Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 53630 |
| ensemblid | ENSG00000135697.10 |
| hgncid | 13815 |
| symbol | BCO1 |
| name | beta-carotene oxygenase 1 |
| refseq_nuc | NM_017429.3 |
| refseq_prot | NP_059125.2 |
| ensembl_nuc | ENST00000258168.7 |
| ensembl_prot | ENSP00000258168.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 81238689 |
| end | 81291142 |
| strand | + |
| ver | v1.2 |
| region | chr16:81238689-81291142 |
| region5000 | chr16:81233689-81296142 |
| regionname0 | BCO1_chr16_81238689_81291142 |
| regionname5000 | BCO1_chr16_81233689_81296142 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 547 | 263 | 80 | 40 | 113 | 4 | 24 | 82 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0002 | 0/0 | 547 | 68 | 8 | 22 | 22 | 8 | 8 | 16 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0003 | 0/0 | 547 | 55 | 1 | 10 | 30 | 5 | 9 | 20 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0004 | 0/0 | 547 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0005 | 0/0 | 547 | 3 | 0 | 1 | 1 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0006 | 0/0 | 547 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0007 | 0/0 | 547 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0008 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0009 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0010 | 0/0 | 547 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0011 | 0/0 | 547 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0012 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0013 | 0/0 | 547 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| a0014 | 0/0 | 547 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | MDIIF others(542): Show |
chr16 | 81233689 | 81296142 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1641 | 160 | 31 | 26 | 79 | 3 | 20 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0001c0002 | 0/0 | 1641 | 56 | 15 | 4 | 34 | 0 | 3 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0001c0005 | 0/0 | 1641 | 39 | 28 | 9 | 0 | 1 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0001c0007 | 0/0 | 1641 | 5 | 5 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0001c0011 | 0/1 | 1641 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0001c0017 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0001c0018 | 0/0 | 1641 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0002c0004 | 0/0 | 1641 | 45 | 3 | 14 | 20 | 5 | 3 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0002c0006 | 0/0 | 1641 | 21 | 4 | 8 | 2 | 3 | 4 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0002c0020 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0002c0022 | 0/0 | 1641 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0003c0003 | 0/0 | 1641 | 52 | 1 | 10 | 29 | 5 | 7 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0003c0009 | 0/0 | 1641 | 3 | 0 | 0 | 1 | 0 | 2 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0004c0008 | 0/0 | 1641 | 3 | 0 | 3 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0005c0010 | 0/0 | 1641 | 2 | 0 | 0 | 1 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0005c0024 | 0/0 | 1641 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0006c0014 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0006c0016 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0007c0023 | 0/0 | 1641 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0008c0015 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0009c0013 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0010c0019 | 0/0 | 1641 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0011c0021 | 0/0 | 1641 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0012c0012 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0013c0025 | 0/0 | 1641 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 | ||
| a0014c0026 | 0/0 | 1641 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | ATGGA others(1636): Show |
chr16 | 81233689 | 81296142 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2429 | 151 | 31 | 18 | 78 | 3 | 20 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0001c0001t0002 | 0/0 | 2429 | 9 | 0 | 8 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0001c0002t0001 | 0/0 | 2429 | 55 | 15 | 4 | 33 | 0 | 3 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0001c0002t0002 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0001c0005t0001 | 0/0 | 2429 | 39 | 28 | 9 | 0 | 1 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0001c0007t0001 | 0/0 | 2429 | 5 | 5 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0001c0011t0001 | 0/1 | 2429 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0001c0017t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0001c0018t0001 | 0/0 | 2429 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0002c0004t0001 | 0/0 | 2429 | 45 | 3 | 14 | 20 | 5 | 3 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0002c0006t0001 | 0/0 | 2429 | 21 | 4 | 8 | 2 | 3 | 4 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0002c0020t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0002c0022t0001 | 0/0 | 2429 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0003c0003t0001 | 0/0 | 2429 | 52 | 1 | 10 | 29 | 5 | 7 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0003c0009t0001 | 0/0 | 2429 | 3 | 0 | 0 | 1 | 0 | 2 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0004c0008t0001 | 0/0 | 2429 | 3 | 0 | 3 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0005c0010t0001 | 0/0 | 2429 | 2 | 0 | 0 | 1 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0005c0024t0001 | 0/0 | 2429 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0006c0014t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0006c0016t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0007c0023t0001 | 0/0 | 2429 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0008c0015t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0009c0013t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0010c0019t0001 | 0/0 | 2429 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0011c0021t0001 | 0/0 | 2429 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0012c0012t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0013c0025t0001 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| a0014c0026t0001 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | GTGAA others(2424): Show |
chr16 | 81233689 | 81296142 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0007t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0007t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0007t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0007t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0007t0001g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0011t0001g0060 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0017t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0018t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0020t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0022t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0009t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0009t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0009t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0004c0008t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0004c0008t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0004c0008t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0005c0010t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0005c0010t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0005c0024t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0006c0014t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0006c0016t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0007c0023t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0008c0015t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0009c0013t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0010c0019t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0011c0021t0001g0390 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0012c0012t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0013c0025t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0014c0026t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0001 | g0140 | EUR | GBR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00099 | hp2 | a0002 | c0006 | t0001 | g0311 | EUR | GBR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00140 | hp1 | a0002 | c0006 | t0001 | g0249 | EUR | GBR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0331 | EUR | GBR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | FIN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00280 | hp2 | a0001 | c0005 | t0001 | g0021 | EUR | FIN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00323 | hp1 | a0002 | c0004 | t0001 | g0111 | EUR | FIN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00323 | hp2 | a0007 | c0023 | t0001 | g0175 | EUR | FIN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00558 | hp2 | a0002 | c0004 | t0001 | g0146 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00597 | hp1 | a0002 | c0004 | t0001 | g0131 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00609 | hp1 | a0002 | c0004 | t0001 | g0056 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00609 | hp2 | a0002 | c0006 | t0001 | g0377 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0327 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00639 | hp2 | a0001 | c0005 | t0001 | g0118 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0315 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00733 | hp1 | a0001 | c0005 | t0001 | g0027 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0353 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00735 | hp2 | a0001 | c0018 | t0001 | g0275 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00738 | hp1 | a0002 | c0004 | t0001 | g0110 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00738 | hp2 | a0004 | c0008 | t0001 | g0055 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00741 | hp1 | a0004 | c0008 | t0001 | g0085 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00741 | hp2 | a0002 | c0004 | t0001 | g0109 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0007 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0007 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01074 | hp1 | a0002 | c0006 | t0001 | g0313 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01074 | hp2 | a0001 | c0005 | t0001 | g0022 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01081 | hp2 | a0002 | c0004 | t0001 | g0142 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01099 | hp1 | a0002 | c0004 | t0001 | g0093 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0389 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01106 | hp1 | a0005 | c0024 | t0001 | g0383 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01109 | hp1 | a0002 | c0004 | t0001 | g0082 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0106 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0308 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01167 | hp2 | a0002 | c0004 | t0001 | g0104 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01168 | hp1 | a0001 | c0005 | t0001 | g0023 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01169 | hp2 | a0002 | c0004 | t0001 | g0105 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0359 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01192 | hp1 | a0004 | c0008 | t0001 | g0097 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0378 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01243 | hp1 | a0001 | c0005 | t0001 | g0122 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0386 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01255 | hp1 | a0002 | c0006 | t0001 | g0310 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0375 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01256 | hp1 | a0002 | c0006 | t0001 | g0244 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01256 | hp2 | a0001 | c0005 | t0001 | g0024 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01257 | hp1 | a0002 | c0004 | t0001 | g0004 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0384 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01258 | hp1 | a0002 | c0004 | t0001 | g0004 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01258 | hp2 | a0001 | c0005 | t0001 | g0025 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01261 | hp1 | a0001 | c0005 | t0001 | g0026 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01346 | hp1 | a0002 | c0006 | t0001 | g0185 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0381 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01358 | hp1 | a0002 | c0004 | t0001 | g0141 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01358 | hp2 | a0002 | c0006 | t0001 | g0309 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01361 | hp1 | a0002 | c0006 | t0001 | g0388 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01361 | hp2 | a0002 | c0004 | t0001 | g0091 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01433 | hp1 | a0002 | c0004 | t0001 | g0034 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01433 | hp2 | a0001 | c0005 | t0001 | g0137 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0385 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0292 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01515 | hp1 | a0002 | c0004 | t0001 | g0048 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0321 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0323 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0008 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01517 | hp1 | a0002 | c0004 | t0001 | g0049 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0008 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0126 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0031 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0358 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0348 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0345 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0382 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01978 | hp2 | a0002 | c0004 | t0001 | g0143 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0371 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0367 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01993 | hp2 | a0002 | c0004 | t0001 | g0040 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02004 | hp2 | a0003 | c0003 | t0001 | g0302 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0335 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02027 | hp2 | a0003 | c0003 | t0001 | g0319 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02040 | hp1 | a0003 | c0003 | t0001 | g0334 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02055 | hp2 | a0002 | c0006 | t0001 | g0029 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0356 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0376 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02074 | hp1 | a0003 | c0003 | t0001 | g0159 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02083 | hp2 | a0002 | c0004 | t0001 | g0054 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02129 | hp2 | a0005 | c0010 | t0001 | g0096 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0227 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02145 | hp2 | a0001 | c0005 | t0001 | g0156 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02155 | hp1 | a0002 | c0004 | t0001 | g0083 | EAS | CDX | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0300 | EAS | CDX | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02257 | hp2 | a0002 | c0004 | t0001 | g0169 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02258 | hp2 | a0001 | c0005 | t0001 | g0121 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0028 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02293 | hp2 | a0002 | c0006 | t0001 | g0221 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02300 | hp1 | a0002 | c0006 | t0001 | g0151 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0374 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0032 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0124 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0201 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0322 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02602 | hp2 | a0001 | c0005 | t0001 | g0092 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0154 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0120 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02630 | hp1 | a0001 | c0007 | t0001 | g0391 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0312 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02698 | hp1 | a0005 | c0010 | t0001 | g0342 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0157 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02723 | hp2 | a0001 | c0005 | t0001 | g0113 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02738 | hp1 | a0002 | c0004 | t0001 | g0103 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0339 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0132 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0099 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02896 | hp1 | a0002 | c0004 | t0001 | g0010 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0123 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02897 | hp2 | a0002 | c0004 | t0001 | g0012 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02922 | hp1 | a0008 | c0015 | t0001 | g0155 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02965 | hp1 | a0009 | c0013 | t0001 | g0030 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02976 | hp2 | a0006 | c0014 | t0001 | g0098 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03041 | hp2 | a0002 | c0020 | t0001 | g0274 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03098 | hp1 | a0001 | c0007 | t0001 | g0149 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03098 | hp2 | a0002 | c0006 | t0001 | g0164 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03139 | hp1 | a0001 | c0007 | t0001 | g0163 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03195 | hp1 | a0001 | c0005 | t0001 | g0119 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0139 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0133 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0138 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0250 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03453 | hp1 | a0001 | c0007 | t0001 | g0234 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0357 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03490 | hp2 | a0010 | c0019 | t0001 | g0187 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03491 | hp1 | a0002 | c0004 | t0001 | g0135 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03491 | hp2 | a0003 | c0003 | t0001 | g0193 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0195 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03516 | hp1 | a0006 | c0016 | t0001 | g0011 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0116 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03540 | hp2 | a0001 | c0005 | t0001 | g0114 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0112 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03654 | hp2 | a0002 | c0006 | t0001 | g0248 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0128 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03688 | hp1 | a0002 | c0006 | t0001 | g0242 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03704 | hp1 | a0003 | c0003 | t0001 | g0238 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0365 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03831 | hp2 | a0003 | c0009 | t0001 | g0172 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03927 | hp2 | a0002 | c0006 | t0001 | g0247 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03942 | hp1 | a0002 | c0022 | t0001 | g0332 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04184 | hp1 | a0002 | c0004 | t0001 | g0081 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04184 | hp2 | a0011 | c0021 | t0001 | g0390 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04228 | hp2 | a0003 | c0009 | t0001 | g0089 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18522 | hp1 | a0012 | c0012 | t0001 | g0153 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0115 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18939 | hp2 | a0003 | c0003 | t0001 | g0333 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18940 | hp2 | a0003 | c0009 | t0001 | g0053 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18943 | hp1 | a0003 | c0003 | t0001 | g0338 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18945 | hp2 | a0002 | c0004 | t0001 | g0130 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0350 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0366 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18950 | hp2 | a0002 | c0004 | t0001 | g0094 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18952 | hp2 | a0002 | c0004 | t0001 | g0080 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18961 | hp1 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18961 | hp2 | a0013 | c0025 | t0001 | g0301 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0290 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0370 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18964 | hp2 | a0002 | c0004 | t0001 | g0033 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0291 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18968 | hp1 | a0002 | c0004 | t0001 | g0036 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0199 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18973 | hp1 | a0002 | c0004 | t0001 | g0051 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18975 | hp1 | a0002 | c0004 | t0001 | g0067 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18978 | hp2 | a0003 | c0003 | t0001 | g0368 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18982 | hp2 | a0002 | c0004 | t0001 | g0045 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18988 | hp1 | a0002 | c0004 | t0001 | g0100 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18989 | hp1 | a0003 | c0003 | t0001 | g0337 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18990 | hp1 | a0002 | c0006 | t0001 | g0363 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18993 | hp2 | a0003 | c0003 | t0001 | g0362 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18998 | hp2 | a0002 | c0004 | t0001 | g0107 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18999 | hp2 | a0002 | c0004 | t0001 | g0145 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0364 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0318 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19005 | hp1 | a0002 | c0004 | t0001 | g0068 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19009 | hp1 | a0003 | c0003 | t0001 | g0326 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0303 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0125 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19043 | hp1 | a0001 | c0007 | t0001 | g0200 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19043 | hp2 | a0001 | c0017 | t0001 | g0134 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19058 | hp2 | a0002 | c0004 | t0001 | g0052 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19062 | hp1 | a0002 | c0004 | t0001 | g0095 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0336 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19068 | hp1 | a0003 | c0003 | t0001 | g0387 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19070 | hp1 | a0002 | c0004 | t0001 | g0066 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19078 | hp1 | a0003 | c0003 | t0001 | g0245 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19087 | hp1 | a0014 | c0026 | t0001 | g0369 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0013 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0127 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ASW | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ASW | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0325 | EUR | TSI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20752 | hp2 | a0002 | c0006 | t0001 | g0314 | EUR | TSI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0379 | EUR | TSI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20805 | hp2 | a0002 | c0004 | t0001 | g0129 | EUR | TSI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0380 | SAS | GIH | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20905 | hp2 | a0002 | c0006 | t0001 | g0320 | SAS | GIH | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0144 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0117 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0152 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0014 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03471 | hp1 | a0002 | c0006 | t0001 | g0174 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | USA | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0392 | AFR | USA | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20300 | hp1 | a0002 | c0006 | t0001 | g0237 | AFR | USA | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0372 | AFR | USA | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA21309 | hp1 | a0001 | c0005 | t0001 | g0168 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| homoSapiens | chm13v2 | a0001 | c0011 | t0001 | g0060 | REF | REF | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0235 | REF | REF | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81259740 | C | G | 1 | a0014 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.258C>G | p.Asn86Lys | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/11 | 478/2429 | 258/1644 | 86/547 | chr16 | 81259740 | |||
| chr16:81262242 | A | G | 1 | a0013 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.430A>G | p.Ile144Val | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/11 | 650/2429 | 430/1644 | 144/547 | chr16 | 81262242 | |||
| chr16:81264700 | G | C | 1 | a0010 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.532G>C | p.Ala178Pro | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/11 | 752/2429 | 532/1644 | 178/547 | chr16 | 81264700 | |||
| chr16:81264736 | G | A | 1 | a0012 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.568G>A | p.Glu190Lys | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/11 | 788/2429 | 568/1644 | 190/547 | chr16 | 81264736 | |||
| chr16:81268089 | A | T | 3 | a0002 a0005 a0007 |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
missense_variant | MODERATE | c.801A>T | p.Arg267Ser | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/11 | 1021/2429 | 801/1644 | 267/547 | chr16 | 81268089 | |||
| chr16:81270294 | G | A | 1 | a0008 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.979G>A | p.Glu327Lys | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/11 | 1199/2429 | 979/1644 | 327/547 | chr16 | 81270294 | |||
| chr16:81280891 | C | T | 4 | a0003 a0005 a0011 others(1): Show |
60 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
missense_variant | MODERATE | c.1136C>T | p.Ala379Val | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/11 | 1356/2429 | 1136/1644 | 379/547 | chr16 | 81280891 | |||
| chr16:81285618 | G | C | 1 | a0011 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1286G>C | p.Ser429Thr | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/11 | 1506/2429 | 1286/1644 | 429/547 | chr16 | 81285618 | |||
| chr16:81290521 | G | A | 1 | a0009 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.1588G>A | p.Ala530Thr | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 11/11 | 1808/2429 | 1588/1644 | 530/547 | chr16 | 81290521 | |||
| chr16:81290543 | G | A | 1 | a0006 | 2 | HG02976.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.1610G>A | p.Arg537Lys | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 11/11 | 1830/2429 | 1610/1644 | 537/547 | chr16 | 81290543 | |||
| chr16:81290555 | G | A | 2 | a0004 a0007 |
4 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(1): Show |
missense_variant | MODERATE | c.1622G>A | p.Cys541Tyr | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 11/11 | 1842/2429 | 1622/1644 | 541/547 | chr16 | 81290555 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81245515 | T | C | 12 | a0001c0002 a0001c0005 a0001c0017 others(9): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
synonymous_variant | LOW | c.105T>C | p.Asn35Asn | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/11 | 325/2429 | 105/1644 | 35/547 | chr16 | 81245515 | |||
| chr16:81262175 | C | A | 1 | a0001c0018 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.363C>A | p.Thr121Thr | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/11 | 583/2429 | 363/1644 | 121/547 | chr16 | 81262175 | |||
| chr16:81264747 | G | A | 1 | a0002c0020 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.579G>A | p.Lys193Lys | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/11 | 799/2429 | 579/1644 | 193/547 | chr16 | 81264747 | |||
| chr16:81267966 | A | G | 5 | a0001c0005 a0001c0007 a0001c0017 others(2): Show |
47 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(44): Show |
synonymous_variant | LOW | c.678A>G | p.Pro226Pro | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/11 | 898/2429 | 678/1644 | 226/547 | chr16 | 81267966 | |||
| chr16:81270320 | C | T | 1 | a0001c0017 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1005C>T | p.Phe335Phe | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/11 | 1225/2429 | 1005/1644 | 335/547 | chr16 | 81270320 | |||
