Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 731 |
| ensemblid | ENSG00000157131.12 |
| hgncid | 1352 |
| symbol | C8A |
| name | complement C8 alpha chain |
| refseq_nuc | NM_000562.3 |
| refseq_prot | NP_000553.1 |
| ensembl_nuc | ENST00000361249.4 |
| ensembl_prot | ENSP00000354458.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 56854797 |
| end | 56918223 |
| strand | + |
| ver | v1.2 |
| region | chr1:56854797-56918223 |
| region5000 | chr1:56849797-56923223 |
| regionname0 | C8A_chr1_56854797_56918223 |
| regionname5000 | C8A_chr1_56849797_56923223 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 584 | 185 | 48 | 32 | 87 | 7 | 10 | 70 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0002 | 0/1 | 584 | 99 | 5 | 12 | 54 | 6 | 21 | 40 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0003 | 0/0 | 584 | 20 | 12 | 5 | 1 | 0 | 2 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0004 | 0/0 | 584 | 17 | 3 | 1 | 10 | 1 | 2 | 7 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0005 | 0/0 | 584 | 12 | 7 | 0 | 5 | 0 | 0 | 4 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0006 | 0/0 | 584 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0007 | 0/0 | 584 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0008 | 0/0 | 584 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0009 | 0/0 | 584 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0010 | 0/0 | 584 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0011 | 0/0 | 584 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0012 | 0/0 | 584 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0013 | 0/0 | 584 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0014 | 0/0 | 584 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0015 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0016 | 0/0 | 584 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0017 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0018 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0019 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| a0020 | 0/0 | 584 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | MFAVV others(579): Show |
chr1 | 56849797 | 56923223 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1752 | 180 | 45 | 31 | 86 | 7 | 10 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0001c0010 | 0/0 | 1752 | 3 | 3 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0001c0018 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0001c0023 | 0/0 | 1752 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0002c0002 | 0/1 | 1752 | 99 | 5 | 12 | 54 | 6 | 21 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0003c0003 | 0/0 | 1752 | 20 | 12 | 5 | 1 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0004c0004 | 0/0 | 1752 | 17 | 3 | 1 | 10 | 1 | 2 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0005c0005 | 0/0 | 1752 | 9 | 4 | 0 | 5 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0005c0009 | 0/0 | 1752 | 3 | 3 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0006c0006 | 0/0 | 1752 | 9 | 9 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0007c0008 | 0/0 | 1752 | 4 | 0 | 4 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0008c0007 | 0/0 | 1752 | 4 | 0 | 0 | 0 | 0 | 4 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0009c0014 | 0/0 | 1752 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0010c0012 | 0/0 | 1752 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0011c0013 | 0/0 | 1752 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0012c0011 | 0/0 | 1752 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0013c0022 | 0/0 | 1752 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0014c0024 | 0/0 | 1752 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0015c0017 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0016c0016 | 0/0 | 1752 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0017c0020 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0018c0021 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0019c0019 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 | ||
| a0020c0015 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | ATGTT others(1747): Show |
chr1 | 56849797 | 56923223 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2367 | 171 | 36 | 31 | 86 | 7 | 10 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0001c0001t0003 | 0/0 | 2367 | 7 | 7 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0001c0001t0005 | 0/0 | 2367 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0001c0010t0001 | 0/0 | 2367 | 3 | 3 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0001c0018t0001 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0001c0023t0001 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0002c0002t0001 | 0/1 | 2367 | 98 | 5 | 12 | 53 | 6 | 21 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0002c0002t0006 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0003c0003t0002 | 0/0 | 2367 | 20 | 12 | 5 | 1 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0004c0004t0001 | 0/0 | 2367 | 17 | 3 | 1 | 10 | 1 | 2 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0005c0005t0002 | 0/0 | 2367 | 9 | 4 | 0 | 5 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0005c0009t0002 | 0/0 | 2367 | 3 | 3 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0006c0006t0001 | 0/0 | 2367 | 9 | 9 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0007c0008t0001 | 0/0 | 2367 | 4 | 0 | 4 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0008c0007t0004 | 0/0 | 2367 | 4 | 0 | 0 | 0 | 0 | 4 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0009c0014t0001 | 0/0 | 2367 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0010c0012t0001 | 0/0 | 2367 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0011c0013t0002 | 0/0 | 2367 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0012c0011t0001 | 0/0 | 2367 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0013c0022t0002 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0014c0024t0002 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0015c0017t0002 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0016c0016t0001 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0017c0020t0005 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0018c0021t0001 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0019c0019t0001 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| a0020c0015t0007 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | AGATA others(2362): Show |
chr1 | 56849797 | 56923223 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0003 | 0/0 | 7 | 1 | 1 | 2 | 0 | 3 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0010t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0010t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0010t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0018t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0001c0023t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0001 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0002c0002t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0003c0003t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0004c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0005c0005t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0005c0005t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0005c0005t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0005c0005t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0005c0005t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0005c0005t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0005c0005t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0005c0005t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0005c0005t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0005c0009t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0005c0009t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0006c0006t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0006c0006t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0006c0006t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0006c0006t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0006c0006t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0006c0006t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0006c0006t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0006c0006t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0007c0008t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0007c0008t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0007c0008t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0007c0008t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0008c0007t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0008c0007t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0008c0007t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0008c0007t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0009c0014t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0010c0012t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0010c0012t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0011c0013t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0011c0013t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0012c0011t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0012c0011t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0013c0022t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0014c0024t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0015c0017t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0016c0016t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0017c0020t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0018c0021t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0019c0019t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| a0020c0015t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0004 | c0004 | t0001 | g0230 | EUR | FIN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0054 | EUR | FIN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00408 | hp1 | a0004 | c0004 | t0001 | g0007 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00408 | hp2 | a0009 | c0014 | t0001 | g0015 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00558 | hp2 | a0004 | c0004 | t0001 | g0245 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG00738 | hp2 | a0010 | c0012 | t0001 | g0200 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01081 | hp1 | a0010 | c0012 | t0001 | g0174 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01106 | hp2 | a0004 | c0004 | t0001 | g0231 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01109 | hp1 | a0003 | c0003 | t0002 | g0196 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01109 | hp2 | a0003 | c0003 | t0002 | g0080 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01192 | hp2 | a0001 | c0023 | t0001 | g0067 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01243 | hp2 | a0013 | c0022 | t0002 | g0218 | AMR | PUR | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01346 | hp1 | a0003 | c0003 | t0002 | g0250 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01346 | hp2 | a0007 | c0008 | t0001 | g0258 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01358 | hp1 | a0007 | c0008 | t0001 | g0246 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0219 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01496 | hp2 | a0007 | c0008 | t0001 | g0259 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0036 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0032 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0036 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01891 | hp1 | a0003 | c0003 | t0002 | g0041 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01943 | hp1 | a0003 | c0003 | t0002 | g0088 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01975 | hp1 | a0014 | c0024 | t0002 | g0257 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0210 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02004 | hp2 | a0007 | c0008 | t0001 | g0256 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02015 | hp2 | a0005 | c0005 | t0002 | g0166 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02040 | hp2 | a0003 | c0003 | t0002 | g0236 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02055 | hp2 | a0004 | c0004 | t0001 | g0243 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02080 | hp2 | a0004 | c0004 | t0001 | g0268 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | KHV | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02145 | hp1 | a0003 | c0003 | t0002 | g0252 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02145 | hp2 | a0003 | c0003 | t0002 | g0278 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | CDX | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CDX | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0147 | AMR | PEL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02280 | hp2 | a0003 | c0003 | t0002 | g0017 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02451 | hp2 | a0005 | c0005 | t0002 | g0204 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02615 | hp1 | a0001 | c0010 | t0001 | g0261 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02622 | hp2 | a0015 | c0017 | t0002 | g0075 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02630 | hp2 | a0006 | c0006 | t0001 | g0019 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02647 | hp1 | a0005 | c0005 | t0002 | g0198 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02698 | hp2 | a0016 | c0016 | t0001 | g0003 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02735 | hp2 | a0008 | c0007 | t0004 | g0051 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0029 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02809 | hp1 | a0005 | c0009 | t0002 | g0203 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02818 | hp1 | a0017 | c0020 | t0005 | g0267 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02895 | hp1 | a0006 | c0006 | t0001 | g0045 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02896 | hp1 | a0011 | c0013 | t0002 | g0173 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02897 | hp1 | a0011 | c0013 | t0002 | g0172 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02897 | hp2 | a0006 | c0006 | t0001 | g0045 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02922 | hp2 | a0005 | c0005 | t0002 | g0197 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02965 | hp1 | a0006 | c0006 | t0001 | g0078 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02965 | hp2 | a0003 | c0003 | t0002 | g0041 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02976 | hp1 | a0003 | c0003 | t0002 | g0226 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03041 | hp2 | a0006 | c0006 | t0001 | g0263 | AFR | GWD | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03098 | hp1 | a0006 | c0006 | t0001 | g0083 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03098 | hp2 | a0018 | c0021 | t0001 | g0068 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0221 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03139 | hp1 | a0004 | c0004 | t0001 | g0039 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03209 | hp1 | a0019 | c0019 | t0001 | g0207 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03225 | hp2 | a0004 | c0004 | t0001 | g0039 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03490 | hp1 | a0003 | c0003 | t0002 | g0040 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03492 | hp1 | a0003 | c0003 | t0002 | g0040 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0214 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03669 | hp2 | a0008 | c0007 | t0004 | g0049 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0182 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0192 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03831 | hp2 | a0008 | c0007 | t0004 | g0052 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0157 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03942 | hp2 | a0004 | c0004 | t0001 | g0244 | SAS | BEB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0159 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG04228 | hp1 | a0008 | c0007 | t0004 | g0053 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0140 | SAS | STU | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18522 | hp1 | a0001 | c0010 | t0001 | g0260 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0248 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18747 | hp2 | a0020 | c0015 | t0007 | g0050 | EAS | CHB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18906 | hp2 | a0006 | c0006 | t0001 | g0213 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18939 | hp2 | a0012 | c0011 | t0001 | g0241 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18940 | hp2 | a0005 | c0005 | t0002 | g0181 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18952 | hp2 | a0004 | c0004 | t0001 | g0007 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18961 | hp1 | a0005 | c0005 | t0002 | g0180 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18968 | hp2 | a0012 | c0011 | t0001 | g0242 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18977 | hp1 | a0005 | c0005 | t0002 | g0111 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18980 | hp1 | a0005 | c0005 | t0002 | g0186 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18993 | hp1 | a0004 | c0004 | t0001 | g0237 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18995 | hp1 | a0002 | c0002 | t0006 | g0033 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19007 | hp1 | a0009 | c0014 | t0001 | g0015 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19030 | hp2 | a0003 | c0003 | t0002 | g0217 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19066 | hp1 | a0004 | c0004 | t0001 | g0007 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19080 | hp1 | a0001 | c0018 | t0001 | g0120 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19080 | hp2 | a0004 | c0004 | t0001 | g0239 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19084 | hp2 | a0004 | c0004 | t0001 | g0007 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19090 | hp2 | a0004 | c0004 | t0001 | g0238 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19240 | hp1 | a0003 | c0003 | t0002 | g0017 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA19240 | hp2 | a0005 | c0005 | t0002 | g0199 | AFR | YRI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ASW | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0276 | AFR | ASW | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0189 | EUR | TSI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0178 | EUR | TSI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0194 | SAS | GIH | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA20905 | hp2 | a0004 | c0004 | t0001 | g0266 | SAS | GIH | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG01123 | hp2 | a0003 | c0003 | t0002 | g0100 | AMR | CLM | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02486 | hp1 | a0003 | c0003 | t0002 | g0277 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02486 | hp2 | a0005 | c0009 | t0002 | g0037 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02559 | hp1 | a0001 | c0010 | t0001 | g0229 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0211 | AFR | MSL | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG06807 | hp1 | a0005 | c0009 | t0002 | g0037 | AFR | USA | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| HG06807 | hp2 | a0006 | c0006 | t0001 | g0270 | AFR | USA | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18955 | hp1 | a0004 | c0004 | t0001 | g0240 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | USA | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | USA | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA21309 | hp1 | a0006 | c0006 | t0001 | g0071 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0167 | AFR | LWK | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0175 | REF | REF | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0254 | REF | REF | C8A_chr1_56849797_56923223 | C8A | chr1 | 56849797 | 56923223 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:56854927 | T | C | 1 | a0012 | 2 | NA18939.hp2 NA18968.hp2 |
missense_variant | MODERATE | c.26T>C | p.Leu9Ser | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/11 | 131/2367 | 26/1755 | 9/584 | chr1 | 56854927 | |||
| chr1:56867631 | C | T | 2 | a0007 a0014 |
5 | HG01346.hp2 HG01358.hp1 HG01496.hp2 others(2): Show |
missense_variant | MODERATE | c.100C>T | p.Pro34Ser | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/11 | 205/2367 | 100/1755 | 34/584 | chr1 | 56867631 | |||
| chr1:56867638 | C | A | 2 | a0008 a0020 |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
missense_variant | MODERATE | c.107C>A | p.Ala36Glu | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/11 | 212/2367 | 107/1755 | 36/584 | chr1 | 56867638 | |||
| chr1:56874953 | G | A | 1 | a0016 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.176G>A | p.Arg59Gln | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/11 | 281/2367 | 176/1755 | 59/584 | chr1 | 56874953 | |||
| chr1:56875054 | C | A | 4 | a0002 a0005 a0010 others(1): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
missense_variant | MODERATE | c.277C>A | p.Gln93Lys | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/11 | 382/2367 | 277/1755 | 93/584 | chr1 | 56875054 | |||
| chr1:56906790 | C | T | 2 | a0013 a0018 |
2 | HG01243.hp2 HG03098.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1220C>T | p.Thr407Ile | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/11 | 1325/2367 | 1220/1755 | 407/584 | chr1 | 56906790 | |||
| chr1:56908105 | G | A | 3 | a0006 a0015 a0018 |
11 | HG02622.hp2 HG02630.hp2 HG02895.hp1 others(8): Show |
missense_variant | MODERATE | c.1372G>A | p.Asp458Asn | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/11 | 1477/2367 | 1372/1755 | 458/584 | chr1 | 56908105 | |||
| chr1:56912427 | C | T | 1 | a0017 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1405C>T | p.Arg469Trp | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1510/2367 | 1405/1755 | 469/584 | chr1 | 56912427 | |||
| chr1:56912446 | C | G | 1 | a0019 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1424C>G | p.Pro475Arg | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1529/2367 | 1424/1755 | 475/584 | chr1 | 56912446 | |||
| chr1:56912476 | G | T | 6 | a0003 a0005 a0008 others(3): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
missense_variant | MODERATE | c.1454G>T | p.Arg485Leu | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1559/2367 | 1454/1755 | 485/584 | chr1 | 56912476 | |||
| chr1:56917615 | A | G | 1 | a0009 | 2 | HG00408.hp2 NA19007.hp1 |
missense_variant | MODERATE | c.1654A>G | p.Arg552Gly | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1759/2367 | 1654/1755 | 552/584 | chr1 | 56917615 | |||
| chr1:56917622 | G | A | 1 | a0011 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1661G>A | p.Gly554Asp | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1766/2367 | 1661/1755 | 554/584 | chr1 | 56917622 | |||
| chr1:56917642 | G | C | 7 | a0003 a0005 a0008 others(4): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
missense_variant | MODERATE | c.1681G>C | p.Glu561Gln | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1786/2367 | 1681/1755 | 561/584 | chr1 | 56917642 | |||
| chr1:56917685 | C | T | 3 | a0004 a0010 a0020 |
20 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(17): Show |
missense_variant | MODERATE | c.1724C>T | p.Pro575Leu | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1829/2367 | 1724/1755 | 575/584 | chr1 | 56917685 | |||
| chr1:56917703 | C | G | 1 | a0016 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1742C>G | p.Thr581Arg | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1847/2367 | 1742/1755 | 581/584 | chr1 | 56917703 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:56867639 | A | G | 1 | a0001c0023 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.108A>G | p.Ala36Ala | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/11 | 213/2367 | 108/1755 | 36/584 | chr1 | 56867639 | |||
| chr1:56881571 | C | G | 2 | a0008c0007 a0020c0015 |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
