Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 153643 |
| ensemblid | ENSG00000153347.10 |
| hgncid | 26335 |
| symbol | FAM81B |
| name | family with sequence similarity 81 member B |
| refseq_nuc | NM_152548.3 |
| refseq_prot | NP_689761.2 |
| ensembl_nuc | ENST00000283357.10 |
| ensembl_prot | ENSP00000283357.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 95391366 |
| end | 95450441 |
| strand | + |
| ver | v1.2 |
| region | chr5:95391366-95450441 |
| region5000 | chr5:95386366-95455441 |
| regionname0 | FAM81B_chr5_95391366_95450441 |
| regionname5000 | FAM81B_chr5_95386366_95455441 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 452 | 330 | 88 | 66 | 123 | 11 | 40 | 97 | FAM81B_chr5_95386366_95455441 | FAM81B | MQLQF others(447): Show |
chr5 | 95386366 | 95455441 |
| a0002 | 0/0 | 452 | 6 | 0 | 3 | 0 | 1 | 2 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | MQLQF others(447): Show |
chr5 | 95386366 | 95455441 |
| a0003 | 0/0 | 452 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | FAM81B_chr5_95386366_95455441 | FAM81B | MQLQF others(447): Show |
chr5 | 95386366 | 95455441 |
| a0004 | 0/0 | 143 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | MQLQF others(138): Show |
chr5 | 95386366 | 95455441 |
| a0005 | 0/0 | 452 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | MQLQF others(447): Show |
chr5 | 95386366 | 95455441 |
| a0006 | 0/0 | 452 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | MQLQF others(447): Show |
chr5 | 95386366 | 95455441 |
| a0007 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | MQLQF others(447): Show |
chr5 | 95386366 | 95455441 |
| a0008 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | MQLQF others(447): Show |
chr5 | 95386366 | 95455441 |
| a0009 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | MQLQF others(447): Show |
chr5 | 95386366 | 95455441 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1356 | 255 | 63 | 48 | 101 | 8 | 33 | FAM81B_chr5_95386366_95455441 | FAM81B | ATGCA others(1351): Show |
chr5 | 95386366 | 95455441 | ||
| a0001c0002 | 0/0 | 1356 | 75 | 25 | 18 | 22 | 3 | 7 | FAM81B_chr5_95386366_95455441 | FAM81B | ATGCA others(1351): Show |
chr5 | 95386366 | 95455441 | ||
| a0002c0003 | 0/0 | 1356 | 6 | 0 | 3 | 0 | 1 | 2 | FAM81B_chr5_95386366_95455441 | FAM81B | ATGCA others(1351): Show |
chr5 | 95386366 | 95455441 | ||
| a0003c0007 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | ATGCA others(1351): Show |
chr5 | 95386366 | 95455441 | ||
| a0003c0008 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | ATGCA others(1351): Show |
chr5 | 95386366 | 95455441 | ||
| a0004c0004 | 0/0 | 1356 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | ATGCA others(1351): Show |
chr5 | 95386366 | 95455441 | ||
| a0005c0006 | 0/0 | 1356 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | ATGCA others(1351): Show |
chr5 | 95386366 | 95455441 | ||
| a0006c0005 | 0/0 | 1356 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | ATGCA others(1351): Show |
chr5 | 95386366 | 95455441 | ||
| a0007c0009 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | ATGCA others(1351): Show |
chr5 | 95386366 | 95455441 | ||
| a0008c0010 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | ATGCA others(1351): Show |
chr5 | 95386366 | 95455441 | ||
| a0009c0011 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | ATGCA others(1351): Show |
chr5 | 95386366 | 95455441 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1542 | 190 | 31 | 43 | 83 | 7 | 25 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0001c0001t0002 | 0/1 | 1542 | 65 | 32 | 5 | 18 | 1 | 8 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0001c0002t0001 | 0/0 | 1542 | 57 | 14 | 14 | 20 | 3 | 6 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0001c0002t0002 | 0/0 | 1542 | 18 | 11 | 4 | 2 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0002c0003t0001 | 0/0 | 1542 | 5 | 0 | 2 | 0 | 1 | 2 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0002c0003t0002 | 0/0 | 1542 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0003c0007t0001 | 0/0 | 1542 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0003c0008t0002 | 0/0 | 1542 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0004c0004t0001 | 0/0 | 1542 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0004c0004t0002 | 0/0 | 1542 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0005c0006t0001 | 0/0 | 1542 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0006c0005t0002 | 0/0 | 1542 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0007c0009t0001 | 0/0 | 1542 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0008c0010t0001 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| a0009c0011t0001 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | AGAAA others(1537): Show |
chr5 | 95386366 | 95455441 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0302 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0003c0007t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0003c0007t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0003c0008t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0004c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0004c0004t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0005c0006t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0005c0006t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0006c0005t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0006c0005t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0007c0009t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0008c0010t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0009c0011t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | GBR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0053 | EUR | FIN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0014 | EUR | FIN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00733 | hp2 | a0002 | c0003 | t0001 | g0045 