Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 283742 |
| ensemblid | ENSG00000171262.11 |
| hgncid | 26773 |
| symbol | FAM98B |
| name | family with sequence similarity 98 member B |
| refseq_nuc | NM_173611.4 |
| refseq_prot | NP_775882.2 |
| ensembl_nuc | ENST00000397609.6 |
| ensembl_prot | ENSP00000380734.2 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 38454127 |
| end | 38487710 |
| strand | + |
| ver | v1.2 |
| region | chr15:38454127-38487710 |
| region5000 | chr15:38449127-38492710 |
| regionname0 | FAM98B_chr15_38454127_38487710 |
| regionname5000 | FAM98B_chr15_38449127_38492710 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 433 | 357 | 86 | 59 | 159 | 18 | 33 | 123 | FAM98B_chr15_38449127_38492710 | FAM98B | MRGPE others(428): Show |
chr15 | 38449127 | 38492710 |
| a0002 | 0/0 | 430 | 30 | 3 | 9 | 15 | 0 | 3 | 12 | FAM98B_chr15_38449127_38492710 | FAM98B | MRGPE others(425): Show |
chr15 | 38449127 | 38492710 |
| a0003 | 0/0 | 427 | 4 | 0 | 0 | 1 | 0 | 3 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | MRGPE others(422): Show |
chr15 | 38449127 | 38492710 |
| a0004 | 0/0 | 433 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | MRGPE others(428): Show |
chr15 | 38449127 | 38492710 |
| a0005 | 0/0 | 433 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | MRGPE others(428): Show |
chr15 | 38449127 | 38492710 |
| a0006 | 0/0 | 433 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | MRGPE others(428): Show |
chr15 | 38449127 | 38492710 |
| a0007 | 0/0 | 433 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | MRGPE others(428): Show |
chr15 | 38449127 | 38492710 |
| a0008 | 0/0 | 424 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | MRGPE others(419): Show |
chr15 | 38449127 | 38492710 |
| a0009 | 0/0 | 433 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | MRGPE others(428): Show |
chr15 | 38449127 | 38492710 |
| a0010 | 0/0 | 433 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | MRGPE others(428): Show |
chr15 | 38449127 | 38492710 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1299 | 337 | 71 | 56 | 158 | 18 | 32 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1294): Show |
chr15 | 38449127 | 38492710 | ||
| a0001c0003 | 0/0 | 1299 | 12 | 8 | 3 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1294): Show |
chr15 | 38449127 | 38492710 | ||
| a0001c0004 | 0/0 | 1299 | 7 | 7 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1294): Show |
chr15 | 38449127 | 38492710 | ||
| a0001c0014 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1294): Show |
chr15 | 38449127 | 38492710 | ||
| a0002c0002 | 0/0 | 1290 | 29 | 3 | 9 | 15 | 0 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1285): Show |
chr15 | 38449127 | 38492710 | ||
| a0002c0007 | 0/0 | 1290 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1285): Show |
chr15 | 38449127 | 38492710 | ||
| a0003c0005 | 0/0 | 1281 | 4 | 0 | 0 | 1 | 0 | 3 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1276): Show |
chr15 | 38449127 | 38492710 | ||
| a0004c0006 | 0/0 | 1299 | 3 | 0 | 2 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1294): Show |
chr15 | 38449127 | 38492710 | ||
| a0005c0010 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1294): Show |
chr15 | 38449127 | 38492710 | ||
| a0006c0012 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1294): Show |
chr15 | 38449127 | 38492710 | ||
| a0007c0013 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1294): Show |
chr15 | 38449127 | 38492710 | ||
| a0008c0011 | 0/0 | 1272 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1267): Show |
chr15 | 38449127 | 38492710 | ||
| a0009c0009 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1294): Show |
chr15 | 38449127 | 38492710 | ||
| a0010c0008 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ATGAG others(1294): Show |
chr15 | 38449127 | 38492710 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4388 | 136 | 10 | 24 | 82 | 7 | 12 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0002 | 1/0 | 4388 | 110 | 26 | 21 | 50 | 5 | 7 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0003 | 0/0 | 4388 | 25 | 0 | 3 | 21 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0004 | 0/0 | 4388 | 30 | 9 | 7 | 1 | 4 | 9 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0005 | 0/0 | 4388 | 12 | 12 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0007 | 0/0 | 4387 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4382): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0008 | 0/0 | 4388 | 3 | 0 | 0 | 0 | 1 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0009 | 0/0 | 4388 | 3 | 3 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0010 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0011 | 0/0 | 4388 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0012 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0013 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0015 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0016 | 0/0 | 4388 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0017 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0018 | 0/0 | 4388 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0019 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0020 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0021 | 0/0 | 4387 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4382): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0022 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0001t0023 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0003t0002 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0003t0005 | 0/0 | 4388 | 10 | 6 | 3 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0003t0014 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0004t0006 | 0/0 | 4388 | 5 | 5 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0004t0010 | 0/0 | 4388 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0001c0014t0001 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0002c0002t0002 | 0/0 | 4379 | 6 | 3 | 3 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4374): Show |
chr15 | 38449127 | 38492710 |
| a0002c0002t0003 | 0/0 | 4379 | 21 | 0 | 5 | 14 | 0 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4374): Show |
chr15 | 38449127 | 38492710 |
| a0002c0002t0004 | 0/0 | 4379 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4374): Show |
chr15 | 38449127 | 38492710 |
| a0002c0002t0024 | 0/0 | 4379 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4374): Show |
chr15 | 38449127 | 38492710 |
| a0002c0007t0003 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4374): Show |
chr15 | 38449127 | 38492710 |
| a0003c0005t0001 | 0/0 | 4370 | 4 | 0 | 0 | 1 | 0 | 3 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4365): Show |
chr15 | 38449127 | 38492710 |
| a0004c0006t0004 | 0/0 | 4388 | 3 | 0 | 2 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0005c0010t0001 | 0/0 | 4388 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0006c0012t0006 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0007c0013t0003 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0008c0011t0003 | 0/0 | 4361 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4356): Show |
chr15 | 38449127 | 38492710 |
| a0009c0009t0002 | 0/0 | 4388 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| a0010c0008t0001 | 0/0 | 4388 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | ACTTA others(4383): Show |
chr15 | 38449127 | 38492710 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 24 | 2 | 3 | 18 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0017 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0003 | 0/0 | 16 | 0 | 5 | 6 | 2 | 3 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0005 | 0/0 | 7 | 0 | 5 | 1 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0009 | 1/0 | 5 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0003g0002 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0003g0004 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0003g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0005g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0007g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0008g0007 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0011g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0012g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0013g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0016g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0017g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0018g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0019g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0020g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0021g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0022g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0001t0023g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0003t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0003t0005g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0003t0005g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0003t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0003t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0003t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0003t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0003t0014g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0004t0006g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0004t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0004t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0004t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0004t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0001c0014t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0003g0002 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0002t0024g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0002c0007t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0003c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0003c0005t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0003c0005t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0004c0006t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0004c0006t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0004c0006t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0005c0010t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0006c0012t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0007c0013t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0008c0011t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0009c0009t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| a0010c0008t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | GBR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00140 | hp1 | a0001 | c0001 | t0008 | g0007 | EUR | GBR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0174 | EUR | GBR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | FIN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0085 | EUR | FIN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | FIN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0097 | EUR | FIN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00642 | hp1 | a0002 | c0002 | t0003 | g0168 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0073 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG00738 | hp2 | a0002 | c0002 | t0003 | g0169 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01069 | hp1 | a0001 | c0003 | t0005 | g0053 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01071 | hp1 | a0001 | c0003 | t0005 | g0053 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0215 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01106 | hp1 | a0001 | c0001 | t0021 | g0164 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01109 | hp2 | a0001 | c0003 | t0005 | g0015 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01169 | hp1 | a0002 | c0002 | t0004 | g0092 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0095 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0074 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0111 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01433 | hp1 | a0002 | c0002 | t0003 | g0140 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0084 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0030 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01928 | hp2 | a0005 | c0010 | t0001 | g0229 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01981 | hp1 | a0002 | c0002 | t0003 | g0161 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02015 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02055 | hp1 | a0001 | c0003 | t0005 | g0015 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02055 | hp2 | a0006 | c0012 | t0006 | g0057 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02080 | hp1 | a0001 | c0001 | t0020 | g0188 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02129 | hp2 | a0007 | c0013 | t0003 | g0004 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02132 | hp1 | a0001 | c0001 | t0017 | g0207 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02155 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | CDX | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0086 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02258 | hp2 | a0001 | c0004 | t0006 | g0028 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02273 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02280 | hp2 | a0001 | c0003 | t0005 | g0102 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02293 | hp1 | a0008 | c0011 | t0003 | g0162 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02300 | hp1 | a0004 | c0006 | t0004 | g0089 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02523 | hp1 | a0002 | c0002 | t0024 | g0165 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02572 | hp2 | a0001 | c0004 | t0006 | g0027 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02602 | hp1 | a0001 | c0001 | t0008 | g0007 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0108 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0099 