synonymous_variant | LOW | c.591C>G | p.Leu197Leu | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/11 | 696/2367 | 591/1755 | 197/584 | chr1 | 56881571 | |||
| chr1:56885938 | C | T | 1 | a0001c0010 | 3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.867C>T | p.Phe289Phe | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/11 | 972/2367 | 867/1755 | 289/584 | chr1 | 56885938 | |||
| chr1:56912477 | C | T | 7 | a0003c0003 a0005c0005 a0005c0009 others(4): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
synonymous_variant | LOW | c.1455C>T | p.Arg485Arg | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1560/2367 | 1455/1755 | 485/584 | chr1 | 56912477 | |||
| chr1:56912525 | T | C | 7 | a0003c0003 a0005c0005 a0005c0009 others(4): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
synonymous_variant | LOW | c.1503T>C | p.Pro501Pro | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1608/2367 | 1503/1755 | 501/584 | chr1 | 56912525 | |||
| chr1:56912561 | C | T | 1 | a0001c0018 | 1 | NA19080.hp1 | synonymous_variant | LOW | c.1539C>T | p.Thr513Thr | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/11 | 1644/2367 | 1539/1755 | 513/584 | chr1 | 56912561 | |||
| chr1:56917704 | G | T | 2 | a0005c0009 a0013c0022 |
4 | HG01243.hp2 HG02486.hp2 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.1743G>T | p.Thr581Thr | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 1848/2367 | 1743/1755 | 581/584 | chr1 | 56917704 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:56854814 | C | G | 2 | a0008c0007t0004 a0020c0015t0007 |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-88C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/11 | 88 | chr1 | 56854814 | ||||||
| chr1:56917808 | C | G | 1 | a0002c0002t0006 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*92C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 92 | chr1 | 56917808 | ||||||
| chr1:56917859 | G | T | 2 | a0001c0001t0005 a0017c0020t0005 |
3 | HG02818.hp1 HG03579.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*143G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 143 | chr1 | 56917859 | ||||||
| chr1:56918010 | C | T | 8 | a0003c0003t0002 a0005c0005t0002 a0005c0009t0002 others(5): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*294C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 294 | chr1 | 56918010 | ||||||
| chr1:56918192 | A | G | 3 | a0001c0001t0003 a0001c0001t0005 a0017c0020t0005 |
10 | HG02615.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*476A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 11/11 | 476 | chr1 | 56918192 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:56855019 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.77+41A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855019 | |||||||
| chr1:56855389 | C | T | 3 | a0003c0003t0002g0276 a0003c0003t0002g0277 a0003c0003t0002g0278 |
3 | HG02145.hp2 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.77+411C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855389 | |||||||
| chr1:56855391 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.77+413T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855391 | |||||||
| chr1:56855418 | T | TAAGAGTG others(311): Show |
1 | a0001c0001t0001g0275 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.77+454_77+455insCG others(316): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56855418 | ||||||
| chr1:56855488 | G | A | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+510G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855488 | |||||||
| chr1:56855498 | A | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | NA19002.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.77+520A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855498 | |||||||
| chr1:56855540 | T | C | 2 | a0002c0002t0001g0009 a0002c0002t0001g0054 |
4 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+562T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855540 | |||||||
| chr1:56855550 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+572G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855550 | |||||||
| chr1:56855636 | GT | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
252 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(249): Show |
intron_variant | MODIFIER | c.77+670delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56855636 | ||||||
| chr1:56855636 | GTT | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(9): Show |
23 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.77+669_77+670delTT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56855636 | ||||||
| chr1:56855703 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.77+725C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855703 | |||||||
| chr1:56855981 | C | G | 1 | a0013c0022t0002g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.77+1003C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855981 | |||||||
| chr1:56855988 | G | A | 1 | a0001c0023t0001g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.77+1010G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56855988 | |||||||
| chr1:56856017 | T | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0069 others(20): Show |
29 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.77+1039T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856017 | |||||||
| chr1:56856037 | G | T | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+1059G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856037 | |||||||
| chr1:56856044 | G | A | 7 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0003c0003t0002g0017 others(4): Show |
9 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+1066G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856044 | |||||||
| chr1:56856132 | C | T | 1 | a0006c0006t0001g0083 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.77+1154C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856132 | |||||||
| chr1:56856170 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.77+1192G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856170 | |||||||
| chr1:56856187 | G | A | 1 | a0002c0002t0001g0084 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.77+1209G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856187 | |||||||
| chr1:56856356 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.77+1378A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856356 | |||||||
| chr1:56856404 | C | A | 1 | a0002c0002t0001g0085 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.77+1426C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856404 | |||||||
| chr1:56856491 | C | G | 3 | a0003c0003t0002g0276 a0003c0003t0002g0277 a0003c0003t0002g0278 |
3 | HG02145.hp2 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.77+1513C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856491 | |||||||
| chr1:56856557 | T | C | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+1579T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856557 | |||||||
| chr1:56856644 | A | G | 13 | a0001c0001t0001g0047 a0001c0001t0001g0066 a0001c0001t0001g0215 others(10): Show |
15 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.77+1666A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856644 | |||||||
| chr1:56856793 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.77+1815A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856793 | |||||||
| chr1:56856861 | G | A | 4 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0275 others(1): Show |
4 | HG01255.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+1883G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856861 | |||||||
| chr1:56856914 | T | G | 1 | a0002c0002t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.77+1936T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56856914 | |||||||
| chr1:56857057 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.77+2079G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857057 | |||||||
| chr1:56857229 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.77+2251A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857229 | |||||||
| chr1:56857303 | T | TAC | 102 | a0001c0001t0001g0038 a0001c0001t0001g0069 a0001c0001t0001g0070 others(99): Show |
131 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.77+2351_77+2352dup others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56857303 | ||||||
| chr1:56857303 | T | TACAC | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(58): Show |
90 | HG00544.hp2 HG00609.hp2 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.77+2349_77+2352dup others(4): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56857303 | ||||||
| chr1:56857303 | T | TACACAC | 22 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0092 others(19): Show |
28 | HG00408.hp2 HG00621.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.77+2347_77+2352dup others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56857303 | ||||||
| chr1:56857303 | T | TACACACA others(1): Show |
7 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(4): Show |
7 | HG00323.hp1 HG01243.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+2345_77+2352dup others(8): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56857303 | ||||||
| chr1:56857303 | T | TACACACA others(3): Show |
2 | a0003c0003t0002g0088 a0008c0007t0004g0049 |
2 | HG01943.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.77+2343_77+2352dup others(10): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56857303 | ||||||
| chr1:56857442 | A | T | 2 | a0002c0002t0001g0209 a0002c0002t0001g0210 |
2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.77+2464A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857442 | |||||||
| chr1:56857506 | T | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.77+2528T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857506 | |||||||
| chr1:56857691 | G | A | 87 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(84): Show |
111 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.77+2713G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857691 | |||||||
| chr1:56857880 | T | G | 13 | a0001c0001t0001g0047 a0001c0001t0001g0066 a0001c0001t0001g0215 others(10): Show |
15 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.77+2902T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56857880 | |||||||
| chr1:56858022 | G | T | 1 | a0002c0002t0001g0194 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.77+3044G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858022 | |||||||
| chr1:56858090 | C | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
281 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(278): Show |
intron_variant | MODIFIER | c.77+3112C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858090 | |||||||
| chr1:56858417 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.77+3439T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858417 | |||||||
| chr1:56858636 | G | A | 2 | a0013c0022t0002g0218 a0018c0021t0001g0068 |
2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.77+3658G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858636 | |||||||
| chr1:56858749 | C | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
281 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(278): Show |
intron_variant | MODIFIER | c.77+3771C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858749 | |||||||
| chr1:56858785 | C | A | 2 | a0001c0001t0001g0195 a0003c0003t0002g0196 |
2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.77+3807C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858785 | |||||||
| chr1:56858813 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0003c0003t0002g0017 |
4 | HG02280.hp2 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+3835T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858813 | |||||||
| chr1:56858839 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
284 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.77+3861A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56858839 | |||||||
| chr1:56859067 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0060 |
4 | HG02071.hp2 HG02135.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+4089G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859067 | |||||||
| chr1:56859222 | G | A | 1 | a0002c0002t0001g0138 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.77+4244G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859222 | |||||||
| chr1:56859224 | A | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(18): Show |
32 | HG00408.hp2 HG01168.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.77+4246A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859224 | |||||||
| chr1:56859586 | T | A | 2 | a0001c0001t0001g0195 a0003c0003t0002g0196 |
2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.77+4608T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859586 | |||||||
| chr1:56859715 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.77+4737C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859715 | |||||||
| chr1:56859761 | A | AC | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
284 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.77+4783_77+4784ins others(1): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859761 | |||||||
| chr1:56859791 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.77+4813G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859791 | |||||||
| chr1:56859904 | A | T | 1 | a0004c0004t0001g0039 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.77+4926A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56859904 | |||||||
| chr1:56860018 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.77+5040G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860018 | |||||||
| chr1:56860074 | T | A | 100 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(97): Show |
125 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.77+5096T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860074 | |||||||
| chr1:56860182 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
250 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.77+5204A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860182 | |||||||
| chr1:56860208 | G | A | 1 | a0002c0002t0001g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.77+5230G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860208 | |||||||
| chr1:56860209 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.77+5231C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860209 | |||||||
| chr1:56860313 | G | A | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+5335G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860313 | |||||||
| chr1:56860400 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0003g0018 a0001c0001t0003g0072 others(1): Show |
8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.77+5422A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860400 | |||||||
| chr1:56860451 | A | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.77+5473A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860451 | |||||||
| chr1:56860491 | T | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0228 |
3 | HG00735.hp1 HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.77+5513T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860491 | |||||||
| chr1:56860562 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(9): Show |
23 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.77+5584G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860562 | |||||||
| chr1:56860750 | T | C | 1 | a0019c0019t0001g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.77+5772T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860750 | |||||||
| chr1:56860761 | G | A | 3 | a0002c0002t0001g0140 a0002c0002t0001g0141 a0002c0002t0001g0142 |
3 | HG02738.hp1 HG03834.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.77+5783G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860761 | |||||||
| chr1:56860779 | C | T | 1 | a0004c0004t0001g0268 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.77+5801C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860779 | |||||||
| chr1:56860877 | A | G | 1 | a0019c0019t0001g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.77+5899A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56860877 | |||||||
| chr1:56861027 | G | A | 1 | a0003c0003t0002g0276 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.77+6049G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861027 | |||||||
| chr1:56861160 | T | A | 2 | a0001c0001t0001g0195 a0003c0003t0002g0196 |
2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.77+6182T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861160 | |||||||
| chr1:56861264 | A | G | 14 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(11): Show |
14 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+6286A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861264 | |||||||
| chr1:56861338 | G | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(10): Show |
24 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.78-6271G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861338 | |||||||
| chr1:56861462 | CA | C | 2 | a0001c0001t0001g0038 a0003c0003t0002g0211 |
3 | HG02572.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.78-6146delA | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861462 | |||||||
| chr1:56861498 | G | T | 1 | a0001c0023t0001g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.78-6111G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861498 | |||||||
| chr1:56861526 | T | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(9): Show |
23 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.78-6083T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861526 | |||||||
| chr1:56861547 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.78-6062C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861547 | |||||||
| chr1:56861570 | A | T | 1 | a0017c0020t0005g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.78-6039A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861570 | |||||||
| chr1:56861611 | T | A | 2 | a0013c0022t0002g0218 a0018c0021t0001g0068 |
2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.78-5998T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861611 | |||||||
| chr1:56861698 | T | C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0047 a0001c0001t0001g0074 others(12): Show |
16 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.78-5911T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861698 | |||||||
| chr1:56861792 | T | C | 4 | a0001c0001t0001g0066 a0001c0001t0005g0214 a0003c0003t0002g0040 others(1): Show |
5 | HG03490.hp1 HG03492.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-5817T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56861792 | |||||||
| chr1:56862122 | C | T | 1 | a0004c0004t0001g0266 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.78-5487C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862122 | |||||||
| chr1:56862197 | A | G | 7 | a0001c0001t0001g0038 a0001c0001t0001g0227 a0001c0001t0001g0264 others(4): Show |
8 | HG02572.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.78-5412A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862197 | |||||||
| chr1:56862310 | C | T | 90 | a0001c0001t0001g0193 a0002c0002t0001g0001 a0002c0002t0001g0009 others(87): Show |
115 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.78-5299C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862310 | |||||||
| chr1:56862321 | A | G | 1 | a0002c0002t0001g0192 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.78-5288A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862321 | |||||||
| chr1:56862449 | C | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
235 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.78-5160C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862449 | |||||||
| chr1:56862622 | C | T | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-4987C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56862622 | |||||||
| chr1:56863029 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.78-4580G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863029 | |||||||
| chr1:56863057 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.78-4552C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863057 | |||||||
| chr1:56863092 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.78-4517G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863092 | |||||||
| chr1:56863115 | A | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.78-4494A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863115 | |||||||
| chr1:56863192 | G | T | 1 | a0006c0006t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.78-4417G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863192 | |||||||
| chr1:56863253 | T | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
237 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.78-4356T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863253 | |||||||
| chr1:56863729 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.78-3880C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863729 | |||||||
| chr1:56863831 | TC | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(10): Show |
24 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.78-3775delC | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56863831 | ||||||
| chr1:56863831 | TCCCTCTC others(18): Show |
T | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.78-3768_78-3744del others(25): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56863831 | ||||||
| chr1:56863885 | CCCTT | C | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG00558.hp1 HG01168.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-3707_78-3704del others(4): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 56863885 | ||||||
| chr1:56863886 | C | T | 1 | a0002c0002t0001g0001 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.78-3723C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56863886 | |||||||
| chr1:56864044 | G | C | 1 | a0001c0010t0001g0229 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.78-3565G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864044 | |||||||
| chr1:56864129 | G | A | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-3480G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864129 | |||||||
| chr1:56864264 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.78-3345G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864264 | |||||||
| chr1:56864361 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.78-3248C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864361 | |||||||
| chr1:56864376 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.78-3233A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864376 | |||||||
| chr1:56864389 | G | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(18): Show |
32 | HG00408.hp2 HG01168.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.78-3220G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864389 | |||||||
| chr1:56864443 | T | A | 6 | a0001c0001t0001g0227 a0001c0001t0001g0264 a0001c0001t0001g0265 others(3): Show |
6 | HG02818.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-3166T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864443 | |||||||
| chr1:56864578 | G | A | 1 | a0002c0002t0001g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.78-3031G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864578 | |||||||
| chr1:56864739 | G | T | 1 | a0001c0001t0001g0106 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.78-2870G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864739 | |||||||
| chr1:56864740 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.78-2869A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56864740 | |||||||
| chr1:56865052 | C | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
85 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.78-2557C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865052 | |||||||
