Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57613 |
| ensemblid | ENSG00000084444.14 |
| hgncid | 29288 |
| symbol | FAM234B |
| name | family with sequence similarity 234 member B |
| refseq_nuc | NM_020853.2 |
| refseq_prot | NP_065904.1 |
| ensembl_nuc | ENST00000197268.13 |
| ensembl_prot | ENSP00000197268.8 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 13044381 |
| end | 13083449 |
| strand | + |
| ver | v1.2 |
| region | chr12:13044381-13083449 |
| region5000 | chr12:13039381-13088449 |
| regionname0 | FAM234B_chr12_13044381_13083449 |
| regionname5000 | FAM234B_chr12_13039381_13088449 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 622 | 388 | 70 | 68 | 191 | 15 | 42 | 149 | FAM234B_chr12_13039381_13088449 | FAM234B | MATVL others(617): Show |
chr12 | 13039381 | 13088449 |
| a0002 | 0/0 | 622 | 21 | 21 | 0 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | MATVL others(617): Show |
chr12 | 13039381 | 13088449 |
| a0003 | 0/0 | 622 | 11 | 0 | 0 | 9 | 1 | 1 | 8 | FAM234B_chr12_13039381_13088449 | FAM234B | MATVL others(617): Show |
chr12 | 13039381 | 13088449 |
| a0004 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | MATVL others(617): Show |
chr12 | 13039381 | 13088449 |
| a0005 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | MATVL others(617): Show |
chr12 | 13039381 | 13088449 |
| a0006 | 0/0 | 622 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | MATVL others(617): Show |
chr12 | 13039381 | 13088449 |
| a0007 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | MATVL others(617): Show |
chr12 | 13039381 | 13088449 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1866 | 225 | 19 | 48 | 116 | 13 | 28 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0001c0002 | 0/0 | 1866 | 130 | 24 | 17 | 73 | 2 | 14 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0001c0004 | 0/0 | 1866 | 16 | 14 | 2 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0001c0006 | 0/0 | 1866 | 8 | 6 | 1 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0001c0007 | 1/0 | 1866 | 4 | 3 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0001c0008 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0001c0010 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0001c0014 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0001c0015 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0001c0016 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0002c0003 | 0/0 | 1866 | 21 | 21 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0003c0005 | 0/0 | 1866 | 11 | 0 | 0 | 9 | 1 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0004c0012 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0005c0011 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0006c0013 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 | ||
| a0007c0009 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | ATGGC others(1861): Show |
chr12 | 13039381 | 13088449 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4710 | 173 | 14 | 34 | 97 | 8 | 19 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0002 | 0/0 | 4711 | 25 | 4 | 6 | 7 | 3 | 5 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0003 | 0/0 | 4709 | 8 | 0 | 1 | 7 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4704): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0005 | 0/0 | 4710 | 7 | 0 | 4 | 0 | 2 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0007 | 0/0 | 4710 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0008 | 0/0 | 4710 | 2 | 0 | 1 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0009 | 0/0 | 4710 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0010 | 0/0 | 4710 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0013 | 0/0 | 4710 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0014 | 0/0 | 4710 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0017 | 0/0 | 4710 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0018 | 0/0 | 4710 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0019 | 0/0 | 4710 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0001t0020 | 0/0 | 4711 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0001c0002t0001 | 0/0 | 4710 | 63 | 10 | 5 | 43 | 2 | 3 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0002t0002 | 0/0 | 4711 | 48 | 10 | 0 | 29 | 0 | 9 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0001c0002t0003 | 0/0 | 4709 | 4 | 0 | 4 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4704): Show |
chr12 | 13039381 | 13088449 |
| a0001c0002t0004 | 0/0 | 4710 | 8 | 0 | 6 | 0 | 0 | 2 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0002t0006 | 0/0 | 4711 | 4 | 4 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0001c0002t0023 | 0/0 | 4711 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0001c0002t0024 | 0/0 | 4709 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4704): Show |
chr12 | 13039381 | 13088449 |
| a0001c0002t0025 | 0/0 | 4711 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0001c0004t0001 | 0/0 | 4710 | 12 | 10 | 2 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0004t0002 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0001c0004t0003 | 0/0 | 4709 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4704): Show |
chr12 | 13039381 | 13088449 |
| a0001c0004t0006 | 0/0 | 4711 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0001c0006t0001 | 0/0 | 4710 | 2 | 1 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0006t0002 | 0/0 | 4711 | 4 | 3 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0001c0006t0015 | 0/0 | 4710 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0006t0016 | 0/0 | 4710 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0007t0001 | 0/0 | 4710 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0007t0002 | 1/0 | 4711 | 3 | 2 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0001c0008t0012 | 0/0 | 4696 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4691): Show |
chr12 | 13039381 | 13088449 |
| a0001c0010t0003 | 0/0 | 4709 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4704): Show |
chr12 | 13039381 | 13088449 |
| a0001c0014t0001 | 0/0 | 4710 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0015t0001 | 0/0 | 4710 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0001c0016t0011 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4690): Show |
chr12 | 13039381 | 13088449 |
| a0002c0003t0001 | 0/0 | 4710 | 14 | 14 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0002c0003t0002 | 0/0 | 4711 | 4 | 4 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0002c0003t0003 | 0/0 | 4709 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4704): Show |
chr12 | 13039381 | 13088449 |
| a0002c0003t0022 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0003c0005t0001 | 0/0 | 4710 | 11 | 0 | 0 | 9 | 1 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0004c0012t0001 | 0/0 | 4710 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| a0005c0011t0021 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0006c0013t0002 | 0/0 | 4711 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4706): Show |
chr12 | 13039381 | 13088449 |
| a0007c0009t0001 | 0/0 | 4710 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | GCACG others(4705): Show |
chr12 | 13039381 | 13088449 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 30 | 0 | 4 | 26 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0003 | 0/0 | 24 | 0 | 1 | 16 | 3 | 4 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 8 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 1 | 0 | 2 | 2 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0005g0015 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0005g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0008g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0010g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0014g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0017g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0019g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0001t0020g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0002 | 0/0 | 20 | 0 | 0 | 20 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0004 | 0/0 | 11 | 1 | 0 | 8 | 0 | 2 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0003g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0004g0002 | 0/0 | 8 | 0 | 6 | 0 | 0 | 2 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0006g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0023g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0024g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0002t0025g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0004t0001g0007 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0004t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0004t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0004t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0004t0006g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0006t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0006t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0006t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0006t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0006t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0006t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0006t0015g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0006t0016g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0007t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0007t0002g0035 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0007t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0008t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0010t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0014t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0015t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0001c0016t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0001g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0002c0003t0022g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0003c0005t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0003c0005t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0003c0005t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0003c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0003c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0003c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0003c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0003c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0004c0012t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0005c0011t0021g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0006c0013t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| a0007c0009t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | GBR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0023 | EUR | GBR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0015 | EUR | FIN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00544 | hp2 | a0004 | c0012 | t0001 | g0112 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00609 | hp1 | a0003 | c0005 | t0001 | g0032 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0154 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01074 | hp1 | a0001 | c0001 | t0017 | g0204 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0161 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01109 | hp1 | a0001 | c0006 | t0002 | g0123 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0113 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01167 | hp2 | a0001 | c0001 | t0010 | g0141 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01257 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01258 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01496 | hp1 | a0001 | c0002 | t0024 | g0012 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0155 | EUR | IBS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01516 | hp1 | a0003 | c0005 | t0001 | g0032 | EUR | IBS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0017 | EUR | IBS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0017 | EUR | IBS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0062 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0067 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01928 | hp2 | a0001 | c0002 | t0025 | g0002 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01934 | hp2 | a0001 | c0004 | t0001 | g0007 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01975 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01981 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0086 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02071 | hp2 | a0001 | c0001 | t0008 | g0175 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02148 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CDX | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02257 | hp1 | a0005 | c0011 | t0021 | g0224 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0059 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02451 | hp2 | a0001 | c0004 | t0006 | g0044 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0090 