Item | Value |
---|---|
geneid | 285203 |
ensemblid | ENSG00000163378.14 |
hgncid | 28526 |
symbol | EOGT |
name | EGF domain specific O-linked N-acetylglucosamine transferase |
refseq_nuc | NM_001278689.2 |
refseq_prot | NP_001265618.1 |
ensembl_nuc | ENST00000383701.8 |
ensembl_prot | ENSP00000373206.3 |
mane_status | MANE Select |
chr | chr3 |
start | 68975225 |
end | 69013684 |
strand | - |
ver | v1.2 |
region | chr3:68975225-69013684 |
region5000 | chr3:68970225-69018684 |
regionname0 | EOGT_chr3_68975225_69013684 |
regionname5000 | EOGT_chr3_68970225_69018684 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 527 | 424 | 92 | 60 | 210 | 14 | 46 | 166 | EOGT_chr3_68970225_69018684 | EOGT | MLMLF others(522): Show |
chr3 | 68970225 | 69018684 |
a0002 | 0/0 | 527 | 13 | 0 | 13 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | MLMLF others(522): Show |
chr3 | 68970225 | 69018684 |
a0003 | 0/0 | 527 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | MLMLF others(522): Show |
chr3 | 68970225 | 69018684 |
a0004 | 0/0 | 527 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | MLMLF others(522): Show |
chr3 | 68970225 | 69018684 |
a0005 | 0/0 | 527 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | MLMLF others(522): Show |
chr3 | 68970225 | 69018684 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1581 | 164 | 37 | 29 | 68 | 8 | 20 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0002 | 0/0 | 1581 | 155 | 26 | 22 | 88 | 3 | 16 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0003 | 0/0 | 1581 | 72 | 7 | 8 | 49 | 3 | 5 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0004 | 0/0 | 1581 | 13 | 13 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0007 | 0/0 | 1581 | 5 | 4 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0009 | 0/0 | 1581 | 5 | 0 | 0 | 5 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0010 | 0/0 | 1581 | 2 | 0 | 0 | 0 | 0 | 2 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0011 | 0/0 | 1581 | 2 | 0 | 0 | 0 | 0 | 2 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0012 | 0/0 | 1581 | 2 | 2 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0014 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0015 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0016 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0001c0017 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0002c0005 | 0/0 | 1581 | 7 | 0 | 7 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0002c0006 | 0/0 | 1581 | 6 | 0 | 6 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0003c0008 | 0/0 | 1581 | 5 | 4 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0004c0018 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 | ||
a0005c0013 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | ATGTT others(1576): Show |
chr3 | 68970225 | 69018684 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4443 | 34 | 2 | 1 | 25 | 1 | 4 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0002 | 0/1 | 4453 | 37 | 5 | 15 | 2 | 5 | 9 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0003 | 0/0 | 4459 | 11 | 0 | 4 | 4 | 0 | 3 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4454): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0004 | 0/0 | 4461 | 7 | 0 | 0 | 5 | 0 | 2 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4456): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0005 | 0/0 | 4451 | 10 | 9 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0006 | 0/0 | 4463 | 4 | 0 | 1 | 3 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4458): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0007 | 0/0 | 4449 | 5 | 1 | 3 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4444): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0009 | 0/0 | 4455 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0010 | 0/0 | 4457 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4452): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0011 | 0/0 | 4455 | 3 | 0 | 0 | 3 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0012 | 0/0 | 4455 | 4 | 3 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0013 | 0/0 | 4453 | 4 | 0 | 0 | 4 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0014 | 0/0 | 4465 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4460): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0016 | 0/0 | 4453 | 4 | 4 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0018 | 0/0 | 4445 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4440): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0020 | 0/0 | 4451 | 4 | 0 | 0 | 4 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0021 | 0/0 | 4445 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4440): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0023 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0024 | 0/0 | 4451 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0025 | 0/0 | 4457 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4452): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0026 | 0/0 | 4445 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4440): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0027 | 0/0 | 4453 | 3 | 1 | 2 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0028 | 0/0 | 4461 | 2 | 2 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4456): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0029 | 0/0 | 4455 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0030 | 0/0 | 4453 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0031 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4444): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0032 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4444): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0033 | 0/0 | 4459 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4454): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0034 | 0/0 | 4459 | 2 | 2 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4454): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0039 | 0/0 | 4445 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4440): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0040 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4456): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0042 | 0/0 | 4457 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4452): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0043 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0044 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4456): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0045 | 0/0 | 4459 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4454): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0047 | 0/0 | 4453 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0055 | 0/0 | 4462 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4457): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0057 | 0/0 | 4455 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0060 | 0/0 | 4455 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0001t0064 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0001 | 0/0 | 4443 | 76 | 4 | 14 | 47 | 1 | 10 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0002 | 0/0 | 4453 | 4 | 1 | 1 | 0 | 1 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0003 | 0/0 | 4459 | 9 | 0 | 3 | 5 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4454): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0004 | 0/0 | 4461 | 7 | 0 | 0 | 6 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4456): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0005 | 0/0 | 4451 | 8 | 8 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0006 | 0/0 | 4463 | 5 | 0 | 0 | 5 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4458): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0008 | 0/0 | 4443 | 8 | 0 | 0 | 8 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0009 | 0/0 | 4455 | 2 | 0 | 0 | 0 | 0 | 2 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0010 | 0/0 | 4457 | 2 | 0 | 2 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4452): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0011 | 0/0 | 4455 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0014 | 0/0 | 4465 | 3 | 3 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4460): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0015 | 0/0 | 4459 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4454): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0018 | 0/0 | 4445 | 4 | 0 | 0 | 4 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4440): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0019 | 0/0 | 4441 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4436): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0021 | 0/0 | 4445 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4440): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0022 | 0/0 | 4445 | 4 | 0 | 0 | 4 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4440): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0023 | 0/0 | 4451 | 2 | 2 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0024 | 0/0 | 4451 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0025 | 0/0 | 4457 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4452): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0026 | 0/0 | 4445 | 2 | 1 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4440): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0031 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4444): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0037 | 0/0 | 4443 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0046 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0048 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0049 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0051 | 0/0 | 4443 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0052 | 0/0 | 4471 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4466): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0053 | 0/0 | 4469 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4464): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0056 | 0/0 | 4459 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4454): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0059 | 0/0 | 4443 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
a0001c0002t0062 | 0/0 | 4453 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0001 | 0/0 | 4443 | 8 | 0 | 0 | 7 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0002 | 0/0 | 4453 | 6 | 1 | 4 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0003 | 0/0 | 4459 | 25 | 0 | 0 | 24 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4454): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0004 | 0/0 | 4461 | 11 | 0 | 1 | 9 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4456): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0006 | 0/0 | 4463 | 2 | 1 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4458): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0007 | 0/0 | 4449 | 2 | 0 | 2 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4444): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0009 | 0/0 | 4455 | 4 | 0 | 1 | 0 | 3 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0011 | 0/0 | 4455 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0012 | 0/0 | 4455 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0014 | 0/0 | 4465 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4460): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0015 | 0/0 | 4459 | 4 | 4 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4454): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0019 | 0/0 | 4441 | 4 | 0 | 0 | 4 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4436): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0021 | 0/0 | 4445 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4440): Show |
chr3 | 68970225 | 69018684 |
a0001c0003t0050 | 0/0 | 4443 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
a0001c0004t0007 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4444): Show |
chr3 | 68970225 | 69018684 |
a0001c0004t0012 | 0/0 | 4455 | 2 | 2 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0004t0013 | 0/0 | 4453 | 3 | 3 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0004t0014 | 0/0 | 4465 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4460): Show |
chr3 | 68970225 | 69018684 |
a0001c0004t0016 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0004t0020 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0001c0004t0035 | 0/0 | 4457 | 2 | 2 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4452): Show |
chr3 | 68970225 | 69018684 |
a0001c0004t0038 | 0/0 | 4455 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0007t0017 | 0/0 | 4453 | 5 | 4 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0001c0009t0004 | 0/0 | 4461 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4456): Show |
chr3 | 68970225 | 69018684 |
a0001c0009t0006 | 0/0 | 4463 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4458): Show |
chr3 | 68970225 | 69018684 |
a0001c0009t0054 | 0/0 | 4467 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4462): Show |
chr3 | 68970225 | 69018684 |
a0001c0009t0061 | 0/0 | 4455 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0001c0010t0001 | 0/0 | 4443 | 2 | 0 | 0 | 0 | 0 | 2 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
a0001c0011t0004 | 0/0 | 4461 | 2 | 0 | 0 | 0 | 0 | 2 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4456): Show |
chr3 | 68970225 | 69018684 |
a0001c0012t0036 | 0/0 | 4457 | 2 | 2 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4452): Show |
chr3 | 68970225 | 69018684 |
a0001c0014t0058 | 0/0 | 4445 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4440): Show |
chr3 | 68970225 | 69018684 |
a0001c0015t0003 | 0/0 | 4459 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4454): Show |
chr3 | 68970225 | 69018684 |
a0001c0016t0005 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0001c0017t0041 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4448): Show |
chr3 | 68970225 | 69018684 |
a0002c0005t0004 | 0/0 | 4461 | 6 | 0 | 6 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4456): Show |
chr3 | 68970225 | 69018684 |
a0002c0005t0006 | 0/0 | 4463 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4458): Show |
chr3 | 68970225 | 69018684 |
a0002c0006t0004 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4456): Show |
chr3 | 68970225 | 69018684 |
a0002c0006t0010 | 0/0 | 4457 | 5 | 0 | 5 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4452): Show |
chr3 | 68970225 | 69018684 |
a0003c0008t0001 | 0/0 | 4443 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
a0003c0008t0005 | 0/0 | 4451 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0003c0008t0029 | 0/0 | 4455 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4450): Show |
chr3 | 68970225 | 69018684 |
a0003c0008t0032 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4444): Show |
chr3 | 68970225 | 69018684 |
a0003c0008t0063 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4446): Show |
chr3 | 68970225 | 69018684 |
a0004c0018t0001 | 0/0 | 4443 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
a0005c0013t0001 | 0/0 | 4443 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | GCCCG others(4438): Show |
chr3 | 68970225 | 69018684 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0001g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0002g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0003g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0004g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0006g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0007g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0007g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0007g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0007g0382 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0009g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0009g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0010g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0011g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0011g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0011g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0012g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0012g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0013g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0013g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0014g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0016g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0016g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0016g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0016g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0018g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0020g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0020g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0020g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0021g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0021g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0023g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0024g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0024g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0025g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0026g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0027g0007 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0028g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0028g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0029g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0030g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0031g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0032g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0033g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0033g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0034g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0034g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0039g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0040g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0042g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0043g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0044g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0045g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0047g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0055g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0057g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0060g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0001t0064g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0001 | 0/0 | 12 | 0 | 2 | 9 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0003g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0006g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0006g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0008g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0008g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0008g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0008g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0008g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0008g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0009g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0009g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0010g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0010g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0011g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0014g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0014g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0015g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0018g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0018g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0018g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0018g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0019g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0021g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0022g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0022g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0022g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0022g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0023g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0023g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0024g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0025g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0025g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0026g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0026g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0031g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0037g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0046g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0048g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0049g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0051g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0052g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0053g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0056g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0059g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0002t0062g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0004g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0006g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0007g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0009g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0009g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0009g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0009g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0011g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0011g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0012g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0014g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0015g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0015g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0019g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0019g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0019g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0019g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0021g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0003t0050g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0012g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0013g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0013g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0014g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0016g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0020g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0035g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0035g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0004t0038g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0007t0017g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0007t0017g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0007t0017g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0007t0017g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0007t0017g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0009t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0009t0004g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0009t0006g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0009t0054g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0009t0061g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0010t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0010t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0011t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0011t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0012t0036g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0014t0058g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0015t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0016t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0001c0017t0041g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0002c0005t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0002c0005t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0002c0005t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0002c0005t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0002c0005t0006g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0002c0006t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0002c0006t0010g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0002c0006t0010g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0002c0006t0010g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0003c0008t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0003c0008t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0003c0008t0029g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0003c0008t0032g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0003c0008t0063g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0004c0018t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