| chr1:56865068 | T | C | 5 | a0001c0001t0001g0216 a0001c0001t0001g0271 a0003c0003t0002g0276 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-2541T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865068 | |||||||
| chr1:56865296 | C | A | 1 | a0005c0005t0002g0197 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.78-2313C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865296 | |||||||
| chr1:56865353 | T | G | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(25): Show |
37 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.78-2256T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865353 | |||||||
| chr1:56865372 | C | T | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.78-2237C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865372 | |||||||
| chr1:56865409 | G | T | 90 | a0001c0001t0001g0193 a0002c0002t0001g0001 a0002c0002t0001g0009 others(87): Show |
115 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.78-2200G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865409 | |||||||
| chr1:56865454 | G | T | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.78-2155G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865454 | |||||||
| chr1:56865830 | T | C | 6 | a0001c0001t0001g0227 a0001c0001t0001g0264 a0001c0001t0001g0265 others(3): Show |
6 | HG02818.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.78-1779T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865830 | |||||||
| chr1:56865873 | G | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.78-1736G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56865873 | |||||||
| chr1:56866070 | T | A | 5 | a0002c0002t0001g0145 a0002c0002t0001g0146 a0002c0002t0001g0147 others(2): Show |
5 | HG02273.hp2 NA18989.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-1539T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866070 | |||||||
| chr1:56866148 | T | C | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-1461T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866148 | |||||||
| chr1:56866221 | A | C | 1 | a0001c0001t0003g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.78-1388A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866221 | |||||||
| chr1:56866251 | A | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.78-1358A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866251 | |||||||
| chr1:56866598 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.78-1011G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866598 | |||||||
| chr1:56866632 | C | T | 1 | a0005c0005t0002g0111 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.78-977C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866632 | |||||||
| chr1:56866716 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.78-893A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866716 | |||||||
| chr1:56866762 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.78-847G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866762 | |||||||
| chr1:56866812 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.78-797A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866812 | |||||||
| chr1:56866816 | G | T | 2 | a0003c0003t0002g0217 a0019c0019t0001g0207 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.78-793G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866816 | |||||||
| chr1:56866826 | G | A | 1 | a0007c0008t0001g0246 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.78-783G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866826 | |||||||
| chr1:56866831 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.78-778G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866831 | |||||||
| chr1:56866906 | A | T | 1 | a0003c0003t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.78-703A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866906 | |||||||
| chr1:56866945 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0136 |
5 | HG00544.hp2 NA18957.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-664C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56866945 | |||||||
| chr1:56867049 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0224 |
2 | NA18956.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.78-560A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867049 | |||||||
| chr1:56867084 | T | C | 33 | a0001c0001t0001g0105 a0002c0002t0001g0001 a0002c0002t0001g0010 others(30): Show |
47 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.78-525T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867084 | |||||||
| chr1:56867130 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.78-479T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867130 | |||||||
| chr1:56867182 | A | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(18): Show |
32 | HG00408.hp2 HG01168.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.78-427A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867182 | |||||||
| chr1:56867197 | A | G | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.78-412A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867197 | |||||||
| chr1:56867206 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78-403G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 1/10 | chr1 | 56867206 | |||||||
| chr1:56867710 | A | G | 1 | a0003c0003t0002g0211 | 1 | HG03471.hp2 | splice_region_variant&intron_variant | LOW | c.171+8A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867710 | |||||||
| chr1:56867761 | C | T | 6 | a0001c0001t0001g0227 a0001c0001t0001g0264 a0001c0001t0001g0265 others(3): Show |
6 | HG02818.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+59C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867761 | |||||||
| chr1:56867810 | G | T | 13 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(10): Show |
13 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.171+108G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867810 | |||||||
| chr1:56867870 | C | A | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.171+168C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867870 | |||||||
| chr1:56867942 | A | G | 1 | a0002c0002t0001g0165 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.171+240A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867942 | |||||||
| chr1:56867948 | T | C | 1 | a0002c0002t0001g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.171+246T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56867948 | |||||||
| chr1:56868083 | G | A | 1 | a0005c0005t0002g0166 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.171+381G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868083 | |||||||
| chr1:56868086 | A | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
247 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.171+384A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868086 | |||||||
| chr1:56868412 | C | T | 2 | a0002c0002t0001g0138 a0002c0002t0001g0190 |
2 | HG02165.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.171+710C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868412 | |||||||
| chr1:56868482 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
235 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.171+780A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868482 | |||||||
| chr1:56868547 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.171+845G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868547 | |||||||
| chr1:56868595 | G | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(63): Show |
87 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.171+893G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868595 | |||||||
| chr1:56868735 | A | G | 1 | a0003c0003t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.171+1033A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868735 | |||||||
| chr1:56868738 | A | C | 2 | a0003c0003t0002g0217 a0019c0019t0001g0207 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.171+1036A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868738 | |||||||
| chr1:56868773 | C | T | 2 | a0003c0003t0002g0217 a0019c0019t0001g0207 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.171+1071C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868773 | |||||||
| chr1:56868883 | T | C | 1 | a0002c0002t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.171+1181T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56868883 | |||||||
| chr1:56869046 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.171+1344T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869046 | |||||||
| chr1:56869145 | T | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(63): Show |
87 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.171+1443T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869145 | |||||||
| chr1:56869201 | C | T | 6 | a0001c0001t0001g0046 a0007c0008t0001g0246 a0007c0008t0001g0256 others(3): Show |
7 | HG01346.hp2 HG01358.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+1499C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869201 | |||||||
| chr1:56869318 | G | T | 1 | a0001c0001t0001g0274 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.171+1616G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869318 | |||||||
| chr1:56869445 | T | C | 1 | a0002c0002t0001g0168 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.171+1743T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869445 | |||||||
| chr1:56869475 | A | G | 1 | a0003c0003t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.171+1773A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869475 | |||||||
| chr1:56869520 | G | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
347 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(344): Show |
intron_variant | MODIFIER | c.171+1818G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869520 | |||||||
| chr1:56869533 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0038 others(46): Show |
58 | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(55): Show |
intron_variant | MODIFIER | c.171+1831C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869533 | |||||||
| chr1:56869634 | G | A | 89 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0010 others(86): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.171+1932G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869634 | |||||||
| chr1:56869686 | G | C | 1 | a0006c0006t0001g0083 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.171+1984G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869686 | |||||||
| chr1:56869803 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(63): Show |
87 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.171+2101C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869803 | |||||||
| chr1:56869809 | C | T | 1 | a0003c0003t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.171+2107C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869809 | |||||||
| chr1:56869849 | C | T | 4 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0275 others(1): Show |
4 | HG01255.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+2147C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869849 | |||||||
| chr1:56869884 | A | G | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.171+2182A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869884 | |||||||
| chr1:56869908 | G | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(63): Show |
87 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.171+2206G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56869908 | |||||||
| chr1:56870078 | T | G | 2 | a0002c0002t0001g0150 a0002c0002t0001g0151 |
2 | NA18969.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.171+2376T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870078 | |||||||
| chr1:56870085 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.171+2383G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870085 | |||||||
| chr1:56870245 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.171+2543G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870245 | |||||||
| chr1:56870367 | G | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(71): Show |
95 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.171+2665G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870367 | |||||||
| chr1:56870405 | G | A | 4 | a0001c0001t0001g0038 a0001c0010t0001g0229 a0001c0010t0001g0260 others(1): Show |
5 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+2703G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870405 | |||||||
| chr1:56870581 | G | T | 89 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0010 others(86): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.171+2879G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870581 | |||||||
| chr1:56870670 | C | T | 1 | a0005c0005t0002g0111 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.171+2968C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870670 | |||||||
| chr1:56870681 | T | TAAATTAA others(6): Show |
1 | a0001c0001t0001g0271 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.171+2979_171+2980i others(15): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870681 | |||||||
| chr1:56870681 | T | TAAATTAA others(16): Show |
5 | a0001c0001t0001g0107 a0001c0001t0001g0215 a0003c0003t0002g0276 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+2979_171+2980i others(25): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870681 | |||||||
| chr1:56870681 | T | TAAATTAA others(21): Show |
4 | a0001c0001t0001g0216 a0001c0001t0005g0214 a0003c0003t0002g0040 others(1): Show |
5 | HG03139.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+2979_171+2980i others(30): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870681 | |||||||
| chr1:56870681 | T | TAAATTAA others(26): Show |
1 | a0001c0001t0001g0066 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.171+2979_171+2980i others(35): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870681 | |||||||
| chr1:56870683 | T | TAAA | 11 | a0001c0001t0001g0066 a0001c0001t0001g0107 a0001c0001t0001g0215 others(8): Show |
12 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+2981_171+2982i others(5): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870683 | |||||||
| chr1:56870685 | C | T | 11 | a0001c0001t0001g0066 a0001c0001t0001g0107 a0001c0001t0001g0215 others(8): Show |
12 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+2983C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870685 | |||||||
| chr1:56870686 | G | A | 11 | a0001c0001t0001g0066 a0001c0001t0001g0107 a0001c0001t0001g0215 others(8): Show |
12 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+2984G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870686 | |||||||
| chr1:56870687 | T | A | 11 | a0001c0001t0001g0066 a0001c0001t0001g0107 a0001c0001t0001g0215 others(8): Show |
12 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+2985T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870687 | |||||||
| chr1:56870725 | T | C | 1 | a0002c0002t0001g0169 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.171+3023T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870725 | |||||||
| chr1:56870849 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.171+3147A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870849 | |||||||
| chr1:56870887 | G | T | 3 | a0002c0002t0001g0140 a0002c0002t0001g0141 a0002c0002t0001g0142 |
3 | HG02738.hp1 HG03834.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.171+3185G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56870887 | |||||||
| chr1:56871015 | C | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0113 |
3 | NA18961.hp2 NA18965.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.171+3313C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871015 | |||||||
| chr1:56871038 | C | T | 1 | a0004c0004t0001g0245 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.171+3336C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871038 | |||||||
| chr1:56871070 | A | G | 1 | a0001c0001t0001g0025 | 2 | NA18969.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.171+3368A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871070 | |||||||
| chr1:56871102 | G | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(63): Show |
87 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.171+3400G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871102 | |||||||
| chr1:56871157 | G | A | 1 | a0002c0002t0001g0170 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.171+3455G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871157 | |||||||
| chr1:56871197 | G | A | 1 | a0003c0003t0002g0196 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.171+3495G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871197 | |||||||
| chr1:56871317 | C | T | 1 | a0001c0001t0001g0025 | 2 | NA18969.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.171+3615C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871317 | |||||||
| chr1:56871462 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(68): Show |
92 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.172-3487G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871462 | |||||||
| chr1:56871877 | T | A | 1 | a0017c0020t0005g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.172-3072T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871877 | |||||||
| chr1:56871924 | T | C | 2 | a0001c0001t0005g0214 a0006c0006t0001g0213 |
2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.172-3025T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56871924 | |||||||
| chr1:56872087 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.172-2862T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872087 | |||||||
| chr1:56872284 | C | T | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.172-2665C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872284 | |||||||
| chr1:56872357 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.172-2592G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872357 | |||||||
| chr1:56872380 | T | C | 1 | a0002c0002t0001g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.172-2569T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872380 | |||||||
| chr1:56872409 | A | G | 1 | a0002c0002t0001g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.172-2540A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872409 | |||||||
| chr1:56872448 | A | T | 1 | a0001c0001t0001g0133 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.172-2501A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872448 | |||||||
| chr1:56872549 | T | C | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-2400T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872549 | |||||||
| chr1:56872559 | G | A | 2 | a0004c0004t0001g0230 a0004c0004t0001g0231 |
2 | HG00280.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.172-2390G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872559 | |||||||
| chr1:56872905 | A | AAAAG | 10 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0055 others(7): Show |
13 | HG00423.hp1 HG00735.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.172-2032_172-2029d others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 56872905 | ||||||
| chr1:56872905 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.172-2044A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872905 | |||||||
| chr1:56872972 | G | A | 2 | a0001c0001t0005g0214 a0006c0006t0001g0213 |
2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.172-1977G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56872972 | |||||||
| chr1:56873055 | A | G | 4 | a0001c0001t0001g0271 a0003c0003t0002g0276 a0003c0003t0002g0277 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1894A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873055 | |||||||
| chr1:56873212 | A | G | 6 | a0002c0002t0001g0145 a0002c0002t0001g0146 a0002c0002t0001g0147 others(3): Show |
6 | HG00558.hp1 HG02273.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1737A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873212 | |||||||
| chr1:56873252 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.172-1697T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873252 | |||||||
| chr1:56873320 | C | T | 2 | a0013c0022t0002g0218 a0018c0021t0001g0068 |
2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.172-1629C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873320 | |||||||
| chr1:56873361 | A | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
179 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.172-1588A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873361 | |||||||
| chr1:56873458 | C | G | 1 | a0002c0002t0001g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.172-1491C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873458 | |||||||
| chr1:56873487 | T | C | 1 | a0001c0001t0003g0073 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.172-1462T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873487 | |||||||
| chr1:56873514 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0279 |
2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.172-1435G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873514 | |||||||
| chr1:56873612 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.172-1337C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873612 | |||||||
| chr1:56873614 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.172-1335C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873614 | |||||||
| chr1:56873774 | A | G | 11 | a0001c0001t0001g0066 a0001c0001t0001g0107 a0001c0001t0001g0215 others(8): Show |
12 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-1175A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873774 | |||||||
| chr1:56873907 | T | C | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.172-1042T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873907 | |||||||
| chr1:56873979 | C | A | 2 | a0001c0001t0001g0087 a0004c0004t0001g0039 |
3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.172-970C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56873979 | |||||||
| chr1:56874047 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(2): Show |
10 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.172-902C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874047 | |||||||
| chr1:56874186 | A | G | 4 | a0001c0001t0001g0066 a0001c0001t0005g0214 a0003c0003t0002g0040 others(1): Show |
5 | HG03490.hp1 HG03492.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-763A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874186 | |||||||
| chr1:56874299 | C | G | 5 | a0001c0001t0001g0227 a0001c0001t0001g0264 a0001c0001t0001g0265 others(2): Show |
5 | HG02886.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-650C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874299 | |||||||
| chr1:56874468 | G | A | 1 | a0019c0019t0001g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.172-481G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874468 | |||||||
| chr1:56874557 | G | A | 1 | a0005c0005t0002g0111 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.172-392G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874557 | |||||||
| chr1:56874610 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.172-339G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874610 | |||||||
| chr1:56874640 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.172-309T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874640 | |||||||
| chr1:56874660 | G | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0044 a0004c0004t0001g0243 others(2): Show |
8 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.172-289G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874660 | |||||||
| chr1:56874675 | G | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(10): Show |
24 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.172-274G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874675 | |||||||
| chr1:56874699 | C | G | 2 | a0003c0003t0002g0217 a0019c0019t0001g0207 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.172-250C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874699 | |||||||
| chr1:56874708 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(74): Show |
99 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.172-241A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874708 | |||||||