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02622 | hp1 | a0001 | c0006 | t0002 | g0125 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0057 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0107 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0007 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0190 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02809 | hp1 | a0001 | c0006 | t0015 | g0132 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0138 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02818 | hp1 | a0001 | c0007 | t0002 | g0035 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0007 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02886 | hp2 | a0001 | c0008 | t0012 | g0133 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02895 | hp2 | a0001 | c0006 | t0002 | g0122 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02896 | hp1 | a0001 | c0007 | t0002 | g0136 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02896 | hp2 | a0001 | c0002 | t0006 | g0027 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02897 | hp1 | a0001 | c0002 | t0006 | g0027 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02897 | hp2 | a0002 | c0003 | t0003 | g0061 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02922 | hp1 | a0001 | c0006 | t0016 | g0134 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02965 | hp1 | a0001 | c0004 | t0003 | g0139 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02965 | hp2 | a0002 | c0003 | t0003 | g0117 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02970 | hp1 | a0002 | c0003 | t0002 | g0009 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02970 | hp2 | a0001 | c0004 | t0002 | g0222 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0072 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03041 | hp2 | a0002 | c0003 | t0022 | g0060 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03130 | hp2 | a0002 | c0003 | t0002 | g0006 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03139 | hp1 | a0001 | c0004 | t0001 | g0007 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03195 | hp1 | a0001 | c0004 | t0006 | g0044 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0085 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0007 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03225 | hp2 | a0001 | c0002 | t0006 | g0083 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03453 | hp1 | a0002 | c0003 | t0002 | g0058 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03453 | hp2 | a0001 | c0016 | t0011 | g0053 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0007 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03491 | hp2 | a0001 | c0002 | t0004 | g0002 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03492 | hp1 | a0001 | c0002 | t0004 | g0002 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0029 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | ESN | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0227 | AFR | GWD | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03579 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03579 | hp2 | a0001 | c0006 | t0001 | g0124 | AFR | MSL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03654 | hp2 | a0001 | c0001 | t0020 | g0202 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0089 | SAS | STU | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03834 | hp2 | a0001 | c0001 | t0019 | g0001 | SAS | BEB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03942 | hp1 | a0006 | c0013 | t0002 | g0091 | SAS | BEB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0118 | SAS | BEB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0101 | SAS | STU | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | BEB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | STU | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | STU | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG04228 | hp1 | a0001 | c0001 | t0013 | g0003 | SAS | STU | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG04228 | hp2 | a0003 | c0005 | t0001 | g0109 | SAS | STU | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | YRI | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18522 | hp2 | a0001 | c0007 | t0001 | g0135 | AFR | YRI | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18906 | hp1 | a0001 | c0006 | t0002 | g0121 | AFR | YRI | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | YRI | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18939 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18951 | hp2 | a0001 | c0010 | t0003 | g0194 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18957 | hp1 | a0003 | c0005 | t0001 | g0033 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18964 | hp1 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18968 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18978 | hp1 | a0001 | c0006 | t0001 | g0137 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18979 | hp1 | a0003 | c0005 | t0001 | g0028 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18990 | hp2 | a0003 | c0005 | t0001 | g0111 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19012 | hp2 | a0007 | c0009 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | LWK | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | LWK | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19064 | hp2 | a0003 | c0005 | t0001 | g0028 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19072 | hp1 | a0001 | c0002 | t0023 | g0076 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19072 | hp2 | a0003 | c0005 | t0001 | g0115 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19083 | hp2 | a0003 | c0005 | t0001 | g0108 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19086 | hp2 | a0003 | c0005 | t0001 | g0033 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19240 | hp1 | a0001 | c0015 | t0001 | g0066 | AFR | YRI | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0065 | AFR | ASW | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | ASW | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0200 | EUR | TSI | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | TSI | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | GIH | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | GIH | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0007 | AMR | CLM | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02109 | hp1 | a0001 | c0014 | t0001 | g0084 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02559 | hp1 | a0002 | c0003 | t0002 | g0006 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | USA | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | USA | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA18955 | hp2 | a0003 | c0005 | t0001 | g0110 | EAS | JPT | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA20300 | hp1 | a0001 | c0002 | t0006 | g0082 | AFR | USA | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0186 | AFR | USA | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | LWK | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0196 | REF | REF | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| homoSapiens | grch38p0 | a0001 | c0007 | t0002 | g0035 | REF | REF | FAM234B_chr12_13039381_13088449 | FAM234B | chr12 | 13039381 | 13088449 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:13055794 | C | A | 1 | a0005 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.281C>A | p.Ala94Glu | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/13 | 304/4711 | 281/1869 | 94/622 | chr12 | 13055794 | |||
| chr12:13058537 | G | A | 2 | a0003 a0004 |
12 | HG00544.hp2 HG00609.hp1 HG01516.hp1 others(9): Show |
missense_variant | MODERATE | c.520G>A | p.Gly174Arg | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/13 | 543/4711 | 520/1869 | 174/622 | chr12 | 13058537 | |||
| chr12:13062895 | G | A | 1 | a0006 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.772G>A | p.Ala258Thr | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/13 | 795/4711 | 772/1869 | 258/622 | chr12 | 13062895 | |||
| chr12:13066671 | G | A | 1 | a0002 | 21 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(18): Show |
missense_variant | MODERATE | c.884G>A | p.Arg295Gln | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 6/13 | 907/4711 | 884/1869 | 295/622 | chr12 | 13066671 | |||
| chr12:13076042 | C | T | 1 | a0007 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.1541C>T | p.Thr514Ile | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/13 | 1564/4711 | 1541/1869 | 514/622 | chr12 | 13076042 | |||
| chr12:13080627 | C | G | 1 | a0004 | 1 | HG00544.hp2 | missense_variant&splice_region_variant | MODERATE | c.1866C>G | p.Ile622Met | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1889/4711 | 1866/1869 | 622/622 | chr12 | 13080627 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:13055618 | C | T | 9 | a0001c0002 a0001c0014 a0001c0015 others(6): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
synonymous_variant | LOW | c.105C>T | p.Asp35Asp | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/13 | 128/4711 | 105/1869 | 35/622 | chr12 | 13055618 | |||
| chr12:13055744 | C | T | 1 | a0001c0010 | 1 | NA18951.hp2 | synonymous_variant | LOW | c.231C>T | p.Val77Val | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/13 | 254/4711 | 231/1869 | 77/622 | chr12 | 13055744 | |||
| chr12:13055891 | C | T | 1 | a0001c0016 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.378C>T | p.Pro126Pro | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/13 | 401/4711 | 378/1869 | 126/622 | chr12 | 13055891 | |||
| chr12:13055939 | C | T | 1 | a0001c0016 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.426C>T | p.Ser142Ser | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/13 | 449/4711 | 426/1869 | 142/622 | chr12 | 13055939 | |||
| chr12:13058488 | T | C | 1 | a0001c0004 | 16 | HG01123.hp2 HG01934.hp2 HG02257.hp2 others(13): Show |
synonymous_variant | LOW | c.471T>C | p.Asn157Asn | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/13 | 494/4711 | 471/1869 | 157/622 | chr12 | 13058488 | |||
| chr12:13061603 | A | G | 5 | a0001c0001 a0001c0004 a0001c0010 others(2): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
synonymous_variant | LOW | c.561A>G | p.Val187Val | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/13 | 584/4711 | 561/1869 | 187/622 | chr12 | 13061603 | |||
| chr12:13068672 | T | C | 15 | a0001c0001 a0001c0002 a0001c0004 others(12): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
synonymous_variant | LOW | c.1329T>C | p.Asp443Asp | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/13 | 1352/4711 | 1329/1869 | 443/622 | chr12 | 13068672 | |||
| chr12:13071396 | C | T | 1 | a0001c0014 | 1 | HG02109.hp1 | splice_region_variant&synonymous_variant | LOW | c.1524C>T | p.Ser508Ser | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/13 | 1547/4711 | 1524/1869 | 508/622 | chr12 | 13071396 | |||
| chr12:13076091 | C | T | 1 | a0001c0008 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1590C>T | p.Pro530Pro | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/13 | 1613/4711 | 1590/1869 | 530/622 | chr12 | 13076091 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:13080671 | G | T | 1 | a0001c0001t0008 | 2 | HG01071.hp1 HG02071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*41G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 41 | chr12 | 13080671 | ||||||
| chr12:13080965 | T | C | 1 | a0001c0001t0009 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*335T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 335 | chr12 | 13080965 | ||||||
| chr12:13080976 | T | G | 1 | a0001c0001t0010 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*346T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 346 | chr12 | 13080976 | ||||||
| chr12:13081142 | A | G | 3 | a0001c0002t0004 a0001c0002t0024 a0001c0002t0025 |
10 | HG01257.hp2 HG01258.hp1 HG01433.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*512A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 512 | chr12 | 13081142 | ||||||
| chr12:13081274 | T | G | 1 | a0001c0016t0011 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*644T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 644 | chr12 | 13081274 | ||||||
| chr12:13081511 | A | T | 1 | a0001c0002t0023 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*881A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 881 | chr12 | 13081511 | ||||||
| chr12:13081722 | T | A | 1 | a0001c0002t0023 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1092T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1092 | chr12 | 13081722 | ||||||
| chr12:13081949 | CT | C | 24 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(21): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*1345delT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1345 | INFO_REALIGN_3_PRIME | chr12 | 13081949 | |||||
| chr12:13081949 | CTT | C | 6 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0024 others(3): Show |