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02622 | hp1 | a0001 | c0004 | t0010 | g0058 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0008 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02630 | hp1 | a0001 | c0004 | t0006 | g0027 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02647 | hp1 | a0001 | c0004 | t0006 | g0059 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0093 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0172 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0055 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02735 | hp1 | a0001 | c0003 | t0005 | g0231 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02738 | hp1 | a0009 | c0009 | t0002 | g0143 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0141 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0136 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0170 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02896 | hp1 | a0001 | c0003 | t0005 | g0105 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0171 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0126 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0106 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0031 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03017 | hp1 | a0010 | c0008 | t0001 | g0179 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03041 | hp1 | a0001 | c0001 | t0022 | g0061 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03130 | hp1 | a0001 | c0004 | t0006 | g0028 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0078 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0094 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0087 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0007 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03491 | hp1 | a0003 | c0005 | t0001 | g0213 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03492 | hp1 | a0003 | c0005 | t0001 | g0051 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0054 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03669 | hp1 | a0002 | c0002 | t0003 | g0167 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0091 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0096 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03834 | hp1 | a0001 | c0001 | t0016 | g0187 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03834 | hp2 | a0003 | c0005 | t0001 | g0051 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03927 | hp1 | a0002 | c0002 | t0003 | g0166 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03942 | hp2 | a0002 | c0007 | t0003 | g0232 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0090 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG04184 | hp1 | a0004 | c0006 | t0004 | g0088 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0216 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18522 | hp2 | a0001 | c0003 | t0005 | g0103 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18942 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18945 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18956 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18965 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18972 | hp1 | a0002 | c0002 | t0003 | g0070 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18986 | hp2 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18990 | hp2 | a0001 | c0001 | t0012 | g0045 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18999 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19000 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19043 | hp1 | a0001 | c0001 | t0015 | g0173 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19043 | hp2 | a0001 | c0003 | t0014 | g0072 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19055 | hp2 | a0003 | c0005 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19060 | hp1 | a0001 | c0014 | t0001 | g0023 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19079 | hp1 | a0002 | c0002 | t0003 | g0067 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19087 | hp2 | a0001 | c0001 | t0023 | g0005 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19090 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA19240 | hp2 | a0001 | c0003 | t0005 | g0015 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ASW | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA20752 | hp1 | a0001 | c0001 | t0018 | g0138 | EUR | TSI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0118 | EUR | TSI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | TSI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | GIH | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG01123 | hp2 | a0004 | c0006 | t0004 | g0033 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02486 | hp1 | a0001 | c0003 | t0005 | g0015 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG02559 | hp2 | a0001 | c0004 | t0010 | g0056 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03471 | hp1 | a0001 | c0001 | t0019 | g0196 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | USA | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0123 | AFR | USA | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0112 | REF | REF | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0009 | REF | REF | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:38470352 | C | T | 1 | a0007 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.478C>T | p.Pro160Ser | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/8 | 513/4388 | 478/1302 | 160/433 | chr15 | 38470352 | |||
| chr15:38470377 | C | T | 1 | a0006 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.503C>T | p.Pro168Leu | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/8 | 538/4388 | 503/1302 | 168/433 | chr15 | 38470377 | |||
| chr15:38484433 | G | C | 1 | a0010 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1076G>C | p.Trp359Ser | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1111/4388 | 1076/1302 | 359/433 | chr15 | 38484433 | |||
| chr15:38484469 | G | A | 1 | a0004 | 3 | HG01123.hp2 HG02300.hp1 HG04184.hp1 |
missense_variant | MODERATE | c.1112G>A | p.Gly371Glu | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1147/4388 | 1112/1302 | 371/433 | chr15 | 38484469 | |||
| chr15:38484483 | T | G | 1 | a0009 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.1126T>G | p.Trp376Gly | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1161/4388 | 1126/1302 | 376/433 | chr15 | 38484483 | |||
| chr15:38484486 | G | A | 1 | a0005 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1129G>A | p.Gly377Arg | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1164/4388 | 1129/1302 | 377/433 | chr15 | 38484486 | |||
| chr15:38484532 | ATTATGGT others(11): Show |
A | 1 | a0003 | 4 | HG03491.hp1 HG03492.hp1 HG03834.hp2 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.1194_1211delTTATGG others(12): Show |
p.Tyr399_Gly404del | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1229/4388 | 1194/1302 | 398/433 | INFO_REALIGN_3_PRIME | chr15 | 38484532 | ||
| chr15:38484551 | TTATGGTG others(11): Show |
T | 1 | a0008 | 1 | HG02293.hp1 | disruptive_inframe_deletion | MODERATE | c.1209_1226delGGGCTA others(12): Show |
p.Gly404_Gly409del | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1244/4388 | 1209/1302 | 403/433 | INFO_REALIGN_3_PRIME | chr15 | 38484551 | ||
| chr15:38484605 | AGGTGGTG others(2): Show |
A | 2 | a0002 a0008 |
31 | HG00642.hp1 HG00738.hp2 HG01169.hp1 others(28): Show |
disruptive_inframe_deletion | MODERATE | c.1269_1277delTGGTGG others(3): Show |
p.Gly424_Gly426del | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1304/4388 | 1269/1302 | 423/433 | INFO_REALIGN_3_PRIME | chr15 | 38484605 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:38454188 | A | G | 1 | a0001c0014 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.27A>G | p.Gln9Gln | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/8 | 62/4388 | 27/1302 | 9/433 | chr15 | 38454188 | |||
| chr15:38484368 | T | C | 2 | a0001c0003 a0002c0007 |
13 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(10): Show |
synonymous_variant | LOW | c.1011T>C | p.Gly337Gly | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1046/4388 | 1011/1302 | 337/433 | chr15 | 38484368 | |||
| chr15:38484440 | T | C | 2 | a0001c0004 a0006c0012 |
8 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(5): Show |
synonymous_variant | LOW | c.1083T>C | p.Gly361Gly | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1118/4388 | 1083/1302 | 361/433 | chr15 | 38484440 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:38484675 | G | A | 1 | a0001c0001t0012 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 16 | chr15 | 38484675 | ||||||
| chr15:38484810 | A | G | 1 | a0002c0002t0024 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*151A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 151 | chr15 | 38484810 | ||||||
| chr15:38484970 | A | G | 2 | a0001c0001t0012 a0001c0001t0023 |
2 | NA18990.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*311A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 311 | chr15 | 38484970 | ||||||
| chr15:38485057 | A | G | 1 | a0001c0001t0022 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 398 | chr15 | 38485057 | ||||||
| chr15:38485088 | C | T | 1 | a0001c0001t0021 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*429C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 429 | chr15 | 38485088 | ||||||
| chr15:38485142 | C | T | 2 | a0001c0004t0006 a0006c0012t0006 |
6 | HG02055.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*483C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 483 | chr15 | 38485142 | ||||||
| chr15:38485173 | G | A | 1 | a0001c0001t0013 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*514G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 514 | chr15 | 38485173 | ||||||
| chr15:38485180 | T | C | 1 | a0001c0001t0021 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 521 | chr15 | 38485180 | ||||||
| chr15:38485264 | G | A | 1 | a0001c0003t0014 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 605 | chr15 | 38485264 | ||||||
| chr15:38485272 | T | A | 1 | a0001c0001t0015 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*613T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 613 | chr15 | 38485272 | ||||||
| chr15:38485622 | C | T | 1 | a0001c0001t0020 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 963 | chr15 | 38485622 | ||||||
| chr15:38485632 | A | C | 8 | a0001c0001t0003 a0001c0001t0022 a0001c0003t0014 others(5): Show |
52 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*973A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 973 | chr15 | 38485632 | ||||||
| chr15:38486037 | T | G | 1 | a0001c0001t0016 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1378T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1378 | chr15 | 38486037 | ||||||
| chr15:38486273 | GA | G | 2 | a0001c0001t0007 a0001c0001t0021 |
5 | HG01106.hp1 HG02258.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1621delA | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1621 | INFO_REALIGN_3_PRIME | chr15 | 38486273 | |||||
| chr15:38486331 | A | C | 1 | a0001c0001t0019 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1672A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1672 | chr15 | 38486331 | ||||||
| chr15:38486691 | T | C | 1 | a0001c0001t0017 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2032T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2032 | chr15 | 38486691 | ||||||
| chr15:38486839 | G | A | 1 | a0001c0001t0008 | 3 | HG00140.hp1 HG02602.hp1 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2180G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2180 | chr15 | 38486839 | ||||||
| chr15:38486896 | G | A | 1 | a0001c0001t0022 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2237G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2237 | chr15 | 38486896 | ||||||
| chr15:38487116 | C | T | 1 | a0001c0001t0021 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2457C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2457 | chr15 | 38487116 | ||||||
| chr15:38487121 | G | A | 1 | a0001c0001t0007 | 4 | HG02258.hp1 HG02615.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2462G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2462 | chr15 | 38487121 | ||||||
| chr15:38487206 | T | C | 1 | a0001c0001t0003 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2547T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2547 | chr15 | 38487206 | ||||||
| chr15:38487335 | A | C | 2 | a0001c0001t0005 a0001c0003t0005 |
22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2676A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2676 | chr15 | 38487335 | ||||||
| chr15:38487339 | G | T | 2 | a0001c0001t0010 a0001c0004t0010 |
3 | HG02559.hp2 HG02622.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2680G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2680 | chr15 | 38487339 | ||||||
| chr15:38487425 | A | G | 32 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(29): Show |
277 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*2766A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2766 | chr15 | 38487425 | ||||||
| chr15:38487537 | T | C | 10 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0016 others(7): Show |
149 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*2878T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2878 | chr15 | 38487537 | ||||||
| chr15:38487556 | C | G | 1 | a0001c0001t0018 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2897C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2897 | chr15 | 38487556 | ||||||
| chr15:38487589 | T | C | 6 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0011 others(3): Show |
15 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2930T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2930 | chr15 | 38487589 | ||||||