a0005c0013t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0037 | g0034 | EUR | GBR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00099 | hp2 | a0001 | c0001 | t0039 | g0045 | EUR | GBR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0208 | EUR | GBR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | GBR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0220 | EUR | FIN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00323 | hp1 | a0001 | c0001 | t0007 | g0382 | EUR | FIN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0191 | EUR | FIN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0349 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00408 | hp2 | a0001 | c0001 | t0013 | g0011 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0347 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00438 | hp1 | a0001 | c0002 | t0006 | g0280 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00544 | hp1 | a0001 | c0003 | t0004 | g0127 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00544 | hp2 | a0001 | c0001 | t0021 | g0233 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00558 | hp1 | a0001 | c0001 | t0044 | g0264 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00558 | hp2 | a0001 | c0001 | t0013 | g0011 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00597 | hp2 | a0001 | c0003 | t0004 | g0149 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00621 | hp1 | a0001 | c0002 | t0003 | g0351 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00621 | hp2 | a0001 | c0002 | t0003 | g0337 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00639 | hp1 | a0002 | c0006 | t0010 | g0026 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0385 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | CHS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0250 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00735 | hp1 | a0001 | c0003 | t0009 | g0134 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00735 | hp2 | a0003 | c0008 | t0005 | g0036 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00738 | hp1 | a0001 | c0002 | t0003 | g0223 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00741 | hp1 | a0001 | c0002 | t0019 | g0320 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01069 | hp2 | a0002 | c0006 | t0010 | g0316 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01070 | hp1 | a0001 | c0002 | t0003 | g0030 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01070 | hp2 | a0001 | c0001 | t0007 | g0246 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01071 | hp1 | a0002 | c0006 | t0010 | g0026 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0030 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0386 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0331 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01099 | hp1 | a0002 | c0006 | t0010 | g0025 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01099 | hp2 | a0002 | c0005 | t0004 | g0021 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01106 | hp2 | a0001 | c0002 | t0026 | g0298 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0297 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01167 | hp1 | a0001 | c0001 | t0027 | g0007 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01169 | hp1 | a0001 | c0001 | t0027 | g0007 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01192 | hp1 | a0002 | c0006 | t0010 | g0025 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01243 | hp2 | a0001 | c0002 | t0010 | g0267 | AMR | PUR | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0383 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01256 | hp1 | a0001 | c0001 | t0007 | g0221 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01256 | hp2 | a0001 | c0003 | t0007 | g0014 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01258 | hp1 | a0001 | c0003 | t0007 | g0014 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01261 | hp1 | a0001 | c0003 | t0002 | g0133 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01261 | hp2 | a0001 | c0001 | t0006 | g0092 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01346 | hp1 | a0001 | c0001 | t0014 | g0068 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01346 | hp2 | a0001 | c0003 | t0002 | g0124 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01361 | hp1 | a0001 | c0001 | t0007 | g0232 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0330 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0384 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01433 | hp2 | a0001 | c0002 | t0010 | g0353 | AMR | CLM | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0352 | EUR | IBS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01884 | hp1 | a0001 | c0007 | t0017 | g0083 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01884 | hp2 | a0001 | c0004 | t0020 | g0137 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0345 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01934 | hp1 | a0002 | c0005 | t0004 | g0020 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0294 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01952 | hp1 | a0001 | c0007 | t0017 | g0077 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01975 | hp1 | a0002 | c0005 | t0004 | g0217 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01975 | hp2 | a0002 | c0006 | t0004 | g0240 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0216 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01978 | hp2 | a0001 | c0003 | t0004 | g0116 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01981 | hp1 | a0001 | c0001 | t0010 | g0062 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG01981 | hp2 | a0002 | c0005 | t0004 | g0203 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02004 | hp2 | a0001 | c0003 | t0002 | g0229 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0328 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0375 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02027 | hp2 | a0001 | c0001 | t0013 | g0094 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02040 | hp1 | a0001 | c0009 | t0061 | g0350 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02055 | hp2 | a0001 | c0001 | t0016 | g0078 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02056 | hp2 | a0001 | c0003 | t0003 | g0152 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02080 | hp1 | a0001 | c0003 | t0003 | g0015 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02080 | hp2 | a0001 | c0003 | t0003 | g0141 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02083 | hp1 | a0001 | c0003 | t0003 | g0015 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02129 | hp2 | a0001 | c0003 | t0001 | g0164 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02135 | hp2 | a0001 | c0001 | t0030 | g0012 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0346 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02145 | hp2 | a0001 | c0001 | t0040 | g0202 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02148 | hp1 | a0002 | c0005 | t0004 | g0020 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0374 | EAS | CDX | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CDX | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0356 | EAS | CDX | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0381 | EAS | CDX | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02257 | hp1 | a0001 | c0001 | t0064 | g0265 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02257 | hp2 | a0001 | c0004 | t0035 | g0138 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02273 | hp1 | a0002 | c0005 | t0006 | g0244 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02280 | hp1 | a0001 | c0003 | t0006 | g0090 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02280 | hp2 | a0001 | c0001 | t0032 | g0219 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02300 | hp1 | a0001 | c0003 | t0002 | g0107 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02300 | hp2 | a0002 | c0005 | t0004 | g0021 | AMR | PEL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02451 | hp1 | a0001 | c0004 | t0012 | g0104 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02451 | hp2 | a0001 | c0002 | t0005 | g0272 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02523 | hp2 | a0001 | c0001 | t0030 | g0012 | EAS | KHV | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02572 | hp2 | a0001 | c0002 | t0014 | g0023 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0188 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02602 | hp2 | a0001 | c0001 | t0018 | g0063 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02615 | hp1 | a0003 | c0008 | t0029 | g0038 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02615 | hp2 | a0001 | c0002 | t0023 | g0046 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02622 | hp1 | a0001 | c0004 | t0016 | g0120 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02622 | hp2 | a0001 | c0002 | t0023 | g0049 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02630 | hp1 | a0001 | c0002 | t0005 | g0271 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02630 | hp2 | a0001 | c0016 | t0005 | g0282 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02647 | hp1 | a0001 | c0002 | t0046 | g0284 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02647 | hp2 | a0001 | c0004 | t0038 | g0044 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0304 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02698 | hp2 | a0001 | c0002 | t0004 | g0319 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02717 | hp1 | a0001 | c0004 | t0013 | g0087 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0109 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02723 | hp1 | a0001 | c0003 | t0015 | g0259 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02723 | hp2 | a0003 | c0008 | t0001 | g0035 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0111 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0387 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02809 | hp1 | a0001 | c0002 | t0005 | g0306 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02886 | hp1 | a0001 | c0002 | t0014 | g0023 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02886 | hp2 | a0001 | c0003 | t0002 | g0119 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02895 | hp1 | a0001 | c0001 | t0029 | g0047 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0205 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02896 | hp1 | a0001 | c0001 | t0034 | g0117 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02896 | hp2 | a0001 | c0001 | t0012 | g0110 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0206 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0163 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02922 | hp1 | a0001 | c0004 | t0013 | g0086 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02922 | hp2 | a0001 | c0007 | t0017 | g0102 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0275 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02970 | hp1 | a0001 | c0001 | t0034 | g0070 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02970 | hp2 | a0001 | c0001 | t0043 | g0263 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02976 | hp1 | a0001 | c0004 | t0013 | g0079 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02976 | hp2 | a0001 | c0001 | t0026 | g0059 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0225 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0303 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03041 | hp2 | a0001 | c0002 | t0005 | g0273 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03098 | hp1 | a0001 | c0001 | t0028 | g0247 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03098 | hp2 | a0001 | c0002 | t0021 | g0288 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03130 | hp2 | a0001 | c0002 | t0026 | g0305 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03195 | hp1 | a0001 | c0002 | t0005 | g0266 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03195 | hp2 | a0001 | c0012 | t0036 | g0027 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0069 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03225 | hp1 | a0001 | c0002 | t0015 | g0050 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03225 | hp2 | a0001 | c0007 | t0017 | g0055 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0209 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03453 | hp1 | a0001 | c0002 | t0014 | g0289 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03453 | hp2 | a0001 | c0004 | t0007 | g0080 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03486 | hp1 | a0001 | c0001 | t0023 | g0071 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03486 | hp2 | a0001 | c0002 | t0053 | g0290 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03490 | hp2 | a0001 | c0010 | t0001 | g0196 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03491 | hp1 | a0001 | c0002 | t0009 | g0278 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03491 | hp2 | a0001 | c0015 | t0003 | g0067 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03492 | hp2 | a0001 | c0002 | t0009 | g0281 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03516 | hp2 | a0001 | c0004 | t0014 | g0139 | AFR | ESN | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03540 | hp2 | a0001 | c0003 | t0015 | g0008 | AFR | GWD | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03579 | hp1 | a0001 | c0001 | t0028 | g0248 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03579 | hp2 | a0001 | c0002 | t0048 | g0051 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03654 | hp1 | a0001 | c0011 | t0004 | g0105 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03654 | hp2 | a0001 | c0003 | t0002 | g0106 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0310 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03669 | hp2 | a0001 | c0003 | t0006 | g0126 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0088 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03704 | hp2 | a0001 | c0002 | t0062 | g0260 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03710 | hp2 | a0001 | c0003 | t0004 | g0128 | SAS | PJL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03831 | hp1 | a0001 | c0001 | t0047 | g0200 | SAS | BEB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | BEB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0214 | SAS | BEB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0066 | SAS | BEB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03927 | hp1 | a0001 | c0011 | t0004 | g0135 | SAS | BEB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | BEB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0327 | SAS | BEB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | STU | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | STU | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG04184 | hp1 | a0001 | c0003 | t0003 | g0129 | SAS | BEB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG04184 | hp2 | a0001 | c0002 | t0003 | g0291 | SAS | BEB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0161 | SAS | STU | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG04199 | hp2 | a0001 | c0010 | t0001 | g0192 | SAS | STU | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0335 | SAS | STU | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0277 | SAS | STU | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | STU | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0283 | SAS | STU | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | YRI | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18522 | hp2 | a0001 | c0002 | t0005 | g0269 | AFR | YRI | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | CHB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0364 | EAS | CHB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CHB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | CHB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18906 | hp1 | a0001 | c0003 | t0012 | g0076 | AFR | YRI | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18906 | hp2 | a0001 | c0012 | t0036 | g0027 | AFR | YRI | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18939 | hp2 | a0001 | c0003 | t0019 | g0148 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18941 | hp1 | a0001 | c0002 | t0059 | g0286 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18941 | hp2 | a0001 | c0002 | t0008 | g0039 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0370 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18943 | hp1 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18943 | hp2 | a0001 | c0002 | t0008 | g0314 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18944 | hp1 | a0001 | c0001 | t0020 | g0010 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18945 | hp1 | a0001 | c0003 | t0004 | g0004 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18945 | hp2 | a0004 | c0018 | t0001 | g0187 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18948 | hp1 | a0001 | c0002 | t0018 | g0361 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18948 | hp2 | a0001 | c0002 | t0006 | g0024 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18949 | hp1 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18949 | hp2 | a0001 | c0002 | t0018 | g0287 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18950 | hp2 | a0001 | c0002 | t0022 | g0323 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18951 | hp1 | a0001 | c0003 | t0004 | g0145 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18951 | hp2 | a0001 | c0002 | t0004 | g0302 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18953 | hp1 | a0001 | c0001 | t0020 | g0099 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18954 | hp1 | a0001 | c0002 | t0008 | g0315 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0342 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18956 | hp2 | a0001 | c0003 | t0003 | g0160 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18957 | hp1 | a0001 | c0003 | t0003 | g0167 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18957 | hp2 | a0001 | c0001 | t0011 | g0179 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18959 | hp2 | a0001 | c0002 | t0004 | g0357 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18960 | hp2 | a0001 | c0003 | t0003 | g0016 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18961 | hp1 | a0001 | c0003 | t0019 | g0089 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0355 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18962 | hp1 | a0001 | c0002 | t0022 | g0343 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18963 | hp1 | a0001 | c0002 | t0024 | g0333 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18963 | hp2 | a0001 | c0003 | t0019 | g0168 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18964 | hp1 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18966 | hp1 | a0001 | c0001 | t0011 | g0178 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18968 | hp1 | a0001 | c0009 | t0004 | g0363 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18968 | hp2 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18969 | hp2 | a0001 | c0001 | t0009 | g0252 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0380 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18971 | hp2 | a0001 | c0003 | t0011 | g0162 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18972 | hp2 | a0001 | c0001 | t0033 | g0253 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18977 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0366 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18978 | hp2 | a0001 | c0003 | t0003 | g0159 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18979 | hp1 | a0001 | c0002 | t0008 | g0318 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18980 | hp1 | a0001 | c0002 | t0011 | g0033 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18980 | hp2 | a0001 | c0002 | t0004 | g0292 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18981 | hp1 | a0001 | c0001 | t0057 | g0326 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18981 | hp2 | a0001 | c0003 | t0003 | g0151 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18982 | hp2 | a0001 | c0003 | t0003 | g0147 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18983 | hp1 | a0005 | c0013 | t0001 | g0329 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18983 | hp2 | a0001 | c0002 | t0008 | g0296 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18984 | hp1 | a0001 | c0003 | t0011 | g0150 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18985 | hp1 | a0001 | c0002 | t0008 | g0313 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18985 | hp2 | a0001 | c0003 | t0003 | g0158 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18986 | hp1 | a0001 | c0003 | t0004 | g0262 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18986 | hp2 | a0001 | c0002 | t0018 | g0360 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18987 | hp2 | a0001 | c0003 | t0003 | g0154 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18988 | hp1 | a0001 | c0001 | t0024 | g0261 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18989 | hp1 | a0001 | c0003 | t0014 | g0144 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0365 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18990 | hp1 | a0001 | c0002 | t0008 | g0362 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18990 | hp2 | a0001 | c0001 | t0013 | g0093 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18991 | hp1 | a0001 | c0003 | t0003 | g0142 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18991 | hp2 | a0001 | c0002 | t0022 | g0354 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18992 | hp1 | a0001 | c0003 | t0003 | g0146 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18992 | hp2 | a0001 | c0002 | t0031 | g0373 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18993 | hp1 | a0001 | c0002 | t0008 | g0312 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18993 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18994 | hp1 | a0001 | c0003 | t0050 | g0122 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18995 | hp2 | a0001 | c0003 | t0003 | g0118 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18998 | hp1 | a0001 | c0002 | t0006 | g0295 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18998 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18999 | hp1 | a0001 | c0002 | t0025 | g0340 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19000 | hp1 | a0001 | c0001 | t0020 | g0103 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19000 | hp2 | a0001 | c0003 | t0003 | g0155 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19001 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19002 | hp1 | a0001 | c0001 | t0033 | g0254 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19002 | hp2 | a0001 | c0002 | t0022 | g0338 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19003 | hp1 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19003 | hp2 | a0001 | c0003 | t0004 | g0156 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19004 | hp1 | a0001 | c0002 | t0004 | g0279 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19005 | hp1 | a0001 | c0003 | t0004 | g0143 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0377 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19007 | hp1 | a0001 | c0002 | t0011 | g0033 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19007 | hp2 | a0001 | c0001 | t0020 | g0010 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19010 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19011 | hp1 | a0001 | c0001 | t0031 | g0198 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19030 | hp1 | a0001 | c0003 | t0015 | g0008 | AFR | LWK | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19030 | hp2 | a0001 | c0002 | t0052 | g0048 | AFR | LWK | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19043 | hp1 | a0001 | c0004 | t0007 | g0084 | AFR | LWK | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19043 | hp2 | a0003 | c0008 | t0063 | g0388 | AFR | LWK | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19054 | hp2 | a0001 | c0001 | t0021 | g0181 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19058 | hp1 | a0001 | c0003 | t0021 | g0153 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19058 | hp2 | a0001 | c0001 | t0012 | g0098 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19060 | hp1 | a0001 | c0001 | t0055 | g0177 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0379 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19062 | hp1 | a0001 | c0009 | t0054 | g0309 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19062 | hp2 | a0001 | c0001 | t0009 | g0258 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19063 | hp2 | a0001 | c0003 | t0019 | g0157 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19064 | hp1 | a0001 | c0003 | t0003 | g0016 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0359 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19065 | hp2 | a0001 | c0002 | t0006 | g0301 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19066 | hp2 | a0001 | c0009 | t0004 | g0369 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19068 | hp1 | a0001 | c0001 | t0024 | g0185 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19072 | hp1 | a0001 | c0001 | t0011 | g0169 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0372 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19074 | hp1 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19074 | hp2 | a0001 | c0001 | t0045 | g0171 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19077 | hp1 | a0001 | c0003 | t0004 | g0004 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19077 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19079 | hp2 | a0001 | c0002 | t0006 | g0024 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19081 | hp1 | a0001 | c0003 | t0003 | g0140 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19081 | hp2 | a0001 | c0002 | t0003 | g0332 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19082 | hp1 | a0001 | c0002 | t0056 | g0376 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19084 | hp1 | a0001 | c0001 | t0025 | g0255 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19084 | hp2 | a0001 | c0003 | t0004 | g0004 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19085 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19085 | hp2 | a0001 | c0002 | t0003 | g0371 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0378 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19086 | hp2 | a0001 | c0002 | t0051 | g0344 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0358 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19087 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19088 | hp1 | a0001 | c0003 | t0001 | g0125 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19088 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19090 | hp1 | a0001 | c0009 | t0006 | g0368 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19090 | hp2 | a0001 | c0001 | t0060 | g0095 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | YRI | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA19240 | hp2 | a0001 | c0004 | t0035 | g0121 | AFR | YRI | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0073 | AFR | ASW | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA20129 | hp2 | a0001 | c0014 | t0058 | g0108 | AFR | ASW | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA20752 | hp1 | a0001 | c0003 | t0009 | g0091 | EUR | TSI | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA20752 | hp2 | a0001 | c0003 | t0009 | g0136 | EUR | TSI | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA20805 | hp1 | a0001 | c0003 | t0009 | g0132 | EUR | TSI | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | TSI | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02109 | hp1 | a0001 | c0017 | t0041 | g0274 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02109 | hp2 | a0001 | c0002 | t0005 | g0317 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0218 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02486 | hp2 | a0001 | c0001 | t0042 | g0053 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02559 | hp1 | a0001 | c0001 | t0016 | g0082 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG02559 | hp2 | a0001 | c0002 | t0049 | g0052 | AFR | ACB | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0074 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG03471 | hp2 | a0001 | c0002 | t0005 | g0270 | AFR | MSL | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG06807 | hp1 | a0003 | c0008 | t0032 | g0037 | AFR | USA | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
HG06807 | hp2 | a0001 | c0003 | t0015 | g0008 | AFR | USA | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18955 | hp1 | a0001 | c0002 | t0025 | g0367 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA18955 | hp2 | a0001 | c0002 | t0018 | g0339 | EAS | JPT | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA20300 | hp1 | a0001 | c0007 | t0017 | g0081 | AFR | USA | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA20300 | hp2 | a0001 | c0001 | t0016 | g0213 | AFR | USA | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA21309 | hp1 | a0001 | c0004 | t0012 | g0085 | AFR | LWK | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
NA21309 | hp2 | a0001 | c0001 | t0027 | g0007 | AFR | LWK | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0243 | REF | REF | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0176 | REF | REF | EOGT_chr3_68970225_69018684 | EOGT | chr3 | 68970225 | 69018684 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:68982812 | T | C | 1 | a0002 | 13 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
missense_variant&splice_region_variant | MODERATE | c.1213A>G | p.Arg405Gly | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/18 | 1679/4443 | 1213/1584 | 405/527 | chr3 | 68982812 | |||
chr3:69004435 | T | A | 1 | a0003 | 5 | HG00735.hp2 HG02615.hp1 HG02723.hp2 others(2): Show |
missense_variant | MODERATE | c.563A>T | p.Lys188Ile | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/18 | 1029/4443 | 563/1584 | 188/527 | chr3 | 69004435 | |||
chr3:69004436 | T | A | 1 | a0003 | 5 | HG00735.hp2 HG02615.hp1 HG02723.hp2 others(2): Show |
stop_gained | HIGH | c.562A>T | p.Lys188* | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/18 | 1028/4443 | 562/1584 | 188/527 | chr3 | 69004436 | |||
chr3:69007718 | C | T | 1 | a0005 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.415G>A | p.Glu139Lys | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/18 | 881/4443 | 415/1584 | 139/527 | chr3 | 69007718 | |||
chr3:69009680 | T | C | 1 | a0004 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.167A>G | p.His56Arg | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 4/18 | 633/4443 | 167/1584 | 56/527 | chr3 | 69009680 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:68979697 | G | A | 1 | a0001c0010 | 2 | HG03490.hp2 HG04199.hp2 |
synonymous_variant | LOW | c.1305C>T | p.Phe435Phe | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/18 | 1771/4443 | 1305/1584 | 435/527 | chr3 | 68979697 | |||
chr3:68982855 | T | C | 1 | a0001c0007 | 5 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(2): Show |
synonymous_variant | LOW | c.1170A>G | p.Lys390Lys | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/18 | 1636/4443 | 1170/1584 | 390/527 | chr3 | 68982855 | |||
chr3:68987445 | C | T | 1 | a0001c0016 | 1 | HG02630.hp2 | splice_region_variant&synonymous_variant | LOW | c.1152G>A | p.Glu384Glu | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/18 | 1618/4443 | 1152/1584 | 384/527 | chr3 | 68987445 | |||
chr3:68988937 | A | G | 3 | a0001c0003 a0001c0009 a0001c0011 |
79 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(76): Show |
synonymous_variant | LOW | c.912T>C | p.Tyr304Tyr | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 11/18 | 1378/4443 | 912/1584 | 304/527 | chr3 | 68988937 | |||
chr3:68988988 | G | A | 3 | a0001c0007 a0001c0014 a0001c0017 |
7 | HG01884.hp1 HG01952.hp1 HG02109.hp1 others(4): Show |
synonymous_variant | LOW | c.861C>T | p.Ser287Ser | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 11/18 | 1327/4443 | 861/1584 | 287/527 | chr3 | 68988988 | |||
chr3:68989009 | G | A | 2 | a0001c0004 a0001c0012 |
15 | HG01884.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
synonymous_variant | LOW | c.840C>T | p.Tyr280Tyr | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 11/18 | 1306/4443 | 840/1584 | 280/527 | chr3 | 68989009 | |||
chr3:68998059 | G | A | 1 | a0001c0011 | 2 | HG03654.hp1 HG03927.hp1 |
synonymous_variant | LOW | c.783C>T | p.His261His | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/18 | 1249/4443 | 783/1584 | 261/527 | chr3 | 68998059 | |||
chr3:69005184 | G | A | 1 | a0001c0015 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.471C>T | p.Thr157Thr | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/18 | 937/4443 | 471/1584 | 157/527 | chr3 | 69005184 | |||
chr3:69005190 | T | C | 7 | a0001c0002 a0001c0009 a0001c0012 others(4): Show |
171 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(168): Show |
synonymous_variant | LOW | c.465A>G | p.Arg155Arg | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/18 | 931/4443 | 465/1584 | 155/527 | chr3 | 69005190 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:68975335 | G | C | 1 | a0001c0017t0041 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2283C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 2283 | chr3 | 68975335 | ||||||
chr3:68975536 | C | CTT | 65 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(62): Show |
176 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*2080_*2081dupAA | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 2081 | chr3 | 68975536 | ||||||
chr3:68975577 | T | G | 1 | a0001c0003t0050 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2041A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 2041 | chr3 | 68975577 | ||||||
chr3:68975591 | T | G | 9 | a0001c0001t0024 a0001c0001t0030 a0001c0001t0031 others(6): Show |
11 | HG02135.hp2 HG02486.hp2 HG02523.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2027A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 2027 | chr3 | 68975591 | ||||||
chr3:68975621 | T | C | 1 | a0001c0001t0057 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1997A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 1997 | chr3 | 68975621 | ||||||
chr3:68976307 | C | T | 9 | a0001c0001t0024 a0001c0001t0030 a0001c0001t0031 others(6): Show |
11 | HG02135.hp2 HG02486.hp2 HG02523.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1311G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 1311 | chr3 | 68976307 | ||||||
chr3:68976338 | G | A | 2 | a0001c0001t0026 a0001c0002t0026 |
3 | HG01106.hp2 HG02976.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1280C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 1280 | chr3 | 68976338 | ||||||
chr3:68976456 | T | A | 1 | a0001c0002t0051 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1162A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 1162 | chr3 | 68976456 | ||||||
chr3:68976478 | T | C | 55 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(52): Show |
155 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*1140A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 1140 | chr3 | 68976478 | ||||||
chr3:68976563 | G | A | 1 | a0001c0001t0039 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1055C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 1055 | chr3 | 68976563 | ||||||
chr3:68976583 | G | A | 1 | a0001c0001t0047 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1035C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 1035 | chr3 | 68976583 | ||||||
chr3:68976641 | C | CGT | 3 | a0001c0001t0021 a0001c0002t0021 a0001c0003t0021 |
4 | HG00544.hp2 HG03098.hp2 NA19054.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*975_*976dupAC | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CGTGTGT | 8 | a0001c0001t0007 a0001c0001t0031 a0001c0001t0032 others(5): Show |
14 | HG00323.hp1 HG01070.hp2 HG01256.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*971_*976dupACACAC | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CGTGTGTG others(1): Show |
10 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0027 others(7): Show |
33 | HG00733.hp2 HG00735.hp2 HG01167.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*969_*976dupACACAC others(2): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CGTGTGTG others(3): Show |
14 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0030 others(11): Show |
62 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*967_*976dupACACAC others(4): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CGTGTGTG others(5): Show |
17 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0016 others(14): Show |
35 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*965_*976dupACACAC others(6): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CGTGTGTG others(7): Show |
11 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0042 others(8): Show |
59 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*963_*976dupACACAC others(8): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CGTGTGTG others(9): Show |
16 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0028 others(13): Show |
54 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*961_*976dupACACAC others(10): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CGTGTGTG others(11): Show |
7 | a0001c0001t0006 a0001c0001t0040 a0001c0002t0006 others(4): Show |
16 | HG00438.hp1 HG01261.hp2 HG02145.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*959_*976dupACACAC others(12): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CGTGTGTG others(13): Show |
5 | a0001c0001t0014 a0001c0001t0034 a0001c0002t0014 others(2): Show |
8 | HG01346.hp1 HG02572.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*957_*976dupACACAC others(14): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CGTGTGTG others(15): Show |
1 | a0001c0009t0054 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*955_*976dupACACAC others(16): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CGTGTGTG others(17): Show |
1 | a0001c0002t0053 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*953_*976dupACACAC others(18): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CGTGTGTG others(19): Show |
1 | a0001c0002t0052 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*951_*976dupACACAC others(20): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | C | CTGTGTGT others(10): Show |
1 | a0001c0001t0055 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*976_*977insACACAC others(11): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 976 | chr3 | 68976641 | ||||||
chr3:68976641 | CGT | C | 2 | a0001c0002t0019 a0001c0003t0019 |
5 | HG00741.hp1 NA18939.hp2 NA18961.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*975_*976delAC | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 975 | chr3 | 68976641 | ||||||
chr3:68976682 | T | C | 3 | a0001c0001t0016 a0001c0004t0016 a0001c0017t0041 |
6 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*936A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 936 | chr3 | 68976682 | ||||||
chr3:68976779 | C | T | 1 | a0001c0002t0046 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*839G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 839 | chr3 | 68976779 | ||||||
chr3:68976790 | TAC | T | 13 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0020 others(10): Show |
28 | HG00408.hp2 HG00558.hp2 HG01884.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*826_*827delGT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 826 | chr3 | 68976790 | ||||||
chr3:68977119 | C | T | 1 | a0001c0002t0008 | 8 | NA18941.hp2 NA18943.hp2 NA18954.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*499G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 499 | chr3 | 68977119 | ||||||
chr3:68977134 | T | G | 2 | a0001c0001t0032 a0003c0008t0032 |
2 | HG02280.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*484A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 484 | chr3 | 68977134 | ||||||
chr3:68977163 | G | A | 48 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(45): Show |
143 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*455C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 455 | chr3 | 68977163 | ||||||
chr3:68977241 | G | A | 1 | a0001c0002t0059 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 377 | chr3 | 68977241 | ||||||
chr3:68977291 | A | G | 2 | a0001c0001t0044 a0001c0001t0045 |
2 | HG00558.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*327T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 327 | chr3 | 68977291 | ||||||
chr3:68977324 | CAA | C | 31 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0016 others(28): Show |
55 | HG00408.hp2 HG00558.hp2 HG01884.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*292_*293delTT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 292 | chr3 | 68977324 | ||||||
chr3:68977435 | T | C | 11 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0020 others(8): Show |
25 | HG00408.hp2 HG00558.hp2 HG01884.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*183A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 183 | chr3 | 68977435 | ||||||
chr3:68977507 | T | C | 1 | a0001c0009t0061 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*111A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 111 | chr3 | 68977507 | ||||||
chr3:68977521 | C | T | 1 | a0001c0001t0028 | 2 | HG03098.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*97G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 18/18 | 97 | chr3 | 68977521 | ||||||
chr3:69011971 | G | T | 1 | a0001c0001t0039 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-50C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/18 | 2125 | chr3 | 69011971 | ||||||
chr3:69011981 | G | A | 1 | a0001c0002t0062 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/18 | 2135 | chr3 | 69011981 | ||||||
chr3:69012568 | C | A | 1 | a0003c0008t0063 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-124G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/18 | 2722 | chr3 | 69012568 | ||||||
chr3:69012650 | C | T | 1 | a0001c0004t0038 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-206G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/18 | 2804 | chr3 | 69012650 | ||||||
chr3:69012723 | G | A | 1 | a0001c0012t0036 | 2 | HG03195.hp2 NA18906.hp2 |
5_prime_UTR_variant | MODIFIER | c.-279C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/18 | 2877 | chr3 | 69012723 | ||||||
chr3:69012727 | G | A | 1 | a0001c0001t0064 | 1 | HG02257.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-283C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/18 | chr3 | 69012727 | |||||||
chr3:69013659 | A | G | 1 | a0001c0002t0037 | 1 | HG00099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-441T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/18 | 3813 | chr3 | 69013659 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:68978038 | T | G | 1 | a0001c0001t0003g0386 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1438-274A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 17/17 | chr3 | 68978038 | |||||||
chr3:68978155 | T | C | 1 | a0001c0001t0043g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1437+178A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 17/17 | chr3 | 68978155 | |||||||
chr3:68978606 | G | C | 1 | a0001c0001t0011g0179 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1335-171C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68978606 | |||||||