17 | HG01106.hp2 HG01167.hp1 HG01168.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1344_*1345delTT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1344 | INFO_REALIGN_3_PRIME | chr12 | 13081949 | |||||
| chr12:13081949 | CTTTTTTT others(8): Show |
C | 1 | a0001c0008t0012 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1331_*1345delTTTT others(11): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1331 | INFO_REALIGN_3_PRIME | chr12 | 13081949 | |||||
| chr12:13081949 | CTTTTTTT others(9): Show |
C | 1 | a0001c0016t0011 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1330_*1345delTTTT others(12): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1330 | INFO_REALIGN_3_PRIME | chr12 | 13081949 | |||||
| chr12:13081975 | T | G | 2 | a0001c0002t0006 a0001c0004t0006 |
6 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1345T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1345 | chr12 | 13081975 | ||||||
| chr12:13082137 | G | T | 1 | a0001c0001t0019 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1507G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1507 | chr12 | 13082137 | ||||||
| chr12:13082165 | A | G | 1 | a0002c0003t0022 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1535A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1535 | chr12 | 13082165 | ||||||
| chr12:13082347 | C | T | 1 | a0001c0001t0018 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1717C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1717 | chr12 | 13082347 | ||||||
| chr12:13082574 | G | A | 1 | a0001c0001t0020 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1944G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1944 | chr12 | 13082574 | ||||||
| chr12:13082583 | T | G | 1 | a0001c0001t0013 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1953T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1953 | chr12 | 13082583 | ||||||
| chr12:13082605 | G | A | 1 | a0001c0001t0014 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1975G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 1975 | chr12 | 13082605 | ||||||
| chr12:13082762 | A | G | 1 | a0001c0001t0017 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2132A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 2132 | chr12 | 13082762 | ||||||
| chr12:13082840 | C | A | 2 | a0001c0006t0015 a0001c0006t0016 |
2 | HG02809.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2210C>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 2210 | chr12 | 13082840 | ||||||
| chr12:13082858 | G | A | 1 | a0001c0016t0011 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2228G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 2228 | chr12 | 13082858 | ||||||
| chr12:13083010 | A | G | 1 | a0001c0001t0005 | 7 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2380A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 2380 | chr12 | 13083010 | ||||||
| chr12:13083018 | G | A | 1 | a0001c0006t0015 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2388G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 2388 | chr12 | 13083018 | ||||||
| chr12:13083192 | A | G | 2 | a0001c0002t0006 a0001c0004t0006 |
6 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2562A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 2562 | chr12 | 13083192 | ||||||
| chr12:13083244 | C | T | 1 | a0001c0001t0007 | 2 | NA18939.hp1 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2614C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 2614 | chr12 | 13083244 | ||||||
| chr12:13083409 | G | A | 1 | a0005c0011t0021 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2779G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 13/13 | 2779 | chr12 | 13083409 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:13044790 | G | T | 1 | a0001c0002t0001g0231 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.37+350G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13044790 | |||||||
| chr12:13044942 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.37+502C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13044942 | |||||||
| chr12:13045026 | G | C | 104 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(101): Show |
171 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.37+586G>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13045026 | |||||||
| chr12:13045069 | A | C | 1 | a0001c0001t0001g0229 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.37+629A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13045069 | |||||||
| chr12:13045199 | A | G | 1 | a0001c0002t0001g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.37+759A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13045199 | |||||||
| chr12:13045220 | CT | C | 95 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(92): Show |
162 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.37+795delT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 13045220 | ||||||
| chr12:13045435 | C | T | 1 | a0001c0002t0001g0116 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.37+995C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13045435 | |||||||
| chr12:13045437 | A | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
6 | HG01891.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.37+997A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13045437 | |||||||
| chr12:13045601 | A | T | 1 | a0005c0011t0021g0224 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.37+1161A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13045601 | |||||||
| chr12:13045831 | CT | C | 103 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0002g0130 others(100): Show |
170 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.37+1403delT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 13045831 | ||||||
| chr12:13045843 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.37+1403T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13045843 | |||||||
| chr12:13045887 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.37+1447T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13045887 | |||||||
| chr12:13046070 | A | G | 1 | a0003c0005t0001g0115 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.37+1630A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13046070 | |||||||
| chr12:13046134 | AAGAAAAT others(97): Show |
A | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.37+1714_37+1817del | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 13046134 | ||||||
| chr12:13046170 | C | G | 1 | a0001c0001t0001g0039 | 2 | NA18957.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.37+1730C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13046170 | |||||||
| chr12:13046308 | A | G | 1 | a0001c0004t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.37+1868A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13046308 | |||||||
| chr12:13046314 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.37+1874A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13046314 | |||||||
| chr12:13046471 | T | C | 2 | a0001c0004t0001g0138 a0001c0004t0003g0139 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.37+2031T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13046471 | |||||||
| chr12:13046547 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.37+2107G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13046547 | |||||||
| chr12:13046606 | A | G | 1 | a0001c0001t0002g0221 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.37+2166A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13046606 | |||||||
| chr12:13046916 | A | G | 1 | a0001c0002t0002g0114 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.37+2476A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13046916 | |||||||
| chr12:13046944 | A | T | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.37+2504A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13046944 | |||||||
| chr12:13047171 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0140 others(3): Show |
11 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.37+2731G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047171 | |||||||
| chr12:13047189 | A | T | 1 | a0001c0006t0001g0137 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.37+2749A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047189 | |||||||
| chr12:13047250 | G | A | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.37+2810G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047250 | |||||||
| chr12:13047278 | T | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0002t0001g0126 |
3 | HG02486.hp2 NA18522.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.37+2838T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047278 | |||||||
| chr12:13047357 | T | A | 1 | a0001c0002t0001g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.37+2917T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047357 | |||||||
| chr12:13047385 | G | A | 4 | a0001c0002t0001g0026 a0001c0002t0001g0051 a0001c0002t0001g0052 others(1): Show |
5 | HG02615.hp2 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.37+2945G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047385 | |||||||
| chr12:13047396 | A | C | 1 | a0001c0002t0001g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.37+2956A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047396 | |||||||
| chr12:13047398 | C | CCCTTATA others(9): Show |
1 | a0001c0002t0001g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.37+2958_37+2959ins others(16): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047398 | |||||||
| chr12:13047402 | C | A | 1 | a0001c0002t0001g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.37+2962C>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047402 | |||||||
| chr12:13047416 | T | A | 1 | a0001c0002t0001g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.37+2976T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047416 | |||||||
| chr12:13047417 | A | G | 1 | a0001c0002t0001g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.37+2977A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047417 | |||||||
| chr12:13047423 | C | G | 1 | a0001c0002t0001g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.37+2983C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047423 | |||||||
| chr12:13047425 | T | A | 1 | a0001c0002t0001g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.37+2985T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047425 | |||||||
| chr12:13047445 | T | A | 1 | a0001c0002t0001g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.37+3005T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047445 | |||||||
| chr12:13047451 | G | C | 1 | a0001c0002t0001g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.37+3011G>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047451 | |||||||
| chr12:13047480 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.37+3040T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047480 | |||||||
| chr12:13047489 | T | G | 1 | a0001c0002t0001g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.37+3049T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047489 | |||||||
| chr12:13047656 | G | T | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.37+3216G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047656 | |||||||
| chr12:13047884 | G | T | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.37+3444G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047884 | |||||||
| chr12:13047979 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.37+3539T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13047979 | |||||||
| chr12:13048234 | A | G | 1 | a0001c0006t0001g0137 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.37+3794A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048234 | |||||||
| chr12:13048235 | T | C | 4 | a0001c0002t0001g0026 a0001c0002t0001g0051 a0001c0002t0001g0052 others(1): Show |
5 | HG02615.hp2 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.37+3795T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048235 | |||||||
| chr12:13048265 | A | G | 56 | a0001c0002t0001g0014 a0001c0002t0001g0026 a0001c0002t0001g0034 others(53): Show |
82 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.37+3825A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048265 | |||||||
| chr12:13048501 | C | CCA | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.37+4061_37+4062ins others(2): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048501 | |||||||
| chr12:13048504 | TTCTGTTT others(25): Show |
T | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.37+4068_37+4099del others(32): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 13048504 | ||||||
| chr12:13048508 | GTTTTCTG others(8): Show |
G | 2 | a0001c0001t0001g0207 a0001c0001t0002g0219 |
2 | HG03490.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.37+4101_37+4115del others(15): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 13048508 | ||||||
| chr12:13048565 | A | G | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.37+4125A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048565 | |||||||
| chr12:13048580 | T | C | 3 | a0001c0006t0015g0132 a0001c0006t0016g0134 a0001c0008t0012g0133 |