| chr1:56874802 | A | T | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(20): Show |
32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.172-147A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874802 | |||||||
| chr1:56874844 | C | A | 1 | a0003c0003t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.172-105C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874844 | |||||||
| chr1:56874873 | G | A | 4 | a0001c0001t0001g0066 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG01168.hp2 HG01433.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-76G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 2/10 | chr1 | 56874873 | |||||||
| chr1:56875101 | G | A | 5 | a0001c0001t0001g0038 a0001c0010t0001g0229 a0001c0010t0001g0260 others(2): Show |
6 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.316+8G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875101 | |||||||
| chr1:56875187 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(74): Show |
98 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.316+94G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875187 | |||||||
| chr1:56875199 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.316+106G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875199 | |||||||
| chr1:56875233 | A | G | 1 | a0003c0003t0002g0276 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.316+140A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875233 | |||||||
| chr1:56875367 | A | G | 1 | a0004c0004t0001g0268 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.316+274A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875367 | |||||||
| chr1:56875499 | A | T | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+406A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875499 | |||||||
| chr1:56875651 | T | C | 1 | a0002c0002t0001g0152 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.317-411T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875651 | |||||||
| chr1:56875731 | A | G | 1 | a0008c0007t0004g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.317-331A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875731 | |||||||
| chr1:56875952 | A | G | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-110A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875952 | |||||||
| chr1:56875972 | A | T | 2 | a0001c0001t0001g0087 a0004c0004t0001g0039 |
3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.317-90A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56875972 | |||||||
| chr1:56876036 | G | C | 1 | a0003c0003t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.317-26G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 3/10 | chr1 | 56876036 | |||||||
| chr1:56876220 | G | T | 1 | a0002c0002t0001g0164 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.464+11G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876220 | |||||||
| chr1:56876290 | G | C | 1 | a0002c0002t0001g0138 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.464+81G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876290 | |||||||
| chr1:56876445 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.464+236C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876445 | |||||||
| chr1:56876505 | C | T | 1 | a0002c0002t0001g0189 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.464+296C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876505 | |||||||
| chr1:56876523 | T | C | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+314T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876523 | |||||||
| chr1:56876749 | C | A | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(20): Show |
32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.464+540C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876749 | |||||||
| chr1:56876752 | T | G | 1 | a0002c0002t0001g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.464+543T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876752 | |||||||
| chr1:56876948 | C | T | 80 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0010 others(77): Show |
104 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.464+739C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56876948 | |||||||
| chr1:56877025 | T | C | 1 | a0015c0017t0002g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.464+816T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877025 | |||||||
| chr1:56877090 | T | G | 2 | a0002c0002t0001g0108 a0002c0002t0001g0109 |
2 | NA18979.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.464+881T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877090 | |||||||
| chr1:56877093 | A | C | 3 | a0003c0003t0002g0276 a0003c0003t0002g0277 a0003c0003t0002g0278 |
3 | HG02145.hp2 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464+884A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877093 | |||||||
| chr1:56877155 | C | A | 1 | a0008c0007t0004g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.464+946C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877155 | |||||||
| chr1:56877160 | A | G | 2 | a0001c0001t0001g0249 a0006c0006t0001g0045 |
3 | HG02895.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.464+951A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877160 | |||||||
| chr1:56877296 | G | T | 1 | a0001c0001t0001g0255 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.464+1087G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877296 | |||||||
| chr1:56877332 | C | T | 2 | a0003c0003t0002g0217 a0019c0019t0001g0207 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.464+1123C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877332 | |||||||
| chr1:56877583 | T | G | 89 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0010 others(86): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.464+1374T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877583 | |||||||
| chr1:56877643 | C | T | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+1434C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877643 | |||||||
| chr1:56877673 | G | A | 1 | a0003c0003t0002g0250 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.464+1464G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877673 | |||||||
| chr1:56877849 | A | G | 89 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0010 others(86): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.464+1640A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877849 | |||||||
| chr1:56877856 | C | A | 1 | a0001c0001t0001g0253 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.464+1647C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877856 | |||||||
| chr1:56877918 | A | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(2): Show |
10 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.464+1709A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56877918 | |||||||
| chr1:56878049 | C | T | 21 | a0002c0002t0001g0028 a0002c0002t0001g0033 a0002c0002t0001g0034 others(18): Show |
25 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.464+1840C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878049 | |||||||
| chr1:56878067 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.464+1858G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878067 | |||||||
| chr1:56878097 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
179 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.464+1888T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878097 | |||||||
| chr1:56878172 | T | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0047 others(11): Show |
22 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.464+1963T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878172 | |||||||
| chr1:56878178 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.464+1969C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878178 | |||||||
| chr1:56878224 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(74): Show |
99 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.464+2015C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878224 | |||||||
| chr1:56878353 | G | A | 2 | a0001c0001t0001g0087 a0004c0004t0001g0039 |
3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.464+2144G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878353 | |||||||
| chr1:56878371 | T | C | 4 | a0001c0001t0001g0066 a0001c0001t0005g0214 a0003c0003t0002g0040 others(1): Show |
5 | HG03490.hp1 HG03492.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+2162T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878371 | |||||||
| chr1:56878489 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(84): Show |
109 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.464+2280G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878489 | |||||||
| chr1:56878577 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.464+2368C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878577 | |||||||
| chr1:56878641 | A | G | 8 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0003c0003t0002g0017 others(5): Show |
10 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.464+2432A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878641 | |||||||
| chr1:56878702 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(84): Show |
109 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.464+2493T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878702 | |||||||
| chr1:56878717 | A | G | 1 | a0001c0010t0001g0261 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.464+2508A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878717 | |||||||
| chr1:56878738 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.464+2529G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56878738 | |||||||
| chr1:56879053 | C | T | 1 | a0005c0005t0002g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.465-2392C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879053 | |||||||
| chr1:56879137 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.465-2308G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879137 | |||||||
| chr1:56879178 | A | T | 2 | a0003c0003t0002g0217 a0019c0019t0001g0207 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.465-2267A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879178 | |||||||
| chr1:56879320 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.465-2125C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879320 | |||||||
| chr1:56879822 | A | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(74): Show |
99 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.465-1623A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879822 | |||||||
| chr1:56879941 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.465-1504G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56879941 | |||||||
| chr1:56880235 | T | C | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.465-1210T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880235 | |||||||
| chr1:56880267 | A | T | 1 | a0003c0003t0002g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.465-1178A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880267 | |||||||
| chr1:56880439 | GTAT | G | 13 | a0002c0002t0001g0033 a0002c0002t0001g0034 a0002c0002t0001g0171 others(10): Show |
14 | HG00423.hp2 HG02015.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.465-999_465-997del others(3): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 56880439 | ||||||
| chr1:56880462 | A | C | 1 | a0002c0002t0001g0191 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.465-983A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880462 | |||||||
| chr1:56880580 | T | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0279 |
2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.465-865T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880580 | |||||||
| chr1:56880741 | C | A | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.465-704C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880741 | |||||||
| chr1:56880867 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0062 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.465-578G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56880867 | |||||||
| chr1:56881161 | A | G | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.465-284A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56881161 | |||||||
| chr1:56881317 | C | T | 1 | a0002c0002t0001g0054 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.465-128C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56881317 | |||||||
| chr1:56881357 | A | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(44): Show |
66 | HG00408.hp2 HG01109.hp2 HG01243.hp2 others(63): Show |
intron_variant | MODIFIER | c.465-88A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 4/10 | chr1 | 56881357 | |||||||
| chr1:56881650 | G | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(48): Show |
70 | HG00408.hp2 HG01109.hp2 HG01243.hp2 others(67): Show |
intron_variant | MODIFIER | c.654+16G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56881650 | |||||||
| chr1:56881814 | A | T | 1 | a0007c0008t0001g0259 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.654+180A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56881814 | |||||||
| chr1:56882036 | A | C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(10): Show |
24 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.654+402A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882036 | |||||||
| chr1:56882061 | A | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0047 others(11): Show |
22 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.654+427A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882061 | |||||||
| chr1:56882194 | T | C | 1 | a0004c0004t0001g0039 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.654+560T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882194 | |||||||
| chr1:56882266 | A | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
293 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.654+632A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882266 | |||||||
| chr1:56882293 | C | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.654+659C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882293 | |||||||
| chr1:56882524 | TAGA | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0275 a0003c0003t0002g0221 |
3 | HG02280.hp1 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.654+897_654+899del others(3): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56882524 | ||||||
| chr1:56882561 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.655-920A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882561 | |||||||
| chr1:56882621 | G | T | 1 | a0003c0003t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.655-860G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882621 | |||||||
| chr1:56882650 | C | T | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(25): Show |
37 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.655-831C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882650 | |||||||
| chr1:56882727 | C | T | 1 | a0018c0021t0001g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.655-754C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882727 | |||||||
| chr1:56882754 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0044 a0004c0004t0001g0243 |
6 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.655-727C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882754 | |||||||
| chr1:56882763 | C | T | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(20): Show |
32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.655-718C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882763 | |||||||
| chr1:56882842 | A | T | 1 | a0001c0001t0001g0275 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.655-639A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56882842 | |||||||
| chr1:56882978 | A | ACAAGGCC others(17): Show |
4 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0003c0003t0002g0226 others(1): Show |
4 | HG02886.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-498_655-475dup others(24): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56882978 | ||||||
| chr1:56883223 | C | CTG | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(67): Show |
91 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.655-235_655-234dup others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56883223 | ||||||
| chr1:56883223 | C | CTGTG | 75 | a0001c0001t0001g0193 a0002c0002t0001g0001 a0002c0002t0001g0009 others(72): Show |
98 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.655-237_655-234dup others(4): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56883223 | ||||||
| chr1:56883223 | C | CTGTGTG | 6 | a0002c0002t0001g0028 a0002c0002t0001g0176 a0002c0002t0001g0177 others(3): Show |
7 | HG00738.hp1 HG01106.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-239_655-234dup others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56883223 | ||||||
| chr1:56883223 | CTG | C | 26 | a0001c0001t0001g0066 a0001c0001t0001g0087 a0001c0001t0001g0092 others(23): Show |
27 | HG01168.hp2 HG01192.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.655-235_655-234del others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 56883223 | ||||||
| chr1:56883297 | T | G | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-184T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56883297 | |||||||
| chr1:56883441 | C | G | 4 | a0001c0001t0001g0082 a0001c0010t0001g0229 a0001c0010t0001g0260 others(1): Show |
4 | HG02559.hp1 HG02615.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-40C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56883441 | |||||||
| chr1:56883445 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.655-36G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 5/10 | chr1 | 56883445 | |||||||
| chr1:56883707 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.855+26C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883707 | |||||||
| chr1:56883734 | A | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(73): Show |
98 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.855+53A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883734 | |||||||
| chr1:56883735 | C | T | 2 | a0012c0011t0001g0241 a0012c0011t0001g0242 |
2 | NA18939.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.855+54C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883735 | |||||||
| chr1:56883791 | T | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(73): Show |
98 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.855+110T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883791 | |||||||
| chr1:56883903 | T | C | 1 | a0002c0002t0001g0110 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.855+222T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883903 | |||||||
| chr1:56883910 | GC | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(74): Show |
99 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.855+237delC | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56883910 | ||||||
| chr1:56883941 | T | C | 90 | a0001c0001t0001g0193 a0002c0002t0001g0001 a0002c0002t0001g0009 others(87): Show |
115 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.855+260T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56883941 | |||||||
| chr1:56884061 | G | A | 1 | a0005c0005t0002g0166 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.855+380G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884061 | |||||||
| chr1:56884067 | T | TA | 7 | a0001c0001t0001g0082 a0001c0001t0001g0117 a0001c0001t0001g0135 others(4): Show |
7 | HG02698.hp1 HG03017.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.855+405dupA | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56884067 | ||||||
| chr1:56884067 | TA | T | 51 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0038 others(48): Show |
54 | HG00323.hp1 HG00673.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.855+405delA | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56884067 | ||||||
| chr1:56884067 | TAA | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0063 others(4): Show |
17 | HG00408.hp2 HG02015.hp1 HG02922.hp2 others(14): Show |
intron_variant | MODIFIER | c.855+404_855+405del others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56884067 | ||||||
| chr1:56884236 | G | A | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+555G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884236 | |||||||
| chr1:56884434 | T | G | 1 | a0003c0003t0002g0250 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.855+753T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884434 | |||||||
| chr1:56884482 | T | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(10): Show |
24 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.855+801T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884482 | |||||||
| chr1:56884832 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.856-1095G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884832 | |||||||
| chr1:56884950 | T | C | 1 | a0003c0003t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.856-977T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56884950 | |||||||
| chr1:56885062 | GAGA | G | 90 | a0001c0001t0001g0193 a0002c0002t0001g0001 a0002c0002t0001g0009 others(87): Show |
115 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.856-860_856-858del others(3): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885062 | ||||||
| chr1:56885070 | C | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(11): Show |
14 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.856-857C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885070 | |||||||
| chr1:56885149 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.856-778G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885149 | |||||||
| chr1:56885242 | G | T | 2 | a0001c0001t0001g0087 a0004c0004t0001g0039 |
3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.856-685G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885242 | |||||||
| chr1:56885269 | T | TATAAATA others(35): Show |
1 | a0001c0001t0001g0251 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.856-647_856-606dup others(42): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885269 | ||||||
| chr1:56885286 | A | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(73): Show |
98 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.856-641A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885286 | |||||||
| chr1:56885303 | TATATTTA others(5): Show |
T | 1 | a0001c0001t0001g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.856-619_856-608del others(12): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885303 | ||||||
| chr1:56885311 | C | A | 1 | a0001c0001t0001g0002 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.856-616C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885311 | |||||||
| chr1:56885312 | A | G | 12 | a0001c0001t0001g0066 a0001c0001t0001g0107 a0001c0001t0001g0215 others(9): Show |
13 | HG01123.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.856-615A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885312 | |||||||
| chr1:56885312 | ATAAATAT others(7): Show |
A | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-605_856-592del others(14): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885312 | ||||||
| chr1:56885315 | A | AAT | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
150 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.856-607_856-606dup others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | ||||||
| chr1:56885315 | A | AATATATA others(81): Show |
1 | a0001c0001t0001g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-606_856-605ins others(88): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | ||||||
| chr1:56885315 | A | AATATATA others(21): Show |
9 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0081 others(6): Show |
9 | HG01109.hp2 HG02109.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-606_856-605ins others(28): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | ||||||
| chr1:56885315 | A | AATATATA others(47): Show |
