot | ENSP00000318690.3 |
mane_status | MANE Select |
chr | chr2 |
start | 75662705 |
end | 75710915 |
strand | - |
ver | v1.2 |
region | chr2:75662705-75710915 |
region5000 | chr2:75657705-75715915 |
regionname0 | GCFC2_chr2_75662705_75710915 |
regionname5000 | GCFC2_chr2_75657705_75715915 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 781 | 166 | 13 | 29 | 100 | 7 | 15 | 82 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0002 | 0/0 | 781 | 142 | 24 | 26 | 68 | 5 | 19 | 55 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0003 | 0/0 | 781 | 34 | 32 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0004 | 0/0 | 781 | 32 | 11 | 5 | 10 | 2 | 4 | 9 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0005 | 0/0 | 781 | 5 | 1 | 2 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0006 | 0/0 | 781 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0007 | 0/0 | 781 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0008 | 0/0 | 781 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0009 | 0/0 | 781 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0010 | 0/0 | 781 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0011 | 0/0 | 781 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0012 | 0/0 | 781 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0013 | 0/0 | 781 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0014 | 0/0 | 781 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0015 | 0/0 | 781 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0016 | 0/0 | 781 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0017 | 0/0 | 781 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0018 | 0/0 | 781 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0019 | 0/0 | 781 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0020 | 0/0 | 781 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
a0021 | 0/0 | 781 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | MAHRP others(776): Show |
chr2 | 75657705 | 75715915 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2343 | 163 | 13 | 27 | 99 | 7 | 15 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0001c0016 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0001c0018 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0001c0025 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0002c0002 | 0/0 | 2343 | 120 | 20 | 20 | 61 | 3 | 16 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0002c0005 | 0/0 | 2343 | 22 | 4 | 6 | 7 | 2 | 3 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0003c0004 | 0/0 | 2343 | 31 | 29 | 2 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0003c0010 | 0/0 | 2343 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0004c0003 | 0/0 | 2343 | 31 | 11 | 4 | 10 | 2 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0004c0013 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0005c0006 | 0/0 | 2343 | 5 | 1 | 2 | 0 | 2 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0006c0007 | 0/0 | 2343 | 4 | 4 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0007c0009 | 0/0 | 2343 | 4 | 4 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0008c0008 | 0/0 | 2343 | 4 | 0 | 0 | 4 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0009c0023 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0010c0019 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0011c0027 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0012c0021 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0013c0020 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0014c0022 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0015c0015 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0016c0011 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0017c0014 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0018c0024 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0019c0017 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0020c0012 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 | ||
a0021c0026 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ATGGC others(2338): Show |
chr2 | 75657705 | 75715915 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4367 | 146 | 11 | 26 | 90 | 7 | 10 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0001c0001t0002 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0001c0001t0006 | 0/0 | 4367 | 5 | 0 | 0 | 4 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0001c0001t0008 | 0/0 | 4368 | 3 | 0 | 0 | 1 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0001c0001t0011 | 0/0 | 4367 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0001c0001t0012 | 0/0 | 4367 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0001c0001t0013 | 0/0 | 4367 | 2 | 0 | 0 | 0 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0001c0001t0019 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0001c0001t0025 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0001c0016t0001 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0001c0018t0001 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0001c0025t0001 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0002c0002t0002 | 0/0 | 4367 | 52 | 2 | 10 | 24 | 3 | 13 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0002c0002t0003 | 0/0 | 4367 | 55 | 14 | 9 | 29 | 0 | 3 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0002c0002t0009 | 0/0 | 4367 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0002c0002t0010 | 0/0 | 4367 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0002c0002t0014 | 0/0 | 4368 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0002c0002t0015 | 0/0 | 4368 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0002c0002t0017 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0002c0002t0020 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0002c0002t0022 | 0/0 | 4366 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4361): Show |
chr2 | 75657705 | 75715915 |
a0002c0002t0023 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0002c0005t0001 | 0/0 | 4367 | 21 | 3 | 6 | 7 | 2 | 3 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0002c0005t0005 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0003c0004t0002 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0003c0004t0004 | 0/0 | 4368 | 18 | 18 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0003c0004t0005 | 0/0 | 4367 | 12 | 11 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0003c0010t0004 | 0/0 | 4368 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0004c0003t0002 | 0/0 | 4367 | 6 | 6 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0004c0003t0004 | 0/0 | 4368 | 22 | 3 | 4 | 9 | 2 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0004c0003t0018 | 0/0 | 4368 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0004c0003t0021 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0004c0003t0026 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4364): Show |
chr2 | 75657705 | 75715915 |
a0004c0013t0004 | 0/0 | 4368 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0005c0006t0001 | 0/0 | 4367 | 5 | 1 | 2 | 0 | 2 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0006c0007t0004 | 0/0 | 4368 | 4 | 4 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0007c0009t0004 | 0/0 | 4368 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0007c0009t0005 | 0/0 | 4367 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0008c0008t0001 | 0/0 | 4367 | 4 | 0 | 0 | 4 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0009c0023t0024 | 0/0 | 4369 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4364): Show |
chr2 | 75657705 | 75715915 |
a0010c0019t0001 | 0/0 | 4367 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0011c0027t0003 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0012c0021t0007 | 0/0 | 4369 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4364): Show |
chr2 | 75657705 | 75715915 |
a0013c0020t0002 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0014c0022t0016 | 0/0 | 4367 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0015c0015t0007 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4364): Show |
chr2 | 75657705 | 75715915 |
a0016c0011t0007 | 0/0 | 4369 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4364): Show |
chr2 | 75657705 | 75715915 |
a0017c0014t0007 | 0/0 | 4369 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4364): Show |
chr2 | 75657705 | 75715915 |
a0018c0024t0003 | 0/0 | 4367 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0019c0017t0001 | 0/0 | 4367 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
a0020c0012t0004 | 0/0 | 4368 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4363): Show |
chr2 | 75657705 | 75715915 |
a0021c0026t0001 | 0/0 | 4367 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | ACTGA others(4362): Show |
chr2 | 75657705 | 75715915 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 14 | 1 | 1 | 10 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0016 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0008g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0008g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0011g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0012g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0012g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0013g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0019g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0001t0025g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0016t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0018t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0001c0025t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0003 | 0/0 | 8 | 0 | 5 | 1 | 1 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0007 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0009g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0010g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0014g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0014g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0015g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0015g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0017g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0020g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0022g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0002t0023g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0002c0005t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0004t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0010t0004g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0003c0010t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0004 | 0/0 | 7 | 0 | 2 | 0 | 1 | 4 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0018g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0021g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0003t0026g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0004c0013t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0005c0006t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0005c0006t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0005c0006t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0006c0007t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0006c0007t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0007c0009t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0007c0009t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0007c0009t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0007c0009t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0008c0008t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0008c0008t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0008c0008t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0009c0023t0024g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0010c0019t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0011c0027t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0012c0021t0007g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0013c0020t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0014c0022t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0015c0015t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0016c0011t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0017c0014t0007g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0018c0024t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0019c0017t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0020c0012t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
a0021c0026t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | FIN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0034 | EUR | FIN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00408 | hp1 | a0002 | c0005 | t0001 | g0235 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00438 | hp2 | a0004 | c0003 | t0021 | g0067 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00621 | hp1 | a0002 | c0002 | t0003 | g0029 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00639 | hp1 | a0004 | c0013 | t0004 | g0055 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00639 | hp2 | a0002 | c0002 | t0020 | g0155 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00735 | hp1 | a0002 | c0002 | t0003 | g0130 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00735 | hp2 | a0003 | c0004 | t0002 | g0285 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00738 | hp1 | a0002 | c0005 | t0001 | g0035 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00738 | hp2 | a0001 | c0001 | t0025 | g0088 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG00741 | hp2 | a0002 | c0005 | t0001 | g0020 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01069 | hp2 | a0002 | c0002 | t0003 | g0097 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01070 | hp1 | a0002 | c0002 | t0003 | g0104 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01074 | hp2 | a0002 | c0002 | t0003 | g0027 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01099 | hp1 | a0004 | c0003 | t0004 | g0061 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01099 | hp2 | a0002 | c0005 | t0001 | g0175 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0148 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01109 | hp1 | a0009 | c0023 | t0024 | g0268 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01109 | hp2 | a0002 | c0002 | t0003 | g0027 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01169 | hp1 | a0005 | c0006 | t0001 | g0015 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01175 | hp2 | a0002 | c0002 | t0003 | g0096 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01192 | hp2 | a0002 | c0005 | t0001 | g0020 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01243 | hp1 | a0001 | c0016 | t0001 | g0172 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01243 | hp2 | a0003 | c0004 | t0005 | g0291 | AMR | PUR | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01257 | hp2 | a0002 | c0005 | t0001 | g0177 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01261 | hp1 | a0004 | c0003 | t0004 | g0060 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01346 | hp1 | a0004 | c0003 | t0004 | g0004 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01358 | hp1 | a0002 | c0002 | t0003 | g0119 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01361 | hp2 | a0002 | c0005 | t0001 | g0230 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01433 | hp1 | a0005 | c0006 | t0001 | g0083 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01496 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0153 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01515 | hp2 | a0002 | c0005 | t0001 | g0020 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0003 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01516 | hp2 | a0005 | c0006 | t0001 | g0015 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01517 | hp1 | a0002 | c0005 | t0001 | g0174 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01517 | hp2 | a0005 | c0006 | t0001 | g0015 | EUR | IBS | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01884 | hp1 | a0002 | c0002 | t0002 | g0093 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01884 | hp2 | a0003 | c0004 | t0005 | g0022 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01891 | hp1 | a0003 | c0010 | t0004 | g0043 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01891 | hp2 | a0003 | c0004 | t0005 | g0293 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01943 | hp2 | a0001 | c0025 | t0001 | g0263 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01975 | hp1 | a0004 | c0003 | t0004 | g0004 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0132 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02040 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02055 | hp1 | a0006 | c0007 | t0004 | g0069 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02055 | hp2 | a0004 | c0003 | t0002 | g0068 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02056 | hp1 | a0002 | c0005 | t0001 | g0164 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02071 | hp1 | a0002 | c0002 | t0014 | g0142 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02080 | hp2 | a0002 | c0002 | t0003 | g0108 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02129 | hp2 | a0002 | c0002 | t0017 | g0136 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02145 | hp2 | a0002 | c0005 | t0001 | g0173 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02155 | hp1 | a0001 | c0001 | t0019 | g0264 | EAS | CDX | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02280 | hp1 | a0003 | c0004 | t0005 | g0289 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02280 | hp2 | a0006 | c0007 | t0004 | g0014 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02293 | hp1 | a0002 | c0002 | t0003 | g0106 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02293 | hp2 | a0010 | c0019 | t0001 | g0267 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02451 | hp1 | a0001 | c0001 | t0011 | g0196 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02451 | hp2 | a0003 | c0004 | t0004 | g0278 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02572 | hp1 | a0002 | c0005 | t0001 | g0223 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02602 | hp1 | a0002 | c0005 | t0001 | g0169 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02602 | hp2 | a0004 | c0003 | t0004 | g0004 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02615 | hp1 | a0003 | c0004 | t0004 | g0284 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02615 | hp2 | a0003 | c0004 | t0004 | g0021 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02622 | hp2 | a0002 | c0002 | t0009 | g0024 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0199 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02647 | hp1 | a0003 | c0004 | t0004 | g0279 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02647 | hp2 | a0004 | c0003 | t0002 | g0052 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02683 | hp1 | a0001 | c0001 | t0006 | g0048 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02683 | hp2 | a0012 | c0021 | t0007 | g0160 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02698 | hp1 | a0004 | c0003 | t0004 | g0004 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0140 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02717 | hp1 | a0003 | c0010 | t0004 | g0043 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02717 | hp2 | a0003 | c0004 | t0004 | g0280 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02723 | hp1 | a0002 | c0002 | t0009 | g0024 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02723 | hp2 | a0003 | c0004 | t0004 | g0282 