chr3:68978681 | CTGCT | C | 103 | a0001c0001t0003g0019 a0001c0001t0003g0043 a0001c0001t0003g0054 others(100): Show |
125 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1335-250_1335-247d others(6): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68978681 | |||||||
chr3:68978687 | CCT | C | 103 | a0001c0001t0003g0019 a0001c0001t0003g0043 a0001c0001t0003g0054 others(100): Show |
125 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1335-254_1335-253d others(4): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68978687 | |||||||
chr3:68978809 | G | A | 5 | a0001c0001t0044g0264 a0001c0001t0045g0171 a0001c0002t0006g0024 others(2): Show |
6 | HG00558.hp1 NA18948.hp2 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.1335-374C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68978809 | |||||||
chr3:68978846 | C | T | 1 | a0001c0003t0004g0116 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1335-411G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68978846 | |||||||
chr3:68978856 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1335-421G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68978856 | |||||||
chr3:68978865 | T | C | 1 | a0001c0001t0043g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1335-430A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68978865 | |||||||
chr3:68978894 | A | G | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1335-459T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68978894 | |||||||
chr3:68978943 | TATATC | T | 88 | a0001c0001t0001g0180 a0001c0001t0003g0019 a0001c0001t0003g0043 others(85): Show |
107 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1335-513_1335-509d others(7): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68978943 | |||||||
chr3:68979040 | C | T | 363 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(360): Show |
411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.1335-605G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68979040 | |||||||
chr3:68979057 | T | C | 3 | a0001c0002t0001g0268 a0001c0002t0005g0270 a0001c0016t0005g0282 |
3 | HG02572.hp1 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1334+611A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68979057 | |||||||
chr3:68979124 | C | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(224): Show |
264 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1334+544G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68979124 | |||||||
chr3:68979237 | G | A | 2 | a0001c0002t0001g0188 a0001c0002t0002g0214 |
2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1334+431C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68979237 | |||||||
chr3:68979330 | T | G | 1 | a0001c0001t0043g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1334+338A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68979330 | |||||||
chr3:68979469 | G | T | 1 | a0001c0001t0004g0173 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1334+199C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68979469 | |||||||
chr3:68979544 | T | C | 2 | a0001c0002t0022g0338 a0001c0002t0022g0343 |
2 | NA18962.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1334+124A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68979544 | |||||||
chr3:68979611 | GCA | G | 7 | a0001c0001t0003g0054 a0001c0001t0003g0057 a0001c0001t0004g0066 others(4): Show |
7 | HG00099.hp2 HG00738.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1334+55_1334+56del others(2): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 16/17 | chr3 | 68979611 | |||||||
chr3:68979809 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1215-22A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68979809 | |||||||
chr3:68979943 | C | T | 2 | a0001c0011t0004g0105 a0001c0011t0004g0135 |
2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1215-156G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68979943 | |||||||
chr3:68979947 | C | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(121): Show |
147 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.1215-160G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68979947 | |||||||
chr3:68980097 | T | C | 19 | a0001c0001t0001g0170 a0001c0001t0002g0195 a0001c0001t0029g0047 others(16): Show |
21 | HG00642.hp2 HG00735.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.1215-310A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980097 | |||||||
chr3:68980187 | A | C | 1 | a0001c0014t0058g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1215-400T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980187 | |||||||
chr3:68980197 | T | C | 5 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(2): Show |
5 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215-410A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980197 | |||||||
chr3:68980218 | T | C | 19 | a0001c0001t0002g0195 a0001c0001t0029g0047 a0001c0001t0030g0012 others(16): Show |
22 | HG00642.hp2 HG00735.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.1215-431A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980218 | |||||||
chr3:68980264 | A | G | 1 | a0003c0008t0001g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1215-477T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980264 | |||||||
chr3:68980266 | A | G | 3 | a0001c0001t0020g0010 a0001c0001t0020g0099 a0001c0001t0020g0103 |
4 | NA18944.hp1 NA18953.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215-479T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980266 | |||||||
chr3:68980334 | C | G | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1215-547G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980334 | |||||||
chr3:68980428 | T | C | 1 | a0001c0001t0042g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1215-641A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980428 | |||||||
chr3:68980492 | G | A | 1 | a0001c0002t0001g0334 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1215-705C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980492 | |||||||
chr3:68980494 | G | A | 1 | a0001c0002t0001g0334 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1215-707C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980494 | |||||||
chr3:68980531 | C | A | 5 | a0001c0001t0029g0047 a0001c0001t0030g0012 a0001c0001t0031g0198 others(2): Show |
6 | HG02135.hp2 HG02523.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215-744G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980531 | |||||||
chr3:68980598 | A | G | 1 | a0001c0004t0035g0121 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1215-811T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980598 | |||||||
chr3:68980647 | C | G | 1 | a0001c0002t0052g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1215-860G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980647 | |||||||
chr3:68980681 | T | C | 7 | a0001c0001t0004g0173 a0001c0001t0029g0047 a0001c0001t0030g0012 others(4): Show |
9 | HG02080.hp1 HG02083.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215-894A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980681 | |||||||
chr3:68980741 | G | A | 1 | a0001c0001t0003g0386 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1215-954C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980741 | |||||||
chr3:68980857 | G | A | 282 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(279): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1215-1070C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980857 | |||||||
chr3:68980878 | G | C | 1 | a0003c0008t0032g0037 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1215-1091C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980878 | |||||||
chr3:68980906 | T | A | 5 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(2): Show |
5 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215-1119A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980906 | |||||||
chr3:68980917 | A | G | 1 | a0001c0001t0012g0109 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1215-1130T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68980917 | |||||||
chr3:68981150 | G | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(168): Show |
195 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1215-1363C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981150 | |||||||
chr3:68981196 | T | C | 2 | a0001c0002t0023g0046 a0001c0002t0023g0049 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1215-1409A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981196 | |||||||
chr3:68981209 | T | C | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1215-1422A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981209 | |||||||
chr3:68981350 | T | A | 4 | a0001c0001t0029g0047 a0001c0001t0030g0012 a0001c0001t0031g0198 others(1): Show |
5 | HG02135.hp2 HG02523.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1214+1461A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981350 | |||||||
chr3:68981365 | G | C | 1 | a0001c0002t0023g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1214+1446C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981365 | |||||||
chr3:68981372 | G | C | 4 | a0001c0001t0029g0047 a0001c0001t0030g0012 a0001c0001t0031g0198 others(1): Show |
5 | HG02135.hp2 HG02523.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1214+1439C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981372 | |||||||
chr3:68981453 | G | C | 1 | a0001c0002t0023g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1214+1358C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981453 | |||||||
chr3:68981514 | C | T | 5 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(2): Show |
5 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1214+1297G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981514 | |||||||
chr3:68981621 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1214+1190G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981621 | |||||||
chr3:68981626 | CTG | C | 3 | a0001c0003t0001g0013 a0001c0003t0001g0165 a0001c0003t0050g0122 |
4 | NA18969.hp1 NA18994.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1214+1183_1214+118 others(6): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981626 | |||||||
chr3:68981836 | T | TTGTTATC others(13): Show |
16 | a0001c0001t0029g0047 a0001c0001t0030g0012 a0001c0001t0031g0198 others(13): Show |
17 | HG01884.hp1 HG01952.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.1214+974_1214+975i others(22): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981836 | |||||||
chr3:68981848 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(134): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1214+963T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981848 | |||||||
chr3:68981857 | T | C | 11 | a0001c0001t0032g0219 a0001c0001t0043g0263 a0001c0002t0015g0050 others(8): Show |
11 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1214+954A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981857 | |||||||
chr3:68981911 | A | AT | 6 | a0001c0001t0002g0191 a0001c0001t0002g0194 a0001c0001t0002g0197 others(3): Show |
6 | HG00323.hp2 HG01167.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214+899dupA | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981911 | |||||||
chr3:68981911 | AT | A | 5 | a0001c0001t0001g0113 a0001c0002t0004g0357 a0001c0003t0003g0147 others(2): Show |
7 | HG02723.hp1 HG03540.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1214+899delA | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981911 | |||||||
chr3:68981915 | T | C | 1 | a0001c0002t0026g0298 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1214+896A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981915 | |||||||
chr3:68981954 | C | T | 15 | a0001c0001t0029g0047 a0001c0001t0030g0012 a0001c0001t0031g0198 others(12): Show |
16 | HG01884.hp1 HG01952.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.1214+857G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981954 | |||||||
chr3:68981955 | G | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(132): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1214+856C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68981955 | |||||||
chr3:68982169 | A | G | 2 | a0001c0002t0008g0039 a0001c0002t0008g0318 |
2 | NA18941.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1214+642T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68982169 | |||||||
chr3:68982208 | C | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(133): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1214+603G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68982208 | |||||||
chr3:68982349 | G | A | 4 | a0001c0001t0029g0047 a0001c0001t0030g0012 a0001c0001t0031g0198 others(1): Show |
5 | HG02135.hp2 HG02523.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1214+462C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68982349 | |||||||
chr3:68982364 | AC | A | 19 | a0001c0001t0005g0204 a0001c0001t0012g0109 a0001c0001t0012g0110 others(16): Show |
19 | HG00735.hp2 HG01884.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1214+446delG | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68982364 | |||||||
chr3:68982430 | G | A | 1 | a0001c0001t0026g0059 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1214+381C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68982430 | |||||||
chr3:68982459 | G | C | 5 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(2): Show |
5 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1214+352C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68982459 | |||||||
chr3:68982534 | A | G | 5 | a0001c0001t0004g0173 a0001c0001t0029g0047 a0001c0001t0030g0012 others(2): Show |
6 | HG02135.hp2 HG02523.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214+277T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68982534 | |||||||
chr3:68982635 | A | C | 5 | a0001c0001t0004g0173 a0001c0001t0029g0047 a0001c0001t0030g0012 others(2): Show |
6 | HG02135.hp2 HG02523.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214+176T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 15/17 | chr3 | 68982635 | |||||||
chr3:68982885 | G | A | 1 | a0001c0002t0004g0302 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1153-13C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68982885 | |||||||
chr3:68983044 | G | A | 11 | a0001c0001t0032g0219 a0001c0001t0043g0263 a0001c0002t0015g0050 others(8): Show |
11 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-172C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983044 | |||||||
chr3:68983117 | T | C | 1 | a0001c0003t0003g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1153-245A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983117 | |||||||
chr3:68983256 | T | C | 17 | a0001c0001t0029g0047 a0001c0001t0030g0012 a0001c0001t0031g0198 others(14): Show |
18 | HG01884.hp1 HG01952.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.1153-384A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983256 | |||||||
chr3:68983333 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(263): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1153-461G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983333 | |||||||
chr3:68983440 | G | C | 11 | a0001c0001t0032g0219 a0001c0001t0043g0263 a0001c0002t0015g0050 others(8): Show |
11 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-568C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983440 | |||||||
chr3:68983462 | A | C | 1 | a0001c0002t0023g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1153-590T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983462 | |||||||
chr3:68983488 | A | G | 1 | a0001c0002t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1153-616T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983488 | |||||||
chr3:68983501 | G | A | 1 | a0001c0002t0001g0310 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1153-629C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983501 | |||||||
chr3:68983624 | C | T | 5 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(2): Show |
5 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-752G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983624 | |||||||
chr3:68983638 | T | C | 1 | a0001c0002t0014g0289 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1153-766A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983638 | |||||||
chr3:68983722 | G | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(132): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1153-850C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983722 | |||||||
chr3:68983734 | C | T | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1153-862G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983734 | |||||||
chr3:68983797 | C | T | 1 | a0001c0002t0002g0345 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1153-925G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983797 | |||||||
chr3:68983937 | T | C | 12 | a0001c0001t0032g0219 a0001c0001t0043g0263 a0001c0002t0015g0050 others(9): Show |
12 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1153-1065A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983937 | |||||||
chr3:68983977 | A | C | 2 | a0001c0011t0004g0105 a0001c0011t0004g0135 |
2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1153-1105T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983977 | |||||||
chr3:68983992 | T | C | 1 | a0001c0002t0005g0306 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1153-1120A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983992 | |||||||
chr3:68983999 | T | G | 2 | a0001c0002t0001g0307 a0001c0002t0001g0308 |
2 | NA18962.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1153-1127A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68983999 | |||||||
chr3:68984005 | T | A | 1 | a0001c0003t0003g0152 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1153-1133A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984005 | |||||||
chr3:68984027 | A | G | 1 | a0001c0002t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1153-1155T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984027 | |||||||
chr3:68984132 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(151): Show |
180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1153-1260G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984132 | |||||||
chr3:68984205 | C | CCT | 138 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(135): Show |
163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1153-1335_1153-133 others(6): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984205 | |||||||
chr3:68984205 | CCT | C | 4 | a0001c0001t0029g0047 a0001c0001t0042g0053 a0003c0008t0001g0035 others(1): Show |
4 | HG00735.hp2 HG02486.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-1335_1153-133 others(6): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984205 | |||||||
chr3:68984205 | CCTCT | C | 18 | a0001c0001t0005g0204 a0001c0001t0012g0109 a0001c0001t0012g0110 others(15): Show |
18 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1153-1337_1153-133 others(8): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984205 | |||||||
chr3:68984221 | T | A | 11 | a0001c0001t0032g0219 a0001c0001t0043g0263 a0001c0002t0015g0050 others(8): Show |
11 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-1349A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984221 | |||||||
chr3:68984223 | A | ACT | 6 | a0001c0001t0032g0219 a0001c0001t0043g0263 a0001c0002t0015g0050 others(3): Show |
6 | HG02280.hp2 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153-1352_1153-135 others(6): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984223 | |||||||
chr3:68984225 | A | T | 5 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(2): Show |
5 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-1353T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984225 | |||||||
chr3:68984227 | T | A | 11 | a0001c0001t0032g0219 a0001c0001t0043g0263 a0001c0002t0015g0050 others(8): Show |
11 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-1355A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984227 | |||||||
chr3:68984273 | T | C | 2 | a0001c0001t0032g0219 a0003c0008t0032g0037 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1153-1401A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984273 | |||||||
chr3:68984395 | G | T | 1 | a0001c0002t0001g0310 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1153-1523C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984395 | |||||||
chr3:68984411 | C | T | 2 | a0001c0001t0002g0211 a0001c0001t0034g0117 |
2 | HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1153-1539G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984411 | |||||||
chr3:68984415 | C | T | 2 | a0001c0001t0003g0058 a0001c0001t0003g0101 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1153-1543G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984415 | |||||||
chr3:68984498 | A | G | 6 | a0001c0001t0004g0173 a0001c0001t0029g0047 a0001c0001t0030g0012 others(3): Show |
8 | HG02080.hp1 HG02083.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1153-1626T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984498 | |||||||
chr3:68984541 | T | A | 1 | a0001c0003t0014g0144 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1153-1669A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984541 | |||||||
chr3:68984646 | A | C | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1153-1774T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984646 | |||||||
chr3:68984690 | T | C | 2 | a0001c0001t0018g0063 a0001c0001t0039g0045 |
2 | HG00099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1153-1818A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984690 | |||||||
chr3:68984777 | AG | A | 28 | a0001c0001t0002g0042 a0001c0001t0005g0205 a0001c0001t0005g0206 others(25): Show |
28 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1153-1906delC | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984777 | |||||||
chr3:68984827 | T | C | 11 | a0001c0001t0032g0219 a0001c0001t0043g0263 a0001c0002t0015g0050 others(8): Show |
11 | HG01884.hp1 HG01952.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-1955A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984827 | |||||||
chr3:68984866 | C | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(162): Show |
194 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1153-1994G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984866 | |||||||
chr3:68984921 | G | T | 6 | a0001c0002t0018g0287 a0001c0002t0018g0339 a0001c0002t0018g0360 others(3): Show |
6 | NA18948.hp1 NA18949.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153-2049C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984921 | |||||||
chr3:68984987 | C | A | 13 | a0001c0001t0005g0205 a0001c0001t0005g0206 a0001c0001t0005g0218 others(10): Show |
13 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1153-2115G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68984987 | |||||||