| chr16:81285598 | T | C | 1 | a0002c0022 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.1266T>C | p.Phe422Phe | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/11 | 1486/2429 | 1266/1644 | 422/547 | chr16 | 81285598 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81290719 | C | A | 2 | a0001c0001t0002 a0001c0002t0002 |
10 | HG01099.hp2 HG01255.hp2 HG01928.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*142C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 11/11 | 142 | chr16 | 81290719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81238991 | A | G | 1 | a0001c0001t0001g0392 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.64+19A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81238991 | |||||||
| chr16:81239020 | A | AT | 30 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0001t0001g0365 others(27): Show |
30 | HG00609.hp2 HG00621.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.64+62dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81239020 | ||||||
| chr16:81239020 | A | T | 2 | a0001c0007t0001g0391 a0011c0021t0001g0390 |
2 | HG02630.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.64+48A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239020 | |||||||
| chr16:81239020 | AT | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(124): Show |
130 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+62delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81239020 | ||||||
| chr16:81239020 | ATT | A | 15 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0017 others(12): Show |
15 | HG00735.hp1 HG01070.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+61_64+62delTT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81239020 | ||||||
| chr16:81239023 | T | A | 8 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0023 others(5): Show |
8 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+51T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239023 | |||||||
| chr16:81239025 | T | A | 11 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0017 others(8): Show |
11 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+53T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239025 | |||||||
| chr16:81239164 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.64+192C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239164 | |||||||
| chr16:81239178 | G | A | 8 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0023 others(5): Show |
8 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+206G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239178 | |||||||
| chr16:81239220 | T | C | 1 | a0003c0003t0001g0159 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.64+248T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239220 | |||||||
| chr16:81239276 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.64+304G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239276 | |||||||
| chr16:81239314 | G | T | 4 | a0001c0005t0001g0154 a0001c0005t0001g0156 a0001c0005t0001g0157 others(1): Show |
4 | HG02145.hp2 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+342G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239314 | |||||||
| chr16:81239444 | T | G | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(2): Show |
5 | HG02647.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+472T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239444 | |||||||
| chr16:81239465 | G | A | 3 | a0001c0002t0002g0035 a0002c0004t0001g0033 a0002c0004t0001g0034 |
3 | HG01433.hp1 HG02071.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.64+493G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239465 | |||||||
| chr16:81239546 | A | G | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64+574A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239546 | |||||||
| chr16:81239652 | C | T | 1 | a0001c0005t0001g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.64+680C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239652 | |||||||
| chr16:81239653 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.64+681G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239653 | |||||||
| chr16:81239903 | G | T | 2 | a0001c0005t0001g0031 a0001c0005t0001g0032 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.64+931G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239903 | |||||||
| chr16:81240264 | T | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(125): Show |
131 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.64+1292T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240264 | |||||||
| chr16:81240373 | C | G | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.64+1401C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240373 | |||||||
| chr16:81240396 | T | C | 2 | a0002c0006t0001g0029 a0002c0006t0001g0174 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.64+1424T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240396 | |||||||
| chr16:81240410 | A | C | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(2): Show |
5 | HG02647.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1438A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240410 | |||||||
| chr16:81240419 | C | T | 1 | a0003c0003t0001g0359 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.64+1447C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240419 | |||||||
| chr16:81240462 | T | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1490T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240462 | |||||||
| chr16:81240464 | C | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(151): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.64+1492C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240464 | |||||||
| chr16:81240594 | A | G | 1 | a0001c0002t0001g0147 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.64+1622A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240594 | |||||||
| chr16:81240631 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(65): Show |
72 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.64+1659G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240631 | |||||||
| chr16:81240780 | G | C | 10 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(7): Show |
10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+1808G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240780 | |||||||
| chr16:81240836 | A | AT | 372 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(369): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.64+1879dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81240836 | ||||||
| chr16:81240836 | A | ATT | 6 | a0001c0001t0002g0389 a0001c0002t0001g0017 a0001c0002t0001g0018 others(3): Show |
6 | HG00558.hp2 HG01099.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+1878_64+1879dup others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81240836 | ||||||
| chr16:81240871 | G | A | 1 | a0011c0021t0001g0390 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64+1899G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240871 | |||||||
| chr16:81240904 | G | T | 47 | a0001c0002t0001g0003 a0001c0002t0001g0124 a0001c0002t0001g0125 others(44): Show |
49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.64+1932G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240904 | |||||||
| chr16:81240973 | G | T | 10 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(7): Show |
10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+2001G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240973 | |||||||
| chr16:81241017 | T | A | 10 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(7): Show |
10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+2045T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241017 | |||||||
| chr16:81241045 | G | C | 1 | a0002c0004t0001g0033 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.64+2073G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241045 | |||||||
| chr16:81241052 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG01106.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.64+2080G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241052 | |||||||
| chr16:81241054 | A | G | 149 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(146): Show |
151 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.64+2082A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241054 | |||||||
| chr16:81241080 | C | A | 10 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(7): Show |
10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+2108C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241080 | |||||||
| chr16:81241081 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64+2109G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241081 | |||||||
| chr16:81241095 | G | A | 1 | a0002c0006t0001g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.64+2123G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241095 | |||||||
| chr16:81241114 | G | A | 10 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(7): Show |
10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+2142G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241114 | |||||||
| chr16:81241175 | A | G | 19 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(16): Show |
19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+2203A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241175 | |||||||
| chr16:81241200 | G | C | 1 | a0003c0003t0001g0238 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.64+2228G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241200 | |||||||
| chr16:81241215 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG00280.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.64+2243G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241215 | |||||||
| chr16:81241228 | A | G | 19 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(16): Show |
19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+2256A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241228 | |||||||
| chr16:81241268 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64+2296G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241268 | |||||||
| chr16:81241277 | T | C | 146 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(143): Show |
148 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.64+2305T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241277 | |||||||
| chr16:81241346 | C | A | 2 | a0001c0002t0001g0017 a0001c0002t0001g0018 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.64+2374C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241346 | |||||||
| chr16:81241417 | T | A | 1 | a0002c0006t0001g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.64+2445T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241417 | |||||||
| chr16:81241444 | G | A | 10 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(7): Show |
10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+2472G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241444 | |||||||
| chr16:81241454 | G | A | 19 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(16): Show |
19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+2482G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241454 | |||||||
| chr16:81241504 | C | T | 19 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(16): Show |
19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+2532C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241504 | |||||||
| chr16:81241583 | G | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2611G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241583 | |||||||
| chr16:81241629 | C | G | 3 | a0001c0005t0001g0031 a0001c0005t0001g0032 a0009c0013t0001g0030 |
3 | HG01884.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.64+2657C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241629 | |||||||
| chr16:81241663 | C | A | 127 | a0001c0002t0001g0003 a0001c0002t0001g0037 a0001c0002t0001g0038 others(124): Show |
129 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.64+2691C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241663 | |||||||
| chr16:81241668 | T | C | 5 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0002c0004t0001g0010 others(2): Show |
5 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2696T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241668 | |||||||
| chr16:81241677 | G | C | 146 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(143): Show |
148 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.64+2705G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241677 | |||||||
| chr16:81241796 | A | G | 158 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(155): Show |
160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.64+2824A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241796 | |||||||
| chr16:81241811 | A | G | 151 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(148): Show |
153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.64+2839A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241811 | |||||||
| chr16:81241852 | A | G | 5 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0002c0004t0001g0010 others(2): Show |
5 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2880A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241852 | |||||||
| chr16:81241854 | G | A | 2 | a0001c0005t0001g0112 a0001c0005t0001g0113 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.64+2882G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241854 | |||||||
| chr16:81241865 | T | G | 132 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(129): Show |
134 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.64+2893T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241865 | |||||||
| chr16:81242143 | T | A | 1 | a0001c0005t0001g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+3171T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242143 | |||||||
| chr16:81242150 | C | T | 3 | a0002c0004t0001g0109 a0002c0004t0001g0110 a0002c0004t0001g0111 |
3 | HG00323.hp1 HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.64+3178C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242150 | |||||||
| chr16:81242192 | C | CT | 34 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(31): Show |
35 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.64+3245dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81242192 | ||||||
| chr16:81242192 | CT | C | 130 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0243 others(127): Show |
132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.64+3245delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81242192 | ||||||
| chr16:81242192 | CTT | C | 18 | a0001c0001t0001g0165 a0001c0002t0001g0043 a0001c0002t0001g0044 others(15): Show |
18 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.64+3244_64+3245del others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81242192 | ||||||
| chr16:81242192 | CTTTTTTT | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0148 others(7): Show |
13 | HG02027.hp1 NA18612.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+3239_64+3245del others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81242192 | ||||||
| chr16:81242192 | CTTTTTTT others(5): Show |
C | 3 | a0002c0006t0001g0363 a0003c0003t0001g0362 a0003c0003t0001g0364 |
3 | NA18990.hp1 NA18993.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.64+3234_64+3245del others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81242192 | ||||||
| chr16:81242239 | G | A | 2 | a0001c0005t0001g0031 a0001c0005t0001g0032 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.65-3236G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242239 | |||||||
| chr16:81242261 | G | A | 1 | a0001c0005t0001g0112 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.65-3214G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242261 | |||||||
| chr16:81242370 | T | G | 6 | a0002c0006t0001g0185 a0002c0006t0001g0242 a0002c0006t0001g0247 others(3): Show |
6 | HG00140.hp1 HG01346.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-3105T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242370 | |||||||
| chr16:81242391 | G | A | 146 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(143): Show |
148 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.65-3084G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242391 | |||||||
| chr16:81242445 | T | C | 158 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(155): Show |
160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.65-3030T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242445 | |||||||
| chr16:81242461 | C | A | 1 | a0001c0001t0001g0166 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.65-3014C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242461 | |||||||
| chr16:81242466 | G | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0148 others(8): Show |
14 | HG02027.hp1 NA18612.hp1 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-3009G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242466 | |||||||
| chr16:81242493 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.65-2982G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242493 | |||||||
| chr16:81242505 | T | G | 2 | a0001c0005t0001g0031 a0001c0005t0001g0032 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.65-2970T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242505 | |||||||
| chr16:81242583 | A | C | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2892A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242583 | |||||||
| chr16:81242714 | T | A | 141 | a0001c0002t0001g0003 a0001c0002t0001g0037 a0001c0002t0001g0038 others(138): Show |
143 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.65-2761T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242714 | |||||||
| chr16:81242794 | C | T | 9 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0023 others(6): Show |
9 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-2681C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242794 | |||||||
| chr16:81242824 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.65-2651C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242824 | |||||||
| chr16:81242859 | G | A | 12 | a0001c0001t0001g0243 a0001c0001t0001g0252 a0001c0001t0001g0253 others(9): Show |
12 | HG01175.hp2 HG02080.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-2616G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242859 | |||||||
| chr16:81242938 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-2537G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242938 | |||||||
| chr16:81243003 | G | C | 1 | a0003c0003t0001g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.65-2472G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243003 | |||||||
| chr16:81243038 | A | T | 2 | a0002c0006t0001g0029 a0002c0006t0001g0174 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.65-2437A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243038 | |||||||
| chr16:81243127 | G | T | 128 | a0001c0002t0001g0003 a0001c0002t0001g0037 a0001c0002t0001g0038 others(125): Show |
130 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.65-2348G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243127 | |||||||
| chr16:81243171 | G | A | 1 | a0001c0002t0001g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.65-2304G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243171 | |||||||
| chr16:81243176 | A | G | 129 | a0001c0002t0001g0003 a0001c0002t0001g0037 a0001c0002t0001g0038 others(126): Show |
131 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.65-2299A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243176 | |||||||
| chr16:81243203 | C | T | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.65-2272C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243203 | |||||||
| chr16:81243210 | T | C | 129 | a0001c0002t0001g0003 a0001c0002t0001g0037 a0001c0002t0001g0038 others(126): Show |
131 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.65-2265T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243210 | |||||||
| chr16:81243246 | A | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0160 a0001c0001t0001g0239 others(62): Show |
67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.65-2229A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243246 | |||||||
| chr16:81243454 | A | ATCAT | 22 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0002t0001g0015 others(19): Show |
23 | HG00735.hp1 HG01070.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.65-1995_65-1992dup others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81243454 | ||||||
| chr16:81243454 | A | ATCATTCA others(1): Show |
112 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(109): Show |
113 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.65-1999_65-1992dup others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81243454 | ||||||
| chr16:81243454 | A | ATCATTCA others(5): Show |
22 | a0001c0002t0001g0003 a0001c0002t0001g0050 a0001c0002t0001g0357 others(19): Show |
23 | HG00323.hp1 HG00733.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.65-2003_65-1992dup others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81243454 | ||||||
| chr16:81243454 | A | ATCATTCA others(9): Show |
2 | a0001c0005t0001g0021 a0001c0005t0001g0022 |
2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.65-2007_65-1992dup others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81243454 | ||||||
| chr16:81243564 | G | A | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-1911G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243564 | |||||||
| chr16:81243574 | T | C | 2 | a0002c0006t0001g0029 a0002c0006t0001g0174 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.65-1901T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243574 | |||||||
| chr16:81243578 | C | T | 2 | a0002c0004t0001g0142 a0002c0004t0001g0143 |
2 | HG01081.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.65-1897C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243578 | |||||||
| chr16:81243582 | T | C | 157 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(154): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.65-1893T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243582 | |||||||
| chr16:81243658 | G | A | 3 | a0002c0004t0001g0051 a0002c0004t0001g0052 a0003c0009t0001g0053 |
3 | NA18940.hp2 NA18973.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.65-1817G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243658 | |||||||
| chr16:81243720 | C | T | 2 | a0001c0001t0001g0360 a0001c0001t0001g0361 |
2 | HG00621.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.65-1755C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243720 | |||||||
| chr16:81243906 | G | A | 1 | a0001c0002t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.65-1569G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243906 | |||||||
| chr16:81244032 | C | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0148 others(8): Show |
14 | HG02027.hp1 NA18612.hp1 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-1443C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244032 | |||||||
| chr16:81244137 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.65-1338G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244137 | |||||||
| chr16:81244179 | G | A | 148 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(145): Show |
150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.65-1296G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244179 | |||||||
| chr16:81244219 | A | C | 5 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0002c0004t0001g0010 others(2): Show |
5 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-1256A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244219 | |||||||
| chr16:81244255 | C | G | 151 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(148): Show |
153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.65-1220C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244255 | |||||||
| chr16:81244299 | C | G | 148 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(145): Show |
150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.65-1176C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244299 | |||||||
| chr16:81244355 | A | G | 127 | a0001c0002t0001g0003 a0001c0002t0001g0037 a0001c0002t0001g0038 others(124): Show |
129 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.65-1120A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244355 | |||||||
| chr16:81244407 | T | TAAAAAAT others(307): Show |
5 | a0002c0006t0001g0151 a0002c0006t0001g0237 a0002c0006t0001g0313 others(2): Show |
5 | HG01074.hp1 HG02300.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-1058_65-1057ins others(314): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244407 | ||||||
| chr16:81244407 | T | TAAAAAAT others(308): Show |
3 | a0002c0006t0001g0310 a0002c0006t0001g0311 a0005c0010t0001g0342 |
3 | HG00099.hp2 HG01255.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.65-1058_65-1057ins others(315): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244407 | ||||||
| chr16:81244407 | T | TAAAAAAT others(309): Show |
2 | a0002c0006t0001g0309 a0002c0006t0001g0388 |
2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.65-1058_65-1057ins others(316): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244407 | ||||||
| chr16:81244533 | T | C | 151 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(148): Show |
153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.65-942T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244533 | |||||||
| chr16:81244623 | T | C | 152 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(149): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.65-852T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244623 | |||||||
| chr16:81244635 | C | G | 9 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0023 others(6): Show |
9 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-840C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244635 | |||||||
| chr16:81244660 | C | T | 152 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(149): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.65-815C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244660 | |||||||
| chr16:81244661 | G | A | 1 | a0005c0024t0001g0383 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.65-814G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244661 | |||||||
| chr16:81244706 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65-769G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244706 | |||||||
| chr16:81244717 | C | CT | 19 | a0001c0001t0001g0307 a0001c0001t0001g0340 a0001c0001t0001g0341 others(16): Show |
19 | HG00738.hp2 HG01167.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.65-739dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244717 | ||||||
| chr16:81244717 | C | CTT | 117 | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0039 others(114): Show |
119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.65-740_65-739dupTT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244717 | ||||||
| chr16:81244717 | C | CTTT | 14 | a0001c0002t0001g0015 a0001c0002t0001g0046 a0001c0002t0001g0101 others(11): Show |
14 | HG00733.hp1 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.65-741_65-739dupTT others(1): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244717 | ||||||
| chr16:81244717 | CT | C | 20 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0188 others(17): Show |
20 | HG00639.hp1 HG00673.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.65-739delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244717 | ||||||
| chr16:81244737 | A | T | 1 | a0002c0004t0001g0100 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.65-738A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244737 | |||||||
| chr16:81244739 | T | A | 1 | a0002c0004t0001g0100 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.65-736T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244739 | |||||||
| chr16:81244752 | G | A | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-723G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244752 | |||||||
| chr16:81244767 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.65-708C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244767 | |||||||
| chr16:81244894 | T | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | NA18966.hp1 NA18973.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.65-581T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244894 | |||||||
| chr16:81244900 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.65-575G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244900 | |||||||
| chr16:81244913 | A | G | 3 | a0001c0002t0001g0150 a0001c0005t0001g0032 a0009c0013t0001g0030 |
3 | HG02280.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.65-562A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244913 | |||||||
| chr16:81244915 | A | T | 1 | a0003c0003t0001g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.65-560A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244915 | |||||||
| chr16:81244920 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG00558.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.65-555C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244920 | |||||||
| chr16:81244921 | G | A | 3 | a0001c0002t0001g0150 a0001c0005t0001g0032 a0009c0013t0001g0030 |
3 | HG02280.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.65-554G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244921 | |||||||
| chr16:81244956 | T | A | 152 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(149): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.65-519T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244956 | |||||||