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0126 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02738 | hp2 | a0002 | c0005 | t0001 | g0035 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02809 | hp1 | a0004 | c0003 | t0004 | g0072 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02809 | hp2 | a0003 | c0004 | t0005 | g0294 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02818 | hp1 | a0003 | c0004 | t0004 | g0281 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02818 | hp2 | a0007 | c0009 | t0004 | g0272 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02886 | hp1 | a0002 | c0002 | t0009 | g0024 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02886 | hp2 | a0004 | c0003 | t0004 | g0071 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02896 | hp1 | a0003 | c0004 | t0004 | g0287 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02896 | hp2 | a0004 | c0003 | t0002 | g0053 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02897 | hp1 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02897 | hp2 | a0003 | c0004 | t0004 | g0045 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02922 | hp1 | a0013 | c0020 | t0002 | g0122 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02922 | hp2 | a0003 | c0004 | t0004 | g0286 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02965 | hp1 | a0004 | c0003 | t0026 | g0054 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02965 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02970 | hp1 | a0002 | c0002 | t0003 | g0094 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02970 | hp2 | a0004 | c0003 | t0002 | g0013 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02976 | hp1 | a0007 | c0009 | t0005 | g0277 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02976 | hp2 | a0002 | c0002 | t0003 | g0102 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03041 | hp1 | a0002 | c0002 | t0023 | g0120 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03041 | hp2 | a0014 | c0022 | t0016 | g0158 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03098 | hp1 | a0002 | c0002 | t0003 | g0095 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03098 | hp2 | a0003 | c0004 | t0004 | g0276 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03130 | hp1 | a0003 | c0004 | t0004 | g0044 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03130 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03139 | hp1 | a0004 | c0003 | t0004 | g0073 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03139 | hp2 | a0004 | c0003 | t0002 | g0013 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03195 | hp1 | a0006 | c0007 | t0004 | g0014 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03195 | hp2 | a0003 | c0004 | t0005 | g0023 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03209 | hp1 | a0002 | c0002 | t0003 | g0101 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03209 | hp2 | a0015 | c0015 | t0007 | g0157 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03225 | hp1 | a0002 | c0002 | t0003 | g0017 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03225 | hp2 | a0016 | c0011 | t0007 | g0051 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03239 | hp1 | a0017 | c0014 | t0007 | g0159 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03453 | hp1 | a0003 | c0004 | t0004 | g0021 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03453 | hp2 | a0004 | c0003 | t0002 | g0013 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03486 | hp1 | a0003 | c0004 | t0005 | g0023 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0017 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03516 | hp1 | a0002 | c0002 | t0003 | g0099 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03516 | hp2 | a0003 | c0010 | t0004 | g0274 | AFR | ESN | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03540 | hp1 | a0007 | c0009 | t0005 | g0288 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03669 | hp1 | a0002 | c0005 | t0001 | g0165 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0147 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0117 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03704 | hp1 | a0001 | c0001 | t0013 | g0026 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0162 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03710 | hp1 | a0004 | c0003 | t0004 | g0004 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0163 | SAS | PJL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03831 | hp1 | a0004 | c0003 | t0004 | g0004 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0116 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0135 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03927 | hp1 | a0001 | c0001 | t0013 | g0026 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03927 | hp2 | a0018 | c0024 | t0003 | g0107 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0150 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03942 | hp2 | a0002 | c0002 | t0003 | g0112 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0127 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04184 | hp2 | a0001 | c0001 | t0008 | g0206 | SAS | BEB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04199 | hp1 | a0019 | c0017 | t0001 | g0229 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04199 | hp2 | a0001 | c0001 | t0008 | g0202 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0121 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18522 | hp1 | a0003 | c0004 | t0004 | g0283 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18747 | hp1 | a0002 | c0002 | t0003 | g0110 | EAS | CHB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18906 | hp2 | a0003 | c0004 | t0005 | g0022 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18939 | hp2 | a0001 | c0018 | t0001 | g0265 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18940 | hp2 | a0001 | c0001 | t0006 | g0046 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18945 | hp2 | a0002 | c0002 | t0010 | g0028 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18947 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18948 | hp1 | a0002 | c0002 | t0003 | g0031 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18948 | hp2 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18949 | hp2 | a0004 | c0003 | t0004 | g0057 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18950 | hp2 | a0008 | c0008 | t0001 | g0040 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18953 | hp2 | a0001 | c0001 | t0012 | g0201 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18956 | hp1 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18957 | hp1 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18957 | hp2 | a0002 | c0005 | t0001 | g0231 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18964 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18965 | hp1 | a0002 | c0002 | t0010 | g0028 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18968 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18969 | hp1 | a0002 | c0005 | t0001 | g0178 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18970 | hp1 | a0004 | c0003 | t0004 | g0066 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18972 | hp2 | a0001 | c0001 | t0012 | g0200 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18973 | hp1 | a0002 | c0002 | t0003 | g0118 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18974 | hp2 | a0004 | c0003 | t0004 | g0064 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18979 | hp1 | a0008 | c0008 | t0001 | g0208 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18979 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18980 | hp1 | a0002 | c0002 | t0014 | g0137 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18982 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18986 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18987 | hp2 | a0001 | c0001 | t0006 | g0050 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18990 | hp2 | a0004 | c0003 | t0004 | g0062 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18992 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18992 | hp2 | a0004 | c0003 | t0004 | g0025 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18993 | hp1 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18993 | hp2 | a0008 | c0008 | t0001 | g0262 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18995 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18997 | hp2 | a0002 | c0002 | t0003 | g0098 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18998 | hp1 | a0002 | c0002 | t0003 | g0105 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19004 | hp1 | a0002 | c0002 | t0003 | g0029 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19004 | hp2 | a0008 | c0008 | t0001 | g0040 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19005 | hp1 | a0002 | c0005 | t0001 | g0234 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19006 | hp2 | a0002 | c0002 | t0003 | g0115 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19043 | hp1 | a0003 | c0004 | t0005 | g0023 | AFR | LWK | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0100 | AFR | LWK | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19054 | hp1 | a0004 | c0003 | t0004 | g0063 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19055 | hp1 | a0020 | c0012 | t0004 | g0056 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19056 | hp1 | a0021 | c0026 | t0001 | g0270 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19057 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19062 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19063 | hp2 | a0002 | c0002 | t0003 | g0103 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19064 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19065 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19068 | hp1 | a0002 | c0005 | t0001 | g0233 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19068 | hp2 | a0004 | c0003 | t0004 | g0058 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19074 | hp2 | a0002 | c0002 | t0003 | g0031 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19079 | hp2 | a0002 | c0002 | t0015 | g0092 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19080 | hp2 | a0004 | c0003 | t0004 | g0025 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19081 | hp1 | a0002 | c0002 | t0015 | g0114 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19082 | hp1 | a0002 | c0002 | t0003 | g0113 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19083 | hp1 | a0004 | c0003 | t0004 | g0065 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19083 | hp2 | a0002 | c0005 | t0001 | g0232 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19087 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19090 | hp1 | a0001 | c0001 | t0008 | g0166 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19091 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19240 | hp1 | a0003 | c0004 | t0005 | g0290 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA19240 | hp2 | a0002 | c0002 | t0003 | g0156 | AFR | YRI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20129 | hp1 | a0002 | c0005 | t0001 | g0176 | AFR | ASW | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20129 | hp2 | a0003 | c0004 | t0005 | g0022 | AFR | ASW | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20752 | hp1 | a0004 | c0003 | t0004 | g0059 | EUR | TSI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20805 | hp1 | a0004 | c0003 | t0004 | g0004 | EUR | TSI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0161 | SAS | GIH | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | GIH | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02109 | hp1 | a0002 | c0005 | t0005 | g0224 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02109 | hp2 | a0004 | c0003 | t0018 | g0070 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02486 | hp1 | a0003 | c0004 | t0004 | g0275 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02486 | hp2 | a0005 | c0006 | t0001 | g0084 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02559 | hp1 | a0011 | c0027 | t0003 | g0271 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03471 | hp1 | a0002 | c0002 | t0003 | g0017 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG03471 | hp2 | a0003 | c0004 | t0004 | g0045 | AFR | MSL | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG06807 | hp1 | a0006 | c0007 | t0004 | g0014 | AFR | USA | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
HG06807 | hp2 | a0003 | c0004 | t0004 | g0044 | AFR | USA | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18955 | hp1 | a0002 | c0002 | t0022 | g0144 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20300 | hp1 | a0003 | c0004 | t0004 | g0021 | AFR | USA | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA20300 | hp2 | a0003 | c0004 | t0005 | g0292 | AFR | USA | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
NA21309 | hp2 | a0007 | c0009 | t0004 | g0273 | AFR | LWK | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0086 | REF | REF | GCFC2_chr2_75657705_75715915 | GCFC2 | chr2 | 75657705 | 75715915 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:75665985 | T | G | 2 | a0012 a0017 |
2 | HG02683.hp2 HG03239.hp1 |
missense_variant | MODERATE | c.2172A>C | p.Glu724Asp | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/17 | 2232/4367 | 2172/2346 | 724/781 | chr2 | 75665985 | |||
chr2:75665999 | T | C | 1 | a0010 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.2158A>G | p.Ile720Val | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/17 | 2218/4367 | 2158/2346 | 720/781 | chr2 | 75665999 | |||
chr2:75671975 | T | C | 1 | a0008 | 4 | NA18950.hp2 NA18979.hp1 NA18993.hp2 others(1): Show |
missense_variant | MODERATE | c.1931A>G | p.Glu644Gly | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/17 | 1991/4367 | 1931/2346 | 644/781 | chr2 | 75671975 | |||
chr2:75680221 | C | G | 1 | a0015 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1784G>C | p.Cys595Ser | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/17 | 1844/4367 | 1784/2346 | 595/781 | chr2 | 75680221 | |||
chr2:75680225 | T | C | 8 | a0003 a0004 a0006 others(5): Show |
75 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(72): Show |
missense_variant | MODERATE | c.1780A>G | p.Thr594Ala | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/17 | 1840/4367 | 1780/2346 | 594/781 | chr2 | 75680225 | |||
chr2:75680282 | T | C | 1 | a0014 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.1723A>G | p.Thr575Ala | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/17 | 1783/4367 | 1723/2346 | 575/781 | chr2 | 75680282 | |||
chr2:75687860 | T | C | 1 | a0009 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1657A>G | p.Ile553Val | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/17 | 1717/4367 | 1657/2346 | 553/781 | chr2 | 75687860 | |||
chr2:75687889 | C | G | 2 | a0018 a0019 |
2 | HG03927.hp2 HG04199.hp1 |
missense_variant | MODERATE | c.1628G>C | p.Ser543Thr | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/17 | 1688/4367 | 1628/2346 | 543/781 | chr2 | 75687889 | |||
chr2:75690035 | G | C | 1 | a0005 | 5 | HG01169.hp1 HG01433.hp1 HG01516.hp2 others(2): Show |
missense_variant | MODERATE | c.1273C>G | p.Gln425Glu | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/17 | 1333/4367 | 1273/2346 | 425/781 | chr2 | 75690035 | |||
chr2:75694315 | G | C | 1 | a0006 | 4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.946C>G | p.Gln316Glu | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/17 | 1006/4367 | 946/2346 | 316/781 | chr2 | 75694315 | |||
chr2:75696287 | T | C | 13 | a0002 a0003 a0004 others(10): Show |
221 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(218): Show |
missense_variant | MODERATE | c.746A>G | p.Asn249Ser | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/17 | 806/4367 | 746/2346 | 249/781 | chr2 | 75696287 | |||
chr2:75702257 | C | G | 1 | a0020 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.561G>C | p.Lys187Asn | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/17 | 621/4367 | 561/2346 | 187/781 | chr2 | 75702257 | |||
chr2:75702387 | C | T | 1 | a0017 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.431G>A | p.Arg144His | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/17 | 491/4367 | 431/2346 | 144/781 | chr2 | 75702387 | |||
chr2:75710663 | G | C | 1 | a0021 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.193C>G | p.Arg65Gly | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 253/4367 | 193/2346 | 65/781 | chr2 | 75710663 | |||
chr2:75710675 | C | T | 4 | a0004 a0006 a0016 others(1): Show |
38 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(35): Show |
missense_variant | MODERATE | c.181G>A | p.Val61Ile | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 241/4367 | 181/2346 | 61/781 | chr2 | 75710675 | |||
chr2:75710683 | G | A | 1 | a0011 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.173C>T | p.Pro58Leu | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 233/4367 | 173/2346 | 58/781 | chr2 | 75710683 | |||
chr2:75710689 | C | T | 1 | a0016 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.167G>A | p.Gly56Glu | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 227/4367 | 167/2346 | 56/781 | chr2 | 75710689 | |||
chr2:75710762 | G | C | 2 | a0003 a0007 |
38 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(35): Show |
missense_variant | MODERATE | c.94C>G | p.Pro32Ala | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 154/4367 | 94/2346 | 32/781 | chr2 | 75710762 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:75665937 | A | G | 1 | a0001c0018 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.2220T>C | p.Ser740Ser | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/17 | 2280/4367 | 2220/2346 | 740/781 | chr2 | 75665937 | |||
chr2:75670221 | G | A | 1 | a0004c0013 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.2020C>T | p.Leu674Leu | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/17 | 2080/4367 | 2020/2346 | 674/781 | chr2 | 75670221 | |||
chr2:75687909 | C | T | 17 | a0001c0016 a0002c0002 a0003c0004 others(14): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
synonymous_variant | LOW | c.1608G>A | p.Val536Val | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/17 | 1668/4367 | 1608/2346 | 536/781 | chr2 | 75687909 | |||
chr2:75691996 | C | T | 1 | a0003c0010 | 3 | HG01891.hp1 HG02717.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1125G>A | p.Thr375Thr | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/17 | 1185/4367 | 1125/2346 | 375/781 | chr2 | 75691996 | |||
chr2:75706554 | G | A | 1 | a0001c0025 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.363C>T | p.Ser121Ser | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/17 | 423/4367 | 363/2346 | 121/781 | chr2 | 75706554 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:75662780 | A | G | 6 | a0002c0002t0003 a0002c0002t0010 a0002c0002t0015 others(3): Show |
62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1886T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1886 | chr2 | 75662780 | ||||||
chr2:75662881 | C | G | 1 | a0002c0002t0020 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1785G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1785 | chr2 | 75662881 | ||||||
chr2:75662904 | T | TA | 16 | a0001c0001t0008 a0002c0002t0003 a0002c0002t0010 others(13): Show |
118 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*1761dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1761 | chr2 | 75662904 | ||||||