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00735 | hp2 | a0004 | c0004 | t0001 | g0063 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00741 | hp2 | a0005 | c0006 | t0001 | g0263 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0309 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01167 | hp2 | a0006 | c0005 | t0002 | g0218 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0089 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01169 | hp1 | a0006 | c0005 | t0002 | g0219 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0320 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01255 | hp1 | a0004 | c0004 | t0002 | g0064 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01257 | hp1 | a0002 | c0003 | t0002 | g0049 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0323 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0173 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01358 | hp2 | a0005 | c0006 | t0001 | g0313 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01361 | hp2 | a0003 | c0008 | t0002 | g0288 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01516 | hp1 | a0002 | c0003 | t0001 | g0050 | EUR | IBS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0282 | EUR | IBS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0187 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CDX | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | CDX | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0052 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0305 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0186 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0311 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0331 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0310 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0324 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0325 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0329 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0330 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0334 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18951 | hp1 | a0007 | c0009 | t0001 | g0166 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18981 | hp2 | a0003 | c0007 | t0001 | g0212 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18985 | hp1 | a0003 | c0007 | t0001 | g0149 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19043 | hp2 | a0008 | c0010 | t0001 | g0183 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ASW | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | ASW | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0328 | EUR | TSI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | TSI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0139 | EUR | TSI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | GIH | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | GIH | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0319 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0308 | AFR | USA | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | USA | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | USA | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | USA | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA21309 | hp2 | a0009 | c0011 | t0001 | g0097 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0302 | REF | REF | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0161 | REF | REF | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95413979 | C | G | 1 | a0009 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.326C>G | p.Thr109Ser | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/10 | 350/1542 | 326/1359 | 109/452 | chr5 | 95413979 | |||
| chr5:95414083 | C | T | 1 | a0004 | 2 | HG00735.hp2 HG01255.hp1 |
stop_gained | HIGH | c.430C>T | p.Gln144* | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/10 | 454/1542 | 430/1359 | 144/452 | chr5 | 95414083 | |||
| chr5:95420306 | C | T | 1 | a0002 | 6 | HG00733.hp2 HG01168.hp2 HG01257.hp1 others(3): Show |
missense_variant | MODERATE | c.560C>T | p.Ala187Val | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/10 | 584/1542 | 560/1359 | 187/452 | chr5 | 95420306 | |||
| chr5:95428662 | G | A | 1 | a0006 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.716G>A | p.Arg239Gln | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/10 | 740/1542 | 716/1359 | 239/452 | chr5 | 95428662 | |||
| chr5:95436872 | G | A | 1 | a0005 | 2 | HG00741.hp2 HG01358.hp2 |
missense_variant | MODERATE | c.859G>A | p.Asp287Asn | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/10 | 883/1542 | 859/1359 | 287/452 | chr5 | 95436872 | |||
| chr5:95448345 | A | C | 1 | a0008 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1106A>C | p.Lys369Thr | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/10 | 1130/1542 | 1106/1359 | 369/452 | chr5 | 95448345 | |||
| chr5:95448422 | A | G | 1 | a0007 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1183A>G | p.Ile395Val | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/10 | 1207/1542 | 1183/1359 | 395/452 | chr5 | 95448422 | |||
| chr5:95450254 | G | A | 1 | a0003 | 2 | NA18981.hp2 NA18985.hp1 |
missense_variant | MODERATE | c.1331G>A | p.Arg444His | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 10/10 | 1355/1542 | 1331/1359 | 444/452 | chr5 | 95450254 | |||
| chr5:95450254 | G | T | 1 | a0003 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.1331G>T | p.Arg444Leu | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 10/10 | 1355/1542 | 1331/1359 | 444/452 | chr5 | 95450254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95414019 | G | A | 4 | a0001c0002 a0002c0003 a0004c0004 others(1): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
synonymous_variant | LOW | c.366G>A | p.Ala122Ala | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/10 | 390/1542 | 366/1359 | 122/452 | chr5 | 95414019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95450438 | C | T | 6 | a0001c0001t0002 a0001c0002t0002 a0002c0003t0002 others(3): Show |