| chr16:81244961 | G | A | 152 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(149): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.65-514G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244961 | |||||||
| chr16:81244965 | G | A | 149 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(146): Show |
151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.65-510G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244965 | |||||||
| chr16:81245013 | C | T | 152 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(149): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.65-462C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245013 | |||||||
| chr16:81245015 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.65-460C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245015 | |||||||
| chr16:81245016 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65-459G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245016 | |||||||
| chr16:81245079 | G | A | 3 | a0001c0002t0001g0150 a0001c0005t0001g0032 a0009c0013t0001g0030 |
3 | HG02280.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.65-396G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245079 | |||||||
| chr16:81245118 | C | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0179 others(7): Show |
13 | HG02027.hp1 NA18612.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-357C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245118 | |||||||
| chr16:81245258 | A | G | 1 | a0002c0006t0001g0185 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.65-217A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245258 | |||||||
| chr16:81245446 | G | A | 1 | a0009c0013t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.65-29G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245446 | |||||||
| chr16:81245773 | C | G | 152 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(149): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.193+170C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245773 | |||||||
| chr16:81245829 | A | G | 153 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(150): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.193+226A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245829 | |||||||
| chr16:81245849 | C | CT | 125 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(122): Show |
127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.193+272dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | ||||||
| chr16:81245849 | C | CTT | 16 | a0001c0001t0001g0009 a0001c0001t0001g0184 a0001c0001t0001g0224 others(13): Show |
17 | HG01169.hp1 HG01175.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.193+271_193+272dup others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | ||||||
| chr16:81245849 | CTTTTTT | C | 119 | a0001c0002t0001g0003 a0001c0002t0001g0037 a0001c0002t0001g0038 others(116): Show |
121 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.193+267_193+272del others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | ||||||
| chr16:81245849 | CTTTTTTT | C | 6 | a0001c0002t0001g0057 a0001c0005t0001g0119 a0001c0005t0001g0120 others(3): Show |
6 | HG00609.hp1 HG01243.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+266_193+272del others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | ||||||
| chr16:81245849 | CTTTTTTT others(1): Show |
C | 19 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(16): Show |
19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.193+265_193+272del others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | ||||||
| chr16:81245849 | CTTTTTTT others(3): Show |
C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+263_193+272del others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | ||||||
| chr16:81245877 | T | C | 151 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0016 others(148): Show |
153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.193+274T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245877 | |||||||
| chr16:81245917 | C | CA | 3 | a0002c0006t0001g0244 a0003c0003t0001g0008 a0003c0003t0001g0308 |
4 | HG01167.hp1 HG01256.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+316dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245917 | ||||||
| chr16:81245920 | T | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+317T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245920 | |||||||
| chr16:81245958 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.193+355G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245958 | |||||||
| chr16:81245982 | C | G | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193+379C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245982 | |||||||
| chr16:81246075 | C | G | 128 | a0001c0002t0001g0003 a0001c0002t0001g0037 a0001c0002t0001g0038 others(125): Show |
130 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.193+472C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246075 | |||||||
| chr16:81246080 | C | T | 4 | a0001c0001t0001g0251 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | NA18955.hp2 NA18966.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+477C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246080 | |||||||
| chr16:81246211 | C | G | 1 | a0001c0001t0001g0355 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.193+608C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246211 | |||||||
| chr16:81246260 | G | A | 10 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0023 others(7): Show |
10 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+657G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246260 | |||||||
| chr16:81246275 | A | G | 4 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0003c0003t0001g0300 others(1): Show |
4 | HG02155.hp2 NA18943.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+672A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246275 | |||||||
| chr16:81246335 | T | C | 46 | a0001c0001t0001g0220 a0001c0001t0001g0246 a0001c0001t0001g0251 others(43): Show |
46 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.193+732T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246335 | |||||||
| chr16:81246412 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.193+809G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246412 | |||||||
| chr16:81246418 | A | G | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+815A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246418 | |||||||
| chr16:81246453 | T | G | 1 | a0001c0001t0001g0317 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.193+850T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246453 | |||||||
| chr16:81246611 | GA | G | 133 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(130): Show |
135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.193+1009delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246611 | |||||||
| chr16:81246641 | G | A | 1 | a0002c0006t0001g0029 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.193+1038G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246641 | |||||||
| chr16:81246758 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.193+1155C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246758 | |||||||
| chr16:81246842 | C | T | 2 | a0002c0006t0001g0029 a0002c0006t0001g0174 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.193+1239C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246842 | |||||||
| chr16:81246850 | C | CA | 10 | a0001c0001t0001g0148 a0001c0001t0001g0192 a0001c0001t0001g0228 others(7): Show |
10 | HG01981.hp1 HG02280.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.193+1265dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | C | CAAA | 55 | a0001c0002t0001g0003 a0001c0002t0001g0057 a0001c0002t0001g0124 others(52): Show |
57 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.193+1263_193+1265d others(5): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | C | CAAAAAAA others(3): Show |
6 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(3): Show |
6 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+1256_193+1265d others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | C | CAAAAAAA others(4): Show |
1 | a0006c0016t0001g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.193+1255_193+1265d others(13): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | C | CAAAAAAA others(5): Show |
1 | a0001c0005t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193+1254_193+1265d others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | C | CAAAAAAA others(6): Show |
1 | a0002c0004t0001g0104 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.193+1253_193+1265d others(15): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | C | CAAAAAAA others(7): Show |
17 | a0001c0005t0001g0092 a0002c0004t0001g0036 a0002c0004t0001g0045 others(14): Show |
17 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+1252_193+1265d others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | C | CAAAAAAA others(8): Show |
24 | a0001c0001t0001g0254 a0001c0002t0001g0037 a0001c0002t0001g0044 others(21): Show |
24 | HG00323.hp1 HG00609.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.193+1251_193+1265d others(17): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | C | CAAAAAAA others(9): Show |
26 | a0001c0002t0001g0038 a0001c0002t0001g0039 a0001c0002t0001g0043 others(23): Show |
26 | HG00423.hp1 HG00438.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.193+1250_193+1265d others(18): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | C | CAAAAAAA others(10): Show |
6 | a0001c0002t0001g0061 a0001c0002t0001g0062 a0001c0002t0001g0063 others(3): Show |
6 | HG00438.hp1 HG01433.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+1249_193+1265d others(19): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | C | CAAAAAAA others(12): Show |
1 | a0001c0002t0001g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.193+1265_193+1266i others(21): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | CA | C | 15 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(12): Show |
15 | HG00280.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.193+1265delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246850 | CAA | C | 8 | a0001c0005t0001g0023 a0001c0005t0001g0024 a0001c0005t0001g0025 others(5): Show |
8 | HG00733.hp1 HG01168.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+1264_193+1265d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | ||||||
| chr16:81246866 | A | G | 2 | a0001c0001t0001g0354 a0003c0003t0001g0353 |
2 | HG00733.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.193+1263A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246866 | |||||||
| chr16:81246869 | G | A | 133 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(130): Show |
135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.193+1266G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246869 | |||||||
| chr16:81246982 | A | C | 150 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0015 others(147): Show |
152 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.193+1379A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246982 | |||||||
| chr16:81247008 | C | T | 8 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(5): Show |
8 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+1405C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247008 | |||||||
| chr16:81247009 | G | A | 1 | a0009c0013t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.193+1406G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247009 | |||||||
| chr16:81247028 | C | G | 1 | a0001c0005t0001g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.193+1425C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247028 | |||||||
| chr16:81247095 | A | G | 139 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0017 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.193+1492A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247095 | |||||||
| chr16:81247216 | G | A | 6 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0268 others(3): Show |
6 | HG01081.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+1613G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247216 | |||||||
| chr16:81247250 | C | T | 3 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0006c0016t0001g0011 |
3 | HG02559.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.193+1647C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247250 | |||||||
| chr16:81247251 | TCA | T | 5 | a0003c0003t0001g0333 a0003c0003t0001g0334 a0003c0003t0001g0335 others(2): Show |
5 | HG02015.hp2 HG02040.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+1649_193+1650d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247251 | |||||||
| chr16:81247275 | G | C | 8 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(5): Show |
8 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+1672G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247275 | |||||||
| chr16:81247292 | T | G | 137 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.193+1689T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247292 | |||||||
| chr16:81247355 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG00558.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.193+1752T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247355 | |||||||
| chr16:81247427 | C | T | 1 | a0009c0013t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.193+1824C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247427 | |||||||
| chr16:81247440 | G | A | 7 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(4): Show |
7 | HG02055.hp2 HG03098.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+1837G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247440 | |||||||
| chr16:81247468 | A | T | 1 | a0009c0013t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.193+1865A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247468 | |||||||
| chr16:81247532 | A | G | 1 | a0002c0006t0001g0151 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.193+1929A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247532 | |||||||
| chr16:81247557 | G | T | 2 | a0001c0005t0001g0137 a0001c0005t0001g0138 |
2 | HG01433.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.193+1954G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247557 | |||||||
| chr16:81247651 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.193+2048C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247651 | |||||||
| chr16:81247783 | C | T | 1 | a0001c0007t0001g0149 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193+2180C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247783 | |||||||
| chr16:81247822 | G | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+2219G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247822 | |||||||
| chr16:81247852 | T | A | 1 | a0001c0005t0001g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.193+2249T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247852 | |||||||
| chr16:81247881 | C | CCCACCAT | 12 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0023 others(9): Show |
12 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.193+2279_193+2280i others(9): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81247881 | ||||||
| chr16:81247937 | C | G | 1 | a0002c0004t0001g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.193+2334C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247937 | |||||||
| chr16:81247978 | T | G | 42 | a0001c0002t0001g0065 a0001c0002t0001g0084 a0001c0002t0001g0108 others(39): Show |
42 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.193+2375T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247978 | |||||||
| chr16:81248008 | G | A | 1 | a0010c0019t0001g0187 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.193+2405G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248008 | |||||||
| chr16:81248040 | A | T | 1 | a0001c0001t0001g0283 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.193+2437A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248040 | |||||||
| chr16:81248264 | G | A | 1 | a0001c0001t0001g0346 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.193+2661G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248264 | |||||||
| chr16:81248287 | C | G | 1 | a0001c0002t0001g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.193+2684C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248287 | |||||||
| chr16:81248337 | C | A | 159 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0015 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.193+2734C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248337 | |||||||
| chr16:81248357 | T | C | 148 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.193+2754T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248357 | |||||||
| chr16:81248366 | G | A | 144 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(141): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.193+2763G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248366 | |||||||
| chr16:81248390 | C | T | 159 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0015 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.193+2787C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248390 | |||||||
| chr16:81248405 | C | CA | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(195): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.193+2823dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | ||||||
| chr16:81248405 | C | CAA | 144 | a0001c0001t0001g0041 a0001c0001t0001g0161 a0001c0001t0001g0162 others(141): Show |
146 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.193+2822_193+2823d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | ||||||
| chr16:81248405 | C | CAAA | 20 | a0001c0002t0001g0057 a0001c0002t0001g0069 a0001c0002t0001g0070 others(17): Show |
20 | HG01243.hp1 HG01361.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.193+2821_193+2823d others(5): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | ||||||
| chr16:81248405 | C | CAAAAAAA others(1): Show |
8 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0023 others(5): Show |
8 | HG00280.hp2 HG01074.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+2816_193+2823d others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | ||||||
| chr16:81248405 | C | CAAAAAAA others(3): Show |
2 | a0001c0005t0001g0028 a0001c0005t0001g0032 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.193+2814_193+2823d others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | ||||||
| chr16:81248405 | C | CAAAAAAA others(5): Show |
1 | a0002c0006t0001g0029 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.193+2812_193+2823d others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | ||||||
| chr16:81248405 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0001g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193+2809_193+2823d others(17): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | ||||||
| chr16:81248405 | C | CAAAAAAA others(10): Show |
4 | a0001c0002t0001g0015 a0001c0005t0001g0013 a0001c0005t0001g0014 others(1): Show |
4 | HG02559.hp2 HG03516.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+2807_193+2823d others(19): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | ||||||
| chr16:81248405 | C | CAAAAAAA others(16): Show |
2 | a0002c0004t0001g0010 a0002c0004t0001g0012 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.193+2823_193+2824i others(25): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | ||||||
| chr16:81248499 | G | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+2896G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248499 | |||||||
| chr16:81248591 | A | C | 159 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0015 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.193+2988A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248591 | |||||||
| chr16:81248663 | T | C | 159 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0015 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.193+3060T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248663 | |||||||
| chr16:81248688 | C | T | 159 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0015 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.193+3085C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248688 | |||||||
| chr16:81248690 | G | T | 135 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(132): Show |
137 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.193+3087G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248690 | |||||||
| chr16:81248747 | C | G | 1 | a0001c0002t0001g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.193+3144C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248747 | |||||||
| chr16:81248774 | A | G | 159 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0015 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.193+3171A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248774 | |||||||
| chr16:81248778 | A | G | 159 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0015 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.193+3175A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248778 | |||||||
| chr16:81248801 | C | T | 1 | a0001c0005t0001g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.193+3198C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248801 | |||||||
| chr16:81248869 | G | A | 12 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0017 others(9): Show |
12 | HG00735.hp1 HG01070.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.193+3266G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248869 | |||||||
| chr16:81248938 | A | G | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+3335A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248938 | |||||||
| chr16:81248986 | T | G | 12 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0017 others(9): Show |
12 | HG00735.hp1 HG01070.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.193+3383T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248986 | |||||||
| chr16:81249006 | C | T | 12 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0017 others(9): Show |
12 | HG00735.hp1 HG01070.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.193+3403C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249006 | |||||||
| chr16:81249049 | C | A | 164 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(161): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.193+3446C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249049 | |||||||
| chr16:81249092 | C | CTT | 12 | a0001c0002t0001g0124 a0001c0005t0001g0021 a0001c0005t0001g0022 others(9): Show |
12 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.193+3504_193+3505d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249092 | ||||||
| chr16:81249092 | C | CTTT | 131 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.193+3503_193+3505d others(5): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249092 | ||||||
| chr16:81249092 | CT | C | 17 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0176 others(14): Show |
17 | HG00323.hp2 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.193+3505delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249092 | ||||||
| chr16:81249112 | A | ATGGAGTC others(18): Show |
1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193+3516_193+3540d others(27): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249112 | ||||||
| chr16:81249215 | G | T | 161 | a0001c0001t0001g0009 a0001c0001t0001g0254 a0001c0002t0001g0003 others(158): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.193+3612G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249215 | |||||||
| chr16:81249238 | A | G | 1 | a0001c0005t0001g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.193+3635A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249238 | |||||||
| chr16:81249239 | T | C | 2 | a0001c0001t0001g0378 a0001c0001t0001g0379 |
2 | HG01192.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.193+3636T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249239 | |||||||
| chr16:81249243 | A | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+3640A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249243 | |||||||
| chr16:81249257 | G | GT | 8 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0005t0001g0013 others(5): Show |
8 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+3663dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249257 | ||||||
| chr16:81249267 | C | CT | 5 | a0001c0001t0001g0009 a0001c0002t0001g0084 a0004c0008t0001g0055 others(2): Show |
6 | HG00738.hp2 HG00741.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+3671dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249267 | ||||||
| chr16:81249336 | A | G | 154 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0015 others(151): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.193+3733A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249336 | |||||||
| chr16:81249393 | A | G | 3 | a0001c0005t0001g0115 a0001c0005t0001g0117 a0001c0005t0001g0118 |
3 | HG00639.hp2 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.193+3790A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249393 | |||||||
| chr16:81249423 | A | T | 1 | a0001c0005t0001g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.193+3820A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249423 | |||||||
| chr16:81249458 | G | A | 1 | a0003c0003t0001g0339 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.193+3855G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249458 | |||||||
| chr16:81249481 | C | T | 1 | a0003c0003t0001g0250 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.193+3878C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249481 | |||||||
| chr16:81249502 | C | T | 1 | a0001c0002t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193+3899C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249502 | |||||||
| chr16:81249519 | A | G | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0228 others(1): Show |
4 | HG01978.hp1 HG01981.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+3916A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249519 | |||||||
| chr16:81249551 | C | T | 1 | a0001c0005t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193+3948C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249551 | |||||||
| chr16:81249552 | G | A | 1 | a0003c0003t0001g0345 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.193+3949G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249552 | |||||||
| chr16:81249575 | T | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+3972T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249575 | |||||||
| chr16:81249592 | G | C | 1 | a0002c0004t0001g0100 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.193+3989G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249592 | |||||||
| chr16:81249595 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.193+3992T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249595 | |||||||
| chr16:81249614 | C | T | 3 | a0001c0001t0001g0196 a0001c0018t0001g0275 a0010c0019t0001g0187 |
3 | HG00735.hp2 HG03239.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.193+4011C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249614 | |||||||
| chr16:81249692 | C | T | 5 | a0002c0004t0001g0056 a0002c0004t0001g0067 a0002c0004t0001g0080 others(2): Show |
5 | HG00609.hp1 HG02129.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+4089C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249692 | |||||||
| chr16:81249701 | G | A | 2 | a0002c0006t0001g0029 a0002c0006t0001g0174 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.193+4098G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249701 | |||||||
| chr16:81249706 | A | G | 1 | a0003c0003t0001g0331 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.193+4103A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249706 | |||||||
| chr16:81249717 | C | T | 156 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0015 others(153): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.193+4114C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249717 | |||||||
| chr16:81249727 | T | C | 156 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0015 others(153): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.193+4124T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249727 | |||||||
| chr16:81249784 | C | A | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+4181C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249784 | |||||||
| chr16:81249800 | G | C | 1 | a0002c0004t0001g0169 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.193+4197G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249800 | |||||||
| chr16:81249839 | G | T | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+4236G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249839 | |||||||
| chr16:81249971 | G | A | 1 | a0002c0004t0001g0091 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.193+4368G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249971 | |||||||
| chr16:81249993 | A | G | 155 | a0001c0001t0001g0254 a0001c0001t0001g0346 a0001c0002t0001g0003 others(152): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.193+4390A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249993 | |||||||
| chr16:81250022 | C | T | 1 | a0003c0003t0001g0008 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.193+4419C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250022 | |||||||
| chr16:81250025 | A | G | 6 | a0001c0002t0001g0015 a0001c0005t0001g0013 a0001c0005t0001g0014 others(3): Show |
6 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+4422A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250025 | |||||||
| chr16:81250026 | G | A | 142 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(139): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.193+4423G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250026 | |||||||