| chr15:38487701 | G | A | 2 | a0001c0001t0009 a0001c0001t0015 |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3042G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 3042 | chr15 | 38487701 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:38454243 | T | C | 1 | a0001c0001t0004g0054 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.71+11T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454243 | |||||||
| chr15:38454407 | T | C | 7 | a0001c0001t0010g0055 a0001c0004t0006g0027 a0001c0004t0006g0028 others(4): Show |
9 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+175T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454407 | |||||||
| chr15:38454449 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.71+217C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454449 | |||||||
| chr15:38454548 | G | T | 1 | a0001c0004t0006g0028 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.71+316G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454548 | |||||||
| chr15:38454671 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.71+439A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454671 | |||||||
| chr15:38454696 | A | G | 3 | a0001c0003t0005g0053 a0001c0003t0005g0231 a0002c0007t0003g0232 |
4 | HG01069.hp1 HG01071.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+464A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454696 | |||||||
| chr15:38454870 | C | G | 1 | a0001c0001t0002g0230 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.71+638C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454870 | |||||||
| chr15:38455077 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.71+845G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455077 | |||||||
| chr15:38455114 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(74): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.71+882A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455114 | |||||||
| chr15:38455223 | G | T | 1 | a0001c0001t0002g0174 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.71+991G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455223 | |||||||
| chr15:38455343 | C | T | 4 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+1111C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455343 | |||||||
| chr15:38455437 | C | CT | 5 | a0002c0002t0003g0166 a0002c0002t0003g0167 a0002c0002t0003g0168 others(2): Show |
5 | HG00642.hp1 HG00738.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+1206dupT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38455437 | ||||||
| chr15:38455477 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.71+1245T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455477 | |||||||
| chr15:38455671 | C | T | 1 | a0001c0001t0001g0052 | 2 | NA18979.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.71+1439C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455671 | |||||||
| chr15:38455685 | C | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71+1453C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455685 | |||||||
| chr15:38456318 | C | T | 4 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+2086C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38456318 | |||||||
| chr15:38456362 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA18944.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.71+2130G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38456362 | |||||||
| chr15:38456385 | G | A | 1 | a0001c0001t0022g0061 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.71+2153G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38456385 | |||||||
| chr15:38456479 | G | A | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71+2247G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38456479 | |||||||
| chr15:38456782 | A | G | 1 | a0001c0001t0002g0163 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.71+2550A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38456782 | |||||||
| chr15:38457058 | T | A | 1 | a0001c0001t0002g0062 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.71+2826T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457058 | |||||||
| chr15:38457171 | T | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71+2939T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457171 | |||||||
| chr15:38457188 | T | A | 1 | a0001c0001t0002g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.71+2956T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457188 | |||||||
| chr15:38457215 | G | T | 2 | a0002c0002t0003g0161 a0008c0011t0003g0162 |
2 | HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.71+2983G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457215 | |||||||
| chr15:38457225 | C | T | 1 | a0005c0010t0001g0229 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.71+2993C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457225 | |||||||
| chr15:38457411 | A | G | 1 | a0001c0001t0005g0160 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.71+3179A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457411 | |||||||
| chr15:38457560 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(46): Show |
95 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.71+3328T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457560 | |||||||
| chr15:38457654 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.71+3422G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457654 | |||||||
| chr15:38457957 | C | CT | 24 | a0001c0001t0001g0208 a0001c0001t0002g0005 a0001c0001t0002g0021 others(21): Show |
36 | HG00597.hp1 HG00673.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.71+3742dupT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38457957 | ||||||
| chr15:38457957 | CT | C | 40 | a0001c0001t0001g0010 a0001c0001t0001g0177 a0001c0001t0001g0178 others(37): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.71+3742delT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38457957 | ||||||
| chr15:38457978 | A | G | 3 | a0001c0003t0005g0053 a0001c0003t0005g0231 a0002c0007t0003g0232 |
4 | HG01069.hp1 HG01071.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+3746A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457978 | |||||||
| chr15:38458158 | G | A | 22 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0013 others(19): Show |
48 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.71+3926G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458158 | |||||||
| chr15:38458541 | A | G | 1 | a0002c0002t0003g0071 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.71+4309A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458541 | |||||||
| chr15:38458581 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4349T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458581 | |||||||
| chr15:38458619 | C | G | 3 | a0001c0001t0001g0228 a0003c0005t0001g0051 a0003c0005t0001g0213 |
4 | HG03017.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+4387C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458619 | |||||||
| chr15:38458733 | GCTTGGAA others(8): Show |
G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4502_71+4516del others(15): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458733 | |||||||
| chr15:38458749 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4517G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458749 | |||||||
| chr15:38458750 | G | T | 4 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+4518G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458750 | |||||||
| chr15:38458764 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4532C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458764 | |||||||
| chr15:38458765 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4533C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458765 | |||||||
| chr15:38458766 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4534C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458766 | |||||||
| chr15:38458771 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4539C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458771 | |||||||
| chr15:38458772 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4540A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458772 | |||||||
| chr15:38458774 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4542G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458774 | |||||||
| chr15:38458776 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4544C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458776 | |||||||
| chr15:38458778 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4546G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458778 | |||||||
| chr15:38458781 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4549A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458781 | |||||||
| chr15:38458784 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4552G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458784 | |||||||
| chr15:38458786 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.71+4554T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458786 | |||||||
| chr15:38458787 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4555G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458787 | |||||||
| chr15:38458789 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4557C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458789 | |||||||
| chr15:38458790 | C | A | 22 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0013 others(19): Show |
48 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.71+4558C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458790 | |||||||
| chr15:38458792 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4560C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458792 | |||||||
| chr15:38458794 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4562G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458794 | |||||||
| chr15:38458796 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4564T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458796 | |||||||
| chr15:38458797 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4565C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458797 | |||||||
| chr15:38458799 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4567G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458799 | |||||||
| chr15:38458800 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4568C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458800 | |||||||
| chr15:38458802 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4570T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458802 | |||||||
| chr15:38458805 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4573C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458805 | |||||||
| chr15:38458807 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4575A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458807 | |||||||
| chr15:38458811 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4579C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458811 | |||||||
| chr15:38458812 | T | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4580T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458812 | |||||||
| chr15:38458813 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4581G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458813 | |||||||
| chr15:38458817 | A | T | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71+4585A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458817 | |||||||
| chr15:38458818 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4586C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458818 | |||||||
| chr15:38458820 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4588G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458820 | |||||||
| chr15:38458821 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4589G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458821 | |||||||
| chr15:38458824 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4592C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458824 | |||||||
| chr15:38458830 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4598C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458830 | |||||||
| chr15:38458832 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4600C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458832 | |||||||
| chr15:38458837 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4605T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458837 | |||||||
| chr15:38458840 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4608G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458840 | |||||||
| chr15:38458842 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4610C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458842 | |||||||
| chr15:38458844 | T | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4612T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458844 | |||||||
| chr15:38458846 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4614T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458846 | |||||||
| chr15:38458849 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4617T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458849 | |||||||
| chr15:38458851 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4619A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458851 | |||||||
| chr15:38458853 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4621A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458853 | |||||||
| chr15:38458855 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4623C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458855 | |||||||
| chr15:38458858 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4626G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458858 | |||||||
| chr15:38458860 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4628C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458860 | |||||||
| chr15:38458861 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4629T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458861 | |||||||
| chr15:38458862 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4630G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458862 | |||||||