87 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*156C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 10/10 | 156 | chr5 | 95450438 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95391648 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.124+135T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95391648 | |||||||
| chr5:95391663 | G | GA | 116 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
121 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.124+159dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 95391663 | ||||||
| chr5:95391673 | C | A | 3 | a0001c0001t0001g0002 a0001c0001t0002g0015 a0001c0002t0001g0014 |
4 | HG00280.hp2 HG02698.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+160C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95391673 | |||||||
| chr5:95391745 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0002g0015 |
3 | HG02698.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.124+232C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95391745 | |||||||
| chr5:95391947 | TTCCTCAA others(5): Show |
T | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.124+436_124+447del others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 95391947 | ||||||
| chr5:95391974 | C | T | 1 | a0001c0001t0001g0335 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.124+461C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95391974 | |||||||
| chr5:95392053 | G | C | 9 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0132 others(6): Show |
9 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.124+540G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392053 | |||||||
| chr5:95392082 | G | A | 1 | a0001c0002t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.124+569G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392082 | |||||||
| chr5:95392141 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0002g0015 a0001c0002t0001g0014 |
4 | HG00280.hp2 HG02698.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+628G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392141 | |||||||
| chr5:95392304 | G | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.125-490G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392304 | |||||||
| chr5:95392374 | A | G | 272 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(269): Show |
283 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.125-420A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392374 | |||||||
| chr5:95392465 | A | G | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(98): Show |
105 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.125-329A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392465 | |||||||
| chr5:95392590 | C | T | 1 | a0001c0002t0002g0334 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.125-204C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392590 | |||||||
| chr5:95392624 | G | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02280.hp1 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.125-170G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392624 | |||||||
| chr5:95392625 | G | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02280.hp1 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.125-169G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392625 | |||||||
| chr5:95392927 | G | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
299 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.228+30G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95392927 | |||||||
| chr5:95393308 | C | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0030 |
2 | HG00733.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.228+411C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95393308 | |||||||
| chr5:95393473 | C | CCT | 272 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(269): Show |
283 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.228+579_228+580dup others(2): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 95393473 | ||||||
| chr5:95393478 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.228+581G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95393478 | |||||||
| chr5:95393758 | A | G | 1 | a0001c0001t0002g0333 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.228+861A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95393758 | |||||||
| chr5:95393829 | A | T | 1 | a0001c0002t0002g0025 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.228+932A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95393829 | |||||||
| chr5:95393935 | T | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(60): Show |
66 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.228+1038T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95393935 | |||||||
| chr5:95394022 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.228+1125C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394022 | |||||||
| chr5:95394062 | T | C | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0026 others(100): Show |
107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.228+1165T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394062 | |||||||
| chr5:95394065 | G | A | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.228+1168G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394065 | |||||||
| chr5:95394097 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.228+1200C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394097 | |||||||
| chr5:95394215 | C | T | 2 | a0001c0002t0002g0023 a0001c0002t0002g0024 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.228+1318C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394215 | |||||||
| chr5:95394467 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.228+1570G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394467 | |||||||
| chr5:95394473 | A | G | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.228+1576A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394473 | |||||||