chr2:75662904 | T | TAA | 7 | a0002c0002t0015 a0004c0003t0026 a0009c0023t0024 others(4): Show |
8 | HG01109.hp1 HG02683.hp2 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1760_*1761dupTT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1761 | chr2 | 75662904 | ||||||
chr2:75662920 | A | C | 1 | a0002c0002t0009 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1746T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1746 | chr2 | 75662920 | ||||||
chr2:75662948 | G | A | 1 | a0002c0002t0023 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1718C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1718 | chr2 | 75662948 | ||||||
chr2:75662967 | A | C | 1 | a0001c0001t0019 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1699T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1699 | chr2 | 75662967 | ||||||
chr2:75663256 | A | G | 1 | a0004c0003t0021 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1410T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1410 | chr2 | 75663256 | ||||||
chr2:75663264 | T | G | 1 | a0001c0001t0013 | 2 | HG03704.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1402A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1402 | chr2 | 75663264 | ||||||
chr2:75663282 | A | G | 35 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0003 others(32): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1384T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1384 | chr2 | 75663282 | ||||||
chr2:75663414 | T | C | 35 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0003 others(32): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1252A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1252 | chr2 | 75663414 | ||||||
chr2:75663422 | A | G | 1 | a0001c0001t0012 | 2 | NA18953.hp2 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1244T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 1244 | chr2 | 75663422 | ||||||
chr2:75663702 | T | A | 27 | a0002c0002t0003 a0002c0002t0009 a0002c0002t0010 others(24): Show |
141 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*964A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 964 | chr2 | 75663702 | ||||||
chr2:75663844 | A | G | 1 | a0004c0003t0018 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 822 | chr2 | 75663844 | ||||||
chr2:75663882 | AT | A | 7 | a0002c0002t0003 a0002c0002t0010 a0002c0002t0015 others(4): Show |
63 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*783delA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 783 | chr2 | 75663882 | ||||||
chr2:75663967 | G | A | 1 | a0009c0023t0024 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*699C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 699 | chr2 | 75663967 | ||||||
chr2:75663973 | A | G | 1 | a0001c0001t0011 | 2 | HG02451.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*693T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 693 | chr2 | 75663973 | ||||||
chr2:75664123 | G | A | 1 | a0001c0001t0025 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*543C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 543 | chr2 | 75664123 | ||||||
chr2:75664144 | C | T | 1 | a0002c0002t0017 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*522G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 522 | chr2 | 75664144 | ||||||
chr2:75664283 | G | A | 1 | a0004c0003t0026 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 383 | chr2 | 75664283 | ||||||
chr2:75664518 | C | T | 1 | a0014c0022t0016 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*148G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 148 | chr2 | 75664518 | ||||||
chr2:75664558 | C | T | 1 | a0002c0002t0010 | 2 | NA18945.hp2 NA18965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*108G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 17/17 | 108 | chr2 | 75664558 | ||||||
chr2:75710871 | G | A | 1 | a0002c0002t0009 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
5_prime_UTR_variant | MODIFIER | c.-16C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 16 | chr2 | 75710871 | ||||||
chr2:75710874 | C | T | 1 | a0001c0001t0006 | 5 | HG02683.hp1 NA18940.hp2 NA18948.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-19G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/17 | 19 | chr2 | 75710874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:75664807 | C | T | 1 | a0002c0002t0002g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2229-24G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75664807 | |||||||
chr2:75664985 | T | C | 41 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(38): Show |
56 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.2229-202A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75664985 | |||||||
chr2:75665029 | T | C | 1 | a0014c0022t0016g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2229-246A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665029 | |||||||
chr2:75665061 | C | T | 25 | a0002c0005t0005g0224 a0003c0004t0004g0021 a0003c0004t0004g0044 others(22): Show |
34 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.2229-278G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665061 | |||||||
chr2:75665193 | T | C | 147 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(144): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.2229-410A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665193 | |||||||
chr2:75665450 | G | A | 1 | a0003c0004t0002g0285 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2228+479C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665450 | |||||||
chr2:75665464 | T | C | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2228+465A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665464 | |||||||
chr2:75665471 | T | G | 1 | a0007c0009t0004g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2228+458A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665471 | |||||||
chr2:75665486 | G | A | 68 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(65): Show |
101 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(98): Show |
intron_variant | MODIFIER | c.2228+443C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665486 | |||||||
chr2:75665539 | C | T | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2228+390G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665539 | |||||||
chr2:75665545 | ATTC | A | 2 | a0006c0007t0004g0014 a0006c0007t0004g0069 |
4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2228+381_2228+383d others(5): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665545 | |||||||
chr2:75665552 | A | G | 2 | a0003c0010t0004g0043 a0003c0010t0004g0274 |
3 | HG01891.hp1 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2228+377T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665552 | |||||||
chr2:75665696 | T | C | 2 | a0007c0009t0004g0272 a0007c0009t0004g0273 |
2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2228+233A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665696 | |||||||
chr2:75665711 | T | C | 18 | a0004c0003t0004g0004 a0004c0003t0004g0025 a0004c0003t0004g0057 others(15): Show |
25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.2228+218A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665711 | |||||||
chr2:75665749 | T | G | 1 | a0004c0003t0004g0059 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2228+180A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665749 | |||||||
chr2:75665801 | T | C | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2228+128A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 16/16 | chr2 | 75665801 | |||||||
chr2:75666110 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2104-57T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666110 | |||||||
chr2:75666131 | T | C | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2104-78A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666131 | |||||||
chr2:75666169 | G | C | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2104-116C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666169 | |||||||
chr2:75666177 | A | T | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2104-124T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666177 | |||||||
chr2:75666344 | T | G | 8 | a0003c0004t0004g0044 a0003c0004t0004g0045 a0003c0004t0004g0275 others(5): Show |
11 | HG01891.hp1 HG02486.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2104-291A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666344 | |||||||
chr2:75666355 | T | A | 1 | a0001c0001t0001g0218 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2104-302A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666355 | |||||||
chr2:75666518 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2104-465A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666518 | |||||||
chr2:75666579 | G | C | 1 | a0002c0002t0003g0106 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2104-526C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666579 | |||||||
chr2:75666633 | C | T | 89 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(86): Show |
129 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.2104-580G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666633 | |||||||
chr2:75666727 | A | AC | 4 | a0002c0002t0002g0126 a0002c0002t0002g0134 a0002c0002t0002g0138 others(1): Show |
4 | HG02738.hp1 NA18943.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.2104-675dupG | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666727 | |||||||
chr2:75666727 | A | C | 38 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(35): Show |
53 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.2104-674T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666727 | |||||||
chr2:75666786 | A | G | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2104-733T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666786 | |||||||
chr2:75666832 | G | C | 1 | a0001c0001t0001g0246 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2104-779C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666832 | |||||||
chr2:75666926 | T | C | 1 | a0004c0003t0021g0067 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2104-873A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666926 | |||||||
chr2:75666951 | C | T | 1 | a0002c0002t0017g0136 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2104-898G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75666951 | |||||||
chr2:75667099 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(62): Show |
95 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2104-1046A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667099 | |||||||
chr2:75667214 | CT | C | 3 | a0002c0002t0003g0105 a0002c0002t0003g0108 a0002c0002t0003g0115 |
3 | HG02080.hp2 NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.2104-1162delA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667214 | |||||||
chr2:75667294 | A | G | 4 | a0004c0003t0004g0057 a0004c0003t0004g0058 a0004c0003t0004g0063 others(1): Show |
4 | NA18949.hp2 NA18970.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.2104-1241T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667294 | |||||||
chr2:75667409 | T | C | 1 | a0002c0005t0001g0165 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2104-1356A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667409 | |||||||
chr2:75667554 | C | CCTCA | 9 | a0002c0002t0003g0009 a0002c0002t0003g0017 a0002c0002t0003g0095 others(6): Show |
14 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.2104-1502_2104-150 others(8): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667554 | |||||||
chr2:75667625 | T | G | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2104-1572A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667625 | |||||||
chr2:75667915 | T | C | 2 | a0012c0021t0007g0160 a0017c0014t0007g0159 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2104-1862A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667915 | |||||||
chr2:75667943 | A | G | 25 | a0002c0005t0005g0224 a0003c0004t0004g0021 a0003c0004t0004g0044 others(22): Show |
34 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.2104-1890T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75667943 | |||||||
chr2:75668136 | A | G | 16 | a0002c0002t0003g0002 a0002c0002t0003g0029 a0002c0002t0003g0030 others(13): Show |
23 | HG00621.hp1 HG01070.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.2103+2002T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668136 | |||||||
chr2:75668240 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2103+1898G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668240 | |||||||
chr2:75668339 | G | GAAAAC | 16 | a0001c0001t0001g0005 a0001c0001t0001g0091 a0001c0001t0001g0180 others(13): Show |
22 | HG00609.hp2 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2103+1794_2103+179 others(9): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668339 | |||||||
chr2:75668339 | G | GAAAACCA others(9): Show |
1 | a0007c0009t0005g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2103+1798_2103+179 others(20): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668339 | |||||||
chr2:75668339 | G | GAAAACCA others(14): Show |
1 | a0007c0009t0005g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2103+1798_2103+179 others(25): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668339 | |||||||
chr2:75668339 | GAAAAC | G | 2 | a0002c0002t0009g0024 a0004c0003t0026g0054 |
4 | HG02622.hp2 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2103+1794_2103+179 others(9): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668339 | |||||||
chr2:75668778 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2103+1360A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668778 | |||||||
chr2:75668852 | C | T | 146 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(143): Show |
205 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.2103+1286G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668852 | |||||||
chr2:75668859 | A | G | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2103+1279T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668859 | |||||||
chr2:75668873 | C | G | 2 | a0006c0007t0004g0014 a0006c0007t0004g0069 |
4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2103+1265G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668873 | |||||||
chr2:75668938 | C | G | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2103+1200G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668938 | |||||||
chr2:75668967 | G | A | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2103+1171C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75668967 | |||||||
chr2:75669198 | T | A | 1 | a0002c0002t0003g0115 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2103+940A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669198 | |||||||
chr2:75669343 | A | G | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2103+795T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669343 | |||||||
chr2:75669504 | C | A | 41 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(38): Show |
56 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.2103+634G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669504 | |||||||
chr2:75669542 | T | A | 1 | a0002c0002t0014g0137 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2103+596A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669542 | |||||||
chr2:75669652 | C | T | 1 | a0002c0005t0001g0234 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2103+486G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669652 | |||||||
chr2:75669775 | C | G | 7 | a0003c0004t0002g0285 a0004c0003t0002g0013 a0004c0003t0002g0052 others(4): Show |
9 | HG00735.hp2 HG02055.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2103+363G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669775 | |||||||
chr2:75669827 | C | T | 1 | a0014c0022t0016g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2103+311G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669827 | |||||||
chr2:75669885 | T | TA | 42 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(39): Show |
57 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.2103+252_2103+253i others(3): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669885 | |||||||
chr2:75669886 | G | C | 42 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(39): Show |
57 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.2103+252C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669886 | |||||||
chr2:75669904 | T | C | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2103+234A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669904 | |||||||
chr2:75669967 | C | T | 2 | a0006c0007t0004g0014 a0006c0007t0004g0069 |
4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2103+171G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75669967 | |||||||
chr2:75670050 | C | G | 98 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(95): Show |
140 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(137): Show |
intron_variant | MODIFIER | c.2103+88G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75670050 | |||||||
chr2:75670073 | T | C | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2103+65A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 15/16 | chr2 | 75670073 | |||||||
chr2:75670409 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1957-125T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670409 | |||||||
chr2:75670439 | C | A | 9 | a0002c0005t0005g0224 a0003c0004t0005g0022 a0003c0004t0005g0023 others(6): Show |
13 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1957-155G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670439 | |||||||
chr2:75670460 | T | C | 2 | a0003c0004t0004g0279 a0003c0004t0004g0282 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1957-176A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670460 | |||||||
chr2:75670580 | C | T | 2 | a0007c0009t0004g0272 a0007c0009t0004g0273 |
2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1957-296G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670580 | |||||||
chr2:75670590 | C | G | 1 | a0001c0001t0001g0253 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1957-306G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670590 | |||||||
chr2:75670756 | G | A | 2 | a0006c0007t0004g0014 a0006c0007t0004g0069 |
4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1957-472C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670756 | |||||||
chr2:75670763 | T | C | 3 | a0002c0002t0003g0009 a0002c0002t0003g0101 a0011c0027t0003g0271 |
6 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1957-479A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670763 | |||||||
chr2:75670813 | A | C | 49 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(46): Show |
66 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1957-529T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670813 | |||||||
chr2:75670927 | T | C | 1 | a0002c0002t0003g0103 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1957-643A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670927 | |||||||
chr2:75670939 | T | C | 1 | a0002c0002t0003g0094 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1957-655A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75670939 | |||||||
chr2:75671179 | T | C | 3 | a0002c0002t0003g0029 a0002c0002t0003g0110 a0002c0002t0003g0118 |
4 | HG00621.hp1 NA18747.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1956+771A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671179 | |||||||
chr2:75671232 | C | A | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1956+718G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671232 | |||||||