| chr15:38458863 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4631C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458863 | |||||||
| chr15:38458864 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4632A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458864 | |||||||
| chr15:38458866 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4634A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458866 | |||||||
| chr15:38458874 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4642C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458874 | |||||||
| chr15:38458876 | T | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4644T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458876 | |||||||
| chr15:38458879 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4647T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458879 | |||||||
| chr15:38458887 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4655G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458887 | |||||||
| chr15:38458888 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4656A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458888 | |||||||
| chr15:38458892 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4660T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458892 | |||||||
| chr15:38458894 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4662T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458894 | |||||||
| chr15:38458898 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4666A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458898 | |||||||
| chr15:38458899 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4667A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458899 | |||||||
| chr15:38458900 | G | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4668G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458900 | |||||||
| chr15:38458902 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4670A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458902 | |||||||
| chr15:38458904 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4672A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458904 | |||||||
| chr15:38458906 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4674A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458906 | |||||||
| chr15:38458912 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4680T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458912 | |||||||
| chr15:38458914 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4682C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458914 | |||||||
| chr15:38458920 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0214 |
3 | NA18945.hp2 NA18994.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.71+4688G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458920 | |||||||
| chr15:38458920 | G | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4688G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458920 | |||||||
| chr15:38458921 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4689A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458921 | |||||||
| chr15:38458922 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.71+4690G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458922 | |||||||
| chr15:38458927 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4695T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458927 | |||||||
| chr15:38458930 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4698C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458930 | |||||||
| chr15:38458931 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4699T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458931 | |||||||
| chr15:38458949 | G | A | 22 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0013 others(19): Show |
48 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.71+4717G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458949 | |||||||
| chr15:38458956 | G | A | 3 | a0001c0001t0004g0030 a0001c0001t0004g0084 a0001c0001t0004g0085 |
4 | HG00280.hp2 HG00735.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+4724G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458956 | |||||||
| chr15:38459017 | C | G | 1 | a0001c0001t0002g0147 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.71+4785C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459017 | |||||||
| chr15:38459025 | C | T | 1 | a0001c0001t0022g0061 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.71+4793C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459025 | |||||||
| chr15:38459038 | C | T | 15 | a0001c0001t0005g0016 a0001c0001t0005g0100 a0001c0001t0005g0101 others(12): Show |
22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.71+4806C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459038 | |||||||
| chr15:38459105 | C | T | 1 | a0001c0004t0010g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.71+4873C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459105 | |||||||
| chr15:38459124 | T | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71+4892T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459124 | |||||||
| chr15:38459277 | C | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0086 |
3 | HG02258.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.72-4755C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459277 | |||||||
| chr15:38459296 | C | T | 2 | a0001c0001t0002g0145 a0001c0001t0002g0146 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.72-4736C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459296 | |||||||
| chr15:38459330 | C | T | 3 | a0001c0001t0007g0031 a0001c0001t0007g0086 a0001c0001t0007g0099 |
4 | HG02258.hp1 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4702C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459330 | |||||||
| chr15:38459461 | G | A | 1 | a0001c0001t0022g0061 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72-4571G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459461 | |||||||
| chr15:38459556 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.72-4476C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459556 | |||||||
| chr15:38459569 | T | G | 1 | a0001c0001t0005g0160 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72-4463T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459569 | |||||||
| chr15:38459597 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72-4435G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459597 | |||||||
| chr15:38459752 | C | G | 1 | a0001c0001t0004g0054 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.72-4280C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459752 | |||||||
| chr15:38459815 | A | C | 22 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0013 others(19): Show |
48 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.72-4217A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459815 | |||||||
| chr15:38459844 | C | G | 2 | a0001c0001t0002g0144 a0009c0009t0002g0143 |
2 | HG00642.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.72-4188C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459844 | |||||||
| chr15:38459886 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.72-4146T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459886 | |||||||
| chr15:38459954 | A | G | 6 | a0001c0001t0002g0044 a0001c0001t0002g0063 a0001c0001t0002g0079 others(3): Show |
7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-4078A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459954 | |||||||
| chr15:38459961 | G | A | 4 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4071G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459961 | |||||||
| chr15:38460072 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.72-3960T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460072 | |||||||
| chr15:38460168 | G | C | 3 | a0001c0001t0007g0031 a0001c0001t0007g0086 a0001c0001t0007g0099 |
4 | HG02258.hp1 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-3864G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460168 | |||||||
| chr15:38460209 | A | C | 3 | a0001c0001t0007g0031 a0001c0001t0007g0086 a0001c0001t0007g0099 |
4 | HG02258.hp1 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-3823A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460209 | |||||||
| chr15:38460382 | GAGA | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.72-3647_72-3645del others(3): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38460382 | ||||||
| chr15:38460408 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-3624A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460408 | |||||||
| chr15:38460409 | GT | G | 23 | a0001c0001t0002g0110 a0001c0001t0003g0002 a0001c0001t0003g0004 others(20): Show |
49 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.72-3612delT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38460409 | ||||||
| chr15:38460433 | A | G | 1 | a0001c0001t0017g0207 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.72-3599A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460433 | |||||||
| chr15:38460498 | T | C | 2 | a0001c0001t0005g0100 a0001c0001t0005g0101 |
2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.72-3534T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460498 | |||||||
| chr15:38460584 | A | G | 4 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-3448A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460584 | |||||||
| chr15:38460594 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-3438A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460594 | |||||||
| chr15:38460600 | T | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-3432T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460600 | |||||||
| chr15:38460619 | G | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-3413G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460619 | |||||||
| chr15:38460664 | C | T | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG01069.hp2 HG03654.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.72-3368C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460664 | |||||||
| chr15:38460675 | C | T | 4 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-3357C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460675 | |||||||
| chr15:38460765 | C | T | 1 | a0001c0001t0011g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.72-3267C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460765 | |||||||
| chr15:38460927 | C | T | 3 | a0001c0004t0006g0027 a0001c0004t0006g0059 a0006c0012t0006g0057 |
4 | HG02055.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-3105C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460927 | |||||||
| chr15:38461180 | GTT | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(32): Show |
68 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.72-2850_72-2849del others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38461180 | ||||||
| chr15:38461309 | C | T | 1 | a0001c0001t0004g0014 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2723C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461309 | |||||||
| chr15:38461539 | A | AAT | 15 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0113 others(12): Show |
19 | HG00280.hp1 HG00735.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.72-2476_72-2475dup others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38461539 | ||||||
| chr15:38461539 | A | AATAT | 2 | a0001c0001t0001g0037 a0002c0002t0002g0111 |
3 | HG01257.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.72-2478_72-2475dup others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38461539 | ||||||
| chr15:38461575 | G | A | 15 | a0001c0001t0005g0016 a0001c0001t0005g0100 a0001c0001t0005g0101 others(12): Show |
22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-2457G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461575 | |||||||
| chr15:38461593 | G | C | 1 | a0001c0001t0005g0199 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72-2439G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461593 | |||||||
| chr15:38461618 | G | C | 1 | a0001c0001t0007g0086 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.72-2414G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461618 | |||||||
| chr15:38461676 | T | C | 1 | a0001c0001t0022g0061 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72-2356T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461676 | |||||||
| chr15:38461739 | C | T | 1 | a0002c0002t0003g0169 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.72-2293C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461739 | |||||||
| chr15:38461792 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.72-2240C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461792 | |||||||
| chr15:38461812 | A | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-2220A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461812 | |||||||
| chr15:38461877 | A | C | 1 | a0001c0001t0001g0176 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.72-2155A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461877 | |||||||
| chr15:38461978 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-2054A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461978 | |||||||
| chr15:38462123 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.72-1909T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462123 | |||||||
| chr15:38462126 | A | AAATGTAT others(11): Show |
11 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
22 | HG00423.hp1 HG00609.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-1905_72-1888dup others(18): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38462126 | ||||||
| chr15:38462223 | A | G | 23 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0013 others(20): Show |
49 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.72-1809A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462223 | |||||||
| chr15:38462431 | C | A | 1 | a0001c0001t0007g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.72-1601C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462431 | |||||||