chr3:68985144 | A | T | 1 | a0001c0002t0001g0322 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1153-2272T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985144 | |||||||
chr3:68985164 | T | C | 191 | a0001c0001t0001g0075 a0001c0001t0001g0096 a0001c0001t0001g0097 others(188): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1152+2281A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985164 | |||||||
chr3:68985223 | T | G | 3 | a0003c0008t0005g0036 a0003c0008t0029g0038 a0003c0008t0032g0037 |
3 | HG00735.hp2 HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1152+2222A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985223 | |||||||
chr3:68985234 | G | T | 149 | a0001c0001t0001g0056 a0001c0001t0001g0123 a0001c0001t0001g0170 others(146): Show |
172 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1152+2211C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985234 | |||||||
chr3:68985271 | C | T | 1 | a0001c0002t0001g0381 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1152+2174G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985271 | |||||||
chr3:68985357 | C | G | 7 | a0001c0001t0012g0109 a0001c0001t0012g0110 a0001c0001t0012g0163 others(4): Show |
8 | HG02135.hp2 HG02523.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1152+2088G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985357 | |||||||
chr3:68985358 | T | G | 10 | a0001c0001t0005g0205 a0001c0001t0005g0206 a0001c0001t0005g0218 others(7): Show |
10 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1152+2087A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985358 | |||||||
chr3:68985384 | T | G | 12 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(9): Show |
14 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1152+2061A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985384 | |||||||
chr3:68985386 | G | T | 283 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(280): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1152+2059C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985386 | |||||||
chr3:68985540 | T | G | 1 | a0001c0003t0004g0262 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1152+1905A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985540 | |||||||
chr3:68985548 | G | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(242): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1152+1897C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985548 | |||||||
chr3:68985697 | A | G | 1 | a0001c0002t0001g0377 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1152+1748T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985697 | |||||||
chr3:68985712 | T | C | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1152+1733A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985712 | |||||||
chr3:68985867 | C | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(158): Show |
190 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1152+1578G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985867 | |||||||
chr3:68985973 | C | T | 1 | a0001c0002t0002g0352 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1152+1472G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985973 | |||||||
chr3:68985998 | C | T | 11 | a0001c0001t0005g0205 a0001c0001t0005g0206 a0001c0001t0005g0218 others(8): Show |
11 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1152+1447G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68985998 | |||||||
chr3:68986011 | C | G | 1 | a0001c0002t0008g0039 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1152+1434G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986011 | |||||||
chr3:68986105 | G | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(139): Show |
170 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1152+1340C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986105 | |||||||
chr3:68986128 | C | T | 105 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(102): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1152+1317G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986128 | |||||||
chr3:68986173 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(160): Show |
192 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1152+1272G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986173 | |||||||
chr3:68986199 | G | T | 105 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(102): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1152+1246C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986199 | |||||||
chr3:68986296 | C | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(159): Show |
191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1152+1149G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986296 | |||||||
chr3:68986323 | G | A | 1 | a0001c0003t0021g0153 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1152+1122C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986323 | |||||||
chr3:68986452 | C | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(160): Show |
192 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1152+993G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986452 | |||||||
chr3:68986461 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(160): Show |
192 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1152+984C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986461 | |||||||
chr3:68986514 | C | T | 2 | a0001c0001t0002g0210 a0001c0001t0002g0220 |
2 | HG00280.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1152+931G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986514 | |||||||
chr3:68986543 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(153): Show |
184 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1152+902T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986543 | |||||||
chr3:68986570 | ACATTTGA others(7): Show |
A | 1 | a0001c0001t0001g0238 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1152+861_1152+874d others(16): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986570 | |||||||
chr3:68986758 | T | C | 1 | a0001c0003t0021g0153 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1152+687A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986758 | |||||||
chr3:68986775 | C | T | 103 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(100): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.1152+670G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986775 | |||||||
chr3:68986813 | C | T | 1 | a0001c0002t0001g0226 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1152+632G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986813 | |||||||
chr3:68986814 | C | T | 1 | a0001c0003t0004g0127 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1152+631G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986814 | |||||||
chr3:68986929 | T | C | 4 | a0003c0008t0005g0036 a0003c0008t0029g0038 a0003c0008t0032g0037 others(1): Show |
4 | HG00735.hp2 HG02615.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+516A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986929 | |||||||
chr3:68986957 | T | G | 128 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(125): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1152+488A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68986957 | |||||||
chr3:68987310 | C | T | 1 | a0001c0001t0047g0200 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1152+135G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68987310 | |||||||
chr3:68987365 | C | T | 8 | a0001c0002t0001g0364 a0001c0002t0001g0365 a0001c0002t0001g0366 others(5): Show |
8 | NA18612.hp2 NA18942.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1152+80G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68987365 | |||||||
chr3:68987373 | G | GA | 13 | a0001c0001t0002g0201 a0001c0001t0002g0249 a0001c0001t0002g0251 others(10): Show |
13 | HG00733.hp2 HG00738.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1152+71dupT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68987373 | |||||||
chr3:68987373 | GA | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(168): Show |
200 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1152+71delT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68987373 | |||||||
chr3:68987400 | A | G | 5 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(2): Show |
5 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152+45T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 14/17 | chr3 | 68987400 | |||||||
chr3:68987527 | G | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(80): Show |
106 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1084-14C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68987527 | |||||||
chr3:68987532 | G | A | 168 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(165): Show |
197 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1084-19C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68987532 | |||||||
chr3:68987556 | G | A | 127 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(124): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1084-43C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68987556 | |||||||
chr3:68987594 | T | A | 1 | a0001c0002t0001g0283 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1084-81A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68987594 | |||||||
chr3:68987631 | G | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(160): Show |
192 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1084-118C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68987631 | |||||||
chr3:68987807 | C | T | 15 | a0001c0003t0006g0090 a0001c0004t0007g0080 a0001c0004t0007g0084 others(12): Show |
16 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-294G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68987807 | |||||||
chr3:68987817 | G | C | 15 | a0001c0003t0006g0090 a0001c0004t0007g0080 a0001c0004t0007g0084 others(12): Show |
16 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084-304C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68987817 | |||||||
chr3:68987840 | A | G | 123 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(120): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1084-327T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68987840 | |||||||
chr3:68987843 | T | G | 4 | a0001c0001t0030g0012 a0001c0001t0031g0198 a0001c0002t0024g0333 others(1): Show |
5 | HG02135.hp2 HG02523.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1084-330A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68987843 | |||||||
chr3:68987906 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(160): Show |
192 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1083+389C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68987906 | |||||||
chr3:68987961 | C | T | 2 | a0001c0003t0001g0166 a0001c0003t0003g0167 |
2 | NA18957.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1083+334G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68987961 | |||||||
chr3:68988049 | G | T | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1083+246C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68988049 | |||||||
chr3:68988050 | G | A | 4 | a0001c0002t0004g0032 a0001c0002t0004g0279 a0001c0002t0004g0292 others(1): Show |
5 | NA18959.hp2 NA18968.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1083+245C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68988050 | |||||||
chr3:68988111 | T | C | 294 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(291): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1083+184A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 13/17 | chr3 | 68988111 | |||||||
chr3:68988411 | A | G | 20 | a0001c0003t0006g0090 a0001c0004t0007g0080 a0001c0004t0007g0084 others(17): Show |
21 | HG01884.hp1 HG01884.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.997-30T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 12/17 | chr3 | 68988411 | |||||||
chr3:68988432 | T | C | 3 | a0001c0002t0015g0050 a0001c0002t0048g0051 a0001c0002t0049g0052 |
3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.997-51A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 12/17 | chr3 | 68988432 | |||||||
chr3:68988482 | G | C | 108 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(105): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.996+24C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 12/17 | chr3 | 68988482 | |||||||
chr3:68988841 | G | A | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.924+84C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 11/17 | chr3 | 68988841 | |||||||
chr3:68989053 | A | G | 2 | a0001c0001t0002g0042 a0001c0001t0043g0263 |
2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.832-36T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989053 | |||||||
chr3:68989066 | A | G | 118 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(115): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.832-49T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989066 | |||||||
chr3:68989245 | T | C | 11 | a0001c0003t0002g0106 a0001c0003t0002g0107 a0001c0003t0002g0119 others(8): Show |
12 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.832-228A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989245 | |||||||
chr3:68989360 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.832-343G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989360 | |||||||
chr3:68989395 | C | G | 1 | a0001c0003t0001g0013 | 2 | NA18969.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.832-378G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989395 | |||||||
chr3:68989415 | T | TA | 292 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(289): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.832-399_832-398ins others(1): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989415 | |||||||
chr3:68989416 | C | A | 1 | a0001c0002t0008g0313 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.832-399G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989416 | |||||||
chr3:68989417 | T | C | 1 | a0001c0002t0008g0313 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.832-400A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989417 | |||||||
chr3:68989433 | A | G | 8 | a0001c0001t0001g0234 a0001c0001t0001g0238 a0001c0001t0001g0241 others(5): Show |
8 | HG00423.hp2 HG00544.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-416T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989433 | |||||||
chr3:68989464 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(160): Show |
192 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.832-447G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989464 | |||||||
chr3:68989513 | C | T | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.832-496G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989513 | |||||||
chr3:68989605 | A | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(160): Show |
192 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.832-588T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989605 | |||||||
chr3:68989625 | A | G | 293 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(290): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.832-608T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989625 | |||||||
chr3:68989626 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(160): Show |
192 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.832-609A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989626 | |||||||
chr3:68989641 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(160): Show |
192 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.832-624C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989641 | |||||||
chr3:68989670 | C | A | 1 | a0001c0001t0002g0387 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.832-653G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989670 | |||||||
chr3:68989736 | G | A | 1 | a0001c0001t0016g0213 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.832-719C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989736 | |||||||
chr3:68989748 | C | CA | 10 | a0001c0001t0002g0384 a0001c0002t0001g0346 a0001c0002t0001g0366 others(7): Show |
10 | HG01433.hp1 HG01978.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.832-732dupT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989748 | |||||||
chr3:68989748 | CA | C | 44 | a0001c0001t0002g0042 a0001c0001t0003g0111 a0001c0001t0005g0205 others(41): Show |
46 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.832-732delT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989748 | |||||||
chr3:68989748 | CAAAAAA | C | 106 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(103): Show |
112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.832-737_832-732del others(6): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989748 | |||||||
chr3:68989899 | C | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(161): Show |
193 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.832-882G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989899 | |||||||
chr3:68989991 | A | G | 293 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(290): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.832-974T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68989991 | |||||||
chr3:68990036 | T | C | 1 | a0001c0003t0009g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.832-1019A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990036 | |||||||
chr3:68990067 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.832-1050T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990067 | |||||||
chr3:68990304 | G | A | 8 | a0001c0003t0001g0013 a0001c0003t0001g0125 a0001c0003t0001g0130 others(5): Show |
11 | HG01346.hp2 HG02129.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.832-1287C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990304 | |||||||
chr3:68990323 | T | G | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.832-1306A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990323 | |||||||
chr3:68990348 | C | CT | 68 | a0001c0001t0001g0241 a0001c0001t0002g0189 a0001c0001t0002g0207 others(65): Show |
78 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.832-1332dupA | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990348 | |||||||
chr3:68990348 | C | CTT | 7 | a0001c0003t0002g0106 a0001c0003t0003g0005 a0001c0003t0003g0118 others(4): Show |
9 | HG03654.hp1 HG03654.hp2 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-1333_832-1332d others(4): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990348 | |||||||
chr3:68990348 | CTT | C | 9 | a0001c0001t0001g0199 a0001c0001t0002g0042 a0001c0002t0001g0268 others(6): Show |
9 | HG02027.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.832-1333_832-1332d others(4): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990348 | |||||||
chr3:68990348 | CTTT | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(164): Show |
197 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.832-1334_832-1332d others(5): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990348 | |||||||
chr3:68990497 | C | T | 6 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(3): Show |
6 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-1480G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990497 | |||||||
chr3:68990513 | C | T | 4 | a0001c0001t0002g0112 a0001c0001t0003g0111 a0001c0002t0001g0277 others(1): Show |
4 | HG01192.hp2 HG02735.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-1496G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990513 | |||||||
chr3:68990598 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG00423.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.832-1581G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990598 | |||||||
chr3:68990630 | A | G | 292 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(289): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.832-1613T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990630 | |||||||
chr3:68990690 | TAAG | T | 6 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(3): Show |
6 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-1676_832-1674d others(5): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990690 | |||||||
chr3:68990765 | T | A | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.832-1748A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990765 | |||||||
chr3:68990806 | A | G | 1 | a0001c0003t0006g0126 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.832-1789T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990806 | |||||||
chr3:68990901 | GA | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(255): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.832-1885delT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990901 | |||||||
chr3:68990901 | GAA | G | 26 | a0001c0001t0002g0042 a0001c0001t0005g0205 a0001c0001t0005g0206 others(23): Show |
26 | HG00735.hp2 HG01884.hp1 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.832-1886_832-1885d others(4): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68990901 | |||||||
chr3:68991062 | T | A | 1 | a0003c0008t0005g0036 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.832-2045A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991062 | |||||||
chr3:68991143 | C | T | 1 | a0001c0001t0009g0252 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.832-2126G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991143 | |||||||
chr3:68991218 | G | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(173): Show |
206 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.832-2201C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991218 | |||||||
chr3:68991236 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.832-2219G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991236 | |||||||
chr3:68991258 | T | C | 104 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.832-2241A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991258 | |||||||
chr3:68991446 | G | T | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-2429C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991446 | |||||||
chr3:68991450 | T | C | 113 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(110): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.832-2433A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991450 | |||||||
chr3:68991486 | G | A | 1 | a0001c0002t0001g0347 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.832-2469C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991486 | |||||||
chr3:68991493 | A | T | 1 | a0001c0007t0017g0083 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.832-2476T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991493 | |||||||
chr3:68991494 | T | A | 1 | a0001c0007t0017g0083 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.832-2477A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991494 | |||||||
chr3:68991508 | C | T | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.832-2491G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991508 | |||||||