| chr16:81250032 | C | A | 7 | a0001c0002t0001g0015 a0001c0005t0001g0013 a0001c0005t0001g0014 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+4429C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250032 | |||||||
| chr16:81250101 | C | T | 7 | a0001c0002t0001g0015 a0001c0005t0001g0013 a0001c0005t0001g0014 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+4498C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250101 | |||||||
| chr16:81250124 | G | A | 2 | a0001c0001t0001g0230 a0003c0003t0001g0199 |
2 | NA18969.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.193+4521G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250124 | |||||||
| chr16:81250224 | C | G | 154 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0254 others(151): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.193+4621C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250224 | |||||||
| chr16:81250234 | G | A | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.193+4631G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250234 | |||||||
| chr16:81250237 | G | A | 131 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.193+4634G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250237 | |||||||
| chr16:81250460 | C | G | 2 | a0002c0006t0001g0029 a0002c0006t0001g0174 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.193+4857C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250460 | |||||||
| chr16:81250470 | C | G | 3 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | HG03017.hp2 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.193+4867C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250470 | |||||||
| chr16:81250492 | C | T | 1 | a0002c0006t0001g0377 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.193+4889C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250492 | |||||||
| chr16:81250578 | C | CT | 132 | a0001c0001t0001g0192 a0001c0001t0001g0229 a0001c0001t0001g0236 others(129): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.193+4995dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81250578 | ||||||
| chr16:81250578 | C | CTT | 11 | a0001c0001t0001g0217 a0001c0002t0001g0136 a0001c0005t0001g0122 others(8): Show |
11 | HG00099.hp2 HG00741.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+4994_193+4995d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81250578 | ||||||
| chr16:81250578 | C | CTTTTTTT others(4): Show |
8 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0023 others(5): Show |
8 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+4985_193+4995d others(13): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81250578 | ||||||
| chr16:81250578 | C | CTTTTTTT others(5): Show |
1 | a0001c0005t0001g0026 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.193+4984_193+4995d others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81250578 | ||||||
| chr16:81250578 | CT | C | 14 | a0001c0001t0001g0225 a0001c0001t0001g0269 a0001c0001t0001g0270 others(11): Show |
14 | HG00323.hp2 HG00558.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.193+4995delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81250578 | ||||||
| chr16:81250697 | C | T | 7 | a0001c0002t0001g0015 a0001c0005t0001g0013 a0001c0005t0001g0014 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+5094C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250697 | |||||||
| chr16:81250773 | G | T | 2 | a0003c0003t0001g0345 a0003c0003t0001g0350 |
2 | HG01943.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.193+5170G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250773 | |||||||
| chr16:81250800 | C | T | 2 | a0001c0001t0001g0216 a0003c0003t0001g0159 |
2 | HG02074.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.193+5197C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250800 | |||||||
| chr16:81250868 | A | C | 1 | a0002c0004t0001g0100 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.193+5265A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250868 | |||||||
| chr16:81250871 | G | A | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.193+5268G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250871 | |||||||
| chr16:81250979 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.193+5376C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250979 | |||||||
| chr16:81251062 | T | C | 2 | a0002c0006t0001g0029 a0002c0006t0001g0174 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.193+5459T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251062 | |||||||
| chr16:81251132 | C | A | 1 | a0001c0001t0001g0287 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.193+5529C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251132 | |||||||
| chr16:81251169 | C | T | 6 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0268 others(3): Show |
6 | HG01081.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+5566C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251169 | |||||||
| chr16:81251220 | T | C | 1 | a0001c0001t0001g0365 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.193+5617T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251220 | |||||||
| chr16:81251414 | T | G | 107 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(104): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.193+5811T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251414 | |||||||
| chr16:81251502 | G | C | 53 | a0001c0001t0001g0220 a0001c0001t0001g0246 a0001c0001t0001g0251 others(50): Show |
53 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.193+5899G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251502 | |||||||
| chr16:81251521 | C | G | 1 | a0003c0003t0001g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.193+5918C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251521 | |||||||
| chr16:81251695 | G | C | 1 | a0003c0003t0001g0319 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.193+6092G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251695 | |||||||
| chr16:81251709 | C | T | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6106C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251709 | |||||||
| chr16:81251836 | A | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6233A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251836 | |||||||
| chr16:81251838 | A | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6235A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251838 | |||||||
| chr16:81251851 | C | T | 1 | a0002c0004t0001g0110 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.193+6248C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251851 | |||||||
| chr16:81251852 | GCA | G | 3 | a0002c0006t0001g0029 a0002c0006t0001g0174 a0002c0020t0001g0274 |
3 | HG02055.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.193+6266_193+6267d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251852 | ||||||
| chr16:81251859 | C | A | 1 | a0001c0001t0001g0355 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.193+6256C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251859 | |||||||
| chr16:81251869 | C | T | 15 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0002t0001g0015 others(12): Show |
15 | HG00735.hp1 HG01070.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.193+6266C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251869 | |||||||
| chr16:81251871 | T | C | 1 | a0001c0007t0001g0234 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193+6268T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251871 | |||||||
| chr16:81251872 | A | ATGTGTGT others(1): Show |
3 | a0001c0007t0001g0163 a0002c0006t0001g0164 a0012c0012t0001g0153 |
3 | HG03098.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.193+6270_193+6271i others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | ||||||
| chr16:81251872 | A | ATGTGTGT others(3): Show |
1 | a0001c0002t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193+6270_193+6271i others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | ||||||
| chr16:81251872 | A | ATGTGTGT others(5): Show |
4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6270_193+6271i others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | ||||||
| chr16:81251872 | A | ATGTGTGT others(7): Show |
3 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0006c0016t0001g0011 |
3 | HG02559.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.193+6270_193+6271i others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | ||||||
| chr16:81251872 | A | ATGTGTGT others(9): Show |
2 | a0002c0004t0001g0010 a0002c0004t0001g0012 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.193+6270_193+6271i others(18): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | ||||||
| chr16:81251872 | A | ATGTGTGT others(15): Show |
1 | a0001c0005t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193+6270_193+6271i others(24): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | ||||||
| chr16:81251874 | A | ATGTG | 34 | a0001c0001t0001g0254 a0001c0002t0001g0037 a0001c0002t0001g0039 others(31): Show |
34 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.193+6285_193+6288d others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251874 | ||||||
| chr16:81251874 | A | ATGTGTG | 64 | a0001c0002t0001g0003 a0001c0002t0001g0124 a0001c0002t0001g0125 others(61): Show |
66 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.193+6283_193+6288d others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251874 | ||||||
| chr16:81251874 | A | ATGTGTGT others(3): Show |
2 | a0001c0005t0001g0028 a0001c0007t0001g0200 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.193+6279_193+6288d others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251874 | ||||||
| chr16:81251874 | A | ATGTGTGT others(5): Show |
1 | a0001c0005t0001g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.193+6277_193+6288d others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251874 | ||||||
| chr16:81251874 | A | G | 17 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0002t0001g0015 others(14): Show |
17 | HG00735.hp1 HG01070.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+6271A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251874 | |||||||
| chr16:81251892 | A | G | 7 | a0001c0001t0001g0165 a0001c0002t0001g0016 a0001c0002t0001g0150 others(4): Show |
8 | HG01257.hp1 HG01258.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+6289A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251892 | |||||||
| chr16:81251894 | A | G | 1 | a0003c0003t0001g0238 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.193+6291A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251894 | |||||||
| chr16:81251900 | C | G | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6297C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251900 | |||||||
| chr16:81251978 | G | A | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | NA18944.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.193+6375G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251978 | |||||||
| chr16:81252085 | G | C | 1 | a0001c0005t0001g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+6482G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252085 | |||||||
| chr16:81252195 | T | A | 1 | a0001c0001t0001g0287 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.193+6592T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252195 | |||||||
| chr16:81252204 | T | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6601T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252204 | |||||||
| chr16:81252396 | C | G | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | NA18984.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.193+6793C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252396 | |||||||
| chr16:81252413 | G | C | 1 | a0001c0005t0001g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.193+6810G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252413 | |||||||
| chr16:81252536 | G | A | 12 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.193+6933G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252536 | |||||||
| chr16:81252545 | A | G | 1 | a0001c0001t0001g0381 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.193+6942A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252545 | |||||||
| chr16:81252608 | G | A | 2 | a0001c0002t0001g0017 a0001c0002t0001g0018 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193+7005G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252608 | |||||||
| chr16:81252738 | G | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-6938G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252738 | |||||||
| chr16:81252745 | C | G | 8 | a0001c0002t0001g0003 a0001c0002t0001g0357 a0001c0002t0001g0358 others(5): Show |
9 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.194-6931C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252745 | |||||||
| chr16:81252856 | T | C | 170 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(167): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.194-6820T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252856 | |||||||
| chr16:81252867 | A | G | 122 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.194-6809A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252867 | |||||||
| chr16:81252995 | C | G | 3 | a0002c0006t0001g0029 a0002c0006t0001g0174 a0002c0020t0001g0274 |
3 | HG02055.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.194-6681C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252995 | |||||||
| chr16:81253090 | C | T | 1 | a0001c0002t0002g0035 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.194-6586C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253090 | |||||||
| chr16:81253139 | C | G | 1 | a0001c0002t0001g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-6537C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253139 | |||||||
| chr16:81253193 | G | A | 1 | a0002c0004t0001g0067 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.194-6483G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253193 | |||||||
| chr16:81253344 | C | G | 1 | a0001c0002t0001g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-6332C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253344 | |||||||
| chr16:81253545 | C | G | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.194-6131C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253545 | |||||||
| chr16:81253840 | A | G | 122 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.194-5836A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253840 | |||||||
| chr16:81253894 | T | C | 108 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0254 others(105): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.194-5782T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253894 | |||||||
| chr16:81254037 | C | G | 14 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(11): Show |
14 | HG00735.hp1 HG01070.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.194-5639C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254037 | |||||||
| chr16:81254171 | C | G | 4 | a0001c0001t0001g0251 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | NA18955.hp2 NA18966.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-5505C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254171 | |||||||
| chr16:81254185 | A | G | 1 | a0001c0002t0001g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-5491A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254185 | |||||||
| chr16:81254243 | C | T | 118 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(115): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.194-5433C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254243 | |||||||
| chr16:81254269 | T | A | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.194-5407T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254269 | |||||||
| chr16:81254270 | G | A | 10 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0002t0001g0016 others(7): Show |
10 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-5406G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254270 | |||||||
| chr16:81254277 | T | C | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.194-5399T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254277 | |||||||
| chr16:81254289 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.194-5387C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254289 | |||||||
| chr16:81254295 | A | AT | 165 | a0001c0001t0001g0009 a0001c0001t0001g0177 a0001c0001t0001g0182 others(162): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.194-5354dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254295 | ||||||
| chr16:81254295 | A | ATT | 39 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0001g0246 others(36): Show |
39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.194-5355_194-5354d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254295 | ||||||
| chr16:81254295 | AT | A | 6 | a0001c0001t0001g0186 a0001c0001t0001g0284 a0001c0001t0001g0329 others(3): Show |
6 | HG01515.hp2 HG02886.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-5354delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254295 | ||||||
| chr16:81254295 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.194-5364_194-5354d others(13): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254295 | ||||||
| chr16:81254332 | G | A | 103 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(100): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.194-5344G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254332 | |||||||
| chr16:81254359 | C | A | 2 | a0001c0001t0001g0384 a0001c0001t0001g0385 |
2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.194-5317C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254359 | |||||||
| chr16:81254370 | C | T | 1 | a0001c0005t0001g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.194-5306C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254370 | |||||||
| chr16:81254426 | C | G | 1 | a0001c0001t0001g0355 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.194-5250C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254426 | |||||||
| chr16:81254429 | G | A | 1 | a0001c0007t0001g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.194-5247G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254429 | |||||||
| chr16:81254450 | A | AT | 9 | a0001c0001t0001g0231 a0001c0001t0001g0233 a0001c0001t0001g0287 others(6): Show |
9 | HG00735.hp1 HG01070.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-5213dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254450 | ||||||
| chr16:81254450 | AT | A | 13 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0261 others(10): Show |
13 | HG02055.hp2 HG02451.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.194-5213delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254450 | ||||||
| chr16:81254493 | G | A | 1 | a0009c0013t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.194-5183G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254493 | |||||||
| chr16:81254537 | A | G | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.194-5139A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254537 | |||||||
| chr16:81254607 | A | C | 2 | a0002c0004t0001g0104 a0002c0004t0001g0105 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.194-5069A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254607 | |||||||
| chr16:81254671 | A | G | 1 | a0002c0004t0001g0091 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.194-5005A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254671 | |||||||
| chr16:81254851 | C | T | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-4825C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254851 | |||||||
| chr16:81254891 | G | A | 3 | a0001c0005t0001g0028 a0001c0005t0001g0152 a0001c0007t0001g0200 |
3 | HG02280.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.194-4785G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254891 | |||||||
| chr16:81254892 | G | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0282 |
2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.194-4784G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254892 | |||||||
| chr16:81254915 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.194-4761G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254915 | |||||||
| chr16:81255058 | C | T | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-4618C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255058 | |||||||
| chr16:81255076 | C | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0202 a0001c0001t0001g0224 others(1): Show |
5 | HG01071.hp2 HG01261.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-4600C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255076 | |||||||
| chr16:81255117 | G | A | 2 | a0002c0004t0001g0010 a0002c0004t0001g0012 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.194-4559G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255117 | |||||||
| chr16:81255125 | C | G | 11 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.194-4551C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255125 | |||||||
| chr16:81255313 | G | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-4363G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255313 | |||||||
| chr16:81255324 | C | G | 5 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(2): Show |
5 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-4352C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255324 | |||||||
| chr16:81255493 | AT | A | 10 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(7): Show |
10 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-4174delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81255493 | ||||||
| chr16:81255497 | T | A | 5 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(2): Show |
5 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-4179T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255497 | |||||||
| chr16:81255509 | TA | T | 11 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(8): Show |
11 | HG02280.hp2 HG02602.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.194-4166delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255509 | |||||||
| chr16:81255510 | A | T | 99 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(96): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.194-4166A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255510 | |||||||
| chr16:81255803 | C | A | 1 | a0002c0020t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.194-3873C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255803 | |||||||
| chr16:81255827 | T | G | 3 | a0002c0006t0001g0363 a0003c0003t0001g0362 a0003c0003t0001g0364 |
3 | NA18990.hp1 NA18993.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.194-3849T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255827 | |||||||
| chr16:81255911 | C | T | 1 | a0001c0001t0002g0374 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.194-3765C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255911 | |||||||
| chr16:81255947 | G | C | 1 | a0003c0003t0001g0319 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.194-3729G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255947 | |||||||
| chr16:81255967 | G | C | 118 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(115): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.194-3709G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255967 | |||||||
| chr16:81255979 | A | AT | 101 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(98): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.194-3689dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81255979 | ||||||
| chr16:81255996 | A | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
12 | HG01884.hp2 HG02257.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.194-3680A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255996 | |||||||
| chr16:81256117 | A | AT | 35 | a0001c0001t0001g0181 a0001c0001t0001g0189 a0001c0001t0001g0233 others(32): Show |
36 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.194-3546dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81256117 | ||||||
| chr16:81256220 | G | C | 8 | a0001c0002t0001g0016 a0001c0005t0001g0028 a0001c0005t0001g0152 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-3456G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256220 | |||||||
| chr16:81256255 | G | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0252 a0001c0001t0001g0343 |
3 | HG03704.hp2 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.194-3421G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256255 | |||||||
| chr16:81256546 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.194-3130A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256546 | |||||||
| chr16:81256576 | T | C | 1 | a0001c0002t0001g0061 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.194-3100T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256576 | |||||||
| chr16:81256642 | C | A | 2 | a0002c0006t0001g0029 a0002c0006t0001g0174 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.194-3034C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256642 | |||||||
| chr16:81256690 | C | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-2986C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256690 | |||||||
| chr16:81256739 | T | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-2937T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256739 | |||||||
| chr16:81256821 | G | C | 101 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(98): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.194-2855G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256821 | |||||||
| chr16:81256866 | C | T | 3 | a0001c0005t0001g0028 a0001c0005t0001g0152 a0001c0007t0001g0200 |
3 | HG02280.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.194-2810C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256866 | |||||||
| chr16:81256980 | C | T | 1 | a0001c0002t0001g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-2696C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256980 | |||||||
| chr16:81256989 | G | A | 2 | a0001c0001t0001g0165 a0001c0002t0001g0150 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.194-2687G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256989 | |||||||
| chr16:81257000 | G | A | 98 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(95): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.194-2676G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257000 | |||||||
| chr16:81257026 | T | A | 117 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(114): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.194-2650T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257026 | |||||||
| chr16:81257259 | C | T | 103 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(100): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.194-2417C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257259 | |||||||
| chr16:81257285 | G | C | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.194-2391G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257285 | |||||||
| chr16:81257287 | C | T | 74 | a0001c0001t0001g0254 a0001c0002t0001g0003 a0001c0002t0001g0037 others(71): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.194-2389C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257287 | |||||||
| chr16:81257289 | G | T | 3 | a0001c0002t0001g0003 a0001c0002t0001g0357 a0001c0002t0001g0358 |
4 | HG01891.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-2387G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257289 | |||||||
| chr16:81257296 | G | T | 2 | a0001c0001t0001g0381 a0001c0001t0001g0392 |
2 | HG01346.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.194-2380G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257296 | |||||||
| chr16:81257299 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.194-2377C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257299 | |||||||
| chr16:81257513 | C | T | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.194-2163C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257513 | |||||||
| chr16:81257606 | A | AGGCAAAC others(17): Show |
1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.194-2069_194-2046d others(26): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81257606 | ||||||
| chr16:81257674 | G | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-2002G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257674 | |||||||
| chr16:81257695 | G | A | 1 | a0002c0004t0001g0066 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.194-1981G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257695 | |||||||
| chr16:81257773 | G | A | 1 | a0009c0013t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.194-1903G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257773 | |||||||
| chr16:81257858 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.194-1818T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257858 | |||||||
| chr16:81257872 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.194-1804T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257872 | |||||||
| chr16:81257879 | C | CA | 9 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0002t0001g0086 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-1780dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81257879 | ||||||
| chr16:81257879 | CA | C | 7 | a0001c0001t0001g0225 a0001c0002t0001g0047 a0001c0005t0001g0099 others(4): Show |
7 | HG00558.hp1 HG01099.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.194-1780delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81257879 | ||||||