| chr15:38462657 | A | C | 2 | a0001c0001t0005g0107 a0001c0001t0005g0108 |
2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.72-1375A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462657 | |||||||
| chr15:38462694 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.72-1338T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462694 | |||||||
| chr15:38462735 | A | G | 1 | a0001c0001t0022g0061 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72-1297A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462735 | |||||||
| chr15:38462798 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.72-1234A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462798 | |||||||
| chr15:38462835 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.72-1197A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462835 | |||||||
| chr15:38462858 | A | G | 1 | a0001c0001t0002g0159 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.72-1174A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462858 | |||||||
| chr15:38463018 | A | G | 1 | a0001c0001t0002g0062 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.72-1014A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463018 | |||||||
| chr15:38463132 | A | T | 1 | a0001c0001t0022g0061 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72-900A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463132 | |||||||
| chr15:38463284 | C | T | 1 | a0010c0008t0001g0179 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.72-748C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463284 | |||||||
| chr15:38463322 | T | A | 1 | a0001c0001t0005g0160 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72-710T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463322 | |||||||
| chr15:38463446 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(45): Show |
94 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.72-586G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463446 | |||||||
| chr15:38463487 | C | T | 1 | a0002c0007t0003g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.72-545C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463487 | |||||||
| chr15:38463491 | A | AAAAAT | 41 | a0001c0001t0002g0020 a0001c0001t0002g0038 a0001c0001t0002g0039 others(38): Show |
66 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.72-499_72-495dupAA others(3): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463491 | ||||||
| chr15:38463491 | A | AAAAATAA others(3): Show |
32 | a0001c0001t0003g0004 a0001c0001t0003g0013 a0001c0001t0003g0064 others(29): Show |
44 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.72-504_72-495dupAA others(8): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463491 | ||||||
| chr15:38463491 | A | AAAAATAA others(8): Show |
6 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0084 others(3): Show |
8 | HG00735.hp2 HG00738.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-509_72-495dupAA others(13): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463491 | ||||||
| chr15:38463491 | AAAAAT | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.72-499_72-495delAA others(3): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463491 | ||||||
| chr15:38463491 | AAAAATAA others(8): Show |
A | 5 | a0001c0001t0001g0024 a0001c0001t0005g0016 a0001c0001t0005g0106 others(2): Show |
10 | HG01884.hp1 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-509_72-495delAA others(13): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463491 | ||||||
| chr15:38463523 | A | AAATAGAA others(3): Show |
1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-505_72-504insGA others(8): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463523 | ||||||
| chr15:38463528 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-504A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463528 | |||||||
| chr15:38463533 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-499A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463533 | |||||||
| chr15:38463667 | G | T | 1 | a0001c0001t0018g0138 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.72-365G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463667 | |||||||
| chr15:38463700 | A | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(4): Show |
17 | HG02273.hp2 NA18747.hp2 NA18950.hp2 others(14): Show |
intron_variant | MODIFIER | c.72-332A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463700 | |||||||
| chr15:38463913 | G | T | 1 | a0001c0001t0011g0087 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72-119G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463913 | |||||||
| chr15:38464009 | A | G | 2 | a0001c0001t0001g0195 a0001c0001t0019g0196 |
2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.72-23A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38464009 | |||||||
| chr15:38464232 | C | T | 1 | a0001c0001t0001g0049 | 2 | HG01168.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.217+55C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464232 | |||||||
| chr15:38464233 | G | A | 15 | a0001c0001t0005g0016 a0001c0001t0005g0100 a0001c0001t0005g0101 others(12): Show |
22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.217+56G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464233 | |||||||
| chr15:38464419 | T | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG00099.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.217+242T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464419 | |||||||
| chr15:38464452 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.217+275T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464452 | |||||||
| chr15:38464710 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(44): Show |
93 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.217+533A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464710 | |||||||
| chr15:38464725 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218-544A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464725 | |||||||
| chr15:38464730 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218-539A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464730 | |||||||
| chr15:38464749 | G | T | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218-520G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464749 | |||||||
| chr15:38464841 | A | G | 5 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(2): Show |
5 | HG02717.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.218-428A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464841 | |||||||
| chr15:38464861 | C | T | 6 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(3): Show |
6 | HG01106.hp1 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-408C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464861 | |||||||
| chr15:38464922 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.218-347C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464922 | |||||||
| chr15:38464959 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.218-310C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464959 | |||||||
| chr15:38465112 | A | G | 1 | a0001c0001t0005g0199 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-157A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38465112 | |||||||
| chr15:38465586 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.352+183C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465586 | |||||||
| chr15:38465718 | C | T | 1 | a0001c0001t0004g0014 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.352+315C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465718 | |||||||
| chr15:38465736 | A | T | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.352+333A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465736 | |||||||
| chr15:38465761 | G | A | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.352+358G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465761 | |||||||
| chr15:38465765 | A | G | 1 | a0001c0001t0011g0087 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.352+362A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465765 | |||||||
| chr15:38465827 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(44): Show |
93 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.352+424G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465827 | |||||||
| chr15:38465848 | T | A | 22 | a0001c0001t0002g0021 a0001c0001t0002g0046 a0001c0001t0002g0062 others(19): Show |
32 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.352+445T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465848 | |||||||
| chr15:38465849 | A | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0113 a0001c0001t0003g0069 others(3): Show |
7 | HG01106.hp1 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+446A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465849 | |||||||
| chr15:38465872 | T | G | 1 | a0002c0002t0002g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.352+469T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465872 | |||||||
| chr15:38465928 | A | G | 1 | a0001c0001t0011g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.352+525A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465928 | |||||||
| chr15:38466136 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.352+733C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466136 | |||||||
| chr15:38466165 | T | G | 1 | a0001c0001t0004g0014 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.352+762T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466165 | |||||||
| chr15:38466182 | T | TTG | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0041 others(8): Show |
20 | HG01106.hp2 HG01934.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.352+815_352+816dup others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | ||||||
| chr15:38466182 | T | TTGTG | 3 | a0001c0001t0005g0104 a0001c0001t0011g0141 a0001c0003t0005g0105 |
3 | HG02818.hp1 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.352+813_352+816dup others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | ||||||
| chr15:38466182 | T | TTGTGTG | 8 | a0001c0001t0002g0047 a0001c0001t0002g0151 a0001c0001t0002g0152 others(5): Show |
12 | HG00597.hp1 HG01109.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.352+811_352+816dup others(6): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | ||||||
| chr15:38466182 | T | TTGTGTGT others(1): Show |
2 | a0001c0003t0005g0053 a0002c0007t0003g0232 |
3 | HG01069.hp1 HG01071.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.352+809_352+816dup others(8): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | ||||||
| chr15:38466182 | T | TTGTGTGT others(3): Show |
3 | a0001c0001t0005g0016 a0001c0001t0005g0106 a0001c0001t0005g0160 |
6 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.352+807_352+816dup others(10): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | ||||||
| chr15:38466182 | T | TTGTGTGT others(5): Show |
3 | a0001c0001t0005g0100 a0001c0001t0005g0101 a0001c0001t0005g0107 |
3 | HG01891.hp2 HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.352+805_352+816dup others(12): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | ||||||
| chr15:38466182 | TTG | T | 58 | a0001c0001t0002g0044 a0001c0001t0002g0063 a0001c0001t0002g0157 others(55): Show |
91 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.352+815_352+816del others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | ||||||
| chr15:38466182 | TTGTG | T | 6 | a0001c0001t0002g0150 a0001c0001t0007g0031 a0001c0001t0007g0086 others(3): Show |
7 | HG02258.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+813_352+816del others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | ||||||
| chr15:38466182 | TTGTGTG | T | 4 | a0001c0001t0022g0061 a0001c0004t0006g0028 a0002c0002t0003g0167 others(1): Show |
5 | HG00642.hp1 HG02258.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+811_352+816del others(6): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | ||||||
| chr15:38466182 | TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0001g0221 a0001c0001t0021g0164 |
2 | HG01106.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.352+807_352+816del others(10): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | ||||||
| chr15:38466182 | TTGTGTGT others(5): Show |
T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.352+805_352+816del others(12): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | ||||||
| chr15:38466264 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.352+861T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466264 | |||||||
| chr15:38466425 | C | T | 4 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+1022C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466425 | |||||||
| chr15:38466550 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.352+1147A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466550 | |||||||
| chr15:38466699 | G | A | 1 | a0001c0001t0011g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.352+1296G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466699 | |||||||
| chr15:38466813 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.352+1410T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466813 | |||||||
| chr15:38466824 | C | T | 1 | a0001c0003t0014g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352+1421C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466824 | |||||||
| chr15:38466955 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0211 others(3): Show |
11 | HG00423.hp1 HG00609.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.352+1552C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466955 | |||||||
| chr15:38467026 | A | T | 1 | a0001c0001t0001g0178 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.352+1623A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467026 | |||||||
| chr15:38467108 | T | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.352+1705T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467108 | |||||||
| chr15:38467150 | T | C | 2 | a0001c0003t0005g0053 a0002c0007t0003g0232 |