chr3:68991511 | G | A | 5 | a0001c0001t0029g0047 a0003c0008t0005g0036 a0003c0008t0029g0038 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-2494C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991511 | |||||||
chr3:68991633 | A | G | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.832-2616T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991633 | |||||||
chr3:68991640 | G | A | 293 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(290): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.832-2623C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991640 | |||||||
chr3:68991855 | G | A | 111 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(108): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.832-2838C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991855 | |||||||
chr3:68991855 | G | C | 1 | a0001c0001t0003g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.832-2838C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991855 | |||||||
chr3:68991858 | G | A | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.832-2841C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991858 | |||||||
chr3:68991882 | T | C | 294 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(291): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.832-2865A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991882 | |||||||
chr3:68991886 | A | G | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.832-2869T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991886 | |||||||
chr3:68991890 | G | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(81): Show |
107 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.832-2873C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991890 | |||||||
chr3:68991970 | A | T | 1 | a0001c0001t0011g0169 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.832-2953T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68991970 | |||||||
chr3:68992036 | G | A | 181 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(178): Show |
211 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.832-3019C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992036 | |||||||
chr3:68992124 | G | A | 8 | a0001c0003t0001g0013 a0001c0003t0001g0125 a0001c0003t0001g0130 others(5): Show |
11 | HG01346.hp2 HG02129.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.832-3107C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992124 | |||||||
chr3:68992168 | C | T | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-3151G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992168 | |||||||
chr3:68992171 | A | G | 108 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(105): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.832-3154T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992171 | |||||||
chr3:68992283 | C | A | 287 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(284): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.832-3266G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992283 | |||||||
chr3:68992295 | C | T | 1 | a0003c0008t0032g0037 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.832-3278G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992295 | |||||||
chr3:68992327 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.832-3310G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992327 | |||||||
chr3:68992328 | G | A | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.832-3311C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992328 | |||||||
chr3:68992336 | T | C | 358 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(355): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.832-3319A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992336 | |||||||
chr3:68992337 | G | A | 54 | a0001c0003t0001g0013 a0001c0003t0001g0125 a0001c0003t0001g0130 others(51): Show |
65 | HG00544.hp1 HG00597.hp2 HG01346.hp2 others(62): Show |
intron_variant | MODIFIER | c.832-3320C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992337 | |||||||
chr3:68992345 | T | C | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-3328A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992345 | |||||||
chr3:68992356 | A | G | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-3339T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992356 | |||||||
chr3:68992384 | G | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(172): Show |
205 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.832-3367C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992384 | |||||||
chr3:68992471 | A | G | 293 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(290): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.832-3454T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992471 | |||||||
chr3:68992567 | C | A | 1 | a0001c0001t0004g0088 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.832-3550G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992567 | |||||||
chr3:68992567 | C | T | 15 | a0001c0003t0006g0090 a0001c0004t0007g0080 a0001c0004t0007g0084 others(12): Show |
16 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.832-3550G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992567 | |||||||
chr3:68992750 | C | G | 1 | a0001c0001t0003g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.832-3733G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992750 | |||||||
chr3:68992781 | A | G | 294 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(291): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.832-3764T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992781 | |||||||
chr3:68992789 | A | C | 6 | a0001c0001t0030g0012 a0001c0001t0031g0198 a0001c0002t0024g0333 others(3): Show |
7 | HG01106.hp2 HG02135.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-3772T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992789 | |||||||
chr3:68992846 | C | T | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-3829G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992846 | |||||||
chr3:68992914 | C | G | 7 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(4): Show |
7 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-3897G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992914 | |||||||
chr3:68992947 | C | T | 4 | a0001c0001t0009g0252 a0001c0004t0012g0104 a0001c0004t0013g0079 others(1): Show |
4 | HG02451.hp1 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-3930G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992947 | |||||||
chr3:68992985 | C | T | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.832-3968G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68992985 | |||||||
chr3:68993004 | T | C | 109 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(106): Show |
115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.832-3987A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993004 | |||||||
chr3:68993023 | C | T | 183 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(180): Show |
213 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.832-4006G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993023 | |||||||
chr3:68993062 | G | A | 2 | a0001c0002t0005g0306 a0001c0002t0005g0317 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.832-4045C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993062 | |||||||
chr3:68993104 | G | A | 1 | a0001c0002t0001g0228 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.832-4087C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993104 | |||||||
chr3:68993115 | G | T | 285 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(282): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.832-4098C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993115 | |||||||
chr3:68993196 | A | G | 1 | a0001c0002t0062g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.832-4179T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993196 | |||||||
chr3:68993203 | A | T | 1 | a0001c0002t0001g0303 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.832-4186T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993203 | |||||||
chr3:68993243 | C | T | 8 | a0001c0001t0002g0042 a0001c0001t0043g0263 a0001c0007t0017g0055 others(5): Show |
8 | HG01884.hp1 HG01952.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.832-4226G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993243 | |||||||
chr3:68993473 | A | G | 297 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(294): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.832-4456T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993473 | |||||||
chr3:68993501 | T | C | 3 | a0003c0008t0005g0036 a0003c0008t0029g0038 a0003c0008t0032g0037 |
3 | HG00735.hp2 HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.832-4484A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993501 | |||||||
chr3:68993590 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.831+4421T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993590 | |||||||
chr3:68993769 | G | A | 1 | a0001c0002t0004g0319 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.831+4242C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993769 | |||||||
chr3:68993857 | T | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(182): Show |
216 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.831+4154A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993857 | |||||||
chr3:68993861 | T | C | 107 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(104): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.831+4150A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993861 | |||||||
chr3:68993870 | C | G | 9 | a0001c0001t0002g0042 a0001c0001t0043g0263 a0001c0007t0017g0055 others(6): Show |
9 | HG01884.hp1 HG01952.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+4141G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993870 | |||||||
chr3:68993876 | T | C | 12 | a0001c0001t0002g0131 a0001c0003t0002g0106 a0001c0003t0002g0107 others(9): Show |
13 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.831+4135A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993876 | |||||||
chr3:68993880 | G | A | 1 | a0001c0002t0001g0348 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.831+4131C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993880 | |||||||
chr3:68993911 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.831+4100C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68993911 | |||||||
chr3:68994047 | A | G | 1 | a0001c0012t0036g0027 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.831+3964T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994047 | |||||||
chr3:68994196 | T | C | 2 | a0001c0001t0002g0042 a0001c0001t0043g0263 |
2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.831+3815A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994196 | |||||||
chr3:68994337 | T | C | 2 | a0001c0001t0002g0042 a0001c0001t0043g0263 |
2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.831+3674A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994337 | |||||||
chr3:68994375 | G | A | 1 | a0001c0002t0001g0303 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.831+3636C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994375 | |||||||
chr3:68994395 | G | A | 1 | a0001c0002t0005g0266 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.831+3616C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994395 | |||||||
chr3:68994495 | T | C | 1 | a0001c0001t0002g0064 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.831+3516A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994495 | |||||||
chr3:68994496 | A | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(175): Show |
208 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.831+3515T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994496 | |||||||
chr3:68994560 | G | C | 283 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(280): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.831+3451C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994560 | |||||||
chr3:68994566 | C | T | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.831+3445G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994566 | |||||||
chr3:68994682 | T | C | 1 | a0001c0004t0020g0137 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.831+3329A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994682 | |||||||
chr3:68994694 | G | A | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.831+3317C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994694 | |||||||
chr3:68994763 | C | G | 1 | a0001c0003t0015g0259 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.831+3248G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994763 | |||||||
chr3:68994978 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(172): Show |
205 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.831+3033G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68994978 | |||||||
chr3:68995029 | A | G | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.831+2982T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995029 | |||||||
chr3:68995051 | TC | T | 2 | a0001c0003t0015g0008 a0001c0003t0015g0259 |
4 | HG02723.hp1 HG03540.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+2959delG | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995051 | |||||||
chr3:68995245 | G | C | 5 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(2): Show |
5 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+2766C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995245 | |||||||
chr3:68995319 | A | C | 3 | a0001c0002t0015g0050 a0001c0002t0048g0051 a0001c0002t0049g0052 |
3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.831+2692T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995319 | |||||||
chr3:68995337 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(77): Show |
103 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.831+2674C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995337 | |||||||
chr3:68995364 | C | G | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.831+2647G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995364 | |||||||
chr3:68995376 | A | T | 8 | a0001c0001t0002g0042 a0001c0001t0043g0263 a0001c0007t0017g0055 others(5): Show |
8 | HG01884.hp1 HG01952.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.831+2635T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995376 | |||||||
chr3:68995383 | G | A | 1 | a0001c0001t0003g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.831+2628C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995383 | |||||||
chr3:68995434 | C | T | 1 | a0001c0002t0001g0334 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.831+2577G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995434 | |||||||
chr3:68995456 | C | T | 3 | a0001c0001t0003g0058 a0001c0001t0003g0101 a0001c0001t0004g0088 |
3 | HG01168.hp1 HG01169.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.831+2555G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995456 | |||||||
chr3:68995472 | T | C | 1 | a0001c0002t0001g0380 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.831+2539A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995472 | |||||||
chr3:68995507 | T | G | 1 | a0001c0002t0025g0367 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.831+2504A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995507 | |||||||
chr3:68995633 | A | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(292): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.831+2378T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995633 | |||||||
chr3:68995773 | G | A | 6 | a0001c0001t0034g0117 a0001c0007t0017g0055 a0001c0007t0017g0077 others(3): Show |
6 | HG01884.hp1 HG01952.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+2238C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995773 | |||||||
chr3:68995826 | A | T | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.831+2185T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68995826 | |||||||
chr3:68996007 | G | A | 1 | a0001c0014t0058g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.831+2004C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996007 | |||||||
chr3:68996009 | C | T | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.831+2002G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996009 | |||||||
chr3:68996329 | T | C | 1 | a0001c0001t0002g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.831+1682A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996329 | |||||||
chr3:68996481 | C | A | 2 | a0001c0002t0001g0293 a0001c0002t0001g0294 |
2 | HG01943.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.831+1530G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996481 | |||||||
chr3:68996494 | G | C | 9 | a0001c0001t0002g0042 a0001c0001t0043g0263 a0001c0007t0017g0055 others(6): Show |
9 | HG01884.hp1 HG01952.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+1517C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996494 | |||||||
chr3:68996559 | C | G | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.831+1452G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996559 | |||||||
chr3:68996646 | C | T | 1 | a0001c0004t0038g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.831+1365G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996646 | |||||||
chr3:68996690 | A | G | 1 | a0001c0002t0001g0358 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.831+1321T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996690 | |||||||
chr3:68996797 | C | T | 101 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.831+1214G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996797 | |||||||
chr3:68996798 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.831+1213C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996798 | |||||||
chr3:68996921 | T | C | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.831+1090A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996921 | |||||||
chr3:68996979 | G | A | 1 | a0001c0003t0004g0116 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.831+1032C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68996979 | |||||||
chr3:68997047 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.831+964G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68997047 | |||||||
chr3:68997138 | A | G | 10 | a0001c0001t0002g0042 a0001c0001t0029g0047 a0001c0001t0043g0263 others(7): Show |
10 | HG01884.hp1 HG01952.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+873T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68997138 | |||||||
chr3:68997211 | C | G | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.831+800G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68997211 | |||||||
chr3:68997360 | T | C | 4 | a0001c0001t0001g0114 a0001c0002t0004g0032 a0001c0002t0004g0279 others(1): Show |
5 | NA18959.hp2 NA18968.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+651A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68997360 | |||||||
chr3:68997371 | C | CT | 52 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0238 others(49): Show |
53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.831+639dupA | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68997371 | |||||||
chr3:68997393 | G | A | 1 | a0001c0002t0049g0052 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.831+618C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68997393 | |||||||
chr3:68997480 | G | A | 3 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0005g0250 |
3 | HG00733.hp2 HG01255.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.831+531C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68997480 | |||||||
chr3:68997822 | C | A | 1 | a0001c0001t0047g0200 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.831+189G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68997822 | |||||||
chr3:68997949 | C | T | 1 | a0001c0001t0060g0095 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.831+62G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68997949 | |||||||
chr3:68997960 | A | G | 1 | a0001c0002t0008g0318 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.831+51T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68997960 | |||||||
chr3:68997990 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(136): Show |
167 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.831+21C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 10/17 | chr3 | 68997990 | |||||||
chr3:68998155 | A | G | 1 | a0001c0002t0004g0319 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.728-41T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998155 | |||||||
chr3:68998325 | A | G | 1 | a0001c0002t0003g0337 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.728-211T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998325 | |||||||
chr3:68998362 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.728-248A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998362 | |||||||
chr3:68998383 | T | C | 1 | a0001c0003t0009g0136 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.728-269A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998383 | |||||||
chr3:68998461 | C | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(292): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.728-347G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998461 | |||||||
chr3:68998476 | A | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(174): Show |
207 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.728-362T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998476 | |||||||
chr3:68998505 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(158): Show |
190 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.728-391C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998505 | |||||||
chr3:68998555 | T | A | 11 | a0001c0001t0005g0205 a0001c0001t0005g0206 a0001c0001t0005g0218 others(8): Show |
11 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.728-441A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998555 | |||||||
chr3:68998560 | A | G | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.728-446T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998560 | |||||||
chr3:68998616 | G | A | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.728-502C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998616 | |||||||
chr3:68998642 | C | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(292): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.728-528G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998642 | |||||||
chr3:68998835 | T | TA | 29 | a0001c0001t0001g0115 a0001c0001t0002g0249 a0001c0001t0002g0251 others(26): Show |
31 | HG00597.hp1 HG00733.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.728-722dupT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998835 | |||||||
chr3:68998835 | T | TAA | 91 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(88): Show |
95 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.728-723_728-722dup others(2): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998835 | |||||||