chr2:75671283 | G | A | 1 | a0012c0021t0007g0160 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1956+667C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671283 | |||||||
chr2:75671373 | G | C | 1 | a0003c0004t0005g0291 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1956+577C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671373 | |||||||
chr2:75671475 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1956+475G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671475 | |||||||
chr2:75671610 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1956+340A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671610 | |||||||
chr2:75671764 | CATTT | C | 91 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(88): Show |
131 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.1956+182_1956+185d others(6): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671764 | |||||||
chr2:75671801 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0219 a0001c0001t0001g0226 others(1): Show |
10 | NA18942.hp2 NA18952.hp1 NA18964.hp1 others(7): Show |
intron_variant | MODIFIER | c.1956+149G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671801 | |||||||
chr2:75671802 | G | A | 1 | a0007c0009t0004g0272 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1956+148C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671802 | |||||||
chr2:75671870 | A | G | 1 | a0004c0003t0004g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1956+80T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671870 | |||||||
chr2:75671902 | C | A | 1 | a0012c0021t0007g0160 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1956+48G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 14/16 | chr2 | 75671902 | |||||||
chr2:75672177 | A | ATTTATAA others(28): Show |
1 | a0012c0021t0007g0160 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1890-196_1890-162d others(37): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672177 | |||||||
chr2:75672177 | A | ATTTATAA others(63): Show |
2 | a0014c0022t0016g0158 a0017c0014t0007g0159 |
2 | HG03041.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1890-231_1890-162d others(72): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672177 | |||||||
chr2:75672177 | ATTTATAA others(28): Show |
A | 62 | a0001c0001t0001g0240 a0001c0001t0001g0242 a0001c0001t0012g0200 others(59): Show |
91 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.1890-196_1890-162d others(37): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672177 | |||||||
chr2:75672177 | ATTTATAA others(63): Show |
A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(209): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1890-231_1890-162d others(72): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672177 | |||||||
chr2:75672177 | ATTTATAA others(98): Show |
A | 5 | a0001c0001t0001g0091 a0002c0002t0002g0123 a0002c0002t0002g0145 others(2): Show |
5 | HG01109.hp1 HG02895.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1890-266_1890-162d others(2): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672177 | |||||||
chr2:75672178 | TTTATAAA others(27): Show |
T | 1 | a0002c0002t0003g0098 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1890-196_1890-163d others(36): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672178 | |||||||
chr2:75672235 | A | AT | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1890-220dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672235 | |||||||
chr2:75672270 | A | AT | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1890-255dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672270 | |||||||
chr2:75672287 | TAAAATAT others(64): Show |
T | 1 | a0002c0002t0002g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1890-342_1890-272d others(73): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672287 | |||||||
chr2:75672291 | ATATATAT others(36): Show |
A | 1 | a0007c0009t0005g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1890-318_1890-276d others(45): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672291 | |||||||
chr2:75672305 | A | AT | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1890-290dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672305 | |||||||
chr2:75672381 | A | G | 4 | a0002c0002t0009g0024 a0007c0009t0005g0277 a0007c0009t0005g0288 others(1): Show |
6 | HG02622.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1890-365T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672381 | |||||||
chr2:75672395 | A | G | 2 | a0007c0009t0004g0272 a0007c0009t0004g0273 |
2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1890-379T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672395 | |||||||
chr2:75672570 | A | G | 2 | a0012c0021t0007g0160 a0017c0014t0007g0159 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1890-554T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672570 | |||||||
chr2:75672606 | C | T | 86 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(83): Show |
124 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.1890-590G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672606 | |||||||
chr2:75672658 | G | A | 1 | a0004c0003t0018g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1890-642C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672658 | |||||||
chr2:75672733 | C | T | 1 | a0002c0002t0003g0094 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1889+711G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672733 | |||||||
chr2:75672737 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(238): Show |
333 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.1889+707A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672737 | |||||||
chr2:75672784 | T | G | 1 | a0007c0009t0004g0272 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1889+660A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75672784 | |||||||
chr2:75673002 | T | C | 1 | a0007c0009t0005g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1889+442A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673002 | |||||||
chr2:75673037 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1889+407C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673037 | |||||||
chr2:75673038 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0012g0200 a0001c0001t0012g0201 |
3 | NA18953.hp2 NA18972.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1889+406G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673038 | |||||||
chr2:75673077 | A | G | 6 | a0001c0001t0001g0167 a0001c0001t0001g0190 a0001c0001t0001g0191 others(3): Show |
7 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1889+367T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673077 | |||||||
chr2:75673081 | C | T | 43 | a0001c0001t0001g0171 a0001c0001t0002g0213 a0002c0002t0002g0003 others(40): Show |
58 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1889+363G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673081 | |||||||
chr2:75673085 | C | T | 43 | a0001c0001t0001g0171 a0001c0001t0002g0213 a0002c0002t0002g0003 others(40): Show |
58 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1889+359G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673085 | |||||||
chr2:75673086 | G | A | 2 | a0001c0001t0001g0240 a0014c0022t0016g0158 |
2 | HG03041.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1889+358C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673086 | |||||||
chr2:75673093 | A | G | 6 | a0001c0001t0001g0167 a0001c0001t0001g0190 a0001c0001t0001g0191 others(3): Show |
6 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1889+351T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673093 | |||||||
chr2:75673106 | C | G | 8 | a0001c0001t0001g0167 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1889+338G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673106 | |||||||
chr2:75673111 | C | T | 1 | a0004c0003t0018g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1889+333G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673111 | |||||||
chr2:75673113 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0194 |
2 | HG04228.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1889+331T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673113 | |||||||
chr2:75673117 | T | C | 1 | a0012c0021t0007g0160 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1889+327A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673117 | |||||||
chr2:75673129 | T | C | 2 | a0004c0003t0018g0070 a0016c0011t0007g0051 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1889+315A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673129 | |||||||
chr2:75673138 | A | G | 13 | a0002c0002t0002g0093 a0003c0004t0002g0285 a0003c0004t0004g0044 others(10): Show |
17 | HG00735.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1889+306T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673138 | |||||||
chr2:75673171 | G | A | 3 | a0001c0001t0001g0222 a0002c0005t0001g0035 a0002c0005t0001g0230 |
4 | HG00738.hp1 HG01361.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1889+273C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673171 | |||||||
chr2:75673173 | G | A | 1 | a0001c0001t0025g0088 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1889+271C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673173 | |||||||
chr2:75673178 | C | T | 3 | a0001c0001t0001g0187 a0001c0001t0001g0222 a0009c0023t0024g0268 |
3 | HG01109.hp1 HG04204.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1889+266G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673178 | |||||||
chr2:75673179 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0193 |
2 | HG01496.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1889+265C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673179 | |||||||
chr2:75673182 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1889+262G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673182 | |||||||
chr2:75673183 | G | A | 2 | a0002c0005t0001g0035 a0002c0005t0001g0230 |
3 | HG00738.hp1 HG01361.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1889+261C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673183 | |||||||
chr2:75673254 | G | T | 43 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(40): Show |
58 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1889+190C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673254 | |||||||
chr2:75673264 | C | T | 1 | a0007c0009t0005g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1889+180G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673264 | |||||||
chr2:75673287 | G | A | 1 | a0002c0002t0002g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1889+157C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673287 | |||||||
chr2:75673383 | TAAAC | T | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1889+57_1889+60del others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673383 | |||||||
chr2:75673392 | C | T | 1 | a0018c0024t0003g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1889+52G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 13/16 | chr2 | 75673392 | |||||||
chr2:75673574 | C | CA | 49 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(46): Show |
66 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1813-55dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673574 | |||||||
chr2:75673631 | G | A | 2 | a0012c0021t0007g0160 a0017c0014t0007g0159 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1813-111C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673631 | |||||||
chr2:75673677 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1813-157A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673677 | |||||||
chr2:75673789 | T | C | 96 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(93): Show |
138 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.1813-269A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673789 | |||||||
chr2:75673847 | A | C | 1 | a0003c0004t0005g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1813-327T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673847 | |||||||
chr2:75673921 | A | C | 1 | a0001c0001t0001g0240 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1813-401T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673921 | |||||||
chr2:75673924 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0251 a0002c0002t0003g0113 |
4 | NA18966.hp1 NA18977.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1813-404G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673924 | |||||||
chr2:75673925 | G | A | 1 | a0002c0002t0003g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1813-405C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673925 | |||||||
chr2:75673943 | A | G | 43 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(40): Show |
58 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1813-423T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75673943 | |||||||
chr2:75674011 | T | C | 39 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(36): Show |
61 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1813-491A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674011 | |||||||
chr2:75674034 | AATTATAG others(9): Show |
A | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1813-530_1813-515d others(18): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674034 | |||||||
chr2:75674140 | T | C | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1813-620A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674140 | |||||||
chr2:75674391 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1813-871A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674391 | |||||||
chr2:75674437 | C | T | 3 | a0003c0004t0004g0276 a0003c0004t0004g0283 a0003c0004t0004g0284 |
3 | HG02615.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1813-917G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674437 | |||||||
chr2:75674502 | GA | G | 3 | a0003c0004t0004g0021 a0003c0004t0004g0278 a0003c0004t0004g0280 |
5 | HG02451.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1813-983delT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674502 | |||||||
chr2:75674505 | A | G | 3 | a0003c0004t0004g0021 a0003c0004t0004g0278 a0003c0004t0004g0280 |
5 | HG02451.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1813-985T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674505 | |||||||
chr2:75674542 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(265): Show |
372 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(369): Show |
intron_variant | MODIFIER | c.1813-1022T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674542 | |||||||
chr2:75674562 | G | A | 2 | a0002c0002t0002g0127 a0002c0002t0002g0147 |
2 | HG03669.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1813-1042C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674562 | |||||||
chr2:75674588 | T | C | 4 | a0002c0002t0009g0024 a0007c0009t0005g0277 a0007c0009t0005g0288 others(1): Show |
6 | HG02622.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1813-1068A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674588 | |||||||
chr2:75674601 | T | G | 1 | a0002c0002t0014g0137 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1813-1081A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674601 | |||||||
chr2:75674678 | A | T | 103 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(100): Show |
147 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.1813-1158T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674678 | |||||||
chr2:75674699 | T | C | 1 | a0002c0002t0003g0156 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1813-1179A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674699 | |||||||
chr2:75674720 | T | C | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1813-1200A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674720 | |||||||
chr2:75674756 | T | C | 1 | a0003c0004t0005g0023 | 3 | HG03195.hp2 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1813-1236A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75674756 | |||||||
chr2:75675153 | G | A | 2 | a0012c0021t0007g0160 a0017c0014t0007g0159 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1813-1633C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675153 | |||||||
chr2:75675254 | C | T | 42 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(39): Show |
57 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1813-1734G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675254 | |||||||
chr2:75675315 | T | G | 1 | a0001c0001t0001g0074 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1813-1795A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675315 | |||||||
chr2:75675379 | ATAC | A | 66 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(63): Show |
99 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(96): Show |
intron_variant | MODIFIER | c.1813-1862_1813-186 others(7): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675379 | |||||||
chr2:75675465 | G | A | 1 | a0002c0002t0002g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1813-1945C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675465 | |||||||
chr2:75675519 | G | T | 3 | a0007c0009t0005g0277 a0007c0009t0005g0288 a0015c0015t0007g0157 |
3 | HG02976.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1813-1999C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675519 | |||||||
chr2:75675576 | C | T | 2 | a0012c0021t0007g0160 a0017c0014t0007g0159 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1813-2056G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675576 | |||||||
chr2:75675741 | C | A | 2 | a0004c0003t0018g0070 a0016c0011t0007g0051 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1813-2221G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675741 | |||||||
chr2:75675741 | C | CA | 20 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0170 others(17): Show |
21 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1813-2222dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675741 | |||||||
chr2:75675741 | C | CAA | 59 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(56): Show |
90 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1813-2223_1813-222 others(6): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675741 | |||||||
chr2:75675741 | C | CAAA | 16 | a0002c0002t0003g0098 a0002c0002t0003g0111 a0002c0002t0003g0117 others(13): Show |
20 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1813-2224_1813-222 others(7): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675741 | |||||||
chr2:75675741 | CA | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0002c0002t0009g0024 others(3): Show |
8 | HG00597.hp1 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1813-2222delT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675741 | |||||||
chr2:75675743 | A | C | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1813-2223T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675743 | |||||||
chr2:75675755 | AAAAC | A | 17 | a0004c0003t0004g0004 a0004c0003t0004g0025 a0004c0003t0004g0058 others(14): Show |
24 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1813-2239_1813-223 others(8): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75675755 | |||||||
chr2:75676044 | A | G | 147 | a0001c0001t0001g0215 a0001c0001t0002g0213 a0002c0002t0002g0003 others(144): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.1813-2524T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676044 | |||||||
chr2:75676289 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1813-2769G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676289 | |||||||