| chr16:81257928 | G | A | 1 | a0002c0004t0001g0091 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.194-1748G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257928 | |||||||
| chr16:81257973 | G | T | 2 | a0001c0007t0001g0163 a0002c0006t0001g0164 |
2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.194-1703G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257973 | |||||||
| chr16:81257999 | C | G | 8 | a0001c0002t0001g0016 a0001c0005t0001g0028 a0001c0005t0001g0152 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-1677C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257999 | |||||||
| chr16:81258033 | G | A | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.194-1643G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258033 | |||||||
| chr16:81258037 | C | T | 2 | a0001c0001t0001g0381 a0001c0001t0001g0392 |
2 | HG01346.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.194-1639C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258037 | |||||||
| chr16:81258124 | T | C | 1 | a0003c0003t0001g0335 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.194-1552T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258124 | |||||||
| chr16:81258134 | A | G | 3 | a0001c0005t0001g0028 a0001c0005t0001g0152 a0001c0007t0001g0200 |
3 | HG02280.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.194-1542A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258134 | |||||||
| chr16:81258258 | C | T | 1 | a0003c0009t0001g0089 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.194-1418C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258258 | |||||||
| chr16:81258290 | G | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-1386G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258290 | |||||||
| chr16:81258416 | G | A | 1 | a0003c0003t0001g0322 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.194-1260G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258416 | |||||||
| chr16:81258453 | C | T | 3 | a0001c0005t0001g0028 a0001c0005t0001g0152 a0001c0007t0001g0200 |
3 | HG02280.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.194-1223C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258453 | |||||||
| chr16:81258478 | T | C | 70 | a0001c0001t0001g0202 a0001c0002t0001g0003 a0001c0002t0001g0124 others(67): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.194-1198T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258478 | |||||||
| chr16:81258501 | G | A | 3 | a0002c0006t0001g0029 a0002c0006t0001g0174 a0002c0020t0001g0274 |
3 | HG02055.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.194-1175G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258501 | |||||||
| chr16:81258602 | G | C | 8 | a0001c0002t0001g0016 a0001c0005t0001g0028 a0001c0005t0001g0152 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-1074G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258602 | |||||||
| chr16:81258611 | G | T | 1 | a0001c0002t0001g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-1065G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258611 | |||||||
| chr16:81258623 | T | C | 2 | a0001c0002t0001g0173 a0001c0005t0001g0114 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.194-1053T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258623 | |||||||
| chr16:81258782 | G | C | 1 | a0002c0006t0001g0174 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.194-894G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258782 | |||||||
| chr16:81258937 | A | AAG | 4 | a0001c0001t0001g0001 a0001c0001t0001g0179 a0001c0001t0001g0181 others(1): Show |
6 | NA18949.hp1 NA18988.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-724_194-723dup others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81258937 | ||||||
| chr16:81259002 | G | T | 3 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0006c0016t0001g0011 |
3 | HG02559.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.194-674G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259002 | |||||||
| chr16:81259019 | C | G | 5 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0003c0003t0001g0312 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-657C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259019 | |||||||
| chr16:81259054 | C | G | 1 | a0001c0001t0001g0317 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.194-622C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259054 | |||||||
| chr16:81259125 | C | G | 71 | a0001c0001t0001g0202 a0001c0001t0001g0325 a0001c0002t0001g0016 others(68): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.194-551C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259125 | |||||||
| chr16:81259143 | A | C | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | NA18944.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.194-533A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259143 | |||||||
| chr16:81259218 | G | C | 1 | a0003c0003t0001g0366 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.194-458G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259218 | |||||||
| chr16:81259245 | G | A | 8 | a0001c0002t0001g0016 a0001c0005t0001g0028 a0001c0005t0001g0152 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-431G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259245 | |||||||
| chr16:81259351 | G | T | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.194-325G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259351 | |||||||
| chr16:81259355 | G | A | 6 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(3): Show |
6 | HG02280.hp2 HG02647.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-321G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259355 | |||||||
| chr16:81259363 | G | A | 1 | a0003c0003t0001g0322 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.194-313G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259363 | |||||||
| chr16:81259438 | G | A | 1 | a0003c0003t0001g0323 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.194-238G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259438 | |||||||
| chr16:81259457 | A | G | 8 | a0001c0002t0001g0016 a0001c0005t0001g0028 a0001c0005t0001g0152 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-219A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259457 | |||||||
| chr16:81259493 | A | T | 3 | a0001c0005t0001g0154 a0001c0005t0001g0157 a0008c0015t0001g0155 |
3 | HG02615.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.194-183A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259493 | |||||||
| chr16:81259516 | A | G | 1 | a0002c0006t0001g0185 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.194-160A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259516 | |||||||
| chr16:81259579 | A | T | 1 | a0002c0004t0001g0141 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.194-97A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259579 | |||||||
| chr16:81259602 | A | G | 8 | a0001c0002t0001g0016 a0001c0005t0001g0028 a0001c0005t0001g0152 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-74A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259602 | |||||||
| chr16:81259630 | C | T | 2 | a0001c0001t0001g0231 a0001c0002t0001g0038 |
2 | NA18968.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.194-46C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259630 | |||||||
| chr16:81259655 | A | T | 1 | a0001c0005t0001g0099 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.194-21A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259655 | |||||||
| chr16:81260064 | G | A | 7 | a0001c0002t0001g0016 a0001c0005t0001g0028 a0001c0005t0001g0152 others(4): Show |
7 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.323+259G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260064 | |||||||
| chr16:81260119 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.323+314A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260119 | |||||||
| chr16:81260196 | C | G | 103 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(100): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.323+391C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260196 | |||||||
| chr16:81260225 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.323+420C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260225 | |||||||
| chr16:81260308 | G | GA | 11 | a0001c0001t0001g0224 a0001c0001t0001g0228 a0001c0001t0001g0233 others(8): Show |
11 | HG01255.hp2 HG01981.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.323+518dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 81260308 | ||||||
| chr16:81260308 | GA | G | 46 | a0001c0001t0001g0009 a0001c0001t0001g0160 a0001c0001t0001g0212 others(43): Show |
49 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.323+518delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 81260308 | ||||||
| chr16:81260387 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.323+582A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260387 | |||||||
| chr16:81260401 | G | C | 2 | a0001c0001t0001g0360 a0001c0001t0001g0361 |
2 | HG00621.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.323+596G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260401 | |||||||
| chr16:81260485 | T | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
13 | HG01081.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.323+680T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260485 | |||||||
| chr16:81260518 | A | G | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.323+713A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260518 | |||||||
| chr16:81260659 | C | G | 2 | a0001c0001t0001g0346 a0001c0001t0001g0373 |
2 | NA19074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.323+854C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260659 | |||||||
| chr16:81260715 | A | C | 1 | a0009c0013t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.323+910A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260715 | |||||||
| chr16:81260764 | A | C | 1 | a0009c0013t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.323+959A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260764 | |||||||
| chr16:81260837 | A | C | 2 | a0001c0005t0001g0099 a0006c0014t0001g0098 |
2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.323+1032A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260837 | |||||||
| chr16:81260839 | T | G | 1 | a0009c0013t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.323+1034T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260839 | |||||||
| chr16:81261114 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0224 a0001c0001t0002g0203 |
4 | HG01071.hp2 HG02004.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-1022G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261114 | |||||||
| chr16:81261216 | T | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-920T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261216 | |||||||
| chr16:81261232 | G | A | 2 | a0001c0001t0001g0165 a0001c0002t0001g0150 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.324-904G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261232 | |||||||
| chr16:81261282 | A | G | 2 | a0002c0006t0001g0029 a0002c0006t0001g0174 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.324-854A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261282 | |||||||
| chr16:81261284 | T | G | 1 | a0001c0002t0001g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324-852T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261284 | |||||||
| chr16:81261288 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(245): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.324-848T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261288 | |||||||
| chr16:81261403 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-733T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261403 | |||||||
| chr16:81261408 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-728T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261408 | |||||||
| chr16:81261409 | C | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-727C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261409 | |||||||
| chr16:81261412 | G | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-724G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261412 | |||||||
| chr16:81261415 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-721T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261415 | |||||||
| chr16:81261416 | A | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-720A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261416 | |||||||
| chr16:81261453 | A | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-683A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261453 | |||||||
| chr16:81261507 | C | T | 1 | a0002c0004t0001g0004 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.324-629C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261507 | |||||||
| chr16:81261523 | T | C | 1 | a0002c0020t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.324-613T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261523 | |||||||
| chr16:81261527 | G | A | 1 | a0006c0014t0001g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324-609G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261527 | |||||||
| chr16:81261554 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-582T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261554 | |||||||
| chr16:81261581 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-555T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261581 | |||||||
| chr16:81261582 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-554T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261582 | |||||||
| chr16:81261584 | G | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-552G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261584 | |||||||
| chr16:81261586 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-550G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261586 | |||||||
| chr16:81261587 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-549G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261587 | |||||||
| chr16:81261589 | G | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-547G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261589 | |||||||
| chr16:81261594 | G | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-542G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261594 | |||||||
| chr16:81261597 | G | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-539G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261597 | |||||||
| chr16:81261598 | G | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-538G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261598 | |||||||
| chr16:81261600 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-536T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261600 | |||||||
| chr16:81261603 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-533G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261603 | |||||||
| chr16:81261604 | C | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-532C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261604 | |||||||
| chr16:81261614 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-522T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261614 | |||||||
| chr16:81261650 | C | T | 1 | a0001c0002t0001g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.324-486C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261650 | |||||||
| chr16:81261652 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-484T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261652 | |||||||
| chr16:81261653 | G | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-483G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261653 | |||||||
| chr16:81261654 | G | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-482G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261654 | |||||||
| chr16:81261659 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-477G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261659 | |||||||
| chr16:81261660 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-476T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261660 | |||||||
| chr16:81261661 | C | T | 1 | a0009c0013t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.324-475C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261661 | |||||||
| chr16:81261662 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-474T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261662 | |||||||
| chr16:81261663 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-473T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261663 | |||||||
| chr16:81261665 | G | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-471G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261665 | |||||||
| chr16:81261668 | G | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-468G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261668 | |||||||
| chr16:81261670 | G | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-466G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261670 | |||||||
| chr16:81261674 | G | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-462G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261674 | |||||||
| chr16:81261686 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-450T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261686 | |||||||
| chr16:81261696 | G | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-440G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261696 | |||||||
| chr16:81261706 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-430G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261706 | |||||||
| chr16:81261709 | C | A | 1 | a0002c0020t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.324-427C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261709 | |||||||
| chr16:81261714 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-422T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261714 | |||||||
| chr16:81261715 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-421G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261715 | |||||||
| chr16:81261716 | C | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-420C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261716 | |||||||
| chr16:81261723 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-413T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261723 | |||||||
| chr16:81261742 | C | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-394C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261742 | |||||||
| chr16:81261743 | A | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-393A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261743 | |||||||
| chr16:81261783 | C | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-353C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261783 | |||||||
| chr16:81261785 | A | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-351A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261785 | |||||||
| chr16:81261790 | G | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-346G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261790 | |||||||
| chr16:81261791 | G | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-345G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261791 | |||||||
| chr16:81261792 | A | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-344A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261792 | |||||||
| chr16:81261795 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-341G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261795 | |||||||
| chr16:81261797 | A | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-339A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261797 | |||||||
| chr16:81261799 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-337T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261799 | |||||||
| chr16:81261800 | G | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-336G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261800 | |||||||
| chr16:81261801 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-335G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261801 | |||||||
| chr16:81261838 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-298T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261838 | |||||||
| chr16:81261845 | C | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-291C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261845 | |||||||
| chr16:81261846 | A | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-290A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261846 | |||||||
| chr16:81261848 | T | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-288T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261848 | |||||||
| chr16:81261854 | G | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-282G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261854 | |||||||
| chr16:81261863 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-273T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261863 | |||||||
| chr16:81261883 | A | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-253A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261883 | |||||||
| chr16:81261884 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-252G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261884 | |||||||
| chr16:81261893 | C | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-243C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261893 | |||||||
| chr16:81261902 | CGGCTGAT others(25): Show |
C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-231_324-200del others(32): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 81261902 | ||||||
| chr16:81261938 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-198T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261938 | |||||||
| chr16:81261942 | C | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-194C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261942 | |||||||
| chr16:81261946 | G | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-190G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261946 | |||||||
| chr16:81261949 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-187G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261949 | |||||||
| chr16:81261965 | A | T | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-171A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261965 | |||||||
| chr16:81261975 | C | A | 1 | a0001c0002t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-161C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261975 | |||||||
| chr16:81262032 | A | G | 1 | a0001c0005t0001g0092 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.324-104A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81262032 | |||||||
| chr16:81262297 | T | C | 99 | a0001c0001t0001g0254 a0001c0001t0001g0281 a0001c0002t0001g0003 others(96): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.471+14T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262297 | |||||||
| chr16:81262423 | C | T | 2 | a0003c0003t0001g0334 a0003c0003t0001g0337 |
2 | HG02040.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.471+140C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262423 | |||||||
| chr16:81262434 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.471+151C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262434 | |||||||
| chr16:81262633 | GC | G | 10 | a0001c0002t0001g0136 a0001c0005t0001g0115 a0001c0005t0001g0117 others(7): Show |
10 | HG00639.hp2 HG01433.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.471+352delC | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81262633 | ||||||
| chr16:81262742 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.471+459G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262742 | |||||||
| chr16:81262780 | T | C | 3 | a0001c0005t0001g0028 a0001c0005t0001g0152 a0001c0007t0001g0200 |
3 | HG02280.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.471+497T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262780 | |||||||
| chr16:81262836 | C | A | 1 | a0001c0007t0001g0234 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.471+553C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262836 | |||||||
| chr16:81262836 | CAAAA | C | 8 | a0001c0002t0001g0150 a0001c0005t0001g0028 a0001c0005t0001g0092 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.471+570_471+573del others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81262836 | ||||||
| chr16:81262841 | A | AAC | 94 | a0001c0001t0001g0254 a0001c0001t0001g0281 a0001c0002t0001g0003 others(91): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.471+559_471+560ins others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81262841 | ||||||
| chr16:81262841 | A | AC | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(160): Show |
168 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.471+558_471+559ins others(1): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262841 | |||||||
| chr16:81262841 | A | ACAAAAAC | 7 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0268 others(4): Show |
7 | HG01081.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+558_471+559ins others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262841 | |||||||
| chr16:81262842 | A | C | 46 | a0001c0001t0001g0009 a0001c0001t0001g0160 a0001c0001t0001g0239 others(43): Show |
49 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.471+559A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262842 | |||||||
| chr16:81262843 | A | C | 1 | a0001c0001t0001g0316 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.471+560A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262843 | |||||||
| chr16:81262845 | A | C | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0002t0001g0170 others(6): Show |
9 | HG00280.hp2 HG01074.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.471+562A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262845 | |||||||
| chr16:81262846 | A | C | 8 | a0001c0002t0001g0150 a0001c0005t0001g0028 a0001c0005t0001g0092 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.471+563A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262846 | |||||||
| chr16:81262870 | T | TA | 12 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0002t0001g0150 others(9): Show |
12 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.471+594dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81262870 | ||||||
| chr16:81262935 | C | A | 1 | a0002c0004t0001g0135 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.471+652C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262935 | |||||||
| chr16:81262998 | C | T | 7 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0258 others(4): Show |
7 | HG00673.hp1 HG02080.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+715C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262998 | |||||||
| chr16:81263012 | C | T | 1 | a0002c0020t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.471+729C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263012 | |||||||
| chr16:81263094 | T | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+811T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263094 | |||||||
| chr16:81263108 | C | CT | 22 | a0001c0001t0001g0197 a0001c0001t0001g0258 a0001c0001t0001g0265 others(19): Show |
22 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.471+845dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81263108 | ||||||
| chr16:81263108 | C | CTTTT | 7 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(4): Show |
7 | HG02055.hp2 HG02965.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+842_471+845dup others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81263108 | ||||||
| chr16:81263108 | CT | C | 7 | a0001c0001t0001g0268 a0001c0001t0001g0341 a0001c0002t0001g0037 others(4): Show |
7 | HG00280.hp2 HG01081.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+845delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81263108 | ||||||
| chr16:81263108 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0224 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.471+836_471+845del others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81263108 | ||||||
| chr16:81263162 | G | C | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | NA18944.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.471+879G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263162 | |||||||
| chr16:81263188 | G | A | 1 | a0002c0006t0001g0244 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.471+905G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263188 | |||||||
| chr16:81263196 | C | T | 6 | a0001c0002t0001g0015 a0001c0005t0001g0013 a0001c0005t0001g0014 others(3): Show |
6 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+913C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263196 | |||||||
| chr16:81263197 | G | A | 1 | a0001c0005t0001g0092 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.471+914G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263197 | |||||||
| chr16:81263259 | T | G | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.471+976T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263259 | |||||||
| chr16:81263279 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.471+996T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263279 | |||||||
| chr16:81263301 | G | A | 1 | a0001c0005t0001g0092 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.471+1018G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263301 | |||||||
| chr16:81263311 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.471+1028C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263311 | |||||||