chr3:68998835 | T | TAAA | 16 | a0001c0001t0002g0061 a0001c0001t0002g0189 a0001c0001t0002g0239 others(13): Show |
18 | HG01099.hp2 HG01258.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.728-724_728-722dup others(3): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998835 | |||||||
chr3:68998835 | TA | T | 8 | a0001c0002t0003g0030 a0001c0002t0010g0353 a0001c0007t0017g0055 others(5): Show |
9 | HG01070.hp1 HG01071.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.728-722delT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998835 | |||||||
chr3:68998855 | G | GA | 291 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(288): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.728-742dupT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998855 | |||||||
chr3:68998870 | A | G | 106 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(103): Show |
112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.728-756T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998870 | |||||||
chr3:68998924 | T | C | 1 | a0001c0002t0018g0360 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.728-810A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998924 | |||||||
chr3:68998964 | C | T | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.728-850G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68998964 | |||||||
chr3:68999277 | A | T | 1 | a0001c0001t0001g0199 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.728-1163T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68999277 | |||||||
chr3:68999287 | G | A | 6 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(3): Show |
6 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.728-1173C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68999287 | |||||||
chr3:68999310 | T | G | 1 | a0001c0002t0002g0352 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.728-1196A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68999310 | |||||||
chr3:68999597 | C | G | 294 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(291): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.728-1483G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68999597 | |||||||
chr3:68999667 | C | G | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.728-1553G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68999667 | |||||||
chr3:68999749 | C | T | 2 | a0001c0002t0003g0030 a0001c0002t0010g0353 |
3 | HG01070.hp1 HG01071.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.728-1635G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68999749 | |||||||
chr3:68999884 | T | C | 1 | a0001c0001t0043g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.727+1724A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68999884 | |||||||
chr3:68999964 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(157): Show |
189 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.727+1644C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 68999964 | |||||||
chr3:69000000 | T | C | 1 | a0001c0002t0001g0349 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.727+1608A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000000 | |||||||
chr3:69000121 | C | G | 359 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(356): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.727+1487G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000121 | |||||||
chr3:69000143 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.727+1465A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000143 | |||||||
chr3:69000488 | A | G | 1 | a0001c0001t0032g0219 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.727+1120T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000488 | |||||||
chr3:69000620 | G | C | 108 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(105): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.727+988C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000620 | |||||||
chr3:69000791 | A | G | 1 | a0001c0002t0001g0327 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.727+817T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000791 | |||||||
chr3:69000922 | C | T | 6 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(3): Show |
6 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.727+686G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000922 | |||||||
chr3:69000957 | A | AT | 6 | a0001c0001t0002g0190 a0001c0001t0002g0256 a0001c0001t0003g0057 others(3): Show |
6 | HG02027.hp2 HG02523.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.727+650dupA | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000957 | |||||||
chr3:69000957 | AT | A | 9 | a0001c0002t0001g0300 a0001c0002t0001g0308 a0001c0002t0001g0355 others(6): Show |
9 | HG02109.hp1 HG02809.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.727+650delA | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000957 | |||||||
chr3:69000958 | T | A | 1 | a0001c0009t0061g0350 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.727+650A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000958 | |||||||
chr3:69000958 | T | C | 1 | a0001c0003t0004g0149 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.727+650A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000958 | |||||||
chr3:69000980 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(162): Show |
195 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.727+628G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69000980 | |||||||
chr3:69001020 | G | A | 12 | a0001c0004t0007g0080 a0001c0004t0007g0084 a0001c0004t0012g0085 others(9): Show |
12 | HG02257.hp2 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.727+588C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69001020 | |||||||
chr3:69001059 | C | T | 1 | a0001c0001t0047g0200 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.727+549G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69001059 | |||||||
chr3:69001250 | G | A | 12 | a0001c0004t0007g0080 a0001c0004t0007g0084 a0001c0004t0012g0085 others(9): Show |
12 | HG02257.hp2 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.727+358C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69001250 | |||||||
chr3:69001253 | C | A | 6 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(3): Show |
6 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.727+355G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69001253 | |||||||
chr3:69001367 | G | C | 6 | a0001c0007t0017g0055 a0001c0007t0017g0077 a0001c0007t0017g0081 others(3): Show |
6 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.727+241C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69001367 | |||||||
chr3:69001368 | T | A | 1 | a0001c0001t0002g0194 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.727+240A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69001368 | |||||||
chr3:69001482 | G | A | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.727+126C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69001482 | |||||||
chr3:69001500 | C | G | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.727+108G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69001500 | |||||||
chr3:69001510 | T | C | 1 | a0001c0001t0029g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.727+98A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 9/17 | chr3 | 69001510 | |||||||
chr3:69001728 | T | A | 1 | a0001c0012t0036g0027 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.621-14A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69001728 | |||||||
chr3:69001797 | T | C | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.621-83A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69001797 | |||||||
chr3:69001929 | A | C | 293 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(290): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.621-215T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69001929 | |||||||
chr3:69002062 | C | T | 1 | a0001c0002t0003g0332 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.621-348G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002062 | |||||||
chr3:69002063 | G | A | 1 | a0005c0013t0001g0329 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.621-349C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002063 | |||||||
chr3:69002092 | C | T | 293 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(290): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.621-378G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002092 | |||||||
chr3:69002262 | C | G | 1 | a0003c0008t0005g0036 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.621-548G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002262 | |||||||
chr3:69002319 | A | G | 1 | a0001c0002t0001g0224 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.621-605T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002319 | |||||||
chr3:69002429 | C | T | 3 | a0001c0002t0015g0050 a0001c0002t0048g0051 a0001c0002t0049g0052 |
3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.621-715G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002429 | |||||||
chr3:69002444 | T | C | 3 | a0003c0008t0005g0036 a0003c0008t0029g0038 a0003c0008t0032g0037 |
3 | HG00735.hp2 HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.621-730A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002444 | |||||||
chr3:69002531 | T | C | 6 | a0001c0001t0016g0069 a0001c0001t0016g0078 a0001c0001t0016g0082 others(3): Show |
6 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.621-817A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002531 | |||||||
chr3:69002608 | C | A | 1 | a0001c0003t0003g0160 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.621-894G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002608 | |||||||
chr3:69002628 | C | CA | 7 | a0001c0001t0024g0261 a0001c0007t0017g0055 a0001c0007t0017g0077 others(4): Show |
7 | HG01884.hp1 HG01952.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.621-915dupT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002628 | |||||||
chr3:69002661 | C | CT | 172 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(169): Show |
203 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.621-948dupA | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002661 | |||||||
chr3:69002729 | A | T | 1 | a0001c0014t0058g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.621-1015T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002729 | |||||||
chr3:69002786 | C | G | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.621-1072G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002786 | |||||||
chr3:69002879 | G | C | 3 | a0001c0002t0015g0050 a0001c0002t0048g0051 a0001c0002t0049g0052 |
3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.621-1165C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69002879 | |||||||
chr3:69003016 | T | C | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.621-1302A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003016 | |||||||
chr3:69003134 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.620+1244C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003134 | |||||||
chr3:69003212 | A | C | 3 | a0001c0002t0023g0046 a0001c0002t0023g0049 a0001c0002t0052g0048 |
3 | HG02615.hp2 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.620+1166T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003212 | |||||||
chr3:69003276 | C | T | 1 | a0001c0002t0001g0321 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.620+1102G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003276 | |||||||
chr3:69003280 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.620+1098C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003280 | |||||||
chr3:69003320 | T | C | 3 | a0001c0009t0004g0363 a0001c0009t0004g0369 a0001c0009t0006g0368 |
3 | NA18968.hp1 NA19066.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.620+1058A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003320 | |||||||
chr3:69003372 | T | C | 6 | a0001c0002t0004g0302 a0001c0002t0006g0024 a0001c0002t0006g0280 others(3): Show |
7 | HG00438.hp1 NA18948.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.620+1006A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003372 | |||||||
chr3:69003414 | T | A | 1 | a0001c0002t0001g0041 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.620+964A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003414 | |||||||
chr3:69003423 | C | A | 1 | a0001c0001t0016g0078 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.620+955G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003423 | |||||||
chr3:69003442 | T | C | 14 | a0001c0004t0007g0080 a0001c0004t0007g0084 a0001c0004t0012g0085 others(11): Show |
14 | HG01884.hp2 HG02257.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.620+936A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003442 | |||||||
chr3:69003535 | T | C | 1 | a0001c0001t0009g0258 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.620+843A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003535 | |||||||
chr3:69003636 | A | AT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(9): Show |
20 | HG02135.hp2 HG02523.hp2 HG02717.hp2 others(17): Show |
intron_variant | MODIFIER | c.620+741dupA | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003636 | |||||||
chr3:69003776 | T | C | 1 | a0001c0016t0005g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.620+602A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003776 | |||||||
chr3:69003995 | T | A | 20 | a0001c0002t0001g0276 a0001c0002t0001g0297 a0001c0002t0001g0303 others(17): Show |
22 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.620+383A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69003995 | |||||||
chr3:69004022 | G | A | 1 | a0001c0002t0002g0352 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.620+356C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69004022 | |||||||
chr3:69004026 | C | G | 1 | a0001c0003t0050g0122 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.620+352G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69004026 | |||||||
chr3:69004080 | A | G | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.620+298T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69004080 | |||||||
chr3:69004123 | G | C | 1 | a0001c0009t0004g0363 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.620+255C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69004123 | |||||||
chr3:69004293 | T | C | 19 | a0001c0001t0001g0056 a0001c0001t0002g0009 a0001c0001t0002g0060 others(16): Show |
20 | HG00099.hp2 HG00738.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.620+85A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69004293 | |||||||
chr3:69004296 | A | T | 118 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(115): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.620+82T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69004296 | |||||||
chr3:69004361 | C | T | 5 | a0003c0008t0001g0035 a0003c0008t0005g0036 a0003c0008t0029g0038 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.620+17G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 8/17 | chr3 | 69004361 | |||||||
chr3:69004609 | T | A | 2 | a0003c0008t0029g0038 a0003c0008t0032g0037 |
2 | HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.516-127A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/17 | chr3 | 69004609 | |||||||
chr3:69004742 | C | G | 1 | a0001c0016t0005g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.516-260G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/17 | chr3 | 69004742 | |||||||
chr3:69004825 | A | C | 5 | a0002c0005t0004g0020 a0002c0005t0004g0021 a0002c0005t0004g0203 others(2): Show |
7 | HG01099.hp2 HG01934.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.515+315T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/17 | chr3 | 69004825 | |||||||
chr3:69004976 | C | A | 5 | a0001c0004t0014g0139 a0001c0004t0016g0120 a0001c0004t0035g0121 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.515+164G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/17 | chr3 | 69004976 | |||||||
chr3:69005051 | G | C | 8 | a0001c0001t0029g0047 a0001c0001t0042g0053 a0001c0003t0012g0076 others(5): Show |
8 | HG00735.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.515+89C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/17 | chr3 | 69005051 | |||||||
chr3:69005061 | C | CA | 13 | a0001c0001t0006g0184 a0001c0001t0029g0047 a0001c0001t0042g0053 others(10): Show |
13 | HG00735.hp2 HG02486.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.515+78dupT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/17 | chr3 | 69005061 | |||||||
chr3:69005061 | CA | C | 238 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(235): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.515+78delT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/17 | chr3 | 69005061 | |||||||
chr3:69005061 | CAA | C | 9 | a0001c0001t0002g0256 a0001c0001t0003g0101 a0001c0001t0004g0066 others(6): Show |
9 | HG01169.hp2 HG01981.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.515+77_515+78delTT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/17 | chr3 | 69005061 | |||||||
chr3:69005114 | G | T | 3 | a0001c0004t0016g0120 a0001c0004t0035g0121 a0001c0004t0038g0044 |
3 | HG02622.hp1 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.515+26C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/17 | chr3 | 69005114 | |||||||
chr3:69005115 | A | AT | 157 | a0001c0001t0029g0047 a0001c0001t0042g0053 a0001c0002t0001g0001 others(154): Show |
179 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.515+24dupA | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 7/17 | chr3 | 69005115 | |||||||
chr3:69005263 | C | T | 2 | a0001c0001t0002g0383 a0001c0001t0002g0384 |
2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.421-29G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69005263 | |||||||
chr3:69005460 | A | G | 157 | a0001c0001t0029g0047 a0001c0001t0042g0053 a0001c0002t0001g0001 others(154): Show |
179 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.421-226T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69005460 | |||||||
chr3:69005471 | C | T | 1 | a0001c0001t0043g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.421-237G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69005471 | |||||||
chr3:69005606 | A | G | 1 | a0001c0001t0024g0261 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.421-372T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69005606 | |||||||
chr3:69005691 | A | G | 1 | a0001c0002t0001g0364 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.421-457T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69005691 | |||||||
chr3:69005985 | G | A | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.421-751C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69005985 | |||||||
chr3:69006043 | G | C | 1 | a0001c0002t0018g0361 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.421-809C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006043 | |||||||
chr3:69006048 | T | C | 31 | a0001c0003t0001g0166 a0001c0003t0003g0005 a0001c0003t0003g0006 others(28): Show |
37 | HG00597.hp2 HG02056.hp2 HG02080.hp1 others(34): Show |
intron_variant | MODIFIER | c.421-814A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006048 | |||||||
chr3:69006112 | G | A | 1 | a0001c0003t0001g0161 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.421-878C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006112 | |||||||
chr3:69006139 | A | G | 273 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(270): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.421-905T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006139 | |||||||
chr3:69006150 | A | G | 1 | a0001c0001t0023g0071 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.421-916T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006150 | |||||||
chr3:69006255 | C | G | 1 | a0001c0003t0002g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.421-1021G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006255 | |||||||
chr3:69006260 | C | G | 116 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(113): Show |
122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.421-1026G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006260 | |||||||
chr3:69006277 | T | C | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.421-1043A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006277 | |||||||
chr3:69006315 | G | A | 6 | a0001c0002t0015g0050 a0001c0002t0023g0046 a0001c0002t0023g0049 others(3): Show |
6 | HG02559.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-1081C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006315 | |||||||
chr3:69006406 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
12 | NA18939.hp1 NA18944.hp2 NA18960.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-1172C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006406 | |||||||
chr3:69006481 | T | G | 130 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(127): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.420+1232A>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006481 | |||||||
chr3:69006510 | G | C | 4 | a0003c0008t0001g0035 a0003c0008t0005g0036 a0003c0008t0029g0038 others(1): Show |
4 | HG00735.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+1203C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006510 | |||||||
chr3:69006755 | C | G | 130 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(127): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.420+958G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006755 | |||||||
chr3:69006763 | C | T | 127 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(124): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.420+950G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006763 | |||||||
chr3:69006781 | T | C | 3 | a0001c0001t0029g0047 a0001c0001t0042g0053 a0001c0003t0012g0076 |
3 | HG02486.hp2 HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.420+932A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006781 | |||||||
chr3:69006885 | T | C | 130 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(127): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.420+828A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006885 | |||||||
chr3:69006948 | A | G | 1 | a0001c0011t0004g0105 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.420+765T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006948 | |||||||
chr3:69006970 | G | A | 9 | a0001c0001t0001g0193 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.420+743C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69006970 | |||||||
chr3:69007023 | G | C | 1 | a0001c0002t0001g0356 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.420+690C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007023 | |||||||
chr3:69007084 | G | A | 2 | a0001c0002t0026g0298 a0001c0002t0026g0305 |
2 | HG01106.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.420+629C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007084 | |||||||