| chr5:95394636 | G | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
280 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.229-1475G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394636 | |||||||
| chr5:95394780 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.229-1331C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394780 | |||||||
| chr5:95394844 | T | C | 2 | a0001c0002t0002g0023 a0001c0002t0002g0024 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.229-1267T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394844 | |||||||
| chr5:95394875 | A | G | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(100): Show |
107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.229-1236A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394875 | |||||||
| chr5:95395240 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.229-871C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395240 | |||||||
| chr5:95395253 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.229-858C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395253 | |||||||
| chr5:95395315 | C | T | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(98): Show |
105 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.229-796C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395315 | |||||||
| chr5:95395318 | C | G | 1 | a0001c0002t0002g0025 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.229-793C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395318 | |||||||
| chr5:95395400 | G | A | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(100): Show |
107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.229-711G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395400 | |||||||
| chr5:95395442 | C | CA | 224 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(221): Show |
233 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(230): Show |
intron_variant | MODIFIER | c.229-650dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 95395442 | ||||||
| chr5:95395442 | C | CAA | 28 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(25): Show |
29 | HG00621.hp1 HG00621.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.229-651_229-650dup others(2): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 95395442 | ||||||
| chr5:95395643 | A | G | 156 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0125 others(153): Show |
162 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.229-468A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395643 | |||||||
| chr5:95395682 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0028 others(4): Show |
7 | HG00741.hp1 HG01255.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.229-429C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395682 | |||||||
| chr5:95395716 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.229-395G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395716 | |||||||
| chr5:95395763 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.229-348C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395763 | |||||||
| chr5:95395921 | T | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0002g0018 others(3): Show |
6 | HG00741.hp1 HG01255.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.229-190T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395921 | |||||||
| chr5:95395934 | T | A | 3 | a0001c0001t0002g0018 a0001c0002t0002g0019 a0001c0002t0002g0020 |
3 | HG02615.hp2 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.229-177T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395934 | |||||||
| chr5:95396057 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0028 others(4): Show |
7 | HG00741.hp1 HG01255.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.229-54A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95396057 | |||||||
| chr5:95396585 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.293+410T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95396585 | |||||||
| chr5:95396845 | C | T | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.293+670C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95396845 | |||||||
| chr5:95396850 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.293+675C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95396850 | |||||||
| chr5:95397052 | T | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(157): Show |
167 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.293+877T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95397052 | |||||||
| chr5:95397446 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
118 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.293+1271C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95397446 | |||||||
| chr5:95397497 | G | A | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(100): Show |
107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.293+1322G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95397497 | |||||||
| chr5:95397551 | C | T | 8 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
9 | NA18974.hp1 NA18984.hp2 NA19004.hp2 others(6): Show |
intron_variant | MODIFIER | c.293+1376C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95397551 | |||||||
| chr5:95397688 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0176 |
3 | NA18943.hp2 NA18954.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.293+1513G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95397688 | |||||||
| chr5:95398000 | T | C | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(100): Show |
107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.293+1825T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398000 | |||||||
| chr5:95398030 | C | T | 3 | a0001c0001t0002g0190 a0001c0002t0001g0191 a0001c0002t0001g0192 |
3 | HG02559.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.293+1855C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398030 | |||||||