3 | HG02809.hp1 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.37+4140T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048580 | |||||||
| chr12:13048658 | G | A | 1 | a0001c0016t0011g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.37+4218G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048658 | |||||||
| chr12:13048750 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
5 | HG00438.hp1 NA18973.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.37+4310G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048750 | |||||||
| chr12:13048753 | A | G | 2 | a0001c0002t0001g0017 a0001c0002t0001g0118 |
4 | HG01516.hp2 HG01517.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+4313A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048753 | |||||||
| chr12:13048839 | A | G | 9 | a0001c0006t0001g0124 a0001c0006t0001g0137 a0001c0006t0002g0121 others(6): Show |
9 | HG01109.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.37+4399A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048839 | |||||||
| chr12:13048846 | A | C | 56 | a0001c0002t0001g0014 a0001c0002t0001g0026 a0001c0002t0001g0034 others(53): Show |
82 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.37+4406A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048846 | |||||||
| chr12:13048907 | G | T | 2 | a0001c0002t0001g0034 a0001c0002t0003g0113 |
3 | HG01167.hp1 HG01169.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.37+4467G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13048907 | |||||||
| chr12:13049085 | C | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(73): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.37+4645C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049085 | |||||||
| chr12:13049167 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.37+4727T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049167 | |||||||
| chr12:13049218 | C | T | 2 | a0001c0016t0011g0053 a0005c0011t0021g0224 |
2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.37+4778C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049218 | |||||||
| chr12:13049360 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(54): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.37+4920A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049360 | |||||||
| chr12:13049368 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.37+4928C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049368 | |||||||
| chr12:13049377 | G | A | 3 | a0001c0002t0006g0027 a0001c0002t0006g0082 a0001c0002t0006g0083 |
4 | HG02896.hp2 HG02897.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+4937G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049377 | |||||||
| chr12:13049389 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0149 |
3 | NA18973.hp2 NA18985.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.37+4949G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049389 | |||||||
| chr12:13049426 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.37+4986C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049426 | |||||||
| chr12:13049433 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.37+4993G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049433 | |||||||
| chr12:13049460 | G | A | 1 | a0001c0014t0001g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.37+5020G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049460 | |||||||
| chr12:13049767 | A | G | 4 | a0001c0002t0001g0126 a0001c0002t0006g0027 a0001c0002t0006g0082 others(1): Show |
5 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.37+5327A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049767 | |||||||
| chr12:13049861 | G | C | 5 | a0001c0006t0001g0124 a0001c0006t0002g0121 a0001c0006t0002g0122 others(2): Show |
5 | HG01109.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+5421G>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049861 | |||||||
| chr12:13049874 | A | G | 42 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(39): Show |
77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.37+5434A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13049874 | |||||||
| chr12:13050108 | T | C | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-5443T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13050108 | |||||||
| chr12:13050132 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.38-5419A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13050132 | |||||||
| chr12:13050183 | T | C | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-5368T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13050183 | |||||||
| chr12:13050304 | T | A | 3 | a0001c0002t0002g0018 a0001c0002t0002g0085 a0001c0002t0002g0086 |
5 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-5247T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13050304 | |||||||
| chr12:13050338 | T | C | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-5213T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13050338 | |||||||
| chr12:13050669 | A | T | 9 | a0001c0002t0001g0014 a0001c0002t0001g0026 a0001c0002t0001g0034 others(6): Show |
13 | HG01099.hp1 HG01167.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.38-4882A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13050669 | |||||||
| chr12:13050851 | T | A | 1 | a0003c0005t0001g0028 | 2 | NA18979.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.38-4700T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13050851 | |||||||
| chr12:13050953 | A | G | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-4598A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13050953 | |||||||
| chr12:13051123 | T | C | 2 | a0001c0002t0001g0034 a0001c0002t0003g0113 |
3 | HG01167.hp1 HG01169.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.38-4428T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13051123 | |||||||
| chr12:13051318 | G | A | 1 | a0001c0016t0011g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.38-4233G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13051318 | |||||||
| chr12:13051342 | C | G | 43 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0016 others(40): Show |
84 | HG00408.hp2 HG00597.hp1 HG01081.hp2 others(81): Show |
intron_variant | MODIFIER | c.38-4209C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13051342 | |||||||
| chr12:13052102 | T | G | 1 | a0001c0002t0001g0054 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.38-3449T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13052102 | |||||||
| chr12:13052284 | G | T | 1 | a0001c0001t0002g0187 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.38-3267G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13052284 | |||||||
| chr12:13052422 | GAT | G | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-3114_38-3113del others(2): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 13052422 | ||||||
| chr12:13052485 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(242): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.38-3066C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13052485 | |||||||
| chr12:13052504 | A | G | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-3047A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13052504 | |||||||
| chr12:13052574 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.38-2977A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13052574 | |||||||
| chr12:13052660 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0192 |
2 | NA18966.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.38-2891T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13052660 | |||||||
| chr12:13052729 | TG | T | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-2821delG | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13052729 | |||||||
| chr12:13052806 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(242): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.38-2745C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13052806 | |||||||
| chr12:13052877 | C | G | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-2674C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13052877 | |||||||
| chr12:13053013 | A | G | 2 | a0001c0016t0011g0053 a0005c0011t0021g0224 |
2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.38-2538A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13053013 | |||||||
| chr12:13053042 | T | C | 1 | a0001c0002t0001g0055 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.38-2509T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13053042 | |||||||
| chr12:13053149 | T | C | 1 | a0001c0006t0015g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.38-2402T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13053149 | |||||||
| chr12:13053159 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.38-2392T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13053159 | |||||||
| chr12:13053166 | T | C | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-2385T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13053166 | |||||||
| chr12:13053237 | A | AT | 10 | a0001c0002t0002g0018 a0001c0002t0002g0085 a0001c0002t0002g0086 others(7): Show |
21 | HG01123.hp2 HG01934.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.38-2306dupT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 13053237 | ||||||
| chr12:13053380 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.38-2171G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13053380 | |||||||
| chr12:13053430 | G | A | 1 | a0001c0008t0012g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.38-2121G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13053430 | |||||||
| chr12:13053568 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.38-1983G>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13053568 | |||||||
| chr12:13053637 | G | A | 1 | a0001c0002t0001g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.38-1914G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13053637 | |||||||
| chr12:13054008 | C | T | 1 | a0004c0012t0001g0112 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.38-1543C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054008 | |||||||
| chr12:13054118 | A | G | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-1433A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054118 | |||||||
| chr12:13054190 | A | G | 25 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0016 others(22): Show |
57 | HG00408.hp2 HG00597.hp1 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.38-1361A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054190 | |||||||
| chr12:13054198 | G | C | 1 | a0001c0004t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.38-1353G>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054198 | |||||||
| chr12:13054230 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.38-1321G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054230 | |||||||
| chr12:13054233 | A | G | 44 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0016 others(41): Show |
85 | HG00408.hp2 HG00597.hp1 HG01081.hp2 others(82): Show |
intron_variant | MODIFIER | c.38-1318A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054233 | |||||||
| chr12:13054257 | T | TC | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-1294_38-1293ins others(1): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054257 | |||||||
| chr12:13054461 | A | G | 1 | a0001c0006t0015g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.38-1090A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054461 | |||||||
| chr12:13054522 | C | T | 1 | a0001c0004t0003g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.38-1029C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054522 | |||||||
| chr12:13054636 | A | G | 1 | a0001c0014t0001g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.38-915A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054636 | |||||||
| chr12:13054810 | T | C | 9 | a0001c0002t0001g0014 a0001c0002t0001g0026 a0001c0002t0001g0034 others(6): Show |
13 | HG01099.hp1 HG01167.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.38-741T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054810 | |||||||
| chr12:13054974 | A | G | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.38-577A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13054974 | |||||||
| chr12:13055012 | A | T | 1 | a0005c0011t0021g0224 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.38-539A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13055012 | |||||||
| chr12:13055260 | T | C | 1 | a0001c0002t0002g0087 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.38-291T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13055260 | |||||||
| chr12:13055319 | C | G | 1 | a0005c0011t0021g0224 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.38-232C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 1/12 | chr12 | 13055319 | |||||||
| chr12:13056156 | G | A | 1 | a0001c0002t0001g0055 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.433+210G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13056156 | |||||||