chr2:75676399 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1813-2879T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676399 | |||||||
chr2:75676410 | T | C | 18 | a0004c0003t0004g0004 a0004c0003t0004g0025 a0004c0003t0004g0057 others(15): Show |
25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1813-2890A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676410 | |||||||
chr2:75676466 | C | CT | 9 | a0001c0001t0001g0038 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
10 | HG02155.hp1 HG02258.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.1813-2947dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676466 | |||||||
chr2:75676466 | CT | C | 49 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(46): Show |
68 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1813-2947delA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676466 | |||||||
chr2:75676484 | C | G | 1 | a0002c0002t0002g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1813-2964G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676484 | |||||||
chr2:75676535 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1813-3015G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676535 | |||||||
chr2:75676718 | G | A | 2 | a0004c0003t0018g0070 a0016c0011t0007g0051 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1813-3198C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676718 | |||||||
chr2:75676738 | T | C | 146 | a0001c0001t0002g0213 a0002c0002t0002g0003 a0002c0002t0002g0007 others(143): Show |
205 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.1813-3218A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676738 | |||||||
chr2:75676810 | G | C | 2 | a0012c0021t0007g0160 a0017c0014t0007g0159 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1813-3290C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676810 | |||||||
chr2:75676973 | G | A | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1812+3220C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676973 | |||||||
chr2:75676976 | G | T | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1812+3217C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75676976 | |||||||
chr2:75677086 | A | G | 1 | a0014c0022t0016g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1812+3107T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677086 | |||||||
chr2:75677484 | G | A | 51 | a0003c0004t0002g0285 a0003c0004t0004g0021 a0003c0004t0004g0044 others(48): Show |
71 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.1812+2709C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677484 | |||||||
chr2:75677775 | A | G | 20 | a0001c0001t0001g0080 a0002c0002t0003g0030 a0004c0003t0004g0004 others(17): Show |
28 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1812+2418T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677775 | |||||||
chr2:75677777 | T | G | 20 | a0001c0001t0001g0080 a0002c0002t0003g0030 a0004c0003t0004g0004 others(17): Show |
28 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1812+2416A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677777 | |||||||
chr2:75677805 | C | T | 1 | a0017c0014t0007g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1812+2388G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677805 | |||||||
chr2:75677806 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1812+2387C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677806 | |||||||
chr2:75677832 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1812+2361C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677832 | |||||||
chr2:75677870 | C | G | 18 | a0004c0003t0004g0004 a0004c0003t0004g0025 a0004c0003t0004g0057 others(15): Show |
25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1812+2323G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75677870 | |||||||
chr2:75678015 | A | C | 1 | a0002c0002t0003g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1812+2178T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678015 | |||||||
chr2:75678018 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0248 |
2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1812+2175C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678018 | |||||||
chr2:75678048 | A | AGGT | 38 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(35): Show |
60 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.1812+2142_1812+214 others(7): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678048 | |||||||
chr2:75678048 | A | T | 1 | a0002c0002t0003g0098 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1812+2145T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678048 | |||||||
chr2:75678143 | C | T | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1812+2050G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678143 | |||||||
chr2:75678153 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1812+2040A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678153 | |||||||
chr2:75678240 | T | C | 2 | a0012c0021t0007g0160 a0017c0014t0007g0159 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1812+1953A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678240 | |||||||
chr2:75678403 | G | A | 1 | a0003c0004t0004g0284 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1812+1790C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678403 | |||||||
chr2:75678593 | C | T | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1812+1600G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678593 | |||||||
chr2:75678822 | A | G | 1 | a0001c0016t0001g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1812+1371T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75678822 | |||||||
chr2:75679020 | G | T | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1812+1173C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679020 | |||||||
chr2:75679085 | GTGTT | G | 93 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(90): Show |
135 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(132): Show |
intron_variant | MODIFIER | c.1812+1104_1812+110 others(8): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679085 | |||||||
chr2:75679331 | C | T | 1 | a0002c0005t0005g0224 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1812+862G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679331 | |||||||
chr2:75679498 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(225): Show |
320 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.1812+695G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679498 | |||||||
chr2:75679793 | A | AT | 41 | a0001c0016t0001g0172 a0002c0002t0003g0002 a0002c0002t0003g0006 others(38): Show |
63 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.1812+399dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679793 | |||||||
chr2:75679846 | G | A | 42 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(39): Show |
57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1812+347C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679846 | |||||||
chr2:75679868 | T | G | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1812+325A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679868 | |||||||
chr2:75679935 | T | A | 1 | a0003c0004t0004g0275 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1812+258A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75679935 | |||||||
chr2:75680010 | AT | A | 41 | a0001c0016t0001g0172 a0002c0002t0003g0002 a0002c0002t0003g0006 others(38): Show |
63 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.1812+182delA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75680010 | |||||||
chr2:75680079 | C | T | 4 | a0002c0002t0003g0027 a0002c0002t0003g0097 a0002c0002t0003g0106 others(1): Show |
5 | HG00735.hp1 HG01069.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1812+114G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75680079 | |||||||
chr2:75680091 | T | C | 1 | a0004c0003t0004g0061 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1812+102A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75680091 | |||||||
chr2:75680172 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1812+21G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 12/16 | chr2 | 75680172 | |||||||
chr2:75680862 | A | G | 1 | a0002c0002t0022g0144 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1691-548T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75680862 | |||||||
chr2:75681180 | C | T | 1 | a0002c0002t0002g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1691-866G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681180 | |||||||
chr2:75681252 | T | C | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1691-938A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681252 | |||||||
chr2:75681314 | GGAAGCAC others(2198): Show |
G | 2 | a0004c0003t0002g0052 a0004c0003t0002g0068 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1691-3205_1691-100 others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681314 | |||||||
chr2:75681339 | T | C | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1691-1025A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681339 | |||||||
chr2:75681370 | C | T | 2 | a0010c0019t0001g0267 a0015c0015t0007g0157 |
2 | HG02293.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1691-1056G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681370 | |||||||
chr2:75681394 | C | G | 1 | a0002c0002t0002g0152 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1691-1080G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681394 | |||||||
chr2:75681420 | G | A | 1 | a0012c0021t0007g0160 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1691-1106C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681420 | |||||||
chr2:75681433 | G | A | 1 | a0007c0009t0005g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1691-1119C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681433 | |||||||
chr2:75681433 | G | C | 1 | a0001c0001t0001g0226 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1691-1119C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681433 | |||||||
chr2:75681501 | G | A | 1 | a0014c0022t0016g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1691-1187C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681501 | |||||||
chr2:75681758 | C | T | 1 | a0002c0002t0009g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1691-1444G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681758 | |||||||
chr2:75681795 | G | A | 24 | a0003c0004t0004g0021 a0003c0004t0004g0044 a0003c0004t0004g0045 others(21): Show |
33 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1691-1481C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681795 | |||||||
chr2:75681826 | C | T | 6 | a0004c0003t0004g0057 a0004c0003t0004g0058 a0004c0003t0004g0062 others(3): Show |
6 | NA18949.hp2 NA18970.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1691-1512G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681826 | |||||||
chr2:75681835 | C | T | 3 | a0002c0002t0003g0009 a0002c0002t0003g0101 a0011c0027t0003g0271 |
6 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1691-1521G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75681835 | |||||||
chr2:75682106 | C | G | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1691-1792G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682106 | |||||||
chr2:75682157 | C | G | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1691-1843G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682157 | |||||||
chr2:75682281 | C | T | 8 | a0003c0004t0005g0022 a0003c0004t0005g0023 a0003c0004t0005g0289 others(5): Show |
12 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1691-1967G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682281 | |||||||
chr2:75682390 | A | T | 1 | a0001c0001t0006g0048 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1691-2076T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682390 | |||||||
chr2:75682655 | AG | A | 3 | a0003c0004t0004g0276 a0003c0004t0004g0283 a0003c0004t0004g0284 |
3 | HG02615.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1691-2342delC | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682655 | |||||||
chr2:75682998 | G | T | 1 | a0002c0002t0002g0161 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1691-2684C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75682998 | |||||||
chr2:75683029 | T | G | 2 | a0003c0004t0004g0044 a0003c0004t0004g0286 |
3 | HG02922.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1691-2715A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683029 | |||||||
chr2:75683081 | G | A | 1 | a0002c0002t0002g0149 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1691-2767C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683081 | |||||||
chr2:75683239 | G | A | 1 | a0004c0003t0018g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1691-2925C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683239 | |||||||
chr2:75683381 | G | A | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1691-3067C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683381 | |||||||
chr2:75683384 | A | T | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1691-3070T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683384 | |||||||
chr2:75683530 | C | T | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1691-3216G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683530 | |||||||
chr2:75683666 | C | G | 1 | a0002c0002t0003g0111 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1691-3352G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683666 | |||||||
chr2:75683690 | C | T | 1 | a0014c0022t0016g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1691-3376G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683690 | |||||||
chr2:75683771 | C | CA | 37 | a0001c0001t0001g0012 a0001c0001t0001g0188 a0001c0001t0001g0219 others(34): Show |
51 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(48): Show |
intron_variant | MODIFIER | c.1691-3458dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683771 | |||||||
chr2:75683771 | CA | C | 23 | a0001c0001t0001g0261 a0002c0002t0003g0100 a0002c0002t0003g0109 others(20): Show |
30 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1691-3458delT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683771 | |||||||
chr2:75683786 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1691-3472T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683786 | |||||||
chr2:75683920 | C | G | 42 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(39): Show |
57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1691-3606G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683920 | |||||||
chr2:75683941 | G | A | 2 | a0004c0003t0026g0054 a0007c0009t0005g0277 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1691-3627C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75683941 | |||||||
chr2:75684050 | G | A | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1691-3736C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684050 | |||||||
chr2:75684141 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1690+3686A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684141 | |||||||
chr2:75684142 | A | G | 1 | a0002c0002t0003g0108 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1690+3685T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684142 | |||||||
chr2:75684229 | G | A | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1690+3598C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684229 | |||||||
chr2:75684259 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(265): Show |
372 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(369): Show |
intron_variant | MODIFIER | c.1690+3568A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684259 | |||||||
chr2:75684380 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1690+3447G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684380 | |||||||
chr2:75684447 | C | G | 1 | a0002c0002t0003g0116 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1690+3380G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684447 | |||||||
chr2:75684523 | G | A | 2 | a0002c0005t0001g0233 a0002c0005t0001g0234 |
2 | NA19005.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1690+3304C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684523 | |||||||
chr2:75684645 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1690+3182C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684645 | |||||||
chr2:75684651 | T | C | 1 | a0001c0001t0001g0041 | 2 | NA18945.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1690+3176A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684651 | |||||||
chr2:75684724 | T | C | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1690+3103A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684724 | |||||||
chr2:75684766 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1690+3061A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684766 | |||||||
chr2:75684851 | G | A | 141 | a0001c0016t0001g0172 a0002c0002t0002g0003 a0002c0002t0002g0007 others(138): Show |
200 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.1690+2976C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684851 | |||||||
chr2:75684859 | T | C | 141 | a0001c0016t0001g0172 a0002c0002t0002g0003 a0002c0002t0002g0007 others(138): Show |
200 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.1690+2968A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684859 | |||||||
chr2:75684955 | C | T | 1 | a0006c0007t0004g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1690+2872G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75684955 | |||||||
chr2:75685063 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0187 |
2 | NA18955.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1690+2764C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685063 | |||||||
chr2:75685237 | C | T | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1690+2590G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685237 | |||||||
chr2:75685358 | A | G | 1 | a0007c0009t0004g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1690+2469T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685358 | |||||||
chr2:75685482 | T | C | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1690+2345A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685482 | |||||||
chr2:75685686 | C | T | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1690+2141G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685686 | |||||||
chr2:75685732 | T | C | 40 | a0001c0016t0001g0172 a0002c0002t0003g0002 a0002c0002t0003g0006 others(37): Show |
62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1690+2095A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685732 | |||||||
chr2:75685753 | CCTTTAAG others(5): Show |
C | 54 | a0003c0004t0002g0285 a0003c0004t0004g0021 a0003c0004t0004g0044 others(51): Show |
74 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.1690+2062_1690+207 others(16): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685753 | |||||||
chr2:75685766 | T | A | 54 | a0003c0004t0002g0285 a0003c0004t0004g0021 a0003c0004t0004g0044 others(51): Show |
74 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.1690+2061A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685766 | |||||||
chr2:75685769 | A | G | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1690+2058T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685769 | |||||||
chr2:75685844 | T | C | 2 | a0002c0002t0003g0116 a0002c0002t0003g0117 |