| chr16:81263385 | C | A | 1 | a0001c0002t0001g0090 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.471+1102C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263385 | |||||||
| chr16:81263393 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.471+1110G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263393 | |||||||
| chr16:81263441 | G | C | 1 | a0001c0001t0001g0288 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.471+1158G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263441 | |||||||
| chr16:81263534 | A | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0007t0001g0163 others(1): Show |
4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-1106A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263534 | |||||||
| chr16:81263785 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0211 |
2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.472-855A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263785 | |||||||
| chr16:81263837 | C | T | 4 | a0001c0001t0001g0202 a0003c0003t0001g0250 a0003c0003t0001g0345 others(1): Show |
4 | HG01261.hp2 HG01943.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-803C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263837 | |||||||
| chr16:81263876 | T | A | 1 | a0001c0001t0001g0204 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.472-764T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263876 | |||||||
| chr16:81263902 | C | T | 1 | a0001c0002t0001g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.472-738C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263902 | |||||||
| chr16:81263909 | G | C | 1 | a0001c0002t0001g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.472-731G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263909 | |||||||
| chr16:81263971 | A | C | 1 | a0002c0004t0001g0091 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.472-669A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263971 | |||||||
| chr16:81264085 | C | G | 1 | a0001c0002t0001g0090 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.472-555C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264085 | |||||||
| chr16:81264091 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
161 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.472-549G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264091 | |||||||
| chr16:81264097 | A | G | 79 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0325 others(76): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.472-543A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264097 | |||||||
| chr16:81264205 | C | A | 4 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0003c0003t0001g0312 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-435C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264205 | |||||||
| chr16:81264270 | G | T | 5 | a0003c0003t0001g0333 a0003c0003t0001g0334 a0003c0003t0001g0335 others(2): Show |
5 | HG02015.hp2 HG02040.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-370G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264270 | |||||||
| chr16:81264390 | C | T | 2 | a0002c0004t0001g0036 a0002c0004t0001g0107 |
2 | NA18968.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.472-250C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264390 | |||||||
| chr16:81264428 | A | G | 43 | a0001c0001t0001g0325 a0002c0004t0001g0033 a0002c0004t0001g0034 others(40): Show |
43 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.472-212A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264428 | |||||||
| chr16:81264472 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.472-168G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264472 | |||||||
| chr16:81264531 | C | T | 1 | a0001c0002t0001g0069 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.472-109C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264531 | |||||||
| chr16:81264860 | G | A | 1 | a0001c0002t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.619+73G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81264860 | |||||||
| chr16:81264932 | C | G | 8 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0196 others(5): Show |
8 | HG00735.hp2 HG01106.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.619+145C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81264932 | |||||||
| chr16:81264983 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.619+196C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81264983 | |||||||
| chr16:81265034 | A | G | 3 | a0001c0001t0001g0276 a0001c0001t0001g0278 a0001c0001t0001g0297 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.619+247A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265034 | |||||||
| chr16:81265046 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.619+259C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265046 | |||||||
| chr16:81265142 | A | C | 1 | a0001c0001t0001g0217 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.619+355A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265142 | |||||||
| chr16:81265177 | C | G | 1 | a0002c0004t0001g0091 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.619+390C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265177 | |||||||
| chr16:81265204 | TCACCCAT others(12): Show |
T | 1 | a0001c0005t0001g0127 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.619+430_619+448del others(19): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 81265204 | ||||||
| chr16:81265213 | C | T | 1 | a0001c0005t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.619+426C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265213 | |||||||
| chr16:81265221 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.619+434G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265221 | |||||||
| chr16:81265469 | A | G | 9 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0001c0005t0001g0028 others(6): Show |
9 | HG02280.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.619+682A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265469 | |||||||
| chr16:81265475 | C | T | 1 | a0001c0002t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.619+688C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265475 | |||||||
| chr16:81265482 | C | T | 52 | a0001c0002t0001g0003 a0001c0002t0001g0136 a0001c0002t0001g0358 others(49): Show |
53 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.619+695C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265482 | |||||||
| chr16:81265514 | C | G | 1 | a0001c0007t0001g0163 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.619+727C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265514 | |||||||
| chr16:81265564 | T | A | 1 | a0002c0004t0001g0040 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.619+777T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265564 | |||||||
| chr16:81265574 | T | A | 73 | a0001c0002t0001g0003 a0001c0002t0001g0136 a0001c0002t0001g0358 others(70): Show |
75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.619+787T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265574 | |||||||
| chr16:81265676 | G | A | 1 | a0001c0001t0001g0329 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.619+889G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265676 | |||||||
| chr16:81265676 | G | C | 9 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0001c0005t0001g0028 others(6): Show |
9 | HG02280.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.619+889G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265676 | |||||||
| chr16:81265740 | C | A | 1 | a0001c0005t0001g0092 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.619+953C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265740 | |||||||
| chr16:81265758 | G | C | 71 | a0001c0002t0001g0003 a0001c0002t0001g0136 a0001c0002t0001g0358 others(68): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.619+971G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265758 | |||||||
| chr16:81265782 | TCCACCAT others(51): Show |
T | 61 | a0001c0002t0001g0003 a0001c0002t0001g0136 a0001c0002t0001g0358 others(58): Show |
63 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.619+1004_619+1061d others(60): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 81265782 | ||||||
| chr16:81265844 | C | T | 6 | a0001c0001t0001g0009 a0001c0002t0001g0084 a0001c0002t0001g0108 others(3): Show |
7 | HG00738.hp2 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.619+1057C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265844 | |||||||
| chr16:81265887 | C | T | 1 | a0001c0005t0001g0133 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.619+1100C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265887 | |||||||
| chr16:81265895 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.619+1108C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265895 | |||||||
| chr16:81265948 | C | A | 6 | a0001c0001t0001g0241 a0001c0001t0001g0263 a0001c0001t0001g0272 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.619+1161C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265948 | |||||||
| chr16:81266034 | T | C | 3 | a0002c0004t0001g0091 a0002c0004t0001g0104 a0002c0004t0001g0105 |
3 | HG01167.hp2 HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.619+1247T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266034 | |||||||
| chr16:81266079 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.619+1292A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266079 | |||||||
| chr16:81266081 | A | C | 49 | a0001c0002t0001g0003 a0001c0002t0001g0136 a0001c0002t0001g0358 others(46): Show |
50 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.619+1294A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266081 | |||||||
| chr16:81266113 | C | T | 1 | a0001c0005t0001g0113 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.619+1326C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266113 | |||||||
| chr16:81266186 | C | T | 39 | a0001c0002t0001g0003 a0001c0002t0001g0136 a0001c0002t0001g0358 others(36): Show |
40 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.619+1399C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266186 | |||||||
| chr16:81266191 | C | T | 39 | a0001c0002t0001g0003 a0001c0002t0001g0136 a0001c0002t0001g0358 others(36): Show |
40 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.619+1404C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266191 | |||||||
| chr16:81266397 | A | G | 1 | a0002c0004t0001g0140 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.620-1511A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266397 | |||||||
| chr16:81266619 | C | G | 3 | a0001c0001t0001g0162 a0002c0006t0001g0164 a0002c0020t0001g0274 |
3 | HG03041.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.620-1289C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266619 | |||||||
| chr16:81266788 | G | T | 38 | a0001c0002t0001g0003 a0001c0002t0001g0136 a0001c0002t0001g0358 others(35): Show |
39 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.620-1120G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266788 | |||||||
| chr16:81266820 | C | T | 1 | a0002c0006t0001g0244 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.620-1088C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266820 | |||||||
| chr16:81266886 | C | G | 39 | a0001c0002t0001g0003 a0001c0002t0001g0136 a0001c0002t0001g0358 others(36): Show |
40 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.620-1022C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266886 | |||||||
| chr16:81266995 | G | A | 2 | a0001c0001t0001g0270 a0001c0002t0001g0124 |
2 | HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.620-913G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266995 | |||||||
| chr16:81267026 | C | T | 47 | a0001c0002t0001g0003 a0001c0002t0001g0358 a0001c0005t0001g0013 others(44): Show |
48 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.620-882C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267026 | |||||||
| chr16:81267029 | G | A | 5 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0002c0004t0001g0010 others(2): Show |
5 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.620-879G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267029 | |||||||
| chr16:81267159 | G | A | 1 | a0002c0006t0001g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.620-749G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267159 | |||||||
| chr16:81267293 | C | T | 1 | a0001c0002t0001g0018 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.620-615C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267293 | |||||||
| chr16:81267348 | C | T | 3 | a0002c0004t0001g0010 a0002c0004t0001g0012 a0002c0020t0001g0274 |
3 | HG02896.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.620-560C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267348 | |||||||
| chr16:81267411 | G | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0252 a0001c0001t0001g0343 |
3 | HG03704.hp2 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.620-497G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267411 | |||||||
| chr16:81267568 | G | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0190 a0001c0001t0001g0204 others(6): Show |
10 | HG01071.hp2 HG02004.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.620-340G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267568 | |||||||
| chr16:81267622 | G | T | 4 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0282 others(1): Show |
4 | HG03688.hp2 HG03704.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-286G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267622 | |||||||
| chr16:81267671 | G | A | 2 | a0002c0006t0001g0029 a0002c0006t0001g0174 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.620-237G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267671 | |||||||
| chr16:81267805 | G | T | 1 | a0001c0001t0001g0180 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.620-103G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267805 | |||||||
| chr16:81267810 | T | C | 1 | a0002c0006t0001g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.620-98T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267810 | |||||||
| chr16:81267855 | G | C | 109 | a0001c0001t0001g0160 a0001c0001t0001g0223 a0001c0001t0001g0254 others(106): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.620-53G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267855 | |||||||
| chr16:81268222 | TGGCATGG others(4): Show |
T | 47 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0001c0005t0001g0021 others(44): Show |
47 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.843+94_843+104delC others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81268222 | ||||||
| chr16:81268326 | C | T | 2 | a0001c0005t0001g0092 a0002c0006t0001g0164 |
2 | HG02602.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.843+195C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268326 | |||||||
| chr16:81268358 | C | T | 38 | a0001c0001t0001g0160 a0001c0001t0001g0223 a0001c0001t0001g0254 others(35): Show |
39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.843+227C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268358 | |||||||
| chr16:81268404 | A | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0239 a0001c0001t0001g0240 others(46): Show |
52 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.843+273A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268404 | |||||||
| chr16:81268439 | C | A | 1 | a0001c0007t0001g0163 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.843+308C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268439 | |||||||
| chr16:81268460 | C | T | 1 | a0001c0005t0001g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.843+329C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268460 | |||||||
| chr16:81268486 | C | T | 7 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0001c0005t0001g0028 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.843+355C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268486 | |||||||
| chr16:81268524 | C | CG | 3 | a0001c0002t0001g0078 a0001c0005t0001g0144 a0002c0004t0001g0036 |
3 | HG02109.hp1 NA18968.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.843+395dupG | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81268524 | ||||||
| chr16:81268636 | G | A | 2 | a0001c0001t0001g0384 a0001c0001t0001g0385 |
2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.843+505G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268636 | |||||||
| chr16:81268650 | T | C | 1 | a0001c0002t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.843+519T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268650 | |||||||
| chr16:81268679 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(77): Show |
84 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.843+548A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268679 | |||||||
| chr16:81268737 | A | T | 1 | a0003c0003t0001g0331 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.843+606A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268737 | |||||||
| chr16:81268739 | G | A | 3 | a0001c0001t0001g0196 a0001c0018t0001g0275 a0010c0019t0001g0187 |
3 | HG00735.hp2 HG03239.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.843+608G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268739 | |||||||
| chr16:81268827 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.843+696G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268827 | |||||||
| chr16:81269065 | C | CT | 39 | a0001c0001t0001g0186 a0001c0001t0001g0196 a0001c0001t0001g0197 others(36): Show |
39 | HG00735.hp2 HG01123.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.843+957dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | ||||||
| chr16:81269065 | C | CTTT | 28 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0023 others(25): Show |
28 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.843+955_843+957dup others(3): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | ||||||
| chr16:81269065 | C | CTTTT | 9 | a0001c0005t0001g0025 a0001c0005t0001g0120 a0001c0005t0001g0121 others(6): Show |
9 | HG01258.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.843+954_843+957dup others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | ||||||
| chr16:81269065 | CT | C | 44 | a0001c0001t0001g0160 a0001c0001t0001g0223 a0001c0001t0001g0241 others(41): Show |
45 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.843+957delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | ||||||
| chr16:81269065 | CTTT | C | 8 | a0002c0004t0001g0004 a0002c0004t0001g0040 a0002c0004t0001g0066 others(5): Show |
9 | HG00140.hp1 HG01074.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+955_843+957del others(3): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | ||||||
| chr16:81269065 | CTTTT | C | 51 | a0002c0004t0001g0033 a0002c0004t0001g0034 a0002c0004t0001g0045 others(48): Show |
51 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.843+954_843+957del others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | ||||||
| chr16:81269070 | T | A | 38 | a0001c0001t0001g0160 a0001c0001t0001g0223 a0001c0001t0001g0254 others(35): Show |
39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.843+939T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269070 | |||||||
| chr16:81269074 | T | A | 38 | a0001c0001t0001g0160 a0001c0001t0001g0223 a0001c0001t0001g0254 others(35): Show |
39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.843+943T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269074 | |||||||
| chr16:81269167 | C | G | 48 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0001c0005t0001g0021 others(45): Show |
48 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.844-992C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269167 | |||||||
| chr16:81269171 | T | C | 39 | a0001c0001t0001g0160 a0001c0001t0001g0223 a0001c0001t0001g0254 others(36): Show |
40 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.844-988T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269171 | |||||||
| chr16:81269301 | C | CT | 52 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0191 others(49): Show |
52 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.844-844dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269301 | ||||||
| chr16:81269311 | T | G | 1 | a0002c0006t0001g0310 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.844-848T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269311 | |||||||
| chr16:81269342 | G | C | 7 | a0001c0005t0001g0013 a0001c0005t0001g0014 a0001c0005t0001g0028 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-817G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269342 | |||||||
| chr16:81269351 | G | A | 48 | a0001c0001t0001g0009 a0001c0001t0001g0239 a0001c0001t0001g0240 others(45): Show |
51 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.844-808G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269351 | |||||||
| chr16:81269434 | T | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0239 a0001c0001t0001g0240 others(45): Show |
51 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.844-725T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269434 | |||||||
| chr16:81269444 | C | T | 3 | a0001c0005t0001g0092 a0001c0007t0001g0234 a0001c0007t0001g0391 |
3 | HG02602.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.844-715C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269444 | |||||||
| chr16:81269522 | C | T | 37 | a0001c0005t0001g0021 a0001c0005t0001g0022 a0001c0005t0001g0023 others(34): Show |
37 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.844-637C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269522 | |||||||
| chr16:81269534 | C | G | 2 | a0002c0006t0001g0029 a0002c0006t0001g0174 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.844-625C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269534 | |||||||
| chr16:81269719 | C | T | 2 | a0002c0004t0001g0100 a0002c0006t0001g0363 |
2 | NA18988.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.844-440C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269719 | |||||||
| chr16:81269758 | T | C | 2 | a0002c0004t0001g0100 a0002c0006t0001g0363 |
2 | NA18988.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.844-401T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269758 | |||||||
| chr16:81269911 | CAA | C | 3 | a0002c0004t0001g0010 a0002c0004t0001g0012 a0002c0020t0001g0274 |
3 | HG02896.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.844-246_844-245del others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269911 | ||||||
| chr16:81270000 | T | C | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.844-159T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81270000 | |||||||
| chr16:81270020 | G | A | 38 | a0001c0001t0001g0160 a0001c0001t0001g0254 a0001c0001t0001g0258 others(35): Show |
39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.844-139G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81270020 | |||||||
| chr16:81270154 | T | C | 67 | a0001c0001t0001g0210 a0001c0001t0001g0317 a0001c0002t0001g0128 others(64): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
splice_region_variant&intron_variant | LOW | c.844-5T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81270154 | |||||||
| chr16:81270464 | C | T | 80 | a0001c0001t0001g0254 a0001c0001t0001g0258 a0001c0001t0002g0203 others(77): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1101+48C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270464 | |||||||
| chr16:81270535 | A | G | 1 | a0003c0003t0001g0106 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1101+119A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270535 | |||||||
| chr16:81270586 | T | TAGAAAAT others(321): Show |
1 | a0003c0003t0001g0323 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1101+186_1101+187i others(330): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270586 | ||||||
| chr16:81270586 | T | TAGAAAAT others(337): Show |
1 | a0003c0003t0001g0331 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1101+186_1101+187i others(346): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270586 | ||||||
| chr16:81270682 | C | CTTTCTGT others(1): Show |
5 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0259 others(2): Show |
5 | HG01175.hp2 HG03017.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1101+267_1101+268i others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270682 | ||||||
| chr16:81270686 | C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0254 a0001c0002t0001g0039 a0001c0002t0001g0043 others(4): Show |
7 | HG00423.hp1 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1101+275_1101+276i others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270686 | ||||||
| chr16:81270686 | C | CTGTGTGT others(7): Show |
1 | a0001c0001t0001g0316 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1101+275_1101+276i others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270686 | ||||||
| chr16:81270692 | C | CTCTGTG | 6 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
7 | HG00597.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1101+277_1101+278i others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTCTGTGT others(1): Show |
58 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0160 others(55): Show |
59 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1101+277_1101+278i others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTCTGTGT others(3): Show |
91 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0148 others(88): Show |
94 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.1101+277_1101+278i others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTCTGTGT others(5): Show |
13 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0261 others(10): Show |
13 | HG00621.hp1 HG01081.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1101+277_1101+278i others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTCTGTGT others(7): Show |
4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0384 others(1): Show |
4 | HG01106.hp2 HG01257.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+277_1101+278i others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTGTG | 43 | a0001c0001t0001g0272 a0001c0005t0001g0013 a0001c0005t0001g0014 others(40): Show |
43 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1101+301_1101+304d others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTGTGTG | 6 | a0001c0005t0001g0113 a0001c0005t0001g0157 a0002c0004t0001g0145 others(3): Show |
6 | HG00558.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+299_1101+304d others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTGTGTGT others(1): Show |
41 | a0001c0001t0001g0258 a0001c0001t0002g0203 a0001c0002t0001g0003 others(38): Show |
42 | HG00438.hp1 HG00609.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1101+297_1101+304d others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTGTGTGT others(3): Show |
31 | a0001c0001t0001g0317 a0001c0002t0001g0016 a0001c0002t0001g0057 others(28): Show |
32 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1101+295_1101+304d others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTGTGTGT others(5): Show |
26 | a0001c0001t0001g0009 a0001c0002t0001g0069 a0002c0004t0001g0033 others(23): Show |
27 | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1101+293_1101+304d others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTGTGTGT others(7): Show |
36 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0324 others(33): Show |
38 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1101+291_1101+304d others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTGTGTGT others(9): Show |
7 | a0001c0002t0001g0084 a0001c0002t0001g0108 a0002c0004t0001g0104 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1101+289_1101+304d others(18): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | CTGTGTGT others(11): Show |
2 | a0001c0001t0001g0328 a0011c0021t0001g0390 |
2 | HG04184.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1101+287_1101+304d others(20): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | ||||||
| chr16:81270692 | C | G | 13 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0257 others(10): Show |
13 | HG00423.hp1 HG01175.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1101+276C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270692 | |||||||
| chr16:81270703 | T | G | 1 | a0001c0001t0001g0180 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1101+287T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270703 | |||||||
| chr16:81270749 | AT | A | 74 | a0001c0001t0001g0254 a0001c0001t0001g0258 a0001c0001t0001g0276 others(71): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1101+346delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270749 | ||||||
| chr16:81270812 | T | C | 1 | a0002c0006t0001g0244 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1101+396T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270812 | |||||||
| chr16:81270827 | C | G | 1 | a0001c0007t0001g0163 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1101+411C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270827 | |||||||
| chr16:81271033 | T | C | 9 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0268 others(6): Show |
9 | HG01081.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1101+617T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271033 | |||||||
| chr16:81271112 | A | AT | 18 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(15): Show |
19 | HG01081.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1101+707dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81271112 | ||||||
| chr16:81271115 | T | TA | 45 | a0001c0001t0001g0009 a0001c0001t0001g0239 a0001c0001t0001g0240 others(42): Show |
48 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1101+699_1101+700i others(3): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271115 | |||||||