| chr12:13056357 | A | G | 9 | a0003c0005t0001g0028 a0003c0005t0001g0032 a0003c0005t0001g0033 others(6): Show |
12 | HG00544.hp2 HG00609.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.433+411A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13056357 | |||||||
| chr12:13056387 | G | T | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.433+441G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13056387 | |||||||
| chr12:13056519 | A | G | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.433+573A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13056519 | |||||||
| chr12:13056785 | A | G | 1 | a0001c0002t0001g0055 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.433+839A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13056785 | |||||||
| chr12:13056810 | C | T | 1 | a0001c0002t0002g0107 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.433+864C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13056810 | |||||||
| chr12:13056914 | A | G | 1 | a0001c0016t0011g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.433+968A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13056914 | |||||||
| chr12:13056931 | G | T | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.433+985G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13056931 | |||||||
| chr12:13056978 | C | CT | 68 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0041 others(65): Show |
97 | HG00438.hp1 HG00558.hp2 HG01099.hp1 others(94): Show |
intron_variant | MODIFIER | c.433+1049dupT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 13056978 | ||||||
| chr12:13056978 | C | CTT | 15 | a0001c0002t0001g0051 a0001c0002t0001g0052 a0001c0002t0001g0103 others(12): Show |
20 | HG00544.hp1 HG00673.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.433+1048_433+1049d others(4): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 13056978 | ||||||
| chr12:13057046 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.433+1100C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13057046 | |||||||
| chr12:13057078 | G | A | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.433+1132G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13057078 | |||||||
| chr12:13057227 | C | T | 1 | a0001c0016t0011g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.434-1224C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13057227 | |||||||
| chr12:13057247 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0153 |
4 | HG01256.hp1 HG01258.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-1204G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13057247 | |||||||
| chr12:13057375 | A | G | 2 | a0001c0004t0001g0138 a0001c0004t0003g0139 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.434-1076A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13057375 | |||||||
| chr12:13057456 | CT | C | 102 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(99): Show |
169 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.434-984delT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 13057456 | ||||||
| chr12:13057516 | T | C | 1 | a0001c0004t0006g0044 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.434-935T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13057516 | |||||||
| chr12:13057517 | G | T | 1 | a0001c0004t0006g0044 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.434-934G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13057517 | |||||||
| chr12:13057518 | C | T | 1 | a0001c0004t0006g0044 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.434-933C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13057518 | |||||||
| chr12:13057768 | C | T | 9 | a0001c0002t0001g0014 a0001c0002t0001g0026 a0001c0002t0001g0034 others(6): Show |
13 | HG01099.hp1 HG01167.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.434-683C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13057768 | |||||||
| chr12:13057924 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.434-527A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13057924 | |||||||
| chr12:13057983 | T | C | 101 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.434-468T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13057983 | |||||||
| chr12:13058027 | C | A | 100 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(97): Show |
167 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.434-424C>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13058027 | |||||||
| chr12:13058111 | T | C | 100 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(97): Show |
167 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.434-340T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13058111 | |||||||
| chr12:13058146 | C | T | 1 | a0001c0002t0001g0056 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.434-305C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13058146 | |||||||
| chr12:13058278 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(242): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.434-173G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13058278 | |||||||
| chr12:13058310 | C | T | 1 | a0001c0002t0001g0055 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.434-141C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 2/12 | chr12 | 13058310 | |||||||
| chr12:13058561 | GT | G | 99 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(96): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.532+19delT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 13058561 | ||||||
| chr12:13058601 | G | A | 33 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0094 others(30): Show |
51 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.532+52G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13058601 | |||||||
| chr12:13058782 | A | G | 47 | a0001c0002t0001g0014 a0001c0002t0001g0026 a0001c0002t0001g0034 others(44): Show |
70 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.532+233A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13058782 | |||||||
| chr12:13058979 | C | T | 1 | a0005c0011t0021g0224 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.532+430C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13058979 | |||||||
| chr12:13058981 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.532+432C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13058981 | |||||||
| chr12:13058988 | G | A | 3 | a0003c0005t0001g0028 a0003c0005t0001g0108 a0003c0005t0001g0115 |
4 | NA18979.hp1 NA19064.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.532+439G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13058988 | |||||||
| chr12:13059203 | A | G | 99 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(96): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.532+654A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13059203 | |||||||
| chr12:13059292 | G | A | 99 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(96): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.532+743G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13059292 | |||||||
| chr12:13059484 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.532+935T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13059484 | |||||||
| chr12:13059504 | A | C | 1 | a0001c0001t0001g0039 | 2 | NA18957.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.532+955A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13059504 | |||||||
| chr12:13059567 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.532+1018G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13059567 | |||||||
| chr12:13059575 | G | T | 1 | a0001c0002t0002g0114 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.532+1026G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13059575 | |||||||
| chr12:13059624 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.532+1075C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13059624 | |||||||
| chr12:13059715 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(242): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.532+1166A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13059715 | |||||||
| chr12:13059750 | G | C | 2 | a0001c0002t0001g0055 a0001c0002t0001g0056 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.532+1201G>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13059750 | |||||||
| chr12:13059935 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.532+1386G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13059935 | |||||||
| chr12:13060144 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.533-1431C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13060144 | |||||||
| chr12:13060306 | T | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0002g0130 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-1269T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13060306 | |||||||
| chr12:13060525 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.533-1050A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13060525 | |||||||
| chr12:13060590 | CAT | C | 46 | a0001c0002t0001g0014 a0001c0002t0001g0026 a0001c0002t0001g0034 others(43): Show |
69 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.533-978_533-977del others(2): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 13060590 | ||||||
| chr12:13060670 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0192 |
2 | NA18966.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.533-905C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13060670 | |||||||
| chr12:13060748 | T | G | 2 | a0001c0001t0008g0154 a0001c0001t0008g0175 |
2 | HG01071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.533-827T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13060748 | |||||||
| chr12:13060825 | A | G | 15 | a0001c0002t0001g0064 a0001c0002t0002g0063 a0001c0002t0002g0067 others(12): Show |
24 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.533-750A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13060825 | |||||||
| chr12:13060955 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.533-620C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13060955 | |||||||
| chr12:13061207 | G | T | 11 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0046 others(8): Show |
17 | HG00597.hp2 HG02155.hp1 NA18939.hp2 others(14): Show |
intron_variant | MODIFIER | c.533-368G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13061207 | |||||||
| chr12:13061216 | C | T | 2 | a0001c0002t0002g0085 a0001c0002t0002g0086 |
2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.533-359C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13061216 | |||||||
| chr12:13061447 | G | T | 1 | a0001c0001t0002g0173 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.533-128G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 3/12 | chr12 | 13061447 | |||||||
| chr12:13061857 | G | A | 99 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(96): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.721+94G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | chr12 | 13061857 | |||||||
| chr12:13061997 | GA | G | 99 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(96): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.721+237delA | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 13061997 | ||||||
| chr12:13062197 | A | G | 1 | a0001c0014t0001g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.721+434A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | chr12 | 13062197 | |||||||
| chr12:13062217 | A | G | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0179 |
3 | NA18947.hp1 NA18956.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.721+454A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | chr12 | 13062217 | |||||||
| chr12:13062298 | C | T | 24 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0016 others(21): Show |
56 | HG00408.hp2 HG00597.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.721+535C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | chr12 | 13062298 | |||||||
| chr12:13062308 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.722-537C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | chr12 | 13062308 | |||||||
| chr12:13062396 | A | G | 1 | a0002c0003t0001g0065 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.722-449A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | chr12 | 13062396 | |||||||
| chr12:13062434 | A | G | 1 | a0001c0002t0002g0106 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.722-411A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | chr12 | 13062434 | |||||||
| chr12:13062679 | G | A | 10 | a0001c0002t0001g0231 a0003c0005t0001g0028 a0003c0005t0001g0032 others(7): Show |
13 | HG00544.hp2 HG00609.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.722-166G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | chr12 | 13062679 | |||||||
| chr12:13062682 | T | C | 100 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(97): Show |
167 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.722-163T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | chr12 | 13062682 | |||||||