1 | a0001c0001t0001g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.856-606_856-605ins others(54): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | ||||||
| chr1:56885315 | A | AATATATA others(73): Show |
1 | a0015c0017t0002g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.856-606_856-605ins others(80): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | ||||||
| chr1:56885315 | A | AATATATA others(233): Show |
1 | a0001c0001t0001g0002 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.856-606_856-605ins others(240): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885315 | ||||||
| chr1:56885316 | A | ATATATAT others(101): Show |
1 | a0001c0001t0001g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.856-606_856-605ins others(108): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885316 | ||||||
| chr1:56885316 | A | ATATATAT others(17): Show |
3 | a0003c0003t0002g0041 a0006c0006t0001g0071 a0017c0020t0005g0267 |
4 | HG01891.hp1 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-606_856-605ins others(24): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885316 | ||||||
| chr1:56885316 | A | ATATATAT others(195): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0062 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.856-606_856-605ins others(202): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885316 | ||||||
| chr1:56885316 | ATATATTT others(47): Show |
A | 1 | a0002c0002t0001g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.856-586_856-533del others(54): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885316 | ||||||
| chr1:56885317 | T | TATATATT others(23): Show |
1 | a0001c0001t0001g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.856-606_856-605ins others(30): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885317 | ||||||
| chr1:56885325 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.856-602T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885325 | |||||||
| chr1:56885326 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.856-601T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885326 | |||||||
| chr1:56885326 | T | G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0234 a0001c0001t0001g0269 others(3): Show |
7 | HG02155.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-601T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885326 | |||||||
| chr1:56885341 | C | T | 5 | a0001c0001t0001g0087 a0008c0007t0004g0049 a0008c0007t0004g0051 others(2): Show |
5 | HG01192.hp1 HG02735.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.856-586C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885341 | |||||||
| chr1:56885342 | A | G | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(77): Show |
102 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.856-585A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885342 | |||||||
| chr1:56885342 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.856-585A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885342 | |||||||
| chr1:56885345 | AAT | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | NA18940.hp1 NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.856-575_856-574del others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885345 | ||||||
| chr1:56885346 | ATATATAT others(17): Show |
A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(68): Show |
93 | HG00323.hp1 HG00544.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.856-575_856-552del others(24): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885346 | ||||||
| chr1:56885348 | ATATATTT others(15): Show |
A | 2 | a0001c0001t0001g0131 a0008c0007t0004g0052 |
2 | HG00609.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.856-569_856-548del others(22): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885348 | ||||||
| chr1:56885354 | TTATGTAA others(59): Show |
T | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.856-569_856-504del others(66): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885354 | ||||||
| chr1:56885357 | T | C | 6 | a0001c0001t0001g0047 a0001c0001t0001g0087 a0008c0007t0004g0049 others(3): Show |
7 | HG01192.hp1 HG01891.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-570T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885357 | |||||||
| chr1:56885358 | G | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0010t0001g0229 others(2): Show |
6 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.856-569G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885358 | |||||||
| chr1:56885358 | G | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(183): Show |
242 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.856-569G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885358 | |||||||
| chr1:56885361 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.856-566A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885361 | |||||||
| chr1:56885363 | T | TTTACATA others(51): Show |
1 | a0001c0001t0001g0076 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.856-564_856-563ins others(58): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885363 | |||||||
| chr1:56885364 | ATATATT | A | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-553_856-548del others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885364 | ||||||
| chr1:56885365 | T | A | 1 | a0002c0002t0001g0010 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.856-562T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885365 | |||||||
| chr1:56885366 | AT | A | 3 | a0001c0001t0003g0205 a0001c0001t0003g0206 a0003c0003t0002g0080 |
3 | HG01109.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.856-560delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885366 | |||||||
| chr1:56885367 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.856-560T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885367 | |||||||
| chr1:56885370 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.856-557T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885370 | |||||||
| chr1:56885370 | T | TTACATAA others(3): Show |
7 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0062 others(4): Show |
8 | HG01891.hp1 HG02818.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-555_856-554ins others(10): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTACATAA others(57): Show |
1 | a0006c0006t0001g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.856-555_856-554ins others(64): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTATATTT others(9): Show |
1 | a0001c0001t0001g0264 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.856-548_856-533dup others(16): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTATATTT others(25): Show |
3 | a0002c0002t0001g0191 a0004c0004t0001g0230 a0004c0004t0001g0231 |
3 | HG00280.hp1 HG00558.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.856-528_856-497dup others(32): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTATATTT others(25): Show |
3 | a0001c0001t0001g0019 a0001c0001t0001g0077 a0015c0017t0002g0075 |
3 | HG02622.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.856-533_856-532ins others(32): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTATATTT others(301): Show |
1 | a0001c0001t0001g0061 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.856-533_856-532ins others(308): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTATATTT others(271): Show |
1 | a0001c0001t0001g0016 | 2 | NA18942.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.856-533_856-532ins others(278): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTATATTT others(207): Show |
1 | a0001c0001t0001g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.856-533_856-532ins others(214): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTATATTT others(239): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0225 others(1): Show |
10 | HG00408.hp2 NA18944.hp2 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.856-533_856-532ins others(246): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTATATTT others(271): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0112 |
4 | HG02015.hp1 NA18992.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-533_856-532ins others(278): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTATATTT others(271): Show |
1 | a0001c0001t0001g0060 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.856-533_856-532ins others(278): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTATATTT others(271): Show |
1 | a0001c0001t0001g0059 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.856-533_856-532ins others(278): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885370 | T | TTATATTT others(143): Show |
1 | a0001c0001t0001g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.856-533_856-532ins others(150): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885370 | ||||||
| chr1:56885373 | T | C | 7 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0128 others(4): Show |
7 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.856-554T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885373 | |||||||
| chr1:56885374 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.856-553A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885374 | |||||||
| chr1:56885374 | ATTTATT | A | 7 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0128 others(4): Show |
7 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.856-551_856-546del others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885374 | ||||||
| chr1:56885380 | T | A | 5 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 others(2): Show |
6 | HG02559.hp1 HG02615.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.856-547T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885380 | |||||||
| chr1:56885387 | T | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | NA18940.hp1 NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.856-540T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885387 | |||||||
| chr1:56885392 | TTAAATAA others(21): Show |
T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0003c0003t0002g0217 others(1): Show |
4 | HG01168.hp2 HG01433.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-532_856-505del others(28): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885392 | ||||||
| chr1:56885395 | A | AATAAATA others(57): Show |
3 | a0001c0001t0001g0265 a0003c0003t0002g0226 a0006c0006t0001g0263 |
3 | HG02976.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.856-501_856-500ins others(64): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885395 | ||||||
| chr1:56885395 | A | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
166 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.856-532A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885395 | |||||||
| chr1:56885395 | A | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG02559.hp1 NA18940.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-532A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885395 | |||||||
| chr1:56885396 | A | G | 9 | a0001c0001t0001g0103 a0001c0001t0001g0128 a0001c0001t0001g0129 others(6): Show |
9 | HG00621.hp1 HG02735.hp2 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.856-531A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885396 | |||||||
| chr1:56885396 | ATAAATAT others(21): Show |
A | 2 | a0001c0001t0001g0013 a0002c0002t0001g0028 |
3 | HG00423.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.856-516_856-489del others(28): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885396 | ||||||
| chr1:56885399 | AATATATA others(25): Show |
A | 1 | a0010c0012t0001g0200 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.856-523_856-492del others(32): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885399 | ||||||
| chr1:56885403 | T | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(70): Show |
95 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.856-524T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885403 | |||||||
| chr1:56885408 | TTATTTAA others(5): Show |
T | 29 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0066 others(26): Show |
32 | HG00642.hp2 HG00673.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.856-499_856-488del others(12): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885408 | ||||||
| chr1:56885411 | T | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | NA18940.hp1 NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.856-516T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885411 | |||||||
| chr1:56885412 | T | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | NA18940.hp1 NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.856-515T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885412 | |||||||
| chr1:56885417 | TATATATT others(55): Show |
T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | NA18940.hp1 NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.856-503_856-442del others(62): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885417 | ||||||
| chr1:56885424 | T | TTACGTAA others(15): Show |
1 | a0008c0007t0004g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.856-501_856-500ins others(22): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885424 | ||||||
| chr1:56885427 | A | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
94 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.856-500A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885427 | |||||||
| chr1:56885427 | AAT | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(6): Show |
10 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.856-493_856-492del others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885427 | ||||||
| chr1:56885428 | A | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
67 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.856-499A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885428 | |||||||
| chr1:56885429 | T | TAAATATA others(23): Show |
1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.856-497_856-496ins others(30): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885429 | ||||||
| chr1:56885429 | T | TAAATATA others(23): Show |
9 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0003g0073 others(6): Show |
9 | HG01109.hp2 HG02109.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-497_856-496ins others(30): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885429 | ||||||
| chr1:56885429 | T | TAAATATA others(55): Show |
5 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0003c0003t0002g0017 others(2): Show |
6 | HG01243.hp2 HG02280.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.856-497_856-496ins others(62): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885429 | ||||||
| chr1:56885429 | T | TAAATATA others(55): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(2): Show |
10 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.856-497_856-496ins others(62): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885429 | ||||||
| chr1:56885431 | T | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
67 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.856-496T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885431 | |||||||
| chr1:56885433 | TATTTAAG others(39): Show |
T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
67 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.856-491_856-446del others(46): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885433 | ||||||
| chr1:56885439 | A | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(201): Show |
260 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.856-488A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885439 | |||||||
| chr1:56885440 | G | GTAAATAT others(29): Show |
1 | a0004c0004t0001g0007 | 2 | HG00408.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.856-475_856-440dup others(36): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885440 | ||||||
| chr1:56885441 | T | G | 2 | a0002c0002t0001g0189 a0008c0007t0004g0052 |
2 | HG03831.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.856-486T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885441 | |||||||
| chr1:56885443 | AAT | A | 35 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0066 others(32): Show |
38 | HG00642.hp2 HG00673.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.856-473_856-472del others(2): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885443 | ||||||
| chr1:56885458 | C | A | 1 | a0008c0007t0004g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.856-469C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885458 | |||||||
| chr1:56885460 | GTAAA | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.856-464_856-461del others(4): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885460 | ||||||
| chr1:56885467 | TATATTTA others(25): Show |
T | 25 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0066 others(22): Show |
28 | HG00642.hp2 HG00673.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.856-455_856-424del others(32): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885467 | ||||||
| chr1:56885475 | T | A | 1 | a0008c0007t0004g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.856-452T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885475 | |||||||
| chr1:56885476 | T | A | 1 | a0008c0007t0004g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.856-451T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885476 | |||||||
| chr1:56885490 | A | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(48): Show |
70 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.856-437A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885490 | |||||||
| chr1:56885492 | G | A | 1 | a0003c0003t0002g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.856-435G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885492 | |||||||
| chr1:56885499 | C | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(58): Show |
80 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.856-428C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885499 | |||||||
| chr1:56885555 | G | GT | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(81): Show |
107 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.856-363dupT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 56885555 | ||||||
| chr1:56885565 | G | T | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG01168.hp2 HG01433.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.856-362G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885565 | |||||||
| chr1:56885629 | G | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(11): Show |
14 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.856-298G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885629 | |||||||
| chr1:56885665 | C | T | 1 | a0002c0002t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.856-262C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885665 | |||||||
| chr1:56885772 | G | A | 10 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0055 others(7): Show |
13 | HG00423.hp1 HG00735.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.856-155G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885772 | |||||||
| chr1:56885815 | G | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(48): Show |
70 | HG00408.hp2 HG01109.hp2 HG01243.hp2 others(67): Show |
intron_variant | MODIFIER | c.856-112G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885815 | |||||||
| chr1:56885908 | C | T | 2 | a0003c0003t0002g0217 a0019c0019t0001g0207 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.856-19C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885908 | |||||||
| chr1:56885915 | G | A | 1 | a0018c0021t0001g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.856-12G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 6/10 | chr1 | 56885915 | |||||||
| chr1:56886270 | T | C | 4 | a0002c0002t0001g0009 a0002c0002t0001g0029 a0002c0002t0001g0054 others(1): Show |
7 | HG00280.hp2 HG00642.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096+103T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886270 | |||||||
| chr1:56886286 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1096+119T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886286 | |||||||
| chr1:56886313 | T | G | 1 | a0002c0002t0001g0010 | 3 | NA18943.hp1 NA18960.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1096+146T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886313 | |||||||
| chr1:56886415 | T | A | 3 | a0001c0001t0001g0005 a0001c0001t0003g0018 a0001c0001t0003g0072 |
7 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096+248T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886415 | |||||||
| chr1:56886520 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(73): Show |
98 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.1096+353C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886520 | |||||||
| chr1:56886600 | A | T | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+433A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886600 | |||||||
| chr1:56886625 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1096+458C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886625 | |||||||
| chr1:56886681 | A | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(83): Show |
108 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1096+514A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886681 | |||||||
| chr1:56886876 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1096+709G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886876 | |||||||
| chr1:56886998 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1096+831A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56886998 | |||||||
| chr1:56887084 | T | A | 1 | a0001c0001t0001g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1096+917T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887084 | |||||||
| chr1:56887183 | A | G | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+1016A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887183 | |||||||
| chr1:56887321 | C | A | 2 | a0002c0002t0001g0138 a0002c0002t0001g0190 |
2 | HG02165.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1096+1154C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887321 | |||||||
| chr1:56887321 | C | T | 4 | a0001c0001t0001g0087 a0002c0002t0001g0148 a0002c0002t0001g0149 others(1): Show |
5 | HG01192.hp1 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+1154C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887321 | |||||||
| chr1:56887469 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1096+1302T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887469 | |||||||
| chr1:56887664 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1096+1497C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887664 | |||||||
| chr1:56887738 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1096+1571G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887738 | |||||||
| chr1:56887829 | T | C | 2 | a0001c0001t0001g0087 a0004c0004t0001g0039 |
3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1096+1662T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887829 | |||||||
| chr1:56887848 | C | T | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1096+1681C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887848 | |||||||
| chr1:56887922 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1096+1755G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887922 | |||||||
| chr1:56887982 | G | A | 1 | a0008c0007t0004g0051 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1096+1815G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56887982 | |||||||
| chr1:56888049 | T | A | 1 | a0001c0001t0001g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1096+1882T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888049 | |||||||
| chr1:56888121 | T | A | 1 | a0003c0003t0002g0041 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1096+1954T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888121 | |||||||
| chr1:56888162 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(83): Show |
108 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1096+1995C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888162 | |||||||