3 | HG01069.hp1 HG01071.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.352+1747T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467150 | |||||||
| chr15:38467153 | A | T | 1 | a0001c0001t0002g0148 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.352+1750A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467153 | |||||||
| chr15:38467202 | C | G | 1 | a0001c0001t0001g0049 | 2 | HG01168.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.352+1799C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467202 | |||||||
| chr15:38467307 | C | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0086 |
3 | HG02258.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.352+1904C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467307 | |||||||
| chr15:38467335 | T | C | 1 | a0001c0001t0004g0032 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.352+1932T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467335 | |||||||
| chr15:38467337 | T | A | 5 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(2): Show |
5 | HG02717.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+1934T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467337 | |||||||
| chr15:38467655 | T | C | 1 | a0001c0001t0013g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.352+2252T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467655 | |||||||
| chr15:38467774 | A | G | 5 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(2): Show |
5 | HG02717.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+2371A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467774 | |||||||
| chr15:38467837 | A | T | 1 | a0001c0001t0001g0181 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.353-2390A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467837 | |||||||
| chr15:38467937 | G | A | 1 | a0001c0001t0022g0061 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.353-2290G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467937 | |||||||
| chr15:38467972 | C | A | 1 | a0001c0001t0011g0087 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.353-2255C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467972 | |||||||
| chr15:38468027 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.353-2200A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468027 | |||||||
| chr15:38468299 | G | A | 18 | a0001c0001t0005g0016 a0001c0001t0005g0100 a0001c0001t0005g0101 others(15): Show |
26 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.353-1928G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468299 | |||||||
| chr15:38468383 | C | A | 4 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.353-1844C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468383 | |||||||
| chr15:38468389 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(155): Show |
266 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.353-1838A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468389 | |||||||
| chr15:38468419 | G | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(74): Show |
143 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.353-1808G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468419 | |||||||
| chr15:38468462 | G | C | 1 | a0001c0001t0004g0054 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.353-1765G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468462 | |||||||
| chr15:38468490 | T | G | 1 | a0001c0001t0005g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.353-1737T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468490 | |||||||
| chr15:38468707 | T | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.353-1520T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468707 | |||||||
| chr15:38468755 | G | A | 2 | a0001c0001t0004g0090 a0001c0001t0004g0091 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.353-1472G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468755 | |||||||
| chr15:38468816 | C | T | 1 | a0001c0003t0014g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.353-1411C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468816 | |||||||
| chr15:38468871 | G | A | 5 | a0001c0001t0002g0044 a0001c0001t0002g0063 a0001c0001t0002g0079 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.353-1356G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468871 | |||||||
| chr15:38468904 | GTATT | G | 4 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.353-1315_353-1312d others(6): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38468904 | ||||||
| chr15:38468988 | C | A | 15 | a0001c0001t0005g0016 a0001c0001t0005g0100 a0001c0001t0005g0101 others(12): Show |
22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.353-1239C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468988 | |||||||
| chr15:38469027 | T | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.353-1200T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469027 | |||||||
| chr15:38469053 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.353-1174A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469053 | |||||||
| chr15:38469095 | G | A | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.353-1132G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469095 | |||||||
| chr15:38469145 | A | G | 1 | a0001c0001t0019g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.353-1082A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469145 | |||||||
| chr15:38469152 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.353-1075T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469152 | |||||||
| chr15:38469198 | T | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.353-1029T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469198 | |||||||
| chr15:38469211 | C | CCTACCGT others(11): Show |
76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.353-1016_353-1015i others(20): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469211 | |||||||
| chr15:38469212 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.353-1015A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469212 | |||||||
| chr15:38469319 | G | T | 1 | a0001c0003t0005g0103 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.353-908G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469319 | |||||||
| chr15:38469586 | C | T | 31 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(28): Show |
38 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.353-641C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469586 | |||||||
| chr15:38469587 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.353-640G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469587 | |||||||
| chr15:38469588 | TTCCTGGC others(10): Show |
T | 1 | a0001c0003t0014g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.353-634_353-618del others(17): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38469588 | ||||||
| chr15:38469868 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.353-359G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469868 | |||||||
| chr15:38470179 | G | A | 2 | a0001c0001t0002g0127 a0001c0001t0002g0174 |
2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.353-48G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38470179 | |||||||
| chr15:38470192 | A | G | 15 | a0001c0001t0005g0016 a0001c0001t0005g0100 a0001c0001t0005g0101 others(12): Show |
22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.353-35A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38470192 | |||||||
| chr15:38470204 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.353-23T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38470204 | |||||||
| chr15:38470447 | G | T | 1 | a0001c0001t0004g0014 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+42G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470447 | |||||||
| chr15:38470500 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(74): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.531+95A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470500 | |||||||
| chr15:38470528 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.531+123A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470528 | |||||||
| chr15:38470677 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.531+272A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470677 | |||||||
| chr15:38470682 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.531+277C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470682 | |||||||
| chr15:38470800 | G | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.531+395G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470800 | |||||||
| chr15:38470815 | G | A | 31 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(28): Show |
38 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.531+410G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470815 | |||||||
| chr15:38470950 | AT | A | 15 | a0001c0001t0005g0016 a0001c0001t0005g0100 a0001c0001t0005g0101 others(12): Show |
22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.531+558delT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr15 | 38470950 | ||||||
| chr15:38471074 | C | T | 2 | a0001c0001t0003g0013 a0001c0001t0003g0083 |
5 | NA18969.hp2 NA18985.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.531+669C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471074 | |||||||
| chr15:38471167 | G | A | 1 | a0002c0002t0003g0068 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.531+762G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471167 | |||||||
| chr15:38471209 | G | A | 25 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0022 others(22): Show |
37 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.531+804G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471209 | |||||||
| chr15:38471296 | A | T | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.531+891A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471296 | |||||||
| chr15:38471324 | A | G | 1 | a0001c0001t0015g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.531+919A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471324 | |||||||
| chr15:38471462 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.531+1057C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471462 | |||||||
| chr15:38471507 | T | C | 10 | a0001c0001t0002g0042 a0001c0001t0002g0060 a0001c0001t0002g0076 others(7): Show |
11 | HG00438.hp1 HG00544.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.531+1102T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471507 | |||||||
| chr15:38471575 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0222 |
2 | HG01081.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.531+1170G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471575 | |||||||
| chr15:38471592 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(26): Show |
47 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.531+1187A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471592 | |||||||
| chr15:38471614 | C | T | 24 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(21): Show |
29 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.531+1209C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471614 | |||||||
| chr15:38471616 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.531+1211A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471616 | |||||||
| chr15:38471657 | C | T | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.531+1252C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471657 | |||||||
| chr15:38471677 | A | G | 2 | a0001c0001t0009g0170 a0001c0001t0009g0171 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.531+1272A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471677 | |||||||
| chr15:38471739 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.531+1334C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471739 | |||||||
| chr15:38471926 | A | G | 1 | a0001c0001t0004g0014 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+1521A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471926 | |||||||
| chr15:38472221 | A | T | 1 | a0001c0003t0014g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.532-1284A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472221 | |||||||
| chr15:38472226 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.532-1279T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472226 | |||||||
| chr15:38472297 | T | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.532-1208T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472297 | |||||||
| chr15:38472346 | ATAAAT | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0086 |
3 | HG02258.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.532-1155_532-1151d others(7): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr15 | 38472346 | ||||||
| chr15:38472389 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.532-1116A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472389 | |||||||
| chr15:38472555 | T | A | 1 | a0001c0001t0001g0026 | 3 | NA18951.hp2 NA18962.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.532-950T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472555 | |||||||
| chr15:38472642 | C | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(22): Show |
42 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.532-863C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472642 | |||||||
| chr15:38473078 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.532-427A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38473078 | |||||||
| chr15:38473133 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.532-372G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38473133 | |||||||
| chr15:38473437 | T | G | 1 | a0001c0001t0002g0119 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.532-68T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38473437 | |||||||
| chr15:38473729 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.612+144T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 5/7 | chr15 | 38473729 | |||||||
| chr15:38473782 | G | A | 1 | a0001c0001t0022g0061 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.612+197G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 5/7 | chr15 | 38473782 | |||||||