| chr12:13062732 | G | A | 5 | a0001c0006t0001g0124 a0001c0006t0002g0121 a0001c0006t0002g0122 others(2): Show |
5 | HG01109.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.722-113G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | chr12 | 13062732 | |||||||
| chr12:13062751 | C | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(242): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.722-94C>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 4/12 | chr12 | 13062751 | |||||||
| chr12:13063137 | A | G | 46 | a0001c0002t0001g0014 a0001c0002t0001g0026 a0001c0002t0001g0034 others(43): Show |
69 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.852+162A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13063137 | |||||||
| chr12:13063230 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0209 |
3 | HG01099.hp2 HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.852+255C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13063230 | |||||||
| chr12:13063296 | A | C | 1 | a0001c0002t0002g0107 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.852+321A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13063296 | |||||||
| chr12:13063327 | C | T | 99 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(96): Show |
166 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.852+352C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13063327 | |||||||
| chr12:13063355 | A | G | 1 | a0001c0001t0003g0170 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.852+380A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13063355 | |||||||
| chr12:13063389 | G | T | 1 | a0001c0014t0001g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.852+414G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13063389 | |||||||
| chr12:13063396 | A | G | 2 | a0001c0016t0011g0053 a0005c0011t0021g0224 |
2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.852+421A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13063396 | |||||||
| chr12:13063818 | A | G | 1 | a0001c0006t0001g0137 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+843A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13063818 | |||||||
| chr12:13063847 | G | A | 2 | a0001c0002t0001g0126 a0001c0007t0002g0136 |
2 | HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.852+872G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13063847 | |||||||
| chr12:13063924 | C | G | 1 | a0001c0001t0001g0208 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.852+949C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13063924 | |||||||
| chr12:13064021 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.852+1046T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13064021 | |||||||
| chr12:13064166 | C | G | 1 | a0001c0002t0001g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.852+1191C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13064166 | |||||||
| chr12:13064304 | T | C | 1 | a0001c0002t0002g0088 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.852+1329T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13064304 | |||||||
| chr12:13064312 | T | C | 1 | a0001c0002t0006g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.852+1337T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13064312 | |||||||
| chr12:13064422 | A | G | 6 | a0001c0006t0001g0124 a0001c0006t0002g0121 a0001c0006t0002g0122 others(3): Show |
6 | HG01109.hp1 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+1447A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13064422 | |||||||
| chr12:13064423 | A | C | 1 | a0001c0014t0001g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.852+1448A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13064423 | |||||||
| chr12:13064667 | G | T | 1 | a0001c0002t0001g0100 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.852+1692G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13064667 | |||||||
| chr12:13064723 | C | T | 1 | a0001c0002t0001g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.852+1748C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13064723 | |||||||
| chr12:13065090 | G | A | 1 | a0001c0007t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.853-1550G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13065090 | |||||||
| chr12:13065238 | T | C | 106 | a0001c0001t0001g0188 a0001c0002t0001g0002 a0001c0002t0001g0012 others(103): Show |
173 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.853-1402T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13065238 | |||||||
| chr12:13065326 | A | G | 1 | a0005c0011t0021g0224 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.853-1314A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13065326 | |||||||
| chr12:13065399 | T | C | 4 | a0001c0002t0002g0029 a0001c0002t0002g0089 a0001c0002t0002g0101 others(1): Show |
5 | HG02683.hp2 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-1241T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13065399 | |||||||
| chr12:13065438 | A | G | 2 | a0001c0002t0001g0064 a0001c0002t0002g0063 |
2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.853-1202A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13065438 | |||||||
| chr12:13065648 | G | A | 1 | a0001c0001t0005g0015 | 4 | HG00280.hp1 HG01255.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-992G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13065648 | |||||||
| chr12:13065670 | G | A | 42 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0016 others(39): Show |
83 | HG00408.hp2 HG00597.hp1 HG01081.hp2 others(80): Show |
intron_variant | MODIFIER | c.853-970G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13065670 | |||||||
| chr12:13065675 | C | T | 105 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(102): Show |
172 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.853-965C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13065675 | |||||||
| chr12:13065984 | G | A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(73): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.853-656G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13065984 | |||||||
| chr12:13065990 | T | C | 105 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(102): Show |
172 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.853-650T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13065990 | |||||||
| chr12:13066139 | G | C | 105 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(102): Show |
172 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.853-501G>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13066139 | |||||||
| chr12:13066149 | A | G | 1 | a0001c0008t0012g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.853-491A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13066149 | |||||||
| chr12:13066213 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.853-427C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13066213 | |||||||
| chr12:13066431 | G | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0002g0219 |
3 | HG03490.hp2 HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.853-209G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13066431 | |||||||
| chr12:13066438 | T | A | 105 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0014 others(102): Show |
172 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.853-202T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13066438 | |||||||
| chr12:13066598 | T | C | 2 | a0003c0005t0001g0028 a0003c0005t0001g0108 |
3 | NA18979.hp1 NA19064.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.853-42T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13066598 | |||||||
| chr12:13066622 | C | G | 36 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(33): Show |
80 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.853-18C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 5/12 | chr12 | 13066622 | |||||||
| chr12:13066898 | G | A | 42 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0016 others(39): Show |
83 | HG00408.hp2 HG00597.hp1 HG01081.hp2 others(80): Show |
intron_variant | MODIFIER | c.1000+111G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 6/12 | chr12 | 13066898 | |||||||
| chr12:13066955 | C | A | 1 | a0003c0005t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1000+168C>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 6/12 | chr12 | 13066955 | |||||||
| chr12:13067308 | G | A | 1 | a0002c0003t0001g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1142+12G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 7/12 | chr12 | 13067308 | |||||||
| chr12:13067479 | A | G | 1 | a0001c0002t0002g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1142+183A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 7/12 | chr12 | 13067479 | |||||||
| chr12:13068020 | G | C | 1 | a0001c0014t0001g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1143-284G>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 7/12 | chr12 | 13068020 | |||||||
| chr12:13068205 | G | A | 1 | a0001c0002t0002g0090 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1143-99G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 7/12 | chr12 | 13068205 | |||||||
| chr12:13068590 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1287-40C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 8/12 | chr12 | 13068590 | |||||||
| chr12:13068608 | C | G | 1 | a0005c0011t0021g0224 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1287-22C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 8/12 | chr12 | 13068608 | |||||||
| chr12:13068845 | T | C | 101 | a0001c0001t0001g0188 a0001c0002t0001g0002 a0001c0002t0001g0012 others(98): Show |
168 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.1368+134T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13068845 | |||||||
| chr12:13069323 | T | G | 2 | a0001c0016t0011g0053 a0005c0011t0021g0224 |
2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1368+612T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13069323 | |||||||
| chr12:13069417 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1368+706A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13069417 | |||||||
| chr12:13069462 | C | T | 1 | a0001c0002t0002g0223 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1368+751C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13069462 | |||||||
| chr12:13069572 | C | T | 72 | a0001c0001t0001g0188 a0001c0001t0002g0131 a0001c0002t0001g0026 others(69): Show |
105 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.1368+861C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13069572 | |||||||
| chr12:13069601 | G | A | 1 | a0001c0001t0002g0042 | 2 | HG00642.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1368+890G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13069601 | |||||||
| chr12:13069602 | C | A | 1 | a0001c0001t0002g0042 | 2 | HG00642.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1368+891C>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13069602 | |||||||
| chr12:13069667 | T | C | 1 | a0001c0006t0002g0121 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1368+956T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13069667 | |||||||
| chr12:13069723 | T | A | 1 | a0001c0001t0002g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1368+1012T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13069723 | |||||||
| chr12:13069726 | G | T | 1 | a0001c0001t0003g0170 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1368+1015G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13069726 | |||||||
| chr12:13070164 | T | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(239): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.1369-1077T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13070164 | |||||||
| chr12:13070170 | AAGATATA others(5): Show |
A | 1 | a0001c0001t0001g0168 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1369-1069_1369-105 others(16): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070170 | ||||||
| chr12:13070172 | G | GATATATA others(5): Show |
1 | a0001c0007t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1369-1041_1369-103 others(16): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070172 | ||||||
| chr12:13070172 | G | GATATATA others(7): Show |
1 | a0001c0006t0001g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1369-1043_1369-103 others(18): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070172 | ||||||
| chr12:13070172 | GATAT | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0128 others(2): Show |
5 | HG00408.hp1 HG02055.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1369-1033_1369-103 others(8): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070172 | ||||||
| chr12:13070172 | GATATAT | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(8): Show |
13 | HG00099.hp1 HG01168.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1369-1035_1369-103 others(10): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070172 | ||||||
| chr12:13070172 | GATATATA others(1): Show |
G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(18): Show |