| chr16:81271116 | T | A | 6 | a0001c0002t0001g0016 a0001c0007t0001g0234 a0001c0007t0001g0391 others(3): Show |
6 | HG00323.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1101+700T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271116 | |||||||
| chr16:81271116 | T | TA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.1101+700_1101+701i others(3): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271116 | |||||||
| chr16:81271117 | T | A | 35 | a0001c0001t0001g0272 a0001c0005t0001g0021 a0001c0005t0001g0022 others(32): Show |
35 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1101+701T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271117 | |||||||
| chr16:81271127 | T | G | 1 | a0001c0002t0001g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1101+711T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271127 | |||||||
| chr16:81271526 | C | T | 3 | a0002c0004t0001g0093 a0002c0004t0001g0129 a0002c0004t0001g0140 |
3 | HG00099.hp1 HG01099.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1101+1110C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271526 | |||||||
| chr16:81271789 | G | A | 1 | a0002c0006t0001g0311 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1101+1373G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271789 | |||||||
| chr16:81271804 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0176 a0001c0001t0001g0177 others(5): Show |
9 | HG01106.hp2 HG01978.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1101+1388C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271804 | |||||||
| chr16:81271874 | T | C | 10 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0268 others(7): Show |
10 | HG01081.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1101+1458T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271874 | |||||||
| chr16:81271900 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(296): Show |
307 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.1101+1484C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271900 | |||||||
| chr16:81271995 | C | T | 1 | a0003c0003t0001g0300 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1101+1579C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271995 | |||||||
| chr16:81271996 | C | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
131 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1101+1580C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271996 | |||||||
| chr16:81271999 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1101+1583C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271999 | |||||||
| chr16:81272113 | C | CT | 35 | a0001c0001t0001g0262 a0001c0001t0001g0328 a0001c0002t0001g0150 others(32): Show |
35 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1101+1715dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81272113 | ||||||
| chr16:81272113 | CT | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
242 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.1101+1715delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81272113 | ||||||
| chr16:81272144 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0307 |
2 | NA18940.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1101+1728C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272144 | |||||||
| chr16:81272226 | T | G | 1 | a0001c0005t0001g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1101+1810T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272226 | |||||||
| chr16:81272262 | T | C | 2 | a0001c0001t0001g0349 a0001c0002t0001g0016 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1101+1846T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272262 | |||||||
| chr16:81272293 | AT | A | 4 | a0001c0001t0001g0365 a0001c0001t0001g0378 a0001c0001t0001g0379 others(1): Show |
4 | HG01192.hp2 HG01361.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+1883delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81272293 | ||||||
| chr16:81272309 | A | G | 41 | a0001c0001t0001g0317 a0001c0001t0001g0355 a0001c0002t0001g0017 others(38): Show |
42 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1101+1893A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272309 | |||||||
| chr16:81272393 | C | T | 4 | a0001c0001t0001g0165 a0001c0005t0001g0013 a0001c0005t0001g0014 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+1977C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272393 | |||||||
| chr16:81272441 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1101+2025T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272441 | |||||||
| chr16:81272444 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0180 a0001c0001t0001g0182 others(1): Show |
5 | HG02027.hp1 NA18612.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1101+2028A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272444 | |||||||
| chr16:81272558 | G | A | 381 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(378): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.1101+2142G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272558 | |||||||
| chr16:81272566 | G | A | 2 | a0001c0001t0001g0349 a0001c0002t0001g0016 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1101+2150G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272566 | |||||||
| chr16:81272659 | A | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(277): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1101+2243A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272659 | |||||||
| chr16:81272730 | A | T | 4 | a0001c0007t0001g0234 a0001c0007t0001g0391 a0002c0006t0001g0029 others(1): Show |
4 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+2314A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272730 | |||||||
| chr16:81272742 | C | T | 1 | a0002c0006t0001g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1101+2326C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272742 | |||||||
| chr16:81272817 | C | G | 2 | a0001c0005t0001g0092 a0002c0004t0001g0135 |
2 | HG02602.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1101+2401C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272817 | |||||||
| chr16:81272861 | A | G | 3 | a0001c0002t0001g0015 a0001c0002t0001g0019 a0001c0002t0001g0020 |
3 | HG00735.hp1 HG01070.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1101+2445A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272861 | |||||||
| chr16:81272882 | G | A | 5 | a0003c0003t0001g0366 a0003c0003t0001g0368 a0003c0003t0001g0370 others(2): Show |
5 | NA18947.hp2 NA18964.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1101+2466G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272882 | |||||||
| chr16:81272931 | A | AGACTGGA others(31): Show |
1 | a0002c0004t0001g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1101+2516_1101+255 others(42): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81272931 | ||||||
| chr16:81272949 | G | A | 314 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(311): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1101+2533G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272949 | |||||||
| chr16:81272965 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1101+2549C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272965 | |||||||
| chr16:81272967 | A | T | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1101+2551A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272967 | |||||||
| chr16:81272978 | C | CT | 4 | a0001c0001t0001g0165 a0001c0005t0001g0013 a0001c0005t0001g0014 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+2567dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81272978 | ||||||
| chr16:81273055 | C | T | 1 | a0002c0006t0001g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1101+2639C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273055 | |||||||
| chr16:81273116 | T | C | 381 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(378): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.1101+2700T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273116 | |||||||
| chr16:81273235 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0202 others(106): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1101+2819G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273235 | |||||||
| chr16:81273258 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0202 others(105): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.1101+2842C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273258 | |||||||
| chr16:81273278 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1101+2862C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273278 | |||||||
| chr16:81273279 | G | A | 1 | a0002c0004t0001g0141 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1101+2863G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273279 | |||||||
| chr16:81273305 | G | A | 53 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0381 others(50): Show |
55 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1101+2889G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273305 | |||||||
| chr16:81273345 | G | C | 54 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0381 others(51): Show |
56 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1101+2929G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273345 | |||||||
| chr16:81273401 | G | A | 1 | a0001c0005t0001g0112 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1101+2985G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273401 | |||||||
| chr16:81273470 | C | T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | HG03017.hp2 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1101+3054C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273470 | |||||||
| chr16:81273533 | G | C | 56 | a0001c0001t0001g0381 a0001c0002t0001g0015 a0001c0002t0001g0170 others(53): Show |
58 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1101+3117G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273533 | |||||||
| chr16:81273561 | C | T | 1 | a0001c0002t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1101+3145C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273561 | |||||||
| chr16:81273576 | T | C | 2 | a0003c0003t0001g0312 a0005c0010t0001g0342 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1101+3160T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273576 | |||||||
| chr16:81273582 | G | A | 381 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(378): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.1101+3166G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273582 | |||||||
| chr16:81273639 | C | CT | 107 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(104): Show |
109 | HG00140.hp2 HG00280.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.1101+3235dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81273639 | ||||||
| chr16:81273639 | C | CTTT | 47 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0202 others(44): Show |
50 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1101+3233_1101+323 others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81273639 | ||||||
| chr16:81273656 | T | G | 1 | a0001c0002t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1101+3240T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273656 | |||||||
| chr16:81273885 | C | T | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | NA18944.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1101+3469C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273885 | |||||||
| chr16:81273966 | G | A | 2 | a0003c0003t0001g0312 a0005c0010t0001g0342 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1101+3550G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273966 | |||||||
| chr16:81273979 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(319): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1101+3563C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273979 | |||||||
| chr16:81274011 | G | C | 1 | a0001c0002t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1101+3595G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274011 | |||||||
| chr16:81274099 | A | G | 1 | a0001c0001t0002g0376 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1101+3683A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274099 | |||||||
| chr16:81274258 | C | CT | 6 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0307 others(3): Show |
6 | HG00735.hp1 HG03225.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+3865dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81274258 | ||||||
| chr16:81274258 | CT | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(274): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1101+3865delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81274258 | ||||||
| chr16:81274258 | CTT | C | 9 | a0001c0001t0001g0243 a0001c0001t0001g0285 a0001c0001t0001g0330 others(6): Show |
9 | HG00323.hp2 HG01256.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1101+3864_1101+386 others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81274258 | ||||||
| chr16:81274357 | G | A | 6 | a0001c0001t0001g0272 a0001c0007t0001g0163 a0002c0004t0001g0010 others(3): Show |
6 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1101+3941G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274357 | |||||||
| chr16:81274373 | G | C | 2 | a0003c0003t0001g0193 a0003c0003t0001g0195 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1101+3957G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274373 | |||||||
| chr16:81274382 | G | C | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1101+3966G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274382 | |||||||
| chr16:81274399 | G | T | 2 | a0002c0004t0001g0010 a0002c0004t0001g0012 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1101+3983G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274399 | |||||||
| chr16:81274486 | G | A | 2 | a0001c0001t0001g0262 a0001c0007t0001g0149 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1101+4070G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274486 | |||||||
| chr16:81274500 | G | A | 1 | a0001c0002t0001g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1101+4084G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274500 | |||||||
| chr16:81274521 | T | C | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1101+4105T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274521 | |||||||
| chr16:81274555 | C | T | 1 | a0001c0005t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1101+4139C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274555 | |||||||
| chr16:81274664 | G | T | 6 | a0001c0001t0001g0165 a0001c0005t0001g0013 a0001c0005t0001g0014 others(3): Show |
6 | HG02559.hp2 HG02602.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+4248G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274664 | |||||||
| chr16:81274747 | C | G | 8 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0269 others(5): Show |
8 | HG00735.hp1 HG01070.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101+4331C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274747 | |||||||
| chr16:81274909 | A | C | 4 | a0001c0001t0001g0165 a0001c0005t0001g0013 a0001c0005t0001g0014 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+4493A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274909 | |||||||
| chr16:81274913 | A | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
226 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.1101+4497A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274913 | |||||||
| chr16:81275014 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0202 others(76): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1101+4598T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275014 | |||||||
| chr16:81275081 | C | T | 1 | a0001c0005t0001g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1101+4665C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275081 | |||||||
| chr16:81275219 | A | G | 1 | a0001c0001t0001g0330 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1101+4803A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275219 | |||||||
| chr16:81275244 | C | T | 2 | a0001c0007t0001g0163 a0009c0013t0001g0030 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1101+4828C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275244 | |||||||
| chr16:81275261 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
231 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1101+4845C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275261 | |||||||
| chr16:81275508 | A | T | 230 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(227): Show |
235 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1101+5092A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275508 | |||||||
| chr16:81275758 | T | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1102-5099T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275758 | |||||||
| chr16:81275859 | G | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0278 a0001c0001t0001g0297 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1102-4998G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275859 | |||||||
| chr16:81275879 | C | T | 34 | a0001c0001t0001g0192 a0001c0001t0001g0207 a0001c0001t0001g0222 others(31): Show |
34 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.1102-4978C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275879 | |||||||
| chr16:81275884 | T | A | 5 | a0001c0001t0001g0272 a0001c0007t0001g0163 a0002c0004t0001g0010 others(2): Show |
5 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1102-4973T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275884 | |||||||
| chr16:81275979 | C | A | 1 | a0001c0002t0001g0077 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1102-4878C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275979 | |||||||
| chr16:81276021 | G | A | 2 | a0001c0007t0001g0163 a0009c0013t0001g0030 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-4836G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276021 | |||||||
| chr16:81276064 | G | T | 1 | a0001c0001t0001g0206 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1102-4793G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276064 | |||||||
| chr16:81276065 | G | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1102-4792G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276065 | |||||||
| chr16:81276132 | G | A | 286 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(283): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1102-4725G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276132 | |||||||
| chr16:81276161 | G | A | 1 | a0002c0006t0001g0248 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1102-4696G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276161 | |||||||
| chr16:81276215 | A | G | 1 | a0009c0013t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1102-4642A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276215 | |||||||
| chr16:81276402 | G | A | 291 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(288): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1102-4455G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276402 | |||||||
| chr16:81276457 | C | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0002t0001g0019 others(1): Show |
4 | HG00735.hp1 HG01070.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1102-4400C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276457 | |||||||
| chr16:81276700 | G | A | 5 | a0001c0001t0001g0272 a0001c0007t0001g0163 a0002c0004t0001g0010 others(2): Show |
5 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1102-4157G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276700 | |||||||
| chr16:81276926 | G | T | 1 | a0001c0001t0001g0324 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1102-3931G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276926 | |||||||
| chr16:81277002 | G | A | 1 | a0001c0002t0001g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1102-3855G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277002 | |||||||
| chr16:81277060 | G | A | 380 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(377): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.1102-3797G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277060 | |||||||
| chr16:81277065 | C | CA | 217 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(214): Show |
222 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1102-3773dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81277065 | ||||||
| chr16:81277065 | C | CAA | 10 | a0001c0001t0001g0194 a0001c0001t0001g0210 a0001c0001t0001g0220 others(7): Show |
10 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.1102-3774_1102-377 others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81277065 | ||||||
| chr16:81277097 | A | T | 2 | a0001c0001t0001g0243 a0001c0002t0001g0170 |
2 | HG02922.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1102-3760A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277097 | |||||||
| chr16:81277118 | C | T | 1 | a0001c0007t0001g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1102-3739C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277118 | |||||||
| chr16:81277129 | C | T | 1 | a0003c0003t0001g0106 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1102-3728C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277129 | |||||||
| chr16:81277158 | G | A | 4 | a0001c0001t0001g0269 a0001c0001t0001g0349 a0001c0002t0001g0016 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1102-3699G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277158 | |||||||
| chr16:81277165 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1102-3692T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277165 | |||||||
| chr16:81277197 | T | C | 1 | a0001c0002t0001g0050 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1102-3660T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277197 | |||||||
| chr16:81277342 | C | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.1102-3515C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277342 | |||||||
| chr16:81277349 | C | G | 1 | a0001c0001t0001g0392 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1102-3508C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277349 | |||||||
| chr16:81277420 | C | T | 1 | a0002c0006t0001g0244 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1102-3437C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277420 | |||||||
| chr16:81277543 | A | T | 1 | a0002c0006t0001g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1102-3314A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277543 | |||||||
| chr16:81277610 | G | A | 1 | a0001c0002t0001g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1102-3247G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277610 | |||||||
| chr16:81277718 | G | A | 1 | a0003c0003t0001g0290 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1102-3139G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277718 | |||||||
| chr16:81277728 | T | C | 1 | a0002c0006t0001g0311 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1102-3129T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277728 | |||||||
| chr16:81277812 | A | C | 1 | a0001c0005t0001g0126 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1102-3045A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277812 | |||||||
| chr16:81277880 | G | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0278 a0001c0001t0001g0297 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1102-2977G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277880 | |||||||
| chr16:81278073 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1102-2784G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278073 | |||||||
| chr16:81278091 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1102-2766G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278091 | |||||||
| chr16:81278103 | G | A | 1 | a0001c0007t0001g0163 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1102-2754G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278103 | |||||||
| chr16:81278127 | C | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | NA18944.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1102-2730C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278127 | |||||||
| chr16:81278154 | G | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0002t0001g0037 others(8): Show |
13 | HG00597.hp1 HG00609.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.1102-2703G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278154 | |||||||
| chr16:81278232 | G | A | 2 | a0003c0003t0001g0323 a0003c0003t0001g0331 |
2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1102-2625G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278232 | |||||||
| chr16:81278257 | G | T | 3 | a0001c0001t0001g0269 a0001c0001t0001g0349 a0001c0002t0001g0016 |
3 | HG02895.hp1 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1102-2600G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278257 | |||||||
| chr16:81278280 | G | C | 1 | a0001c0001t0001g0224 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1102-2577G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278280 | |||||||
| chr16:81278303 | A | T | 1 | a0001c0005t0001g0028 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1102-2554A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278303 | |||||||
| chr16:81278425 | C | A | 1 | a0003c0003t0001g0335 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1102-2432C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278425 | |||||||
| chr16:81278470 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1102-2387T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278470 | |||||||
| chr16:81278549 | T | C | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1102-2308T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278549 | |||||||
| chr16:81278609 | A | C | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1102-2248A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278609 | |||||||
| chr16:81278747 | C | T | 2 | a0006c0014t0001g0098 a0006c0016t0001g0011 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1102-2110C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278747 | |||||||
| chr16:81278954 | A | G | 1 | a0001c0002t0001g0050 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1102-1903A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278954 | |||||||
| chr16:81278967 | G | GTTGGTTT others(58): Show |
1 | a0001c0005t0001g0126 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1102-1885_1102-182 others(69): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81278967 | ||||||
| chr16:81279022 | A | G | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1102-1835A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279022 | |||||||
| chr16:81279038 | A | G | 1 | a0003c0003t0001g0359 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1102-1819A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279038 | |||||||
| chr16:81279145 | C | T | 1 | a0003c0003t0001g0007 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1102-1712C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279145 | |||||||
| chr16:81279153 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1102-1704C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279153 | |||||||
| chr16:81279257 | C | T | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1102-1600C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279257 | |||||||
| chr16:81279290 | G | C | 1 | a0001c0005t0001g0126 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1102-1567G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279290 | |||||||
| chr16:81279297 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
7 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1102-1560T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279297 | |||||||
| chr16:81279344 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1102-1513C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279344 | |||||||
| chr16:81279361 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0202 others(85): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1102-1496A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279361 | |||||||
| chr16:81279397 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1102-1460C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279397 | |||||||
| chr16:81279401 | G | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0202 others(84): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1102-1456G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279401 | |||||||
| chr16:81279411 | G | A | 1 | a0003c0003t0001g0366 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1102-1446G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279411 | |||||||
| chr16:81279472 | A | G | 1 | a0001c0001t0001g0330 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1102-1385A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279472 | |||||||
| chr16:81279832 | A | G | 2 | a0002c0004t0001g0104 a0002c0004t0001g0105 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1102-1025A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279832 | |||||||
| chr16:81279853 | G | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0287 |
2 | NA18941.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1102-1004G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279853 | |||||||
| chr16:81279930 | A | G | 2 | a0001c0001t0001g0365 a0001c0001t0001g0380 |
2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1102-927A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279930 | |||||||
| chr16:81279963 | A | T | 213 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(210): Show |