2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1690+1983A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685844 | |||||||
chr2:75685978 | T | C | 1 | a0002c0002t0003g0118 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1690+1849A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75685978 | |||||||
chr2:75686165 | T | C | 1 | a0007c0009t0004g0272 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1690+1662A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686165 | |||||||
chr2:75686170 | T | G | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1690+1657A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686170 | |||||||
chr2:75686206 | A | T | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1690+1621T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686206 | |||||||
chr2:75686345 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(236): Show |
331 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.1690+1482A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686345 | |||||||
chr2:75686347 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(236): Show |
331 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.1690+1480A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686347 | |||||||
chr2:75686348 | G | A | 1 | a0002c0002t0003g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1690+1479C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686348 | |||||||
chr2:75686391 | C | G | 146 | a0001c0016t0001g0172 a0002c0002t0002g0003 a0002c0002t0002g0007 others(143): Show |
205 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.1690+1436G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686391 | |||||||
chr2:75686469 | A | G | 48 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(45): Show |
65 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1690+1358T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686469 | |||||||
chr2:75686515 | A | T | 18 | a0004c0003t0004g0004 a0004c0003t0004g0025 a0004c0003t0004g0057 others(15): Show |
25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+1312T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686515 | |||||||
chr2:75686615 | G | A | 1 | a0002c0002t0003g0006 | 6 | NA18947.hp1 NA18979.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1690+1212C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686615 | |||||||
chr2:75686703 | C | T | 2 | a0003c0004t0004g0283 a0003c0004t0004g0284 |
2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1690+1124G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686703 | |||||||
chr2:75686723 | G | A | 1 | a0002c0002t0002g0141 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1690+1104C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686723 | |||||||
chr2:75686775 | T | A | 8 | a0003c0004t0005g0022 a0003c0004t0005g0023 a0003c0004t0005g0289 others(5): Show |
12 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1690+1052A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686775 | |||||||
chr2:75686780 | C | T | 1 | a0002c0002t0014g0137 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1690+1047G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686780 | |||||||
chr2:75686898 | C | T | 1 | a0014c0022t0016g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1690+929G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686898 | |||||||
chr2:75686918 | A | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(69): Show |
102 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1690+909T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686918 | |||||||
chr2:75686937 | A | AT | 143 | a0001c0001t0001g0197 a0001c0016t0001g0172 a0002c0002t0002g0003 others(140): Show |
202 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.1690+889dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686937 | |||||||
chr2:75686956 | C | T | 1 | a0001c0025t0001g0263 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1690+871G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75686956 | |||||||
chr2:75687004 | G | A | 42 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(39): Show |
57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1690+823C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687004 | |||||||
chr2:75687010 | C | T | 41 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(38): Show |
56 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1690+817G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687010 | |||||||
chr2:75687011 | C | T | 1 | a0007c0009t0004g0272 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1690+816G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687011 | |||||||
chr2:75687036 | G | A | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1690+791C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687036 | |||||||
chr2:75687037 | C | A | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1690+790G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687037 | |||||||
chr2:75687067 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1690+760A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687067 | |||||||
chr2:75687069 | G | C | 1 | a0001c0001t0006g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1690+758C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687069 | |||||||
chr2:75687248 | T | A | 24 | a0003c0004t0004g0021 a0003c0004t0004g0044 a0003c0004t0004g0045 others(21): Show |
33 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1690+579A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687248 | |||||||
chr2:75687250 | A | T | 1 | a0002c0002t0003g0103 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1690+577T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687250 | |||||||
chr2:75687310 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1690+517A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687310 | |||||||
chr2:75687514 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1690+313C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687514 | |||||||
chr2:75687573 | C | G | 1 | a0004c0003t0004g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1690+254G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687573 | |||||||
chr2:75687589 | T | A | 3 | a0004c0003t0004g0057 a0004c0003t0004g0058 a0004c0003t0004g0066 |
3 | NA18949.hp2 NA18970.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1690+238A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687589 | |||||||
chr2:75687684 | T | G | 1 | a0002c0002t0003g0103 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1690+143A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687684 | |||||||
chr2:75687743 | A | C | 4 | a0001c0001t0001g0168 a0001c0001t0001g0197 a0001c0001t0011g0196 others(1): Show |
4 | HG02451.hp1 HG02630.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1690+84T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687743 | |||||||
chr2:75687749 | G | T | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1690+78C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 11/16 | chr2 | 75687749 | |||||||
chr2:75688126 | G | A | 1 | a0002c0002t0002g0135 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1540-149C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688126 | |||||||
chr2:75688243 | G | A | 40 | a0001c0016t0001g0172 a0002c0002t0003g0002 a0002c0002t0003g0006 others(37): Show |
62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1540-266C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688243 | |||||||
chr2:75688244 | C | A | 24 | a0003c0004t0004g0021 a0003c0004t0004g0044 a0003c0004t0004g0045 others(21): Show |
33 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1540-267G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688244 | |||||||
chr2:75688255 | T | C | 1 | a0014c0022t0016g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1540-278A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688255 | |||||||
chr2:75688323 | T | C | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1540-346A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688323 | |||||||
chr2:75688335 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1540-358T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688335 | |||||||
chr2:75688466 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1540-489A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688466 | |||||||
chr2:75688605 | C | T | 5 | a0001c0001t0001g0167 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1539+421G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688605 | |||||||
chr2:75688729 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1539+297G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688729 | |||||||
chr2:75688794 | TA | T | 42 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(39): Show |
57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1539+231delT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688794 | |||||||
chr2:75688796 | A | T | 1 | a0002c0002t0003g0103 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1539+230T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688796 | |||||||
chr2:75688963 | T | C | 1 | a0002c0005t0001g0176 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1539+63A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688963 | |||||||
chr2:75688968 | A | C | 2 | a0004c0003t0002g0052 a0004c0003t0002g0068 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1539+58T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 10/16 | chr2 | 75688968 | |||||||
chr2:75689247 | TTATGCAT others(12): Show |
T | 1 | a0002c0002t0003g0103 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1340-41_1340-23del others(19): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689247 | |||||||
chr2:75689254 | T | A | 1 | a0001c0001t0013g0026 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1340-29A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689254 | |||||||
chr2:75689308 | G | A | 1 | a0002c0002t0002g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1340-83C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689308 | |||||||
chr2:75689452 | C | T | 2 | a0012c0021t0007g0160 a0014c0022t0016g0158 |
2 | HG02683.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1340-227G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689452 | |||||||
chr2:75689457 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1340-232C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689457 | |||||||
chr2:75689799 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0204 a0001c0001t0001g0252 others(2): Show |
8 | HG01192.hp1 HG01346.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1339+170G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689799 | |||||||
chr2:75689862 | C | A | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1339+107G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 9/16 | chr2 | 75689862 | |||||||
chr2:75690159 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1227-78G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 8/16 | chr2 | 75690159 | |||||||
chr2:75690361 | A | G | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1226+277T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 8/16 | chr2 | 75690361 | |||||||
chr2:75690401 | A | G | 1 | a0004c0003t0004g0062 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1226+237T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 8/16 | chr2 | 75690401 | |||||||
chr2:75690486 | G | A | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1226+152C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 8/16 | chr2 | 75690486 | |||||||
chr2:75690763 | G | T | 40 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(37): Show |
62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1145-44C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75690763 | |||||||
chr2:75690846 | A | G | 1 | a0007c0009t0005g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1145-127T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75690846 | |||||||
chr2:75690944 | T | G | 66 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(63): Show |
90 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1145-225A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75690944 | |||||||
chr2:75690960 | T | C | 15 | a0004c0003t0004g0004 a0004c0003t0004g0025 a0004c0003t0004g0057 others(12): Show |
22 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1145-241A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75690960 | |||||||
chr2:75691200 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1145-481A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691200 | |||||||
chr2:75691306 | T | C | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1145-587A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691306 | |||||||
chr2:75691416 | C | T | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1144+561G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691416 | |||||||
chr2:75691445 | G | C | 2 | a0002c0002t0002g0034 a0002c0002t0002g0148 |
3 | HG00323.hp2 HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1144+532C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691445 | |||||||
chr2:75691522 | T | C | 40 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(37): Show |
62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1144+455A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691522 | |||||||
chr2:75691757 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1144+220A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691757 | |||||||
chr2:75691860 | T | TAA | 41 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(38): Show |
56 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1144+115_1144+116d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 7/16 | chr2 | 75691860 | |||||||
chr2:75692146 | A | AAT | 23 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0076 others(20): Show |
33 | HG00140.hp1 HG00609.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.1021-48_1021-47dup others(2): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692146 | |||||||
chr2:75692146 | AAT | A | 8 | a0001c0001t0001g0085 a0001c0001t0001g0216 a0001c0001t0001g0225 others(5): Show |
8 | HG00621.hp2 HG01099.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-48_1021-47del others(2): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692146 | |||||||
chr2:75692146 | AATAT | A | 139 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(136): Show |
196 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.1021-50_1021-47del others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692146 | |||||||
chr2:75692146 | AATATATA others(1): Show |
A | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1021-54_1021-47del others(8): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692146 | |||||||
chr2:75692166 | T | C | 41 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(38): Show |
56 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1021-66A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692166 | |||||||
chr2:75692168 | T | C | 142 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(139): Show |
199 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.1021-68A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692168 | |||||||
chr2:75692170 | T | C | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1021-70A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692170 | |||||||
chr2:75692171 | A | G | 1 | a0007c0009t0004g0272 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1021-71T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692171 | |||||||
chr2:75692228 | A | G | 1 | a0017c0014t0007g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1021-128T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692228 | |||||||
chr2:75692353 | T | C | 3 | a0002c0002t0003g0130 a0012c0021t0007g0160 a0017c0014t0007g0159 |
3 | HG00735.hp1 HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1021-253A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692353 | |||||||
chr2:75692361 | C | T | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1021-261G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692361 | |||||||
chr2:75692374 | AG | A | 142 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(139): Show |
201 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.1021-275delC | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692374 | |||||||
chr2:75692522 | C | G | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1021-422G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692522 | |||||||
chr2:75692827 | G | A | 1 | a0002c0005t0005g0224 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1021-727C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692827 | |||||||
chr2:75692879 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0257 |
2 | NA18972.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1021-779G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692879 | |||||||
chr2:75692891 | T | G | 1 | a0001c0001t0001g0261 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1021-791A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692891 | |||||||
chr2:75692900 | T | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0207 a0001c0001t0001g0209 others(3): Show |
8 | HG00609.hp1 HG01934.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021-800A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75692900 | |||||||
chr2:75693355 | G | A | 1 | a0003c0004t0002g0285 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1020+886C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693355 | |||||||
chr2:75693400 | A | G | 1 | a0004c0003t0004g0061 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1020+841T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693400 | |||||||
chr2:75693426 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1020+815G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693426 | |||||||
chr2:75693525 | A | C | 1 | a0002c0002t0002g0143 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1020+716T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693525 | |||||||
chr2:75693640 | T | G | 2 | a0012c0021t0007g0160 a0017c0014t0007g0159 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1020+601A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693640 | |||||||
chr2:75693735 | A | G | 1 | a0002c0002t0003g0006 | 6 | NA18947.hp1 NA18979.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020+506T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693735 | |||||||
chr2:75693993 | T | A | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1020+248A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75693993 | |||||||
chr2:75694106 | G | GCTTA | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1020+134_1020+135i others(6): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75694106 | |||||||
chr2:75694133 | G | C | 1 | a0001c0001t0001g0252 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1020+108C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 6/16 | chr2 | 75694133 | |||||||
chr2:75694553 | T | C | 1 | a0004c0003t0004g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.834-126A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75694553 | |||||||
chr2:75694841 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0188 |
4 | NA18949.hp1 NA18953.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.834-414C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75694841 | |||||||
chr2:75694997 | TGA | T | 2 | a0002c0002t0003g0009 a0011c0027t0003g0271 |
5 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.834-572_834-571del others(2): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75694997 | |||||||