27 | HG00140.hp1 HG00621.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.1369-1037_1369-103 others(12): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070172 | ||||||
| chr12:13070172 | GATATATA others(3): Show |
G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(72): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1369-1039_1369-103 others(14): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070172 | ||||||
| chr12:13070172 | GATATATA others(5): Show |
G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(48): Show |
90 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1369-1041_1369-103 others(16): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070172 | ||||||
| chr12:13070172 | GATATATA others(7): Show |
G | 9 | a0001c0002t0002g0063 a0001c0002t0006g0027 a0001c0002t0006g0082 others(6): Show |
10 | HG02622.hp1 HG02809.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369-1043_1369-103 others(18): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070172 | ||||||
| chr12:13070172 | GATATATA others(9): Show |
G | 6 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0001c0002t0002g0018 others(3): Show |
6 | HG02280.hp1 HG02970.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1369-1045_1369-103 others(20): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070172 | ||||||
| chr12:13070172 | GATATATA others(11): Show |
G | 79 | a0001c0001t0001g0188 a0001c0001t0002g0131 a0001c0002t0001g0002 others(76): Show |
141 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1369-1047_1369-103 others(22): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070172 | ||||||
| chr12:13070194 | TATATATA others(11): Show |
T | 2 | a0001c0002t0001g0069 a0001c0002t0002g0078 |
2 | NA19012.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1369-1045_1369-102 others(22): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070194 | ||||||
| chr12:13070202 | TATATATA others(3): Show |
T | 1 | a0001c0004t0001g0007 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1369-1037_1369-102 others(14): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070202 | ||||||
| chr12:13070339 | A | G | 3 | a0001c0002t0002g0063 a0001c0006t0002g0121 a0001c0006t0002g0125 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1369-902A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13070339 | |||||||
| chr12:13070680 | A | AT | 8 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0001c0002t0002g0063 others(5): Show |
8 | HG01109.hp1 HG02622.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1369-553dupT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 13070680 | ||||||
| chr12:13070787 | A | G | 2 | a0001c0002t0001g0034 a0001c0002t0003g0113 |
3 | HG01167.hp1 HG01169.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1369-454A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13070787 | |||||||
| chr12:13070897 | C | G | 1 | a0001c0004t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1369-344C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13070897 | |||||||
| chr12:13071093 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0041 others(105): Show |
185 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.1369-148C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 9/12 | chr12 | 13071093 | |||||||
| chr12:13071437 | T | C | 3 | a0001c0001t0002g0159 a0001c0001t0003g0160 a0001c0001t0003g0170 |
3 | HG02083.hp2 NA18992.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1524+41T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13071437 | |||||||
| chr12:13071443 | C | T | 1 | a0001c0001t0017g0204 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1524+47C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13071443 | |||||||
| chr12:13071697 | A | G | 4 | a0001c0002t0006g0027 a0001c0002t0006g0082 a0001c0002t0006g0083 others(1): Show |
6 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+301A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13071697 | |||||||
| chr12:13071832 | C | T | 1 | a0001c0004t0001g0186 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1524+436C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13071832 | |||||||
| chr12:13071880 | A | G | 2 | a0001c0002t0001g0126 a0002c0003t0001g0062 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1524+484A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13071880 | |||||||
| chr12:13071929 | G | A | 1 | a0001c0002t0002g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1524+533G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13071929 | |||||||
| chr12:13072016 | C | G | 2 | a0001c0001t0008g0154 a0001c0001t0008g0175 |
2 | HG01071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1524+620C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072016 | |||||||
| chr12:13072073 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(118): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1524+677C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072073 | |||||||
| chr12:13072074 | G | A | 111 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0041 others(108): Show |
188 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.1524+678G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072074 | |||||||
| chr12:13072449 | C | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0041 others(109): Show |
189 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+1053C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072449 | |||||||
| chr12:13072527 | C | T | 1 | a0001c0006t0016g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1524+1131C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072527 | |||||||
| chr12:13072558 | C | T | 1 | a0001c0002t0001g0099 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1524+1162C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072558 | |||||||
| chr12:13072655 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0209 |
3 | HG01099.hp2 HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1524+1259G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072655 | |||||||
| chr12:13072679 | G | A | 111 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0041 others(108): Show |
188 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.1524+1283G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072679 | |||||||
| chr12:13072689 | A | C | 112 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0041 others(109): Show |
189 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+1293A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072689 | |||||||
| chr12:13072729 | C | CA | 8 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0197 others(5): Show |
8 | HG00438.hp2 HG03831.hp1 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.1524+1351dupA | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 13072729 | ||||||
| chr12:13072729 | CAA | C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0041 others(105): Show |
185 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.1524+1350_1524+135 others(6): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 13072729 | ||||||
| chr12:13072872 | T | A | 1 | a0001c0002t0001g0071 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1524+1476T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072872 | |||||||
| chr12:13072959 | A | C | 15 | a0001c0001t0001g0188 a0001c0001t0002g0131 a0001c0002t0001g0055 others(12): Show |
24 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.1524+1563A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072959 | |||||||
| chr12:13072969 | G | A | 1 | a0001c0001t0001g0046 | 2 | NA18989.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1524+1573G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13072969 | |||||||
| chr12:13073097 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1524+1701G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073097 | |||||||
| chr12:13073130 | A | G | 1 | a0001c0006t0001g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1524+1734A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073130 | |||||||
| chr12:13073153 | C | CT | 9 | a0001c0001t0001g0127 a0001c0001t0001g0230 a0001c0001t0002g0203 others(6): Show |
11 | HG01109.hp2 HG01884.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1524+1771dupT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 13073153 | ||||||
| chr12:13073153 | CT | C | 33 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0016 others(30): Show |
68 | HG00408.hp2 HG00597.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.1524+1771delT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 13073153 | ||||||
| chr12:13073162 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1524+1766T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073162 | |||||||
| chr12:13073215 | G | A | 1 | a0001c0002t0001g0051 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1524+1819G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073215 | |||||||
| chr12:13073292 | G | A | 1 | a0001c0002t0001g0055 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1524+1896G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073292 | |||||||
| chr12:13073349 | A | T | 1 | a0003c0005t0001g0115 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1524+1953A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073349 | |||||||
| chr12:13073669 | A | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(118): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1524+2273A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073669 | |||||||
| chr12:13073670 | ATAT | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(118): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1524+2275_1524+227 others(7): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073670 | |||||||
| chr12:13073681 | C | G | 1 | a0001c0002t0001g0093 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1524+2285C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073681 | |||||||
| chr12:13073741 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1525-2285G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073741 | |||||||
| chr12:13073872 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1525-2154G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073872 | |||||||
| chr12:13073885 | G | A | 1 | a0001c0001t0001g0048 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1525-2141G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073885 | |||||||
| chr12:13073888 | A | C | 2 | a0001c0002t0001g0034 a0001c0002t0003g0113 |
3 | HG01167.hp1 HG01169.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1525-2138A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073888 | |||||||
| chr12:13073921 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0003g0038 |
2 | NA18986.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1525-2105C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13073921 | |||||||
| chr12:13074073 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1525-1953G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13074073 | |||||||
| chr12:13074102 | T | C | 2 | a0001c0001t0001g0144 a0001c0015t0001g0066 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1525-1924T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13074102 | |||||||
| chr12:13074161 | C | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(145): Show |
252 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.1525-1865C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13074161 | |||||||
| chr12:13074285 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1525-1741C>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13074285 | |||||||
| chr12:13074607 | C | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0038 others(52): Show |
100 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1525-1419C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13074607 | |||||||
| chr12:13074688 | A | G | 6 | a0001c0001t0001g0184 a0001c0001t0002g0042 a0001c0001t0002g0043 others(3): Show |
8 | HG00642.hp1 HG01168.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.1525-1338A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13074688 | |||||||
| chr12:13074857 | C | T | 5 | a0001c0001t0002g0159 a0001c0001t0002g0211 a0001c0002t0002g0031 others(2): Show |
6 | HG00544.hp1 HG02080.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1525-1169C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13074857 | |||||||
| chr12:13074881 | C | T | 1 | a0001c0016t0011g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1525-1145C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13074881 | |||||||
| chr12:13074939 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1525-1087G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13074939 | |||||||
| chr12:13075224 | T | C | 1 | a0006c0013t0002g0091 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1525-802T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075224 | |||||||
| chr12:13075297 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(139): Show |
249 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.1525-729G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075297 | |||||||