217 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1102-894A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279963 | |||||||
| chr16:81280004 | T | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0202 others(78): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1102-853T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280004 | |||||||
| chr16:81280138 | C | A | 8 | a0001c0001t0001g0262 a0001c0005t0001g0115 a0001c0005t0001g0117 others(5): Show |
8 | HG00639.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1102-719C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280138 | |||||||
| chr16:81280146 | C | T | 58 | a0003c0003t0001g0007 a0003c0003t0001g0008 a0003c0003t0001g0106 others(55): Show |
60 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1102-711C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280146 | |||||||
| chr16:81280148 | A | C | 1 | a0001c0005t0001g0027 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1102-709A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280148 | |||||||
| chr16:81280152 | A | T | 1 | a0001c0001t0001g0233 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1102-705A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280152 | |||||||
| chr16:81280166 | G | C | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1102-691G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280166 | |||||||
| chr16:81280269 | CA | C | 6 | a0001c0001t0001g0296 a0001c0002t0001g0019 a0001c0002t0001g0020 others(3): Show |
6 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1102-549delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280269 | CAA | C | 11 | a0001c0001t0001g0279 a0001c0001t0001g0392 a0001c0002t0001g0015 others(8): Show |
11 | HG00280.hp2 HG01358.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1102-550_1102-549d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280269 | CAAA | C | 26 | a0001c0001t0001g0202 a0001c0001t0001g0209 a0001c0001t0001g0260 others(23): Show |
27 | HG00099.hp2 HG00597.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1102-551_1102-549d others(5): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280269 | CAAAA | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0256 others(39): Show |
44 | HG00099.hp1 HG00609.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1102-552_1102-549d others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280269 | CAAAAA | C | 42 | a0001c0001t0001g0328 a0001c0005t0001g0024 a0001c0005t0001g0025 others(39): Show |
42 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1102-553_1102-549d others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280269 | CAAAAAA | C | 16 | a0001c0001t0001g0262 a0001c0005t0001g0132 a0001c0007t0001g0200 others(13): Show |
18 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1102-554_1102-549d others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280269 | CAAAAAAA others(1): Show |
C | 10 | a0001c0001t0001g0228 a0001c0001t0001g0269 a0001c0001t0001g0304 others(7): Show |
10 | HG01109.hp1 HG01433.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1102-556_1102-549d others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280269 | CAAAAAAA others(2): Show |
C | 54 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0181 others(51): Show |
54 | HG00140.hp1 HG00423.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1102-557_1102-549d others(11): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280269 | CAAAAAAA others(3): Show |
C | 140 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
144 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1102-558_1102-549d others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280269 | CAAAAAAA others(4): Show |
C | 15 | a0001c0001t0001g0160 a0001c0001t0001g0212 a0001c0001t0001g0216 others(12): Show |
15 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1102-559_1102-549d others(13): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280269 | CAAAAAAA others(10): Show |
C | 5 | a0001c0001t0001g0272 a0001c0005t0001g0092 a0002c0004t0001g0010 others(2): Show |
5 | HG02602.hp2 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102-565_1102-549d others(19): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280269 | CAAAAAAA others(15): Show |
C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
10 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1102-570_1102-549d others(24): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | ||||||
| chr16:81280292 | A | T | 2 | a0001c0007t0001g0163 a0009c0013t0001g0030 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-565A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280292 | |||||||
| chr16:81280293 | A | T | 2 | a0001c0007t0001g0163 a0009c0013t0001g0030 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-564A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280293 | |||||||
| chr16:81280295 | A | C | 2 | a0001c0007t0001g0163 a0009c0013t0001g0030 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-562A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280295 | |||||||
| chr16:81280297 | A | C | 2 | a0001c0007t0001g0163 a0009c0013t0001g0030 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-560A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280297 | |||||||
| chr16:81280298 | AAAAAAAA others(4): Show |
A | 2 | a0001c0007t0001g0163 a0009c0013t0001g0030 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-558_1102-548d others(13): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280298 | |||||||
| chr16:81280310 | T | C | 2 | a0001c0007t0001g0163 a0009c0013t0001g0030 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-547T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280310 | |||||||
| chr16:81280318 | C | G | 59 | a0001c0007t0001g0163 a0003c0003t0001g0007 a0003c0003t0001g0008 others(56): Show |
61 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1102-539C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280318 | |||||||
| chr16:81280320 | C | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1102-537C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280320 | |||||||
| chr16:81280320 | CACAG | C | 57 | a0003c0003t0001g0007 a0003c0003t0001g0008 a0003c0003t0001g0106 others(54): Show |
59 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1102-533_1102-530d others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280320 | ||||||
| chr16:81280322 | C | T | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1102-535C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280322 | |||||||
| chr16:81280324 | G | C | 3 | a0001c0007t0001g0163 a0003c0003t0001g0322 a0009c0013t0001g0030 |
3 | HG02602.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-533G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280324 | |||||||
| chr16:81280324 | G | GACAC | 5 | a0001c0001t0001g0272 a0001c0005t0001g0092 a0002c0004t0001g0010 others(2): Show |
5 | HG02602.hp2 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102-509_1102-506d others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280324 | ||||||
| chr16:81280324 | GAC | G | 292 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1102-507_1102-506d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280324 | ||||||
| chr16:81280326 | C | G | 1 | a0002c0022t0001g0332 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1102-531C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280326 | |||||||
| chr16:81280612 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1102-245A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280612 | |||||||
| chr16:81280680 | C | T | 1 | a0001c0007t0001g0149 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1102-177C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280680 | |||||||
| chr16:81280776 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0202 others(74): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1102-81T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280776 | |||||||
| chr16:81280973 | T | C | 6 | a0001c0001t0001g0230 a0001c0001t0001g0255 a0001c0002t0001g0059 others(3): Show |
6 | HG00408.hp2 HG02080.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207+11T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81280973 | |||||||
| chr16:81281174 | G | A | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1207+212G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281174 | |||||||
| chr16:81281267 | G | A | 7 | a0001c0001t0001g0272 a0001c0005t0001g0092 a0001c0007t0001g0163 others(4): Show |
7 | HG02602.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1207+305G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281267 | |||||||
| chr16:81281280 | T | C | 1 | a0003c0009t0001g0089 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1207+318T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281280 | |||||||
| chr16:81281314 | C | T | 1 | a0003c0003t0001g0308 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1207+352C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281314 | |||||||
| chr16:81281407 | T | C | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1207+445T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281407 | |||||||
| chr16:81281437 | C | G | 1 | a0002c0006t0001g0151 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1207+475C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281437 | |||||||
| chr16:81281753 | A | G | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1207+791A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281753 | |||||||
| chr16:81281795 | C | G | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1207+833C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281795 | |||||||
| chr16:81281824 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1207+862G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281824 | |||||||
| chr16:81281898 | T | C | 2 | a0001c0001t0001g0317 a0002c0006t0001g0237 |
2 | HG01928.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1207+936T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281898 | |||||||
| chr16:81281994 | A | C | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1207+1032A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281994 | |||||||
| chr16:81282015 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1207+1053A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282015 | |||||||
| chr16:81282217 | G | A | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1207+1255G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282217 | |||||||
| chr16:81282282 | G | A | 1 | a0006c0014t0001g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1207+1320G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282282 | |||||||
| chr16:81282377 | A | C | 1 | a0001c0001t0001g0354 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1207+1415A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282377 | |||||||
| chr16:81282482 | T | G | 5 | a0001c0005t0001g0119 a0001c0005t0001g0121 a0001c0005t0001g0122 others(2): Show |
5 | HG01243.hp1 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+1520T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282482 | |||||||
| chr16:81282535 | A | C | 1 | a0002c0004t0001g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1207+1573A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282535 | |||||||
| chr16:81282659 | C | G | 356 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(353): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1207+1697C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282659 | |||||||
| chr16:81282710 | T | G | 5 | a0001c0001t0001g0202 a0002c0004t0001g0004 a0002c0004t0001g0040 others(2): Show |
6 | HG01257.hp1 HG01258.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207+1748T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282710 | |||||||
| chr16:81282717 | A | G | 1 | a0003c0003t0001g0353 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1207+1755A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282717 | |||||||
| chr16:81282787 | G | A | 208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(205): Show |
212 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1207+1825G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282787 | |||||||
| chr16:81282878 | C | T | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1207+1916C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282878 | |||||||
| chr16:81282928 | A | G | 60 | a0001c0001t0001g0202 a0001c0001t0001g0392 a0003c0003t0001g0007 others(57): Show |
62 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.1207+1966A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282928 | |||||||
| chr16:81283320 | T | G | 6 | a0001c0001t0001g0192 a0001c0001t0001g0254 a0001c0002t0001g0039 others(3): Show |
6 | HG00423.hp1 HG01943.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-2220T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283320 | |||||||
| chr16:81283372 | C | T | 1 | a0001c0002t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1208-2168C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283372 | |||||||
| chr16:81283402 | C | T | 1 | a0001c0001t0002g0371 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1208-2138C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283402 | |||||||
| chr16:81283583 | C | T | 2 | a0001c0005t0001g0119 a0002c0006t0001g0174 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1208-1957C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283583 | |||||||
| chr16:81283743 | T | C | 1 | a0003c0003t0001g0291 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1208-1797T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283743 | |||||||
| chr16:81283793 | GTTGGCGG others(4): Show |
G | 1 | a0001c0002t0001g0037 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1208-1746_1208-173 others(15): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283793 | |||||||
| chr16:81283959 | G | A | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1208-1581G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283959 | |||||||
| chr16:81283967 | T | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
7 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-1573T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283967 | |||||||
| chr16:81284020 | C | A | 2 | a0001c0005t0001g0123 a0001c0005t0001g0133 |
2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1208-1520C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284020 | |||||||
| chr16:81284125 | G | A | 1 | a0001c0005t0001g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1208-1415G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284125 | |||||||
| chr16:81284228 | A | T | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1208-1312A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284228 | |||||||
| chr16:81284240 | TTATATAT others(37): Show |
T | 370 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(367): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.1208-1283_1208-124 others(48): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81284240 | ||||||
| chr16:81284261 | T | TTTATATA others(11): Show |
1 | a0002c0004t0001g0012 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1208-1279_1208-127 others(22): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284261 | |||||||
| chr16:81284261 | TATATTTA others(15): Show |
T | 4 | a0001c0001t0001g0272 a0001c0002t0001g0170 a0001c0002t0001g0171 others(1): Show |
4 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-1274_1208-125 others(26): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81284261 | ||||||
| chr16:81284284 | A | ATATT | 3 | a0001c0007t0001g0163 a0002c0004t0001g0010 a0002c0004t0001g0012 |
3 | HG02896.hp1 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1208-1253_1208-125 others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81284284 | ||||||
| chr16:81284284 | A | T | 4 | a0001c0001t0001g0272 a0001c0002t0001g0170 a0001c0002t0001g0171 others(1): Show |
4 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-1256A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284284 | |||||||
| chr16:81284548 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0202 others(81): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1208-992T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284548 | |||||||
| chr16:81284753 | G | A | 1 | a0003c0003t0001g0323 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1208-787G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284753 | |||||||
| chr16:81284766 | T | C | 1 | a0002c0004t0001g0131 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1208-774T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284766 | |||||||
| chr16:81284808 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1208-732T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284808 | |||||||
| chr16:81284819 | G | C | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1208-721G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284819 | |||||||
| chr16:81284819 | G | GTTTTC | 2 | a0001c0001t0001g0001 a0001c0001t0001g0183 |
4 | NA18988.hp2 NA18990.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-701_1208-697d others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81284819 | ||||||
| chr16:81284824 | C | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(15): Show |
19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1208-716C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284824 | |||||||
| chr16:81284839 | C | CT | 10 | a0001c0001t0001g0224 a0001c0001t0001g0269 a0001c0001t0001g0349 others(7): Show |
10 | HG02630.hp1 HG02895.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1208-687dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81284839 | ||||||
| chr16:81284848 | T | C | 4 | a0001c0001t0001g0165 a0001c0005t0001g0013 a0001c0005t0001g0014 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-692T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284848 | |||||||
| chr16:81285039 | C | T | 1 | a0001c0007t0001g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1208-501C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285039 | |||||||
| chr16:81285072 | T | C | 1 | a0001c0001t0001g0365 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1208-468T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285072 | |||||||
| chr16:81285076 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | NA18944.hp1 NA18953.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1208-464G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285076 | |||||||
| chr16:81285146 | C | T | 1 | a0001c0001t0001g0373 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1208-394C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285146 | |||||||
| chr16:81285154 | C | T | 1 | a0001c0007t0001g0163 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1208-386C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285154 | |||||||
| chr16:81285155 | A | T | 1 | a0002c0006t0001g0151 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1208-385A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285155 | |||||||
| chr16:81285160 | A | G | 1 | a0002c0006t0001g0310 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1208-380A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285160 | |||||||
| chr16:81285170 | A | G | 9 | a0001c0001t0001g0269 a0001c0001t0001g0349 a0001c0002t0001g0015 others(6): Show |
9 | HG00735.hp1 HG01070.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1208-370A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285170 | |||||||
| chr16:81285276 | G | C | 1 | a0001c0005t0001g0126 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1208-264G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285276 | |||||||
| chr16:81285277 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0209 others(76): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1208-263A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285277 | |||||||
| chr16:81285445 | G | A | 1 | a0001c0005t0001g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1208-95G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285445 | |||||||
| chr16:81285470 | C | T | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1208-70C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285470 | |||||||
| chr16:81285496 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1208-44C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285496 | |||||||
| chr16:81285733 | G | A | 5 | a0001c0001t0001g0272 a0001c0007t0001g0163 a0002c0004t0001g0010 others(2): Show |
5 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+99G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81285733 | |||||||
| chr16:81285814 | A | C | 6 | a0001c0002t0001g0015 a0001c0002t0001g0019 a0001c0002t0001g0020 others(3): Show |
6 | HG00735.hp1 HG01070.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+180A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81285814 | |||||||
| chr16:81285833 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(94): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1302+199G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81285833 | |||||||
| chr16:81285839 | G | A | 1 | a0002c0020t0001g0274 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1302+205G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81285839 | |||||||
| chr16:81285878 | A | C | 1 | a0003c0003t0001g0007 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1302+244A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81285878 | |||||||
| chr16:81286053 | T | A | 8 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0018t0001g0275 others(5): Show |
8 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+419T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286053 | |||||||
| chr16:81286053 | TA | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(89): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1302+429delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 81286053 | ||||||
| chr16:81286194 | C | T | 1 | a0002c0004t0001g0033 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1302+560C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286194 | |||||||
| chr16:81286314 | T | A | 1 | a0001c0002t0001g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1302+680T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286314 | |||||||
| chr16:81286426 | G | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
7 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+792G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286426 | |||||||
| chr16:81286476 | G | A | 2 | a0006c0014t0001g0098 a0006c0016t0001g0011 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1303-819G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286476 | |||||||
| chr16:81286515 | A | C | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1303-780A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286515 | |||||||
| chr16:81286580 | G | A | 1 | a0002c0004t0001g0135 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1303-715G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286580 | |||||||
| chr16:81286756 | G | A | 1 | a0001c0007t0001g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1303-539G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286756 | |||||||
| chr16:81286802 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1303-493C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286802 | |||||||
| chr16:81286803 | G | A | 2 | a0001c0001t0001g0373 a0002c0004t0001g0130 |
2 | NA18945.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1303-492G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286803 | |||||||
| chr16:81286902 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303-393C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286902 | |||||||
| chr16:81286907 | C | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0209 others(78): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1303-388C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286907 | |||||||
| chr16:81287016 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1303-279A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81287016 | |||||||
| chr16:81287224 | C | T | 2 | a0003c0003t0001g0327 a0003c0003t0001g0338 |
2 | HG00621.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1303-71C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81287224 | |||||||
| chr16:81287225 | A | G | 381 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(378): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.1303-70A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81287225 | |||||||
| chr16:81287282 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
7 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303-13G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81287282 | |||||||
| chr16:81287693 | T | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0202 others(81): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1414+287T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81287693 | |||||||
| chr16:81287918 | T | G | 53 | a0001c0001t0001g0202 a0001c0001t0001g0207 a0001c0005t0001g0092 others(50): Show |
55 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1414+512T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81287918 | |||||||
| chr16:81288055 | C | T | 1 | a0006c0014t0001g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1414+649C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288055 | |||||||
| chr16:81288071 | G | T | 1 | a0002c0004t0001g0140 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1414+665G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288071 | |||||||
| chr16:81288101 | G | A | 1 | a0001c0007t0001g0391 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1414+695G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288101 | |||||||
| chr16:81288173 | G | A | 6 | a0001c0001t0001g0148 a0001c0001t0001g0181 a0001c0001t0001g0213 others(3): Show |
6 | HG00438.hp2 HG00597.hp2 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.1414+767G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288173 | |||||||
| chr16:81288204 | C | T | 225 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(222): Show |
229 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1414+798C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288204 | |||||||
| chr16:81288204 | CATTAA | C | 44 | a0001c0005t0001g0092 a0003c0003t0001g0007 a0003c0003t0001g0008 others(41): Show |
46 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1414+800_1414+804d others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 81288204 | ||||||
| chr16:81288477 | C | T | 1 | a0002c0004t0001g0135 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1414+1071C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288477 | |||||||
| chr16:81288503 | G | A | 1 | a0002c0006t0001g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1414+1097G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288503 | |||||||
| chr16:81288633 | G | A | 3 | a0001c0001t0001g0272 a0002c0004t0001g0010 a0002c0004t0001g0012 |
3 | HG02630.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1414+1227G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288633 | |||||||
| chr16:81288715 | A | C | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1414+1309A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288715 | |||||||
| chr16:81288768 | G | A | 4 | a0004c0008t0001g0055 a0004c0008t0001g0085 a0004c0008t0001g0097 others(1): Show |
4 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414+1362G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288768 | |||||||
| chr16:81288838 | G | C | 1 | a0006c0014t0001g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1414+1432G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288838 | |||||||
| chr16:81288856 | C | T | 1 | a0002c0004t0001g0135 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1414+1450C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288856 | |||||||
| chr16:81289066 | T | C | 381 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(378): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.1415-1282T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289066 | |||||||
| chr16:81289184 | C | T | 1 | a0002c0006t0001g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1415-1164C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289184 | |||||||
| chr16:81289615 | T | C | 1 | a0001c0005t0001g0028 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1415-733T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289615 | |||||||
| chr16:81289772 | G | A | 1 | a0006c0014t0001g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1415-576G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289772 | |||||||
| chr16:81289813 | G | A | 1 | a0012c0012t0001g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1415-535G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289813 | |||||||
| chr16:81289901 | G | A | 1 | a0001c0001t0002g0375 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1415-447G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289901 | |||||||
| chr16:81290015 | C | G | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1415-333C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81290015 | |||||||
| chr16:81290148 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1415-200C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81290148 | |||||||
| chr16:81290245 | T | C | 2 | a0006c0014t0001g0098 a0006c0016t0001g0011 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1415-103T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81290245 | |||||||
| chr16:81290316 | T | C | 2 | a0006c0014t0001g0098 a0006c0016t0001g0011 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1415-32T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81290316 |