chr3:69007149 | C | T | 1 | a0001c0003t0003g0118 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.420+564G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007149 | |||||||
chr3:69007199 | G | T | 1 | a0001c0001t0034g0070 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.420+514C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007199 | |||||||
chr3:69007294 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.420+419C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007294 | |||||||
chr3:69007372 | G | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0060 a0001c0001t0002g0061 others(2): Show |
6 | HG01257.hp2 HG01346.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+341C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007372 | |||||||
chr3:69007390 | C | A | 2 | a0001c0002t0004g0032 a0001c0002t0004g0357 |
3 | NA18959.hp2 NA18968.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.420+323G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007390 | |||||||
chr3:69007415 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.420+298C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007415 | |||||||
chr3:69007419 | G | A | 1 | a0001c0001t0043g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.420+294C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007419 | |||||||
chr3:69007453 | G | A | 137 | a0001c0001t0043g0263 a0001c0001t0064g0265 a0001c0002t0001g0001 others(134): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.420+260C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007453 | |||||||
chr3:69007507 | C | CGGGGGGG others(2): Show |
23 | a0001c0001t0001g0385 a0001c0001t0002g0022 a0001c0001t0002g0197 others(20): Show |
24 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.420+197_420+205dup others(9): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007507 | |||||||
chr3:69007507 | C | CGGGGGGG others(3): Show |
34 | a0001c0001t0001g0100 a0001c0001t0002g0072 a0001c0001t0002g0195 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.420+205_420+206ins others(10): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007507 | |||||||
chr3:69007507 | C | CGGGGGGG others(4): Show |
19 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0193 others(16): Show |
20 | HG00140.hp2 HG00673.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.420+205_420+206ins others(11): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007507 | |||||||
chr3:69007507 | C | CGGGGGGG others(5): Show |
14 | a0001c0001t0002g0009 a0001c0001t0002g0065 a0001c0001t0002g0190 others(11): Show |
16 | HG00323.hp2 HG01261.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.420+205_420+206ins others(12): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007507 | |||||||
chr3:69007507 | C | CGGGGGGG others(6): Show |
17 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0064 others(14): Show |
17 | HG00733.hp2 HG01255.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.420+205_420+206ins others(13): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007507 | |||||||
chr3:69007507 | C | CGGGGGGG others(7): Show |
10 | a0001c0001t0002g0189 a0001c0001t0002g0256 a0001c0001t0003g0054 others(7): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.420+205_420+206ins others(14): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007507 | |||||||
chr3:69007507 | C | CGGGGGGG others(8): Show |
3 | a0001c0001t0001g0056 a0001c0001t0047g0200 a0001c0002t0001g0268 |
3 | HG02572.hp1 HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.420+205_420+206ins others(15): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007507 | |||||||
chr3:69007507 | C | CGGGGGGG others(9): Show |
1 | a0001c0002t0005g0266 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.420+205_420+206ins others(16): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007507 | |||||||
chr3:69007511 | G | GGGGGGGG others(1): Show |
22 | a0001c0001t0029g0047 a0001c0002t0001g0031 a0001c0002t0001g0299 others(19): Show |
24 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.420+201_420+202ins others(8): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007511 | |||||||
chr3:69007511 | G | GGGGGGGG others(2): Show |
81 | a0001c0001t0042g0053 a0001c0002t0001g0001 a0001c0002t0001g0029 others(78): Show |
99 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.420+201_420+202ins others(9): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007511 | |||||||
chr3:69007511 | G | GGGGGGGG others(3): Show |
18 | a0001c0002t0001g0028 a0001c0002t0001g0310 a0001c0002t0001g0327 others(15): Show |
20 | HG00438.hp1 HG01099.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.420+201_420+202ins others(10): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007511 | |||||||
chr3:69007511 | G | GGGGGGGG others(4): Show |
3 | a0001c0002t0001g0277 a0001c0002t0001g0331 a0001c0002t0009g0278 |
3 | HG01074.hp2 HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.420+201_420+202ins others(11): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007511 | |||||||
chr3:69007511 | G | GGGGGGGG others(5): Show |
1 | a0001c0002t0001g0330 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.420+201_420+202ins others(12): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007511 | |||||||
chr3:69007511 | G | GGGGGGGG others(7): Show |
1 | a0001c0002t0023g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.420+201_420+202ins others(14): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007511 | |||||||
chr3:69007511 | G | GGGGGGGG others(9): Show |
1 | a0001c0002t0023g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.420+201_420+202ins others(16): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007511 | |||||||
chr3:69007511 | G | GGGGGGGG others(10): Show |
1 | a0001c0002t0052g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.420+201_420+202ins others(17): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007511 | |||||||
chr3:69007511 | G | GGGGGGGG others(13): Show |
1 | a0001c0001t0064g0265 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.420+201_420+202ins others(20): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007511 | |||||||
chr3:69007512 | G | C | 1 | a0001c0003t0011g0162 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.420+201C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007512 | |||||||
chr3:69007565 | T | C | 1 | a0001c0001t0057g0326 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.420+148A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007565 | |||||||
chr3:69007594 | G | A | 14 | a0001c0001t0016g0078 a0001c0001t0016g0082 a0001c0004t0007g0080 others(11): Show |
14 | HG01884.hp1 HG01952.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.420+119C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 6/17 | chr3 | 69007594 | |||||||
chr3:69007823 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA18978.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.312-2A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 5/17 | chr3 | 69007823 | |||||||
chr3:69007841 | T | C | 1 | a0001c0001t0024g0185 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.312-20A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 5/17 | chr3 | 69007841 | |||||||
chr3:69007888 | T | A | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.312-67A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 5/17 | chr3 | 69007888 | |||||||
chr3:69008026 | C | T | 1 | a0001c0002t0003g0328 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.312-205G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 5/17 | chr3 | 69008026 | |||||||
chr3:69008092 | T | C | 5 | a0001c0001t0064g0265 a0001c0002t0023g0046 a0001c0002t0023g0049 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.312-271A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 5/17 | chr3 | 69008092 | |||||||
chr3:69008354 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.311+74A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 5/17 | chr3 | 69008354 | |||||||
chr3:69008555 | C | A | 1 | a0001c0001t0004g0088 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.211-27G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 4/17 | chr3 | 69008555 | |||||||
chr3:69008587 | A | T | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.211-59T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 4/17 | chr3 | 69008587 | |||||||
chr3:69008674 | C | G | 1 | a0001c0003t0004g0116 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.211-146G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 4/17 | chr3 | 69008674 | |||||||
chr3:69008847 | G | C | 2 | a0001c0002t0008g0362 a0001c0002t0011g0033 |
3 | NA18980.hp1 NA18990.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.211-319C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 4/17 | chr3 | 69008847 | |||||||
chr3:69009426 | A | G | 1 | a0001c0001t0002g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.210+211T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 4/17 | chr3 | 69009426 | |||||||
chr3:69009521 | T | C | 1 | a0001c0002t0026g0305 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.210+116A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 4/17 | chr3 | 69009521 | |||||||
chr3:69009632 | C | T | 128 | a0001c0001t0029g0047 a0001c0001t0042g0053 a0001c0001t0057g0326 others(125): Show |
150 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(147): Show |
splice_region_variant&intron_variant | LOW | c.210+5G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 4/17 | chr3 | 69009632 | |||||||
chr3:69009872 | A | C | 52 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(49): Show |
55 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-14-12T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009872 | |||||||
chr3:69009912 | AAACAAC | A | 4 | a0001c0001t0016g0078 a0001c0001t0016g0082 a0001c0004t0012g0104 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-58_-14-53delGT others(4): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009912 | |||||||
chr3:69009930 | C | A | 2 | a0001c0003t0002g0106 a0001c0003t0002g0107 |
2 | HG02300.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-14-70G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009930 | |||||||
chr3:69009930 | C | CA | 8 | a0001c0001t0011g0178 a0001c0003t0003g0160 a0001c0003t0004g0004 others(5): Show |
9 | HG00544.hp1 HG01884.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-14-71dupT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009930 | |||||||
chr3:69009930 | CAACA | C | 10 | a0001c0001t0001g0238 a0001c0001t0002g0189 a0001c0001t0002g0211 others(7): Show |
10 | HG01261.hp2 HG02027.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-74_-14-71delTG others(2): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009930 | |||||||
chr3:69009930 | CAACAA | C | 99 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0097 others(96): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.-14-75_-14-71delTT others(3): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009930 | |||||||
chr3:69009932 | AC | A | 5 | a0001c0001t0001g0182 a0001c0001t0005g0017 a0001c0001t0006g0184 others(2): Show |
5 | HG02148.hp1 HG02886.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-73delG | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009932 | |||||||
chr3:69009933 | C | A | 93 | a0001c0001t0001g0123 a0001c0001t0001g0170 a0001c0001t0001g0174 others(90): Show |
110 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.-14-73G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009933 | |||||||
chr3:69009935 | A | AC | 4 | a0001c0001t0002g0042 a0001c0001t0043g0263 a0001c0002t0001g0041 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-76_-14-75insG | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009935 | |||||||
chr3:69009936 | A | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0114 others(128): Show |
161 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-14-76T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009936 | |||||||
chr3:69009938 | A | C | 1 | a0001c0002t0001g0327 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-14-78T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009938 | |||||||
chr3:69009939 | A | C | 10 | a0001c0001t0057g0326 a0001c0002t0001g0322 a0001c0002t0001g0324 others(7): Show |
10 | HG00735.hp2 HG02027.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-79T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009939 | |||||||
chr3:69009950 | C | A | 119 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0097 others(116): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-14-90G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69009950 | |||||||
chr3:69010054 | C | T | 1 | a0001c0003t0002g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-14-194G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69010054 | |||||||
chr3:69010064 | T | C | 1 | a0001c0017t0041g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-14-204A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69010064 | |||||||
chr3:69010165 | G | T | 117 | a0001c0001t0057g0326 a0001c0002t0001g0001 a0001c0002t0001g0028 others(114): Show |
139 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-14-305C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69010165 | |||||||
chr3:69010183 | G | T | 1 | a0001c0014t0058g0108 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-14-323C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69010183 | |||||||
chr3:69010419 | T | C | 9 | a0001c0002t0001g0268 a0001c0002t0005g0266 a0001c0002t0005g0269 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-559A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69010419 | |||||||
chr3:69010587 | C | T | 2 | a0001c0003t0002g0106 a0001c0003t0002g0107 |
2 | HG02300.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-14-727G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69010587 | |||||||
chr3:69010591 | G | A | 12 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0100 others(9): Show |
14 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.-14-731C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69010591 | |||||||
chr3:69010770 | A | C | 1 | a0001c0001t0007g0382 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-14-910T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69010770 | |||||||
chr3:69010799 | G | T | 2 | a0001c0001t0029g0047 a0001c0001t0042g0053 |
2 | HG02486.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-14-939C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69010799 | |||||||
chr3:69011064 | A | G | 9 | a0001c0001t0001g0193 a0001c0001t0002g0189 a0001c0001t0002g0190 others(6): Show |
9 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+872T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011064 | |||||||
chr3:69011193 | C | CTTTTTTT others(2): Show |
13 | a0001c0001t0001g0245 a0001c0001t0003g0101 a0001c0001t0003g0386 others(10): Show |
13 | HG01070.hp2 HG01074.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+734_-15+742dup others(9): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011193 | |||||||
chr3:69011193 | C | CTTTTTTT others(3): Show |
202 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0075 others(199): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.-15+733_-15+742dup others(10): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011193 | |||||||
chr3:69011193 | C | CTTTTTTT others(4): Show |
135 | a0001c0001t0003g0054 a0001c0001t0029g0047 a0001c0001t0042g0053 others(132): Show |
157 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.-15+732_-15+742dup others(11): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011193 | |||||||
chr3:69011193 | C | CTTTTTTT others(5): Show |
8 | a0001c0002t0001g0276 a0001c0002t0001g0321 a0001c0002t0005g0266 others(5): Show |
8 | HG00741.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+731_-15+742dup others(12): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011193 | |||||||
chr3:69011272 | G | A | 7 | a0001c0002t0008g0312 a0001c0002t0008g0313 a0001c0002t0008g0314 others(4): Show |
9 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+664C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011272 | |||||||
chr3:69011595 | C | CA | 120 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(117): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.-15+340dupT | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011595 | |||||||
chr3:69011595 | C | CAA | 13 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0002g0387 others(10): Show |
13 | HG00733.hp2 HG01255.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+339_-15+340dup others(2): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011595 | |||||||
chr3:69011595 | C | CAAA | 130 | a0001c0001t0002g0256 a0001c0001t0029g0047 a0001c0001t0057g0326 others(127): Show |
152 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.-15+338_-15+340dup others(3): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011595 | |||||||
chr3:69011595 | C | CAAAA | 12 | a0001c0001t0042g0053 a0001c0001t0064g0265 a0001c0002t0001g0040 others(9): Show |
12 | HG02027.hp1 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-15+337_-15+340dup others(4): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011595 | |||||||
chr3:69011606 | A | AC | 4 | a0003c0008t0001g0035 a0003c0008t0005g0036 a0003c0008t0029g0038 others(1): Show |
4 | HG00735.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+329_-15+330ins others(1): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011606 | |||||||
chr3:69011611 | C | G | 56 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0096 others(53): Show |
59 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-15+325G>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011611 | |||||||
chr3:69011615 | G | C | 2 | a0001c0001t0001g0257 a0001c0001t0009g0258 |
2 | NA19062.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-15+321C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011615 | |||||||
chr3:69011703 | C | T | 142 | a0001c0001t0029g0047 a0001c0001t0042g0053 a0001c0001t0057g0326 others(139): Show |
164 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.-15+233G>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011703 | |||||||
chr3:69011763 | T | A | 2 | a0001c0002t0001g0378 a0001c0002t0001g0379 |
2 | NA19060.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-15+173A>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011763 | |||||||
chr3:69011810 | G | A | 2 | a0001c0003t0015g0008 a0001c0003t0015g0259 |
4 | HG02723.hp1 HG03540.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+126C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 3/17 | chr3 | 69011810 | |||||||
chr3:69012181 | G | A | 1 | a0001c0001t0024g0261 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-70-190C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/17 | chr3 | 69012181 | |||||||
chr3:69012187 | A | T | 1 | a0001c0002t0008g0318 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-70-196T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/17 | chr3 | 69012187 | |||||||
chr3:69012371 | G | C | 1 | a0001c0001t0043g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-71+144C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/17 | chr3 | 69012371 | |||||||
chr3:69012378 | G | A | 1 | a0001c0003t0004g0262 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-71+137C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/17 | chr3 | 69012378 | |||||||
chr3:69012395 | G | A | 1 | a0001c0001t0043g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-71+120C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/17 | chr3 | 69012395 | |||||||
chr3:69012444 | T | C | 1 | a0001c0002t0001g0380 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-71+71A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/17 | chr3 | 69012444 | |||||||
chr3:69012480 | G | A | 1 | a0001c0001t0044g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-71+35C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/17 | chr3 | 69012480 | |||||||
chr3:69012511 | T | C | 1 | a0001c0002t0001g0381 | 1 | HG02165.hp2 | splice_region_variant&intron_variant | LOW | c.-71+4A>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 2/17 | chr3 | 69012511 | |||||||
chr3:69012805 | G | T | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | splice_region_variant&intron_variant | LOW | c.-355-6C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69012805 | |||||||
chr3:69012816 | A | T | 8 | a0001c0002t0001g0268 a0001c0002t0005g0266 a0001c0002t0005g0269 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-355-17T>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69012816 | |||||||
chr3:69012858 | G | A | 9 | a0001c0002t0001g0268 a0001c0002t0005g0266 a0001c0002t0005g0269 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-355-59C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69012858 | |||||||
chr3:69012875 | C | A | 75 | a0001c0001t0057g0326 a0001c0002t0001g0001 a0001c0002t0001g0028 others(72): Show |
92 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.-355-76G>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69012875 | |||||||
chr3:69012893 | CAGAG | C | 123 | a0001c0001t0057g0326 a0001c0002t0001g0001 a0001c0002t0001g0028 others(120): Show |
145 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.-355-98_-355-95del others(4): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69012893 | |||||||
chr3:69012902 | A | C | 1 | a0001c0001t0003g0043 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-355-103T>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69012902 | |||||||
chr3:69012989 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-355-190T>C | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69012989 | |||||||
chr3:69013159 | G | T | 3 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0008g0039 |
3 | NA18941.hp2 NA18952.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-355-360C>A | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69013159 | |||||||
chr3:69013239 | G | A | 4 | a0003c0008t0001g0035 a0003c0008t0005g0036 a0003c0008t0029g0038 others(1): Show |
4 | HG00735.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-356+335C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69013239 | |||||||
chr3:69013445 | G | A | 6 | a0001c0001t0001g0385 a0001c0001t0002g0383 a0001c0001t0002g0384 others(3): Show |
6 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-356+129C>T | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69013445 | |||||||
chr3:69013536 | A | AGCGGGGG others(15): Show |
4 | a0003c0008t0001g0035 a0003c0008t0005g0036 a0003c0008t0029g0038 others(1): Show |
4 | HG00735.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-356+16_-356+37dup others(22): Show |
EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69013536 | |||||||
chr3:69013539 | G | C | 1 | a0003c0008t0063g0388 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-356+35C>G | EOGT | ENSG00000163378.14 | transcript | ENST00000383701.8 | protein_coding | 1/17 | chr3 | 69013539 |