| chr5:95398066 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.293+1891A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398066 | |||||||
| chr5:95398142 | G | T | 1 | a0001c0001t0001g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.293+1967G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398142 | |||||||
| chr5:95398343 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.293+2168C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398343 | |||||||
| chr5:95398346 | G | A | 1 | a0003c0007t0001g0212 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.293+2171G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398346 | |||||||
| chr5:95398418 | C | CTAAA | 169 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(166): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.293+2276_293+2279d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95398418 | ||||||
| chr5:95398418 | C | CTAAATAA others(1): Show |
6 | a0001c0001t0001g0133 a0001c0001t0001g0194 a0001c0001t0001g0210 others(3): Show |
6 | HG01358.hp2 HG02630.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+2272_293+2279d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95398418 | ||||||
| chr5:95398418 | CTAAATAA others(1): Show |
C | 7 | a0001c0001t0001g0181 a0001c0001t0002g0190 a0001c0002t0001g0179 others(4): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.293+2272_293+2279d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95398418 | ||||||
| chr5:95398447 | T | TA | 99 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(96): Show |
103 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.293+2275dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95398447 | ||||||
| chr5:95398451 | T | C | 99 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(96): Show |
103 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.293+2276T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398451 | |||||||
| chr5:95398451 | T | TAAAAC | 4 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0002g0121 others(1): Show |
4 | HG02109.hp2 HG02257.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.293+2280_293+2281i others(7): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95398451 | ||||||
| chr5:95398455 | A | T | 6 | a0001c0001t0001g0316 a0001c0001t0001g0318 a0001c0001t0002g0315 others(3): Show |
6 | HG01243.hp2 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+2280A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398455 | |||||||
| chr5:95398460 | T | G | 1 | a0001c0001t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293+2285T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398460 | |||||||
| chr5:95398511 | C | G | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.293+2336C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398511 | |||||||
| chr5:95398561 | G | A | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(101): Show |
108 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.293+2386G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398561 | |||||||
| chr5:95398624 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0028 others(4): Show |
7 | HG00741.hp1 HG01255.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.293+2449A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398624 | |||||||
| chr5:95398807 | A | G | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(100): Show |
107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.293+2632A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398807 | |||||||
| chr5:95398855 | C | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(54): Show |
59 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.293+2680C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398855 | |||||||
| chr5:95398965 | A | T | 2 | a0001c0001t0002g0319 a0001c0001t0002g0320 |
2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.293+2790A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398965 | |||||||
| chr5:95399005 | C | G | 5 | a0001c0001t0001g0181 a0001c0001t0001g0312 a0001c0002t0001g0179 others(2): Show |
5 | HG01496.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+2830C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399005 | |||||||
| chr5:95399040 | A | T | 106 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0031 others(103): Show |
110 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.293+2865A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399040 | |||||||
| chr5:95399339 | G | C | 125 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(122): Show |
128 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(125): Show |
intron_variant | MODIFIER | c.293+3164G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399339 | |||||||
| chr5:95399480 | G | GC | 15 | a0001c0001t0001g0065 a0001c0001t0001g0080 a0001c0001t0001g0303 others(12): Show |
17 | HG00280.hp2 HG00597.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.293+3314dupC | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95399480 | ||||||
| chr5:95399485 | C | A | 3 | a0001c0001t0002g0307 a0001c0002t0001g0041 a0001c0002t0001g0042 |
3 | NA18962.hp2 NA18969.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.293+3310C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399485 | |||||||
| chr5:95399498 | G | C | 8 | a0001c0001t0002g0018 a0001c0002t0001g0014 a0001c0002t0001g0184 others(5): Show |
8 | HG00280.hp2 HG01255.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.293+3323G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399498 | |||||||
| chr5:95399557 | G | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.293+3382G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399557 | |||||||
| chr5:95399610 | T | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0031 others(11): Show |
15 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.293+3435T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399610 | |||||||
| chr5:95399657 | C | G