chr2:75695083 | C | T | 3 | a0004c0003t0004g0057 a0004c0003t0004g0058 a0004c0003t0004g0066 |
3 | NA18949.hp2 NA18970.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.834-656G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695083 | |||||||
chr2:75695124 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.834-697G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695124 | |||||||
chr2:75695167 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.834-740G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695167 | |||||||
chr2:75695196 | T | C | 2 | a0004c0003t0018g0070 a0016c0011t0007g0051 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.834-769A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695196 | |||||||
chr2:75695314 | ATCCAG | A | 3 | a0007c0009t0004g0272 a0007c0009t0004g0273 a0015c0015t0007g0157 |
3 | HG02818.hp2 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.833+881_833+885del others(5): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695314 | |||||||
chr2:75695485 | T | C | 15 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0181 others(12): Show |
18 | HG00423.hp1 HG00609.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.833+715A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695485 | |||||||
chr2:75695522 | C | T | 2 | a0001c0001t0001g0210 a0002c0002t0017g0136 |
2 | HG02129.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.833+678G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695522 | |||||||
chr2:75695556 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0197 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.833+644G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695556 | |||||||
chr2:75695714 | T | C | 1 | a0002c0002t0002g0127 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.833+486A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695714 | |||||||
chr2:75695901 | G | A | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.833+299C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695901 | |||||||
chr2:75695926 | G | T | 2 | a0007c0009t0004g0272 a0007c0009t0004g0273 |
2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.833+274C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695926 | |||||||
chr2:75695982 | C | T | 1 | a0002c0002t0003g0106 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.833+218G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75695982 | |||||||
chr2:75696172 | T | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0260 |
3 | HG03491.hp2 HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.833+28A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 5/16 | chr2 | 75696172 | |||||||
chr2:75696430 | T | C | 1 | a0002c0005t0001g0176 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.718-115A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696430 | |||||||
chr2:75696600 | G | C | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.718-285C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696600 | |||||||
chr2:75696606 | T | A | 24 | a0003c0004t0004g0021 a0003c0004t0004g0044 a0003c0004t0004g0045 others(21): Show |
33 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.718-291A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696606 | |||||||
chr2:75696694 | C | A | 1 | a0004c0003t0018g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.718-379G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696694 | |||||||
chr2:75696696 | T | A | 1 | a0014c0022t0016g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.718-381A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696696 | |||||||
chr2:75696778 | T | C | 1 | a0002c0002t0002g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.718-463A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696778 | |||||||
chr2:75696849 | A | C | 7 | a0003c0004t0002g0285 a0004c0003t0002g0013 a0004c0003t0002g0052 others(4): Show |
9 | HG00735.hp2 HG02055.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-534T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696849 | |||||||
chr2:75696886 | C | T | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.718-571G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75696886 | |||||||
chr2:75697496 | C | T | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.718-1181G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697496 | |||||||
chr2:75697534 | A | T | 1 | a0002c0002t0002g0135 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.718-1219T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697534 | |||||||
chr2:75697624 | C | T | 1 | a0007c0009t0005g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.718-1309G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697624 | |||||||
chr2:75697690 | A | G | 19 | a0002c0005t0001g0020 a0002c0005t0001g0035 a0002c0005t0001g0164 others(16): Show |
22 | HG00408.hp1 HG00738.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.718-1375T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697690 | |||||||
chr2:75697726 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.718-1411G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697726 | |||||||
chr2:75697739 | G | A | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.718-1424C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697739 | |||||||
chr2:75697787 | T | G | 53 | a0003c0004t0002g0285 a0003c0004t0004g0021 a0003c0004t0004g0044 others(50): Show |
73 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.718-1472A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75697787 | |||||||
chr2:75698407 | G | C | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.718-2092C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698407 | |||||||
chr2:75698508 | G | T | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.718-2193C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698508 | |||||||
chr2:75698518 | CAA | C | 2 | a0003c0004t0004g0044 a0003c0004t0004g0286 |
3 | HG02922.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.718-2205_718-2204d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698518 | |||||||
chr2:75698619 | T | G | 1 | a0002c0002t0002g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.718-2304A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698619 | |||||||
chr2:75698871 | G | C | 1 | a0007c0009t0005g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.717+2319C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698871 | |||||||
chr2:75698887 | G | A | 7 | a0003c0004t0002g0285 a0004c0003t0002g0013 a0004c0003t0002g0052 others(4): Show |
9 | HG00735.hp2 HG02055.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.717+2303C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698887 | |||||||
chr2:75698991 | G | A | 18 | a0002c0005t0001g0020 a0002c0005t0001g0035 a0002c0005t0001g0164 others(15): Show |
21 | HG00408.hp1 HG00738.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.717+2199C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75698991 | |||||||
chr2:75699011 | C | CA | 41 | a0001c0001t0001g0254 a0002c0002t0003g0002 a0002c0002t0003g0006 others(38): Show |
65 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.717+2178dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699011 | |||||||
chr2:75699032 | T | C | 1 | a0007c0009t0004g0272 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.717+2158A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699032 | |||||||
chr2:75699112 | G | C | 94 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(91): Show |
136 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.717+2078C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699112 | |||||||
chr2:75699118 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.717+2072G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699118 | |||||||
chr2:75699417 | G | A | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.717+1773C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699417 | |||||||
chr2:75699439 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(69): Show |
102 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.717+1751A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699439 | |||||||
chr2:75699562 | A | ATATT | 5 | a0003c0004t0005g0023 a0003c0004t0005g0290 a0003c0004t0005g0292 others(2): Show |
7 | HG01891.hp2 HG02809.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1627_717+1628i others(6): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699562 | |||||||
chr2:75699563 | C | T | 21 | a0003c0004t0004g0021 a0003c0004t0004g0044 a0003c0004t0004g0045 others(18): Show |
28 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.717+1627G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699563 | |||||||
chr2:75699608 | ACT | A | 3 | a0007c0009t0004g0272 a0007c0009t0004g0273 a0015c0015t0007g0157 |
3 | HG02818.hp2 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.717+1580_717+1581d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699608 | |||||||
chr2:75699710 | G | C | 5 | a0003c0004t0005g0023 a0003c0004t0005g0290 a0003c0004t0005g0292 others(2): Show |
7 | HG01891.hp2 HG02809.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1480C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699710 | |||||||
chr2:75699724 | C | T | 1 | a0003c0004t0004g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.717+1466G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699724 | |||||||
chr2:75699746 | T | C | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.717+1444A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699746 | |||||||
chr2:75699805 | G | C | 1 | a0004c0003t0004g0064 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.717+1385C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699805 | |||||||
chr2:75699807 | G | C | 3 | a0004c0003t0018g0070 a0006c0007t0004g0014 a0006c0007t0004g0069 |
5 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+1383C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699807 | |||||||
chr2:75699896 | G | GT | 11 | a0001c0001t0001g0238 a0002c0002t0002g0123 a0002c0002t0002g0134 others(8): Show |
12 | HG01891.hp1 HG02015.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.717+1293dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75699896 | |||||||
chr2:75700027 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.717+1163T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700027 | |||||||
chr2:75700027 | A | T | 10 | a0002c0002t0003g0009 a0002c0002t0003g0017 a0002c0002t0003g0094 others(7): Show |
15 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(12): Show |
intron_variant | MODIFIER | c.717+1163T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700027 | |||||||
chr2:75700219 | C | T | 1 | a0007c0009t0005g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+971G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700219 | |||||||
chr2:75700306 | A | G | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.717+884T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700306 | |||||||
chr2:75700391 | C | A | 29 | a0003c0004t0002g0285 a0004c0003t0002g0013 a0004c0003t0002g0052 others(26): Show |
40 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.717+799G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700391 | |||||||
chr2:75700393 | CATA | C | 3 | a0003c0004t0004g0276 a0003c0004t0004g0283 a0003c0004t0004g0284 |
3 | HG02615.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.717+794_717+796del others(3): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700393 | |||||||
chr2:75700410 | T | C | 42 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(39): Show |
57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.717+780A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700410 | |||||||
chr2:75700509 | G | A | 40 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0009 others(37): Show |
62 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.717+681C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700509 | |||||||
chr2:75700514 | G | T | 1 | a0001c0001t0011g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.717+676C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700514 | |||||||
chr2:75700524 | C | A | 2 | a0006c0007t0004g0014 a0006c0007t0004g0069 |
4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+666G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700524 | |||||||
chr2:75700572 | G | A | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.717+618C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700572 | |||||||
chr2:75700632 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.717+558A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700632 | |||||||
chr2:75700757 | T | C | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.717+433A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700757 | |||||||
chr2:75700780 | T | C | 18 | a0004c0003t0004g0004 a0004c0003t0004g0025 a0004c0003t0004g0057 others(15): Show |
25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.717+410A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700780 | |||||||
chr2:75700846 | T | C | 3 | a0004c0003t0004g0071 a0004c0003t0004g0072 a0004c0003t0004g0073 |
3 | HG02809.hp1 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.717+344A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700846 | |||||||
chr2:75700980 | C | T | 1 | a0007c0009t0005g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.717+210G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700980 | |||||||
chr2:75700996 | G | C | 20 | a0002c0002t0002g0003 a0002c0002t0002g0032 a0002c0002t0002g0033 others(17): Show |
30 | HG00323.hp2 HG00639.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.717+194C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75700996 | |||||||
chr2:75701107 | G | A | 2 | a0002c0005t0001g0177 a0002c0005t0005g0224 |
2 | HG01257.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.717+83C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75701107 | |||||||
chr2:75701174 | G | T | 144 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(141): Show |
203 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.717+16C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 4/16 | chr2 | 75701174 | |||||||
chr2:75701648 | T | C | 1 | a0004c0003t0026g0054 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.620-361A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75701648 | |||||||
chr2:75701692 | C | T | 1 | a0007c0009t0005g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.620-405G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75701692 | |||||||
chr2:75701719 | T | C | 1 | a0003c0004t0004g0278 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.620-432A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75701719 | |||||||
chr2:75701821 | A | G | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.619+378T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75701821 | |||||||
chr2:75702004 | C | A | 112 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(109): Show |
160 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.619+195G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75702004 | |||||||
chr2:75702112 | C | A | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.619+87G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75702112 | |||||||
chr2:75702196 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19080.hp1 | splice_region_variant&intron_variant | LOW | c.619+3A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 3/16 | chr2 | 75702196 | |||||||
chr2:75702539 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.395-116A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702539 | |||||||
chr2:75702645 | A | C | 25 | a0003c0004t0002g0285 a0003c0004t0004g0021 a0003c0004t0004g0044 others(22): Show |
34 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.395-222T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702645 | |||||||
chr2:75702682 | C | T | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.395-259G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702682 | |||||||
chr2:75702760 | G | A | 3 | a0002c0002t0002g0129 a0002c0002t0002g0149 a0002c0002t0002g0154 |
3 | HG02027.hp1 NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.395-337C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702760 | |||||||
chr2:75702922 | C | G | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.395-499G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702922 | |||||||
chr2:75702969 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.395-546C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702969 | |||||||
chr2:75702979 | T | C | 2 | a0004c0003t0018g0070 a0016c0011t0007g0051 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.395-556A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75702979 | |||||||
chr2:75703016 | G | A | 1 | a0002c0002t0003g0156 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.395-593C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703016 | |||||||
chr2:75703095 | C | A | 29 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0027 others(26): Show |
46 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.395-672G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703095 | |||||||
chr2:75703211 | G | C | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.395-788C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703211 | |||||||
chr2:75703262 | A | C | 1 | a0005c0006t0001g0084 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.395-839T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703262 | |||||||
chr2:75703464 | T | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0257 |
2 | NA18972.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.395-1041A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703464 | |||||||
chr2:75703686 | C | A | 1 | a0007c0009t0005g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.395-1263G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703686 | |||||||
chr2:75703854 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0179 a0001c0001t0001g0225 |
6 | HG00621.hp2 HG01175.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-1431C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75703854 | |||||||
chr2:75704002 | C | T | 41 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(38): Show |
56 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.395-1579G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704002 | |||||||
chr2:75704049 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.395-1626C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704049 | |||||||
chr2:75704077 | C | T | 1 | a0003c0004t0004g0279 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.395-1654G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704077 | |||||||
chr2:75704080 | G | A | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.395-1657C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704080 | |||||||
chr2:75704086 | G | A | 27 | a0003c0004t0002g0285 a0003c0004t0004g0021 a0003c0004t0004g0044 others(24): Show |
36 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.395-1663C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704086 | |||||||
chr2:75704223 | T | C | 1 | a0003c0004t0005g0294 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.395-1800A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704223 | |||||||
chr2:75704231 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0002g0213 |
2 | HG00423.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.395-1808A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704231 | |||||||