| chr15:38473826 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.612+241A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 5/7 | chr15 | 38473826 | |||||||
| chr15:38474377 | C | A | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+79C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38474377 | |||||||
| chr15:38474603 | G | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+305G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38474603 | |||||||
| chr15:38474809 | G | A | 1 | a0001c0001t0004g0073 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.729+511G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38474809 | |||||||
| chr15:38474814 | G | T | 23 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0013 others(20): Show |
49 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.729+516G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38474814 | |||||||
| chr15:38475066 | T | TTATTTTT others(321): Show |
1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+784_729+785ins others(328): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38475066 | ||||||
| chr15:38475220 | G | A | 1 | a0002c0002t0003g0161 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.729+922G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475220 | |||||||
| chr15:38475221 | G | A | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+923G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475221 | |||||||
| chr15:38475341 | T | C | 1 | a0001c0001t0011g0087 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.729+1043T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475341 | |||||||
| chr15:38475398 | C | A | 1 | a0001c0001t0002g0163 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.729+1100C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475398 | |||||||
| chr15:38475470 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.729+1172G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475470 | |||||||
| chr15:38475564 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0024 others(7): Show |
23 | HG02273.hp2 HG02602.hp2 HG04204.hp2 others(20): Show |
intron_variant | MODIFIER | c.729+1266C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475564 | |||||||
| chr15:38475665 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.729+1367A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475665 | |||||||
| chr15:38475730 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(45): Show |
94 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.729+1432C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475730 | |||||||
| chr15:38475759 | C | T | 1 | a0001c0003t0014g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.729+1461C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475759 | |||||||
| chr15:38475800 | T | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+1502T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475800 | |||||||
| chr15:38475842 | G | T | 25 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(22): Show |
30 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.729+1544G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475842 | |||||||
| chr15:38475866 | C | CT | 34 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(31): Show |
41 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.729+1576dupT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38475866 | ||||||
| chr15:38476280 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.729+1982T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476280 | |||||||
| chr15:38476465 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.729+2167C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476465 | |||||||
| chr15:38476488 | T | A | 1 | a0001c0003t0014g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.729+2190T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476488 | |||||||
| chr15:38476496 | C | T | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+2198C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476496 | |||||||
| chr15:38476514 | T | A | 1 | a0001c0001t0001g0209 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.729+2216T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476514 | |||||||
| chr15:38476617 | T | TAAATTTC others(327): Show |
1 | a0001c0001t0005g0101 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.729+2335_729+2336i others(336): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38476617 | ||||||
| chr15:38476703 | C | CT | 32 | a0001c0001t0001g0220 a0001c0001t0003g0002 a0001c0001t0003g0004 others(29): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.729+2419dupT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38476703 | ||||||
| chr15:38476703 | CT | C | 32 | a0001c0001t0002g0151 a0001c0001t0004g0030 a0001c0001t0004g0032 others(29): Show |
39 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.729+2419delT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38476703 | ||||||
| chr15:38476785 | C | T | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+2487C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476785 | |||||||
| chr15:38476795 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
265 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.729+2497C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476795 | |||||||
| chr15:38476868 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+2570A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476868 | |||||||
| chr15:38476896 | C | T | 1 | a0001c0003t0014g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.729+2598C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476896 | |||||||
| chr15:38477127 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0209 |
4 | NA18978.hp1 NA18997.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+2829G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477127 | |||||||
| chr15:38477225 | G | A | 1 | a0001c0001t0004g0014 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+2927G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477225 | |||||||
| chr15:38477227 | T | TGTGCTGT others(318): Show |
1 | a0001c0001t0004g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.729+2946_729+2947i others(327): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | ||||||
| chr15:38477227 | T | TGTGCTGT others(328): Show |
1 | a0002c0002t0004g0092 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.729+2946_729+2947i others(337): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | ||||||
| chr15:38477227 | T | TGTGCTGT others(329): Show |
2 | a0001c0001t0004g0093 a0001c0001t0004g0094 |
2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.729+2946_729+2947i others(338): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | ||||||
| chr15:38477227 | T | TGTGCTGT others(330): Show |
8 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0036 others(5): Show |
10 | HG00280.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.729+2946_729+2947i others(339): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | ||||||
| chr15:38477227 | T | TGTGCTGT others(331): Show |
6 | a0001c0001t0004g0030 a0001c0001t0004g0034 a0001c0001t0004g0035 others(3): Show |
9 | HG00639.hp2 HG00735.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.729+2946_729+2947i others(340): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | ||||||
| chr15:38477227 | T | TGTGCTGT others(332): Show |
6 | a0001c0001t0004g0054 a0001c0001t0004g0073 a0001c0001t0004g0090 others(3): Show |
6 | HG00733.hp2 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+2946_729+2947i others(341): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | ||||||
| chr15:38477227 | T | TGTGCTGT others(333): Show |
4 | a0001c0001t0004g0091 a0001c0001t0004g0096 a0001c0004t0006g0027 others(1): Show |
5 | HG02300.hp1 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.729+2946_729+2947i others(342): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | ||||||
| chr15:38477227 | T | TGTGCTGT others(334): Show |
2 | a0001c0001t0010g0055 a0001c0004t0006g0028 |
3 | HG02258.hp2 HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.729+2946_729+2947i others(343): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | ||||||
| chr15:38477227 | T | TGTGCTGT others(335): Show |
1 | a0001c0004t0010g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.729+2946_729+2947i others(344): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | ||||||
| chr15:38477227 | T | TGTGCTGT others(337): Show |
1 | a0001c0004t0010g0056 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.729+2946_729+2947i others(346): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | ||||||
| chr15:38477252 | A | G | 1 | a0002c0002t0003g0067 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.729+2954A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477252 | |||||||
| chr15:38477311 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+3013A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477311 | |||||||
| chr15:38477454 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.729+3156T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477454 | |||||||
| chr15:38477521 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.729+3223G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477521 | |||||||
| chr15:38477770 | A | G | 23 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0013 others(20): Show |
49 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.729+3472A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477770 | |||||||
| chr15:38477775 | T | C | 5 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(2): Show |
5 | HG01106.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.729+3477T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477775 | |||||||
| chr15:38477857 | G | A | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.730-3435G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477857 | |||||||
| chr15:38477890 | T | A | 1 | a0001c0001t0002g0117 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.730-3402T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477890 | |||||||
| chr15:38477957 | T | G | 23 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0013 others(20): Show |
49 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.730-3335T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477957 | |||||||
| chr15:38477986 | C | A | 1 | a0001c0001t0002g0120 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.730-3306C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477986 | |||||||
| chr15:38478025 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.730-3267G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478025 | |||||||
| chr15:38478063 | A | G | 1 | a0001c0001t0011g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.730-3229A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478063 | |||||||
| chr15:38478131 | T | C | 2 | a0001c0001t0011g0087 a0001c0001t0011g0141 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.730-3161T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478131 | |||||||
| chr15:38478172 | C | G | 2 | a0001c0001t0002g0144 a0009c0009t0002g0143 |
2 | HG00642.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.730-3120C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478172 | |||||||
| chr15:38478196 | T | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.730-3096T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478196 | |||||||
| chr15:38478364 | G | C | 1 | a0001c0001t0002g0152 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.730-2928G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478364 | |||||||
| chr15:38478427 | C | G | 1 | a0001c0001t0003g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.730-2865C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478427 | |||||||
| chr15:38478433 | T | G | 1 | a0006c0012t0006g0057 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.730-2859T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478433 | |||||||
| chr15:38478473 | A | T | 1 | a0001c0001t0011g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.730-2819A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478473 | |||||||
| chr15:38478763 | C | A | 2 | a0004c0006t0004g0088 a0004c0006t0004g0089 |
2 | HG02300.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.730-2529C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478763 | |||||||
| chr15:38478879 | C | T | 1 | a0001c0003t0014g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.730-2413C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478879 | |||||||
| chr15:38478915 | A | T | 1 | a0002c0002t0003g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.730-2377A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478915 | |||||||
| chr15:38479099 | C | T | 1 | a0001c0001t0002g0131 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.730-2193C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479099 | |||||||
| chr15:38479156 | C | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02132.hp2 NA19009.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.730-2136C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479156 | |||||||
| chr15:38479209 | G | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
267 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.730-2083G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479209 | |||||||
| chr15:38479225 | C | G | 1 | a0001c0001t0003g0065 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.730-2067C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479225 | |||||||
| chr15:38479229 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.730-2063A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479229 | |||||||
| chr15:38479403 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
267 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.730-1889T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479403 | |||||||