| chr12:13075433 | C | CT | 30 | a0001c0001t0001g0167 a0001c0001t0001g0171 a0001c0001t0001g0230 others(27): Show |
40 | HG00639.hp2 HG01109.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.1525-578dupT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 13075433 | ||||||
| chr12:13075433 | C | CTT | 73 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(70): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1525-579_1525-578d others(4): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 13075433 | ||||||
| chr12:13075437 | T | TC | 4 | a0001c0002t0006g0027 a0001c0002t0006g0082 a0001c0002t0006g0083 others(1): Show |
6 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1525-589_1525-588i others(3): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075437 | |||||||
| chr12:13075449 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1525-577A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075449 | |||||||
| chr12:13075610 | C | CT | 27 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0129 others(24): Show |
42 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1525-399dupT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 13075610 | ||||||
| chr12:13075610 | CT | C | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(135): Show |
245 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.1525-399delT | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 13075610 | ||||||
| chr12:13075612 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1525-414T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075612 | |||||||
| chr12:13075629 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1525-397T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075629 | |||||||
| chr12:13075716 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1525-310A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075716 | |||||||
| chr12:13075719 | G | C | 1 | a0001c0002t0001g0094 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1525-307G>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075719 | |||||||
| chr12:13075827 | A | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(95): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1525-199A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075827 | |||||||
| chr12:13075855 | T | C | 1 | a0001c0002t0002g0120 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1525-171T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075855 | |||||||
| chr12:13075898 | A | G | 1 | a0001c0016t0011g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1525-128A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075898 | |||||||
| chr12:13075979 | G | A | 1 | a0001c0007t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1525-47G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075979 | |||||||
| chr12:13075989 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0179 |
3 | NA18947.hp1 NA18956.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1525-37G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13075989 | |||||||
| chr12:13076012 | C | A | 1 | a0001c0002t0001g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1525-14C>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 10/12 | chr12 | 13076012 | |||||||
| chr12:13076155 | T | C | 1 | a0001c0002t0001g0073 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1642+12T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13076155 | |||||||
| chr12:13076372 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(95): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1642+229C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13076372 | |||||||
| chr12:13076511 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1642+368A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13076511 | |||||||
| chr12:13076512 | G | T | 1 | a0001c0006t0016g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1642+369G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13076512 | |||||||
| chr12:13076658 | A | C | 1 | a0001c0001t0002g0159 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1642+515A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13076658 | |||||||
| chr12:13077050 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(239): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.1642+907C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13077050 | |||||||
| chr12:13077421 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1642+1278T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13077421 | |||||||
| chr12:13077421 | T | TC | 47 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0047 others(44): Show |
59 | HG00597.hp2 HG01099.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.1642+1285dupC | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 13077421 | ||||||
| chr12:13077517 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1642+1374C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13077517 | |||||||
| chr12:13077720 | C | T | 1 | a0001c0014t0001g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1642+1577C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13077720 | |||||||
| chr12:13077930 | G | A | 2 | a0001c0002t0002g0029 a0001c0002t0002g0089 |
3 | HG03490.hp1 HG03492.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1642+1787G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13077930 | |||||||
| chr12:13078095 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0162 a0001c0001t0003g0041 |
3 | HG02027.hp2 NA18941.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1643-1694C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078095 | |||||||
| chr12:13078104 | G | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(142): Show |
252 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.1643-1685G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078104 | |||||||
| chr12:13078193 | C | T | 24 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0016 others(21): Show |
56 | HG00408.hp2 HG01081.hp2 HG01257.hp2 others(53): Show |
intron_variant | MODIFIER | c.1643-1596C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078193 | |||||||
| chr12:13078210 | T | G | 29 | a0001c0001t0002g0159 a0001c0001t0002g0191 a0001c0001t0002g0211 others(26): Show |
47 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1643-1579T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078210 | |||||||
| chr12:13078211 | T | TTGTAGGT others(13): Show |
1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-1575_1643-155 others(24): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 13078211 | ||||||
| chr12:13078222 | C | G | 2 | a0001c0002t0002g0018 a0001c0002t0002g0085 |
4 | HG02280.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1643-1567C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078222 | |||||||
| chr12:13078283 | G | A | 1 | a0001c0008t0012g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1643-1506G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078283 | |||||||
| chr12:13078352 | T | G | 4 | a0001c0002t0006g0027 a0001c0002t0006g0082 a0001c0002t0006g0083 others(1): Show |
6 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1643-1437T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078352 | |||||||
| chr12:13078634 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(83): Show |
146 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1643-1155A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078634 | |||||||
| chr12:13078641 | C | T | 1 | a0001c0001t0003g0161 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1643-1148C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078641 | |||||||
| chr12:13078836 | C | A | 1 | a0006c0013t0002g0091 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1643-953C>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078836 | |||||||
| chr12:13078944 | C | A | 1 | a0002c0003t0001g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1643-845C>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078944 | |||||||
| chr12:13078960 | CTGCCCAA others(14): Show |
C | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-827_1643-807d others(23): Show |
FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 13078960 | ||||||
| chr12:13078977 | C | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(241): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
intron_variant | MODIFIER | c.1643-812C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078977 | |||||||
| chr12:13078987 | G | T | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-802G>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078987 | |||||||
| chr12:13078991 | T | G | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-798T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13078991 | |||||||
| chr12:13079005 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-784C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079005 | |||||||
| chr12:13079015 | T | A | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-774T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079015 | |||||||
| chr12:13079016 | C | A | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-773C>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079016 | |||||||
| chr12:13079018 | T | G | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-771T>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079018 | |||||||
| chr12:13079022 | A | C | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-767A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079022 | |||||||
| chr12:13079023 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-766G>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079023 | |||||||
| chr12:13079031 | A | C | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-758A>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079031 | |||||||
| chr12:13079034 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-755A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079034 | |||||||
| chr12:13079052 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1643-737A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079052 | |||||||
| chr12:13079113 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1643-676G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079113 | |||||||
| chr12:13079195 | T | C | 2 | a0001c0002t0001g0074 a0001c0002t0001g0077 |
2 | HG00597.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1643-594T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079195 | |||||||
| chr12:13079232 | G | A | 4 | a0001c0002t0001g0026 a0001c0002t0001g0051 a0001c0002t0001g0052 others(1): Show |
5 | HG02615.hp2 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1643-557G>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079232 | |||||||
| chr12:13079287 | A | G | 1 | a0001c0016t0011g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1643-502A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079287 | |||||||
| chr12:13079325 | C | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02148.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1643-464C>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079325 | |||||||
| chr12:13079379 | A | T | 1 | a0001c0001t0001g0045 | 2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1643-410A>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079379 | |||||||
| chr12:13079480 | C | T | 2 | a0001c0002t0001g0126 a0002c0003t0001g0062 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1643-309C>T | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079480 | |||||||
| chr12:13079562 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1643-227A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079562 | |||||||
| chr12:13079599 | G | C | 1 | a0001c0001t0002g0155 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1643-190G>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079599 | |||||||
| chr12:13079637 | T | C | 1 | a0001c0002t0023g0076 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1643-152T>C | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079637 | |||||||
| chr12:13079743 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1643-46A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079743 | |||||||
| chr12:13079757 | T | A | 1 | a0001c0002t0023g0076 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1643-32T>A | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 11/12 | chr12 | 13079757 | |||||||
| chr12:13080126 | A | G | 1 | a0001c0002t0023g0076 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1863+117A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 12/12 | chr12 | 13080126 | |||||||
| chr12:13080147 | A | G | 1 | a0001c0002t0002g0095 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1863+138A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 12/12 | chr12 | 13080147 | |||||||
| chr12:13080269 | A | G | 1 | a0001c0006t0001g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1863+260A>G | FAM234B | ENSG00000084444.14 | transcript | ENST00000197268.13 | protein_coding | 12/12 | chr12 | 13080269 |