chr2:75704393 | A | G | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.395-1970T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704393 | |||||||
chr2:75704403 | C | T | 1 | a0019c0017t0001g0229 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.395-1980G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704403 | |||||||
chr2:75704432 | G | A | 5 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG00597.hp2 HG02155.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-2009C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704432 | |||||||
chr2:75704463 | T | A | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.395-2040A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704463 | |||||||
chr2:75704470 | G | A | 2 | a0001c0001t0006g0049 a0001c0001t0006g0050 |
2 | NA18987.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.395-2047C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704470 | |||||||
chr2:75704474 | T | G | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.394+2049A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704474 | |||||||
chr2:75704927 | C | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(62): Show |
95 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.394+1596G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704927 | |||||||
chr2:75704936 | A | G | 42 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(39): Show |
57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.394+1587T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75704936 | |||||||
chr2:75705193 | G | A | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.394+1330C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705193 | |||||||
chr2:75705238 | C | T | 1 | a0014c0022t0016g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394+1285G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705238 | |||||||
chr2:75705292 | A | C | 5 | a0007c0009t0004g0272 a0007c0009t0004g0273 a0012c0021t0007g0160 others(2): Show |
5 | HG02683.hp2 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+1231T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705292 | |||||||
chr2:75705345 | C | T | 2 | a0007c0009t0004g0272 a0007c0009t0004g0273 |
2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.394+1178G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705345 | |||||||
chr2:75705361 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(69): Show |
102 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.394+1162G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705361 | |||||||
chr2:75705439 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0183 others(5): Show |
11 | HG00597.hp1 NA18944.hp1 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.394+1084G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705439 | |||||||
chr2:75705501 | T | C | 43 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(40): Show |
58 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.394+1022A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705501 | |||||||
chr2:75705515 | GCTAAGGC others(62): Show |
G | 18 | a0004c0003t0004g0004 a0004c0003t0004g0025 a0004c0003t0004g0057 others(15): Show |
25 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.394+939_394+1007de others(70): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705515 | |||||||
chr2:75705616 | C | CA | 185 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(182): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.394+906dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705616 | |||||||
chr2:75705616 | C | CAA | 42 | a0001c0001t0001g0081 a0001c0001t0001g0182 a0001c0001t0001g0261 others(39): Show |
56 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.394+905_394+906dup others(2): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705616 | |||||||
chr2:75705616 | C | CAAA | 12 | a0002c0002t0002g0123 a0002c0002t0002g0133 a0003c0010t0004g0274 others(9): Show |
13 | HG00438.hp2 HG02015.hp1 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.394+904_394+906dup others(3): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705616 | |||||||
chr2:75705616 | C | CAAAA | 33 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0033 others(30): Show |
47 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.394+903_394+906dup others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705616 | |||||||
chr2:75705616 | C | CAAAAA | 8 | a0002c0002t0002g0032 a0002c0002t0002g0128 a0002c0002t0002g0129 others(5): Show |
9 | HG00735.hp1 HG01256.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.394+902_394+906dup others(5): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705616 | |||||||
chr2:75705720 | C | T | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.394+803G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705720 | |||||||
chr2:75705815 | C | T | 2 | a0002c0002t0002g0032 a0002c0002t0002g0153 |
3 | HG01256.hp1 HG01515.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.394+708G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705815 | |||||||
chr2:75705825 | C | T | 1 | a0007c0009t0004g0272 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394+698G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705825 | |||||||
chr2:75705938 | T | C | 1 | a0004c0003t0004g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.394+585A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75705938 | |||||||
chr2:75706004 | G | A | 43 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(40): Show |
58 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.394+519C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706004 | |||||||
chr2:75706004 | G | C | 1 | a0002c0005t0001g0235 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.394+519C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706004 | |||||||
chr2:75706252 | G | A | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.394+271C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706252 | |||||||
chr2:75706252 | G | GT | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0008g0166 |
3 | NA18969.hp2 NA19081.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.394+270dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706252 | |||||||
chr2:75706315 | T | G | 27 | a0003c0004t0002g0285 a0003c0004t0004g0021 a0003c0004t0004g0044 others(24): Show |
36 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.394+208A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706315 | |||||||
chr2:75706464 | A | G | 28 | a0004c0003t0002g0013 a0004c0003t0002g0052 a0004c0003t0002g0053 others(25): Show |
39 | HG00438.hp2 HG00639.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.394+59T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 2/16 | chr2 | 75706464 | |||||||
chr2:75706655 | A | G | 1 | a0017c0014t0007g0159 | 1 | HG03239.hp1 | splice_region_variant&intron_variant | LOW | c.266-4T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75706655 | |||||||
chr2:75706704 | T | A | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.266-53A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75706704 | |||||||
chr2:75706732 | A | G | 4 | a0004c0003t0004g0004 a0004c0003t0004g0059 a0004c0003t0004g0060 others(1): Show |
10 | HG00639.hp1 HG01261.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.266-81T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75706732 | |||||||
chr2:75706856 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.266-205A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75706856 | |||||||
chr2:75706927 | A | G | 21 | a0003c0004t0004g0021 a0003c0004t0004g0044 a0003c0004t0004g0045 others(18): Show |
30 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.266-276T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75706927 | |||||||
chr2:75707035 | T | C | 6 | a0004c0003t0002g0013 a0004c0003t0002g0052 a0004c0003t0002g0053 others(3): Show |
8 | HG02055.hp2 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.266-384A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707035 | |||||||
chr2:75707050 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.266-399G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707050 | |||||||
chr2:75707229 | C | T | 1 | a0015c0015t0007g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.266-578G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707229 | |||||||
chr2:75707295 | G | A | 1 | a0002c0002t0020g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.266-644C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707295 | |||||||
chr2:75707357 | T | C | 2 | a0004c0003t0018g0070 a0016c0011t0007g0051 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.266-706A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707357 | |||||||
chr2:75707447 | G | C | 1 | a0007c0009t0005g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.266-796C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707447 | |||||||
chr2:75707562 | T | TA | 114 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(111): Show |
162 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.266-912dupT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707562 | |||||||
chr2:75707679 | A | G | 2 | a0006c0007t0004g0014 a0006c0007t0004g0069 |
4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-1028T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707679 | |||||||
chr2:75707742 | T | TAACATGT others(12): Show |
42 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(39): Show |
57 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.266-1092_266-1091i others(21): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707742 | |||||||
chr2:75707912 | C | G | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.266-1261G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707912 | |||||||
chr2:75707958 | CAT | C | 3 | a0002c0002t0003g0156 a0007c0009t0004g0272 a0007c0009t0004g0273 |
3 | HG02818.hp2 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.266-1309_266-1308d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75707958 | |||||||
chr2:75708050 | T | C | 7 | a0002c0005t0001g0164 a0002c0005t0001g0178 a0002c0005t0001g0231 others(4): Show |
7 | HG00408.hp1 HG02056.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-1399A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708050 | |||||||
chr2:75708079 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0179 |
5 | HG01175.hp1 HG01433.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-1428G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708079 | |||||||
chr2:75708156 | A | G | 1 | a0002c0002t0002g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.266-1505T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708156 | |||||||
chr2:75708171 | A | C | 1 | a0002c0002t0002g0131 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.266-1520T>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708171 | |||||||
chr2:75708201 | T | G | 2 | a0002c0002t0002g0151 a0002c0002t0002g0152 |
2 | NA18939.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.266-1550A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708201 | |||||||
chr2:75708303 | C | G | 2 | a0007c0009t0005g0277 a0007c0009t0005g0288 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.266-1652G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708303 | |||||||
chr2:75708405 | G | A | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.266-1754C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708405 | |||||||
chr2:75708463 | C | A | 1 | a0001c0001t0001g0041 | 2 | NA18945.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.266-1812G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708463 | |||||||
chr2:75708488 | A | T | 115 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(112): Show |
165 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.266-1837T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708488 | |||||||
chr2:75708501 | C | CT | 57 | a0001c0001t0001g0074 a0001c0001t0001g0085 a0001c0001t0001g0167 others(54): Show |
75 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.266-1851dupA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | |||||||
chr2:75708501 | C | CTT | 16 | a0002c0002t0002g0121 a0002c0002t0002g0123 a0002c0002t0002g0124 others(13): Show |
18 | HG00735.hp1 HG01433.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.266-1852_266-1851d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | |||||||
chr2:75708501 | CT | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(59): Show |
98 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.266-1851delA | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | |||||||
chr2:75708501 | CTT | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0266 a0001c0001t0019g0264 others(4): Show |
8 | HG00323.hp1 HG02055.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.266-1852_266-1851d others(4): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | |||||||
chr2:75708501 | CTTTTTTT others(1): Show |
C | 32 | a0002c0002t0003g0002 a0002c0002t0003g0009 a0002c0002t0003g0017 others(29): Show |
48 | HG00621.hp1 HG01069.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.266-1858_266-1851d others(10): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | |||||||
chr2:75708501 | CTTTTTTT others(2): Show |
C | 3 | a0002c0002t0003g0006 a0002c0002t0003g0031 a0002c0002t0023g0120 |
9 | HG03041.hp1 NA18947.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.266-1859_266-1851d others(11): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | |||||||
chr2:75708501 | CTTTTTTT others(9): Show |
C | 1 | a0007c0009t0005g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.266-1866_266-1851d others(18): Show |
GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708501 | |||||||
chr2:75708604 | C | T | 39 | a0002c0002t0002g0093 a0002c0002t0003g0002 a0002c0002t0003g0006 others(36): Show |
61 | HG00621.hp1 HG01069.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.266-1953G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708604 | |||||||
chr2:75708760 | C | T | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG00423.hp2 HG00597.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.265+1831G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708760 | |||||||
chr2:75708762 | G | A | 2 | a0012c0021t0007g0160 a0017c0014t0007g0159 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.265+1829C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708762 | |||||||
chr2:75708768 | T | C | 145 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(142): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.265+1823A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708768 | |||||||
chr2:75708774 | G | A | 1 | a0002c0002t0002g0161 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.265+1817C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708774 | |||||||
chr2:75708911 | T | C | 1 | a0010c0019t0001g0267 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.265+1680A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708911 | |||||||
chr2:75708970 | C | A | 2 | a0006c0007t0004g0014 a0006c0007t0004g0069 |
4 | HG02055.hp1 HG02280.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+1621G>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75708970 | |||||||
chr2:75709200 | A | T | 1 | a0002c0002t0015g0092 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.265+1391T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709200 | |||||||
chr2:75709212 | GA | G | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.265+1378delT | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709212 | |||||||
chr2:75709215 | T | G | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.265+1376A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709215 | |||||||
chr2:75709217 | C | T | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.265+1374G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709217 | |||||||
chr2:75709345 | T | G | 1 | a0002c0002t0002g0162 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.265+1246A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709345 | |||||||
chr2:75709347 | T | C | 27 | a0003c0004t0002g0285 a0003c0004t0004g0021 a0003c0004t0004g0044 others(24): Show |
36 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.265+1244A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709347 | |||||||
chr2:75709501 | G | T | 8 | a0003c0004t0005g0022 a0003c0004t0005g0023 a0003c0004t0005g0289 others(5): Show |
12 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.265+1090C>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709501 | |||||||
chr2:75709526 | G | C | 8 | a0003c0004t0005g0022 a0003c0004t0005g0023 a0003c0004t0005g0289 others(5): Show |
12 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.265+1065C>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709526 | |||||||
chr2:75709563 | A | T | 1 | a0002c0002t0009g0024 | 3 | HG02622.hp2 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.265+1028T>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709563 | |||||||
chr2:75709621 | C | G | 1 | a0002c0002t0002g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.265+970G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709621 | |||||||
chr2:75709629 | C | T | 1 | a0002c0005t0001g0164 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.265+962G>A | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709629 | |||||||
chr2:75709635 | G | A | 1 | a0002c0002t0002g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.265+956C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709635 | |||||||
chr2:75709809 | T | A | 118 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(115): Show |
168 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.265+782A>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709809 | |||||||
chr2:75709850 | C | G | 144 | a0002c0002t0002g0003 a0002c0002t0002g0007 a0002c0002t0002g0032 others(141): Show |
201 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.265+741G>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709850 | |||||||
chr2:75709920 | T | C | 27 | a0003c0004t0002g0285 a0003c0004t0004g0021 a0003c0004t0004g0044 others(24): Show |
36 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.265+671A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709920 | |||||||
chr2:75709963 | G | A | 1 | a0009c0023t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.265+628C>T | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75709963 | |||||||
chr2:75710030 | T | C | 1 | a0004c0003t0018g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.265+561A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710030 | |||||||
chr2:75710129 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.265+462T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710129 | |||||||
chr2:75710248 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.265+343T>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710248 | |||||||
chr2:75710261 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(271): Show |
378 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(375): Show |
intron_variant | MODIFIER | c.265+330A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710261 | |||||||
chr2:75710274 | T | G | 1 | a0001c0001t0001g0269 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.265+317A>C | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710274 | |||||||
chr2:75710482 | T | C | 3 | a0004c0003t0004g0071 a0004c0003t0004g0072 a0004c0003t0004g0073 |
3 | HG02809.hp1 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.265+109A>G | GCFC2 | ENSG00000005436.14 | transcript | ENST00000321027.8 | protein_coding | 1/16 | chr2 | 75710482 |