| chr15:38479870 | G | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.730-1422G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479870 | |||||||
| chr15:38480030 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
268 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.730-1262A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480030 | |||||||
| chr15:38480063 | A | G | 1 | a0001c0004t0006g0028 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.730-1229A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480063 | |||||||
| chr15:38480222 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.730-1070T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480222 | |||||||
| chr15:38480223 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.730-1069C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480223 | |||||||
| chr15:38480430 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0209 |
4 | NA18978.hp1 NA18997.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-862A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480430 | |||||||
| chr15:38480522 | G | C | 1 | a0001c0001t0001g0220 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.730-770G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480522 | |||||||
| chr15:38480572 | A | G | 1 | a0001c0001t0015g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.730-720A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480572 | |||||||
| chr15:38480573 | T | C | 1 | a0001c0001t0004g0014 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-719T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480573 | |||||||
| chr15:38480579 | A | AT | 44 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0029 others(41): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.730-703dupT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38480579 | ||||||
| chr15:38480684 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.730-608C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480684 | |||||||
| chr15:38480743 | A | G | 39 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0033 others(36): Show |
47 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.730-549A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480743 | |||||||
| chr15:38480813 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.730-479T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480813 | |||||||
| chr15:38480845 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.730-447A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480845 | |||||||
| chr15:38480996 | G | T | 1 | a0001c0001t0002g0163 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.730-296G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480996 | |||||||
| chr15:38481008 | G | A | 1 | a0002c0002t0003g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.730-284G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38481008 | |||||||
| chr15:38481019 | T | C | 2 | a0001c0001t0002g0039 a0001c0001t0002g0115 |
3 | HG02129.hp1 HG02523.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.730-273T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38481019 | |||||||
| chr15:38481080 | G | A | 2 | a0001c0001t0007g0031 a0001c0001t0007g0086 |
3 | HG02258.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.730-212G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38481080 | |||||||
| chr15:38481583 | G | T | 1 | a0001c0003t0014g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.897+124G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38481583 | |||||||
| chr15:38481793 | G | A | 1 | a0001c0001t0011g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.897+334G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38481793 | |||||||
| chr15:38482239 | G | A | 2 | a0003c0005t0001g0051 a0003c0005t0001g0213 |
3 | HG03491.hp1 HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.897+780G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482239 | |||||||
| chr15:38482310 | A | G | 3 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.897+851A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482310 | |||||||
| chr15:38482441 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0017g0207 |
2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.897+982A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482441 | |||||||
| chr15:38482498 | C | G | 1 | a0001c0001t0002g0154 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.897+1039C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482498 | |||||||
| chr15:38482850 | T | C | 4 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.897+1391T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482850 | |||||||
| chr15:38482863 | C | T | 2 | a0001c0003t0005g0102 a0001c0003t0005g0105 |
2 | HG02280.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.898-1392C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482863 | |||||||
| chr15:38483129 | A | G | 1 | a0001c0001t0001g0048 | 2 | NA18998.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.898-1126A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483129 | |||||||
| chr15:38483134 | T | C | 1 | a0002c0002t0003g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.898-1121T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483134 | |||||||
| chr15:38483159 | C | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-1096C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483159 | |||||||
| chr15:38483205 | A | G | 2 | a0001c0001t0002g0144 a0009c0009t0002g0143 |
2 | HG00642.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.898-1050A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483205 | |||||||
| chr15:38483256 | A | T | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-999A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483256 | |||||||
| chr15:38483277 | G | C | 1 | a0001c0001t0011g0141 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.898-978G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483277 | |||||||
| chr15:38483417 | A | AGCAC | 4 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0009g0172 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-837_898-834dup others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483417 | ||||||
| chr15:38483448 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.898-807C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483448 | |||||||
| chr15:38483483 | G | A | 1 | a0001c0001t0011g0087 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.898-772G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483483 | |||||||
| chr15:38483484 | T | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-771T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483484 | |||||||
| chr15:38483543 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(45): Show |
94 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.898-712G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483543 | |||||||
| chr15:38483552 | A | G | 15 | a0001c0001t0005g0016 a0001c0001t0005g0100 a0001c0001t0005g0101 others(12): Show |
22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.898-703A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483552 | |||||||
| chr15:38483558 | C | T | 2 | a0001c0001t0005g0100 a0001c0001t0005g0101 |
2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.898-697C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483558 | |||||||
| chr15:38483665 | CAA | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(14): Show |
30 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.898-571_898-570del others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483665 | ||||||
| chr15:38483682 | AAAAT | A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0217 a0001c0001t0001g0222 others(5): Show |
11 | HG01069.hp2 HG01081.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.898-571_898-568del others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483682 | ||||||
| chr15:38483682 | AAAATATA others(5): Show |
A | 2 | a0001c0001t0005g0199 a0001c0001t0022g0061 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.898-571_898-560del others(12): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483682 | ||||||
| chr15:38483683 | AAATAT | A | 5 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0040 others(2): Show |
12 | HG00099.hp2 HG00738.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.898-570_898-566del others(5): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483683 | ||||||
| chr15:38483684 | A | T | 4 | a0001c0001t0001g0223 a0001c0001t0002g0009 a0001c0001t0002g0109 others(1): Show |
5 | HG01884.hp2 HG02148.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-571A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483684 | |||||||
| chr15:38483684 | AAT | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0209 a0001c0001t0002g0003 others(1): Show |
6 | HG02145.hp2 NA18978.hp1 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-545_898-544del others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483684 | ||||||
| chr15:38483684 | AATAT | A | 66 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0037 others(63): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.898-547_898-544del others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483684 | ||||||
| chr15:38483684 | AATATATA others(1): Show |
A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(62): Show |
83 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.898-551_898-544del others(8): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483684 | ||||||
| chr15:38483684 | AATATATA others(3): Show |
A | 2 | a0001c0001t0003g0004 a0001c0001t0003g0083 |
2 | HG00544.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.898-553_898-544del others(10): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483684 | ||||||
| chr15:38483685 | ATAT | A | 3 | a0001c0001t0001g0003 a0001c0001t0002g0003 a0001c0001t0011g0141 |
3 | HG01255.hp2 HG01981.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.898-569_898-567del others(3): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483685 | |||||||
| chr15:38483685 | ATATAT | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0045 a0001c0001t0013g0078 others(1): Show |
4 | HG02004.hp1 HG03209.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-569_898-565del others(5): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483685 | |||||||
| chr15:38483685 | ATATATAT | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(42): Show |
85 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.898-569_898-563del others(7): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483685 | |||||||
| chr15:38483685 | ATATATAT others(2): Show |
A | 24 | a0001c0001t0002g0060 a0001c0001t0002g0118 a0001c0001t0003g0002 others(21): Show |
48 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.898-569_898-561del others(9): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483685 | |||||||
| chr15:38483690 | T | A | 4 | a0001c0001t0001g0137 a0001c0001t0002g0041 a0001c0001t0002g0124 others(1): Show |
5 | HG02818.hp1 HG02970.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-565T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483690 | |||||||
| chr15:38483692 | T | A | 3 | a0001c0001t0001g0200 a0001c0001t0004g0216 a0001c0001t0011g0141 |
3 | HG02818.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.898-563T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483692 | |||||||
| chr15:38483694 | T | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(97): Show |
160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.898-561T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483694 | |||||||
| chr15:38483696 | T | A | 35 | a0001c0001t0001g0205 a0001c0001t0002g0042 a0001c0001t0002g0060 others(32): Show |
41 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.898-559T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483696 | |||||||
| chr15:38483698 | T | A | 30 | a0001c0001t0002g0042 a0001c0001t0002g0060 a0001c0001t0002g0077 others(27): Show |
36 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.898-557T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483698 | |||||||
| chr15:38483708 | T | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-547T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483708 | |||||||
| chr15:38483710 | T | C | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-545T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483710 | |||||||
| chr15:38483772 | C | A | 2 | a0001c0001t0002g0120 a0001c0001t0021g0164 |
2 | HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.898-483C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483772 | |||||||
| chr15:38483897 | A | G | 1 | a0001c0001t0020g0188 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.898-358A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483897 | |||||||
| chr15:38483927 | C | T | 26 | a0001c0001t0002g0118 a0001c0001t0003g0002 a0001c0001t0003g0004 others(23): Show |
52 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.898-328C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483927 | |||||||
| chr15:38483952 | G | C | 1 | a0001c0001t0003g0069 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.898-303G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483952 | |||||||
| chr15:38484015 | A | G | 1 | a0001c0001t0021g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-240A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38484015 | |||||||
| chr15:38484059 | G | A | 14 | a0001c0001t0005g0016 a0001c0001t0005g0100 a0001c0001t0005g0101 others(11): Show |
21 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.898-196G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38484059 | |||||||
| chr15:38484129 | T | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(65): Show |
124 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.898-126T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38484129 | |||||||
| chr15:38484161 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0181 |
3 | HG01168.hp1 HG01433.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.898-94T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38484161 |