| chr1:56888175 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01168.hp2 HG01433.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1096+2008G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888175 | |||||||
| chr1:56888175 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1096+2008G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888175 | |||||||
| chr1:56888199 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2032T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888199 | |||||||
| chr1:56888325 | G | A | 1 | a0013c0022t0002g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1096+2158G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888325 | |||||||
| chr1:56888339 | T | G | 2 | a0011c0013t0002g0172 a0011c0013t0002g0173 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1096+2172T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888339 | |||||||
| chr1:56888400 | G | T | 2 | a0003c0003t0002g0217 a0019c0019t0001g0207 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1096+2233G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888400 | |||||||
| chr1:56888417 | T | G | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2250T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888417 | |||||||
| chr1:56888419 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2252G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888419 | |||||||
| chr1:56888421 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2254T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888421 | |||||||
| chr1:56888543 | A | G | 81 | a0001c0001t0001g0193 a0002c0002t0001g0001 a0002c0002t0001g0009 others(78): Show |
105 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1096+2376A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888543 | |||||||
| chr1:56888612 | A | C | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2445A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888612 | |||||||
| chr1:56888613 | C | A | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2446C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888613 | |||||||
| chr1:56888614 | A | C | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2447A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888614 | |||||||
| chr1:56888629 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1096+2462G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888629 | |||||||
| chr1:56888634 | A | T | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1096+2467A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888634 | |||||||
| chr1:56888782 | A | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
293 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.1096+2615A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56888782 | |||||||
| chr1:56889080 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2913G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889080 | |||||||
| chr1:56889082 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1096+2915T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889082 | |||||||
| chr1:56889128 | C | T | 5 | a0001c0001t0001g0232 a0004c0004t0001g0007 a0004c0004t0001g0240 others(2): Show |
8 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096+2961C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889128 | |||||||
| chr1:56889174 | T | C | 1 | a0002c0002t0001g0168 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1096+3007T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889174 | |||||||
| chr1:56889325 | A | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(48): Show |
70 | HG00408.hp2 HG01109.hp2 HG01243.hp2 others(67): Show |
intron_variant | MODIFIER | c.1096+3158A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889325 | |||||||
| chr1:56889396 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1096+3229G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889396 | |||||||
| chr1:56889484 | C | T | 1 | a0001c0001t0001g0013 | 3 | HG00423.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1096+3317C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889484 | |||||||
| chr1:56889489 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1096+3322G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889489 | |||||||
| chr1:56889509 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(74): Show |
99 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.1096+3342T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889509 | |||||||
| chr1:56889762 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0059 others(6): Show |
20 | HG00408.hp2 HG02015.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1096+3595C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889762 | |||||||
| chr1:56889797 | T | G | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+3630T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56889797 | |||||||
| chr1:56890175 | C | T | 7 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0003c0003t0002g0017 others(4): Show |
9 | HG01891.hp1 HG02280.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1096+4008C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890175 | |||||||
| chr1:56890259 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1096+4092C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890259 | |||||||
| chr1:56890290 | C | T | 7 | a0002c0002t0001g0028 a0002c0002t0001g0035 a0002c0002t0001g0036 others(4): Show |
10 | HG00438.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1096+4123C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890290 | |||||||
| chr1:56890551 | C | G | 1 | a0004c0004t0001g0231 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1096+4384C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890551 | |||||||
| chr1:56890605 | G | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(2): Show |
10 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1096+4438G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890605 | |||||||
| chr1:56890707 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1096+4540G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890707 | |||||||
| chr1:56890731 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1096+4564C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890731 | |||||||
| chr1:56890761 | T | C | 2 | a0001c0010t0001g0229 a0001c0010t0001g0260 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1096+4594T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890761 | |||||||
| chr1:56890796 | C | A | 1 | a0001c0018t0001g0120 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1096+4629C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890796 | |||||||
| chr1:56890802 | C | A | 1 | a0001c0001t0003g0205 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1096+4635C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890802 | |||||||
| chr1:56890803 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
174 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(171): Show |
intron_variant | MODIFIER | c.1096+4636A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890803 | |||||||
| chr1:56890822 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1096+4655C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890822 | |||||||
| chr1:56890907 | T | C | 35 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0074 others(32): Show |
37 | HG01109.hp2 HG01192.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.1096+4740T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56890907 | |||||||
| chr1:56891169 | A | G | 2 | a0001c0001t0001g0082 a0002c0002t0001g0202 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1096+5002A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891169 | |||||||
| chr1:56891220 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0095 others(16): Show |
24 | HG01123.hp2 HG01943.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.1096+5053T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891220 | |||||||
| chr1:56891362 | A | C | 1 | a0017c0020t0005g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1096+5195A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891362 | |||||||
| chr1:56891383 | G | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0137 a0004c0004t0001g0039 |
4 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+5216G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891383 | |||||||
| chr1:56891423 | A | G | 1 | a0002c0002t0001g0163 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1096+5256A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891423 | |||||||
| chr1:56891472 | T | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | NA18949.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1096+5305T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891472 | |||||||
| chr1:56891763 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1096+5596T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891763 | |||||||
| chr1:56891844 | G | C | 1 | a0004c0004t0001g0266 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1096+5677G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891844 | |||||||
| chr1:56891848 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1096+5681G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891848 | |||||||
| chr1:56891849 | G | C | 2 | a0003c0003t0002g0211 a0003c0003t0002g0217 |
2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1096+5682G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891849 | |||||||
| chr1:56891976 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG01074.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1096+5809T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891976 | |||||||
| chr1:56891986 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1096+5819G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56891986 | |||||||
| chr1:56892104 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1096+5937C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56892104 | |||||||
| chr1:56892165 | C | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0222 a0001c0001t0003g0233 |
4 | HG01255.hp2 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+5998C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56892165 | |||||||
| chr1:56892405 | G | C | 1 | a0012c0011t0001g0241 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1096+6238G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56892405 | |||||||
| chr1:56892485 | G | A | 2 | a0001c0001t0001g0087 a0004c0004t0001g0039 |
3 | HG01192.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1096+6318G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56892485 | |||||||
| chr1:56892496 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0137 a0004c0004t0001g0039 |
4 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+6329G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56892496 | |||||||
| chr1:56893120 | G | A | 8 | a0001c0001t0001g0087 a0001c0001t0001g0137 a0004c0004t0001g0039 others(5): Show |
9 | HG01192.hp1 HG02451.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096+6953G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893120 | |||||||
| chr1:56893212 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1096+7045T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893212 | |||||||
| chr1:56893488 | T | G | 31 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(28): Show |
40 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1096+7321T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893488 | |||||||
| chr1:56893554 | G | A | 1 | a0010c0012t0001g0174 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1096+7387G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893554 | |||||||
| chr1:56893628 | A | G | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(20): Show |
32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1096+7461A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893628 | |||||||
| chr1:56893642 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1096+7475T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893642 | |||||||
| chr1:56893645 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0137 a0004c0004t0001g0039 |
4 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+7478C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56893645 | |||||||
| chr1:56894056 | A | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0137 a0004c0004t0001g0039 others(5): Show |
9 | HG01192.hp1 HG02451.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096+7889A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894056 | |||||||
| chr1:56894120 | T | C | 1 | a0002c0002t0001g0157 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1096+7953T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894120 | |||||||
| chr1:56894144 | A | G | 1 | a0002c0002t0001g0170 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1096+7977A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894144 | |||||||
| chr1:56894182 | C | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0137 a0004c0004t0001g0039 others(5): Show |
9 | HG01192.hp1 HG02451.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096+8015C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894182 | |||||||
| chr1:56894255 | T | G | 87 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0193 others(84): Show |
112 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1096+8088T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894255 | |||||||
| chr1:56894259 | G | C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0137 a0004c0004t0001g0039 |
4 | HG01192.hp1 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+8092G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894259 | |||||||
| chr1:56894391 | T | C | 1 | a0008c0007t0004g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1096+8224T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894391 | |||||||
| chr1:56894413 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1096+8246A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894413 | |||||||
| chr1:56894635 | C | A | 1 | a0002c0002t0001g0187 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1096+8468C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894635 | |||||||
| chr1:56894660 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1096+8493A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894660 | |||||||
| chr1:56894772 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1096+8605C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894772 | |||||||
| chr1:56894777 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
325 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.1096+8610T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894777 | |||||||
| chr1:56894875 | G | C | 1 | a0019c0019t0001g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1096+8708G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894875 | |||||||
| chr1:56894966 | TAAC | T | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+8801_1096+880 others(7): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 56894966 | ||||||
| chr1:56894969 | C | A | 1 | a0003c0003t0002g0236 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1096+8802C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56894969 | |||||||
| chr1:56895170 | C | T | 2 | a0003c0003t0002g0196 a0003c0003t0002g0221 |
2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1096+9003C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56895170 | |||||||
| chr1:56895351 | T | C | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+9184T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56895351 | |||||||
| chr1:56895546 | A | T | 1 | a0002c0002t0001g0161 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1096+9379A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56895546 | |||||||
| chr1:56895820 | G | A | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1096+9653G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56895820 | |||||||
| chr1:56895940 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(4): Show |
12 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096+9773C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56895940 | |||||||
| chr1:56896004 | A | G | 1 | a0002c0002t0001g0160 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1096+9837A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896004 | |||||||
| chr1:56896229 | A | G | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+10062A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896229 | |||||||
| chr1:56896315 | A | T | 29 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(26): Show |
38 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1096+10148A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896315 | |||||||
| chr1:56896334 | T | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(67): Show |
92 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1096+10167T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896334 | |||||||
| chr1:56896361 | G | A | 1 | a0008c0007t0004g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1096+10194G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896361 | |||||||
| chr1:56896453 | T | C | 1 | a0003c0003t0002g0041 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1097-10214T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896453 | |||||||
| chr1:56896773 | G | A | 3 | a0001c0018t0001g0120 a0002c0002t0001g0150 a0002c0002t0001g0151 |
3 | NA18969.hp2 NA18973.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1097-9894G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896773 | |||||||
| chr1:56896948 | T | C | 1 | a0019c0019t0001g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1097-9719T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56896948 | |||||||
| chr1:56897025 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0044 a0004c0004t0001g0243 |
6 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1097-9642G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897025 | |||||||
| chr1:56897114 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(67): Show |
92 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1097-9553C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897114 | |||||||
| chr1:56897174 | A | G | 26 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0087 others(23): Show |
28 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1097-9493A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897174 | |||||||
| chr1:56897245 | G | A | 21 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0087 others(18): Show |
23 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1097-9422G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897245 | |||||||
| chr1:56897247 | G | A | 1 | a0018c0021t0001g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1097-9420G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897247 | |||||||
| chr1:56897287 | C | T | 2 | a0011c0013t0002g0172 a0011c0013t0002g0173 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1097-9380C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897287 | |||||||
| chr1:56897364 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(1): Show |
9 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1097-9303G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897364 | |||||||
| chr1:56897468 | G | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
200 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1097-9199G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897468 | |||||||
| chr1:56897491 | C | T | 1 | a0001c0001t0001g0025 | 2 | NA18969.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1097-9176C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897491 | |||||||
| chr1:56897536 | C | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(11): Show |
14 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1097-9131C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897536 | |||||||
| chr1:56897572 | T | C | 1 | a0019c0019t0001g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1097-9095T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897572 | |||||||
| chr1:56897663 | C | T | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-9004C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897663 | |||||||
| chr1:56897708 | G | A | 1 | a0004c0004t0001g0039 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1097-8959G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897708 | |||||||
| chr1:56897786 | G | A | 26 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0087 others(23): Show |
28 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1097-8881G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897786 | |||||||
| chr1:56897821 | T | C | 25 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0087 others(22): Show |
27 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1097-8846T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897821 | |||||||
| chr1:56897867 | G | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
90 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1097-8800G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56897867 | |||||||
| chr1:56898115 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1097-8552G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898115 | |||||||
| chr1:56898161 | T | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(1): Show |
9 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1097-8506T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898161 | |||||||
| chr1:56898255 | G | T | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-8412G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898255 | |||||||
| chr1:56898347 | G | C | 20 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0087 others(17): Show |
22 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1097-8320G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898347 | |||||||
| chr1:56898368 | C | T | 25 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(22): Show |
34 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1097-8299C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898368 | |||||||
| chr1:56898377 | G | A | 1 | a0002c0002t0001g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1097-8290G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898377 | |||||||
| chr1:56898382 | T | C | 1 | a0003c0003t0002g0278 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1097-8285T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898382 | |||||||
| chr1:56898455 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1097-8212C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898455 | |||||||
| chr1:56898635 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1097-8032T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898635 | |||||||
| chr1:56898717 | T | C | 1 | a0002c0002t0001g0177 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1097-7950T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898717 | |||||||
| chr1:56898764 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(4): Show |
12 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1097-7903G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898764 | |||||||
| chr1:56898766 | C | G | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-7901C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898766 | |||||||
| chr1:56898767 | T | A | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-7900T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898767 | |||||||
| chr1:56898772 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1097-7895G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898772 | |||||||
| chr1:56898805 | C | T | 1 | a0002c0002t0001g0036 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1097-7862C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898805 | |||||||
| chr1:56898808 | T | A | 3 | a0001c0001t0001g0077 a0001c0001t0003g0205 a0001c0001t0003g0206 |
3 | HG02717.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1097-7859T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898808 | |||||||
| chr1:56898893 | G | A | 2 | a0003c0003t0002g0211 a0003c0003t0002g0217 |
2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1097-7774G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898893 | |||||||
| chr1:56898934 | T | C | 1 | a0002c0002t0001g0150 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1097-7733T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898934 | |||||||
| chr1:56898942 | G | A | 20 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0087 others(17): Show |
22 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1097-7725G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56898942 | |||||||
| chr1:56899089 | C | T | 1 | a0002c0002t0001g0157 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1097-7578C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899089 | |||||||
| chr1:56899139 | G | A | 68 | a0001c0001t0001g0193 a0002c0002t0001g0001 a0002c0002t0001g0010 others(65): Show |
87 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1097-7528G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899139 | |||||||
| chr1:56899145 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1097-7522A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899145 | |||||||
| chr1:56899165 | A | G | 1 | a0002c0002t0001g0194 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1097-7502A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899165 | |||||||
| chr1:56899363 | A | G | 1 | a0004c0004t0001g0243 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1097-7304A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899363 | |||||||
| chr1:56899447 | T | G | 1 | a0005c0005t0002g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1097-7220T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899447 | |||||||
| chr1:56899572 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(5): Show |
13 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1097-7095G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899572 | |||||||
| chr1:56899592 | C | T | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-7075C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899592 | |||||||
| chr1:56899603 | G | C | 25 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0087 others(22): Show |
27 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1097-7064G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899603 | |||||||
| chr1:56899619 | G | A | 2 | a0001c0001t0001g0082 a0002c0002t0001g0202 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1097-7048G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899619 | |||||||
| chr1:56899642 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1097-7025C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899642 | |||||||
| chr1:56899808 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(22): Show |
41 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1097-6859T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56899808 | |||||||
| chr1:56900044 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1097-6623C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900044 | |||||||
| chr1:56900056 | G | A | 25 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0087 others(22): Show |
27 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1097-6611G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900056 | |||||||
| chr1:56900346 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0275 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1097-6321G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900346 | |||||||
| chr1:56900377 | C | T | 1 | a0018c0021t0001g0068 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1097-6290C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900377 | |||||||
| chr1:56900416 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(5): Show |
13 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1097-6251G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900416 | |||||||
| chr1:56900450 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1097-6217T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900450 | |||||||
| chr1:56900581 | C | T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0171 |
3 | NA18951.hp1 NA18971.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1097-6086C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900581 | |||||||
| chr1:56900639 | T | C | 3 | a0003c0003t0002g0041 a0003c0003t0002g0226 a0006c0006t0001g0071 |
4 | HG01891.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-6028T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900639 | |||||||
| chr1:56900644 | C | CATGAG | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.1097-6021_1097-602 others(9): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 56900644 | ||||||
| chr1:56900764 | C | T | 1 | a0015c0017t0002g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1097-5903C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900764 | |||||||
| chr1:56900770 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1097-5897C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900770 | |||||||
| chr1:56900818 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0222 a0001c0001t0003g0233 |
4 | HG01255.hp2 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-5849C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56900818 | |||||||
| chr1:56901195 | A | G | 20 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0087 others(17): Show |
22 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1097-5472A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901195 | |||||||
| chr1:56901276 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(5): Show |
13 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1097-5391G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901276 | |||||||
| chr1:56901288 | T | A | 2 | a0001c0001t0001g0082 a0002c0002t0001g0202 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1097-5379T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901288 | |||||||
| chr1:56901288 | T | G | 1 | a0001c0001t0001g0113 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1097-5379T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901288 | |||||||
| chr1:56901299 | G | A | 1 | a0002c0002t0001g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1097-5368G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901299 | |||||||
| chr1:56901318 | G | A | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-5349G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901318 | |||||||
| chr1:56901357 | G | T | 2 | a0013c0022t0002g0218 a0018c0021t0001g0068 |
2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1097-5310G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901357 | |||||||
| chr1:56901368 | T | A | 25 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0087 others(22): Show |
27 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1097-5299T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901368 | |||||||
| chr1:56901944 | A | G | 25 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0087 others(22): Show |
27 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1097-4723A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56901944 | |||||||
| chr1:56902027 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
325 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.1097-4640T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56902027 | |||||||
| chr1:56902134 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0060 |
4 | HG02071.hp2 HG02135.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1097-4533G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56902134 | |||||||
| chr1:56902378 | C | CT | 75 | a0001c0001t0001g0193 a0002c0002t0001g0001 a0002c0002t0001g0010 others(72): Show |
95 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1097-4283dupT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 56902378 | ||||||
| chr1:56902549 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
150 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1097-4118A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56902549 | |||||||
| chr1:56902584 | G | C | 1 | a0013c0022t0002g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1097-4083G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56902584 | |||||||
| chr1:56903121 | G | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
328 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.1097-3546G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903121 | |||||||
| chr1:56903130 | C | T | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-3537C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903130 | |||||||
| chr1:56903213 | C | G | 8 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1097-3454C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903213 | |||||||
| chr1:56903236 | GGTAATTT others(2): Show |
G | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-3430_1097-342 others(13): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903236 | |||||||
| chr1:56903383 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1097-3284C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903383 | |||||||
| chr1:56903442 | A | G | 1 | a0002c0002t0001g0170 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1097-3225A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903442 | |||||||
| chr1:56903500 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
328 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.1097-3167A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903500 | |||||||
| chr1:56903517 | C | T | 1 | a0001c0001t0005g0248 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1097-3150C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903517 | |||||||
| chr1:56903541 | C | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
201 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1097-3126C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903541 | |||||||
| chr1:56903773 | G | C | 1 | a0007c0008t0001g0259 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1097-2894G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903773 | |||||||
| chr1:56903865 | T | C | 8 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1097-2802T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903865 | |||||||
| chr1:56903982 | G | A | 1 | a0003c0003t0002g0088 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1097-2685G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903982 | |||||||
| chr1:56903984 | G | A | 1 | a0001c0001t0005g0214 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1097-2683G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56903984 | |||||||
| chr1:56904026 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1097-2641T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904026 | |||||||
| chr1:56904049 | T | C | 1 | a0008c0007t0004g0052 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1097-2618T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904049 | |||||||
| chr1:56904158 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1097-2509G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904158 | |||||||
| chr1:56904165 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1097-2502G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904165 | |||||||
| chr1:56904202 | G | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
228 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.1097-2465G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904202 | |||||||
| chr1:56904304 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1097-2363C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904304 | |||||||
| chr1:56904351 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1097-2316C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904351 | |||||||
| chr1:56904398 | T | C | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-2269T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904398 | |||||||
| chr1:56904479 | C | T | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-2188C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904479 | |||||||
| chr1:56904487 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1097-2180C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904487 | |||||||
| chr1:56904607 | G | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0235 |
4 | NA18950.hp2 NA18966.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1097-2060G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904607 | |||||||
| chr1:56904616 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0279 |
2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1097-2051G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904616 | |||||||
| chr1:56904644 | T | A | 29 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(26): Show |
38 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1097-2023T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904644 | |||||||
| chr1:56904726 | A | C | 1 | a0007c0008t0001g0246 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1097-1941A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904726 | |||||||
| chr1:56904762 | A | G | 77 | a0001c0001t0001g0193 a0002c0002t0001g0001 a0002c0002t0001g0010 others(74): Show |
98 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1097-1905A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904762 | |||||||
| chr1:56904917 | A | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0074 others(39): Show |
43 | HG01109.hp2 HG01192.hp1 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.1097-1750A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904917 | |||||||
| chr1:56904969 | G | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0279 |
2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1097-1698G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56904969 | |||||||
| chr1:56905055 | AT | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0272 a0003c0003t0002g0250 |
5 | HG00423.hp1 HG01346.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-1606delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 56905055 | ||||||
| chr1:56905171 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0223 |
3 | NA18943.hp2 NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1097-1496C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905171 | |||||||
| chr1:56905391 | T | C | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-1276T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905391 | |||||||
| chr1:56905460 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0058 others(22): Show |
41 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1097-1207T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905460 | |||||||
| chr1:56905638 | C | T | 2 | a0002c0002t0001g0138 a0002c0002t0001g0190 |
2 | HG02165.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1097-1029C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905638 | |||||||
| chr1:56905822 | T | C | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-845T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905822 | |||||||
| chr1:56905858 | T | G | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1097-809T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905858 | |||||||
| chr1:56905891 | C | G | 4 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 others(1): Show |
4 | HG02735.hp2 HG03669.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097-776C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56905891 | |||||||
| chr1:56906062 | C | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0076 others(11): Show |
14 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1097-605C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906062 | |||||||
| chr1:56906074 | T | C | 5 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0052 others(2): Show |
5 | HG02735.hp2 HG03669.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-593T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906074 | |||||||
| chr1:56906249 | G | A | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-418G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906249 | |||||||
| chr1:56906327 | T | C | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-340T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906327 | |||||||
| chr1:56906443 | T | C | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-224T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906443 | |||||||
| chr1:56906525 | T | C | 3 | a0001c0010t0001g0229 a0001c0010t0001g0260 a0001c0010t0001g0261 |
3 | HG02559.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-142T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 7/10 | chr1 | 56906525 | |||||||
| chr1:56906820 | A | G | 1 | a0002c0002t0001g0147 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1222+28A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56906820 | |||||||
| chr1:56906852 | C | T | 6 | a0001c0001t0001g0038 a0001c0001t0001g0222 a0001c0001t0003g0233 others(3): Show |
7 | HG01255.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+60C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56906852 | |||||||
| chr1:56906868 | AT | A | 4 | a0003c0003t0002g0017 a0003c0003t0002g0041 a0003c0003t0002g0226 others(1): Show |
6 | HG01891.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1222+84delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 56906868 | ||||||
| chr1:56906918 | C | T | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.1222+126C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56906918 | |||||||
| chr1:56907047 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1222+255A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907047 | |||||||
| chr1:56907120 | G | A | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(24): Show |
36 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1222+328G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907120 | |||||||
| chr1:56907124 | G | A | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(24): Show |
36 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1222+332G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907124 | |||||||
| chr1:56907132 | G | A | 1 | a0003c0003t0002g0236 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1222+340G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907132 | |||||||
| chr1:56907231 | G | T | 1 | a0002c0002t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1222+439G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907231 | |||||||
| chr1:56907244 | T | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(70): Show |
96 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1222+452T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907244 | |||||||
| chr1:56907251 | A | G | 1 | a0017c0020t0005g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1222+459A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907251 | |||||||
| chr1:56907275 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0003g0018 others(1): Show |
9 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222+483G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907275 | |||||||
| chr1:56907316 | C | T | 144 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(141): Show |
182 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.1222+524C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907316 | |||||||
| chr1:56907624 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02165.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1223-332G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907624 | |||||||
| chr1:56907666 | A | ATGAG | 7 | a0002c0002t0001g0184 a0003c0003t0002g0088 a0003c0003t0002g0100 others(4): Show |
7 | HG01123.hp2 HG01943.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1223-286_1223-283d others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 56907666 | ||||||
| chr1:56907806 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1223-150G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907806 | |||||||
| chr1:56907827 | GAGA | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0069 others(28): Show |
40 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1223-121_1223-119d others(5): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 56907827 | ||||||
| chr1:56907871 | T | C | 1 | a0002c0002t0001g0194 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1223-85T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 8/10 | chr1 | 56907871 | |||||||
| chr1:56908145 | G | A | 3 | a0005c0009t0002g0037 a0005c0009t0002g0203 a0013c0022t0002g0218 |
4 | HG01243.hp2 HG02486.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380+32G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908145 | |||||||
| chr1:56908327 | A | G | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1380+214A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908327 | |||||||
| chr1:56908332 | G | A | 2 | a0004c0004t0001g0237 a0004c0004t0001g0238 |
2 | NA18993.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1380+219G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908332 | |||||||
| chr1:56908474 | C | A | 1 | a0005c0005t0002g0180 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1380+361C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908474 | |||||||
| chr1:56908609 | T | C | 8 | a0003c0003t0002g0252 a0005c0009t0002g0037 a0005c0009t0002g0203 others(5): Show |
9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1380+496T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908609 | |||||||
| chr1:56908611 | C | T | 28 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(25): Show |
31 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1380+498C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908611 | |||||||
| chr1:56908623 | G | A | 1 | a0001c0001t0003g0233 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1380+510G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908623 | |||||||
| chr1:56908662 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1380+549C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908662 | |||||||
| chr1:56908843 | C | G | 5 | a0003c0003t0002g0252 a0008c0007t0004g0049 a0008c0007t0004g0051 others(2): Show |
5 | HG02145.hp1 HG02735.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+730C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908843 | |||||||
| chr1:56908861 | A | G | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
259 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.1380+748A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908861 | |||||||
| chr1:56908904 | C | T | 2 | a0003c0003t0002g0252 a0008c0007t0004g0052 |
2 | HG02145.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1380+791C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908904 | |||||||
| chr1:56908936 | T | C | 1 | a0001c0001t0005g0214 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1380+823T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56908936 | |||||||
| chr1:56909066 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1380+953C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909066 | |||||||
| chr1:56909080 | G | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0215 a0006c0006t0001g0045 others(5): Show |
12 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+967G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909080 | |||||||
| chr1:56909137 | A | G | 3 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 |
3 | HG02735.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1380+1024A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909137 | |||||||
| chr1:56909502 | T | G | 2 | a0001c0001t0001g0262 a0002c0002t0001g0209 |
2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1380+1389T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909502 | |||||||
| chr1:56909507 | A | T | 1 | a0002c0002t0001g0140 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1380+1394A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909507 | |||||||
| chr1:56909721 | TG | T | 3 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 |
3 | HG02735.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1380+1609delG | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909721 | |||||||
| chr1:56909723 | C | A | 3 | a0008c0007t0004g0049 a0008c0007t0004g0051 a0008c0007t0004g0053 |
3 | HG02735.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1380+1610C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909723 | |||||||
| chr1:56909756 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1380+1643C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909756 | |||||||
| chr1:56909847 | GA | G | 5 | a0003c0003t0002g0252 a0008c0007t0004g0049 a0008c0007t0004g0051 others(2): Show |
5 | HG02145.hp1 HG02735.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+1737delA | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56909847 | ||||||
| chr1:56909864 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1380+1751A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909864 | |||||||
| chr1:56909871 | G | A | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1380+1758G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909871 | |||||||
| chr1:56909883 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1380+1770T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909883 | |||||||
| chr1:56909937 | C | T | 1 | a0002c0002t0001g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1380+1824C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909937 | |||||||
| chr1:56909959 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0060 others(4): Show |
11 | HG02071.hp2 NA18947.hp1 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.1380+1846G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56909959 | |||||||
| chr1:56910045 | C | A | 76 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
98 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1380+1932C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910045 | |||||||
| chr1:56910163 | A | C | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1380+2050A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910163 | |||||||
| chr1:56910198 | G | A | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1380+2085G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910198 | |||||||
| chr1:56910377 | C | T | 28 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(25): Show |
31 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1381-2026C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910377 | |||||||
| chr1:56910410 | C | A | 1 | a0004c0004t0001g0237 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1381-1993C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910410 | |||||||
| chr1:56910611 | C | T | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-1792C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910611 | |||||||
| chr1:56910673 | G | T | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-1730G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910673 | |||||||
| chr1:56910674 | G | T | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-1729G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910674 | |||||||
| chr1:56910837 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1381-1566T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910837 | |||||||
| chr1:56910895 | G | C | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-1508G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910895 | |||||||
| chr1:56910995 | A | AT | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-1408_1381-140 others(5): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56910995 | |||||||
| chr1:56911065 | G | GT | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(148): Show |
200 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.1381-1322dupT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911065 | ||||||
| chr1:56911065 | G | GTT | 19 | a0001c0001t0001g0057 a0001c0001t0001g0081 a0001c0001t0001g0099 others(16): Show |
20 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1381-1323_1381-132 others(6): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911065 | ||||||
| chr1:56911065 | G | GTTTTTT | 13 | a0003c0003t0002g0017 a0003c0003t0002g0041 a0003c0003t0002g0080 others(10): Show |
15 | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1381-1327_1381-132 others(10): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911065 | ||||||
| chr1:56911065 | G | GTTTTTTT | 16 | a0003c0003t0002g0040 a0003c0003t0002g0088 a0003c0003t0002g0100 others(13): Show |
17 | HG01123.hp2 HG01943.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.1381-1328_1381-132 others(11): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911065 | ||||||
| chr1:56911065 | G | T | 1 | a0020c0015t0007g0050 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1381-1338G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911065 | |||||||
| chr1:56911065 | GT | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0137 a0001c0001t0001g0215 others(5): Show |
12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-1322delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911065 | ||||||
| chr1:56911067 | T | G | 1 | a0002c0002t0001g0147 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1381-1336T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911067 | |||||||
| chr1:56911232 | G | C | 2 | a0001c0001t0001g0234 a0001c0001t0001g0269 |
2 | HG02155.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1381-1171G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911232 | |||||||
| chr1:56911409 | A | C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0220 a0001c0001t0001g0275 |
3 | HG01192.hp1 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1381-994A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911409 | |||||||
| chr1:56911423 | C | T | 1 | a0019c0019t0001g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1381-980C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911423 | |||||||
| chr1:56911424 | G | A | 2 | a0011c0013t0002g0172 a0011c0013t0002g0173 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1381-979G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911424 | |||||||
| chr1:56911460 | C | T | 2 | a0001c0001t0001g0082 a0002c0002t0001g0202 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1381-943C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911460 | |||||||
| chr1:56911476 | C | G | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-927C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911476 | |||||||
| chr1:56911499 | T | C | 76 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
98 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1381-904T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911499 | |||||||
| chr1:56911573 | G | A | 1 | a0003c0003t0002g0236 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1381-830G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911573 | |||||||
| chr1:56911631 | A | G | 3 | a0006c0006t0001g0071 a0006c0006t0001g0270 a0018c0021t0001g0068 |
3 | HG03098.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1381-772A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911631 | |||||||
| chr1:56911650 | C | T | 1 | a0003c0003t0002g0221 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1381-753C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911650 | |||||||
| chr1:56911663 | A | G | 1 | a0017c0020t0005g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1381-740A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911663 | |||||||
| chr1:56911687 | T | G | 7 | a0001c0001t0001g0038 a0001c0001t0001g0074 a0001c0001t0001g0222 others(4): Show |
8 | HG01255.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1381-716T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911687 | |||||||
| chr1:56911695 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1381-708T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911695 | |||||||
| chr1:56911699 | A | G | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-704A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911699 | |||||||
| chr1:56911721 | T | C | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-682T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911721 | |||||||
| chr1:56911799 | T | C | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-604T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911799 | |||||||
| chr1:56911810 | GACA | G | 8 | a0003c0003t0002g0252 a0005c0009t0002g0037 a0005c0009t0002g0203 others(5): Show |
9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1381-586_1381-584d others(5): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 56911810 | ||||||
| chr1:56911824 | C | T | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-579C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911824 | |||||||
| chr1:56911853 | G | T | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-550G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911853 | |||||||
| chr1:56911906 | G | A | 76 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
98 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1381-497G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911906 | |||||||
| chr1:56911928 | A | G | 8 | a0003c0003t0002g0252 a0005c0009t0002g0037 a0005c0009t0002g0203 others(5): Show |
9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1381-475A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911928 | |||||||
| chr1:56911933 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1381-470C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911933 | |||||||
| chr1:56911974 | A | G | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-429A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911974 | |||||||
| chr1:56911993 | G | A | 8 | a0003c0003t0002g0252 a0005c0009t0002g0037 a0005c0009t0002g0203 others(5): Show |
9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1381-410G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911993 | |||||||
| chr1:56911997 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0275 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1381-406T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56911997 | |||||||
| chr1:56912019 | C | T | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-384C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912019 | |||||||
| chr1:56912095 | T | C | 1 | a0001c0001t0001g0013 | 3 | HG00423.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1381-308T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912095 | |||||||
| chr1:56912106 | G | C | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-297G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912106 | |||||||
| chr1:56912137 | C | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
314 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(311): Show |
intron_variant | MODIFIER | c.1381-266C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912137 | |||||||
| chr1:56912213 | C | T | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1381-190C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912213 | |||||||
| chr1:56912336 | G | A | 3 | a0005c0009t0002g0037 a0005c0009t0002g0203 a0013c0022t0002g0218 |
4 | HG01243.hp2 HG02486.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-67G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912336 | |||||||
| chr1:56912367 | C | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0123 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1381-36C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 9/10 | chr1 | 56912367 | |||||||
| chr1:56912661 | T | G | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+36T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56912661 | |||||||
| chr1:56912740 | T | C | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
314 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(311): Show |
intron_variant | MODIFIER | c.1603+115T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56912740 | |||||||
| chr1:56912782 | T | G | 9 | a0001c0001t0003g0018 a0001c0001t0003g0072 a0001c0001t0003g0073 others(6): Show |
10 | HG02615.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1603+157T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56912782 | |||||||
| chr1:56912842 | C | T | 1 | a0002c0002t0001g0108 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1603+217C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56912842 | |||||||
| chr1:56913005 | T | A | 8 | a0003c0003t0002g0252 a0005c0009t0002g0037 a0005c0009t0002g0203 others(5): Show |
9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1603+380T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913005 | |||||||
| chr1:56913025 | G | A | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+400G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913025 | |||||||
| chr1:56913064 | A | G | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+439A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913064 | |||||||
| chr1:56913131 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0228 |
2 | HG02280.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1603+506G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913131 | |||||||
| chr1:56913153 | A | T | 1 | a0005c0005t0002g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1603+528A>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913153 | |||||||
| chr1:56913178 | C | T | 5 | a0001c0001t0001g0012 a0002c0002t0001g0032 a0002c0002t0001g0177 others(2): Show |
8 | HG00733.hp2 HG00738.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+553C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913178 | |||||||
| chr1:56913197 | G | A | 1 | a0001c0001t0001g0047 | 2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1603+572G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913197 | |||||||
| chr1:56913292 | G | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0215 a0006c0006t0001g0045 others(5): Show |
12 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+667G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913292 | |||||||
| chr1:56913362 | T | C | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+737T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913362 | |||||||
| chr1:56913460 | C | A | 1 | a0002c0002t0001g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1603+835C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913460 | |||||||
| chr1:56913495 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1603+870G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913495 | |||||||
| chr1:56913651 | C | T | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+1026C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913651 | |||||||
| chr1:56913654 | A | G | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+1029A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913654 | |||||||
| chr1:56913658 | CTGTT | C | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+1037_1603+104 others(8): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 56913658 | ||||||
| chr1:56913691 | G | A | 5 | a0003c0003t0002g0252 a0008c0007t0004g0049 a0008c0007t0004g0051 others(2): Show |
5 | HG02145.hp1 HG02735.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1603+1066G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913691 | |||||||
| chr1:56913728 | T | C | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(64): Show |
90 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1603+1103T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913728 | |||||||
| chr1:56913756 | G | T | 28 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(25): Show |
31 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1603+1131G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913756 | |||||||
| chr1:56913966 | T | C | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+1341T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913966 | |||||||
| chr1:56913987 | G | T | 1 | a0020c0015t0007g0050 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1603+1362G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913987 | |||||||
| chr1:56913988 | C | T | 2 | a0001c0001t0001g0076 a0002c0002t0001g0149 |
2 | HG03486.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1603+1363C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913988 | |||||||
| chr1:56913999 | T | C | 114 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0025 others(111): Show |
140 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1603+1374T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56913999 | |||||||
| chr1:56914019 | C | T | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1603+1394C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914019 | |||||||
| chr1:56914061 | T | C | 21 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(18): Show |
25 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(22): Show |
intron_variant | MODIFIER | c.1603+1436T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914061 | |||||||
| chr1:56914084 | TAAG | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0042 others(14): Show |
23 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1603+1464_1603+146 others(7): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 56914084 | ||||||
| chr1:56914262 | G | A | 1 | a0002c0002t0001g0201 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1603+1637G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914262 | |||||||
| chr1:56914359 | C | T | 37 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(34): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+1734C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914359 | |||||||
| chr1:56914378 | G | T | 3 | a0003c0003t0002g0276 a0003c0003t0002g0277 a0003c0003t0002g0278 |
3 | HG02145.hp2 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1603+1753G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914378 | |||||||
| chr1:56914391 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0042 others(14): Show |
23 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1603+1766C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914391 | |||||||
| chr1:56914479 | T | C | 37 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(34): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+1854T>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914479 | |||||||
| chr1:56914620 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1603+1995A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914620 | |||||||
| chr1:56914734 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1603+2109A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914734 | |||||||
| chr1:56914768 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1603+2143G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914768 | |||||||
| chr1:56914786 | C | T | 37 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(34): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+2161C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914786 | |||||||
| chr1:56914787 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(78): Show |
110 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1603+2162G>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914787 | |||||||
| chr1:56914797 | C | A | 2 | a0001c0001t0001g0082 a0002c0002t0001g0202 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1603+2172C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914797 | |||||||
| chr1:56914886 | C | T | 37 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(34): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+2261C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914886 | |||||||
| chr1:56914953 | C | T | 37 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(34): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+2328C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56914953 | |||||||
| chr1:56914983 | CT | C | 37 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(34): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1603+2361delT | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 56914983 | ||||||
| chr1:56915179 | C | G | 5 | a0003c0003t0002g0252 a0008c0007t0004g0049 a0008c0007t0004g0051 others(2): Show |
5 | HG02145.hp1 HG02735.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1604-2386C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915179 | |||||||
| chr1:56915181 | A | C | 3 | a0001c0001t0003g0073 a0001c0001t0003g0205 a0001c0001t0003g0206 |
3 | HG02717.hp1 HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1604-2384A>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915181 | |||||||
| chr1:56915212 | A | G | 1 | a0003c0003t0002g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1604-2353A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915212 | |||||||
| chr1:56915291 | T | A | 37 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(34): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1604-2274T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915291 | |||||||
| chr1:56915312 | A | G | 36 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1604-2253A>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915312 | |||||||
| chr1:56915757 | T | G | 8 | a0003c0003t0002g0252 a0005c0009t0002g0037 a0005c0009t0002g0203 others(5): Show |
9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1604-1808T>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915757 | |||||||
| chr1:56915779 | C | T | 37 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(34): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1604-1786C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56915779 | |||||||
| chr1:56916060 | G | C | 1 | a0002c0002t0001g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1604-1505G>C | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916060 | |||||||
| chr1:56916060 | G | T | 4 | a0002c0002t0001g0009 a0002c0002t0001g0029 a0002c0002t0001g0054 others(1): Show |
7 | HG00280.hp2 HG00642.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1604-1505G>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916060 | |||||||
| chr1:56916231 | C | T | 2 | a0004c0004t0001g0230 a0004c0004t0001g0231 |
2 | HG00280.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1604-1334C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916231 | |||||||
| chr1:56916274 | C | T | 29 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(26): Show |
32 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.1604-1291C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916274 | |||||||
| chr1:56916790 | ACTCAGGC others(4): Show |
A | 8 | a0003c0003t0002g0252 a0005c0009t0002g0037 a0005c0009t0002g0203 others(5): Show |
9 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1604-773_1604-763d others(13): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 56916790 | ||||||
| chr1:56916869 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0215 a0006c0006t0001g0045 others(4): Show |
11 | HG02622.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1604-696C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916869 | |||||||
| chr1:56916880 | C | G | 37 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(34): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1604-685C>G | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916880 | |||||||
| chr1:56916897 | C | T | 37 | a0003c0003t0002g0017 a0003c0003t0002g0040 a0003c0003t0002g0041 others(34): Show |
41 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1604-668C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916897 | |||||||
| chr1:56916959 | T | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0228 others(3): Show |
10 | HG00323.hp2 HG00735.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1604-606T>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56916959 | |||||||
| chr1:56917045 | CTG | C | 17 | a0001c0001t0001g0216 a0004c0004t0001g0007 a0004c0004t0001g0039 others(14): Show |
21 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1604-516_1604-515d others(4): Show |
C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 56917045 | ||||||
| chr1:56917059 | C | A | 1 | a0002c0002t0001g0191 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1604-506C>A | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56917059 | |||||||
| chr1:56917072 | C | T | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
87 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.1604-493C>T | C8A | ENSG00000157131.12 | transcript | ENST00000361249.4 | protein_coding | 10/10 | chr1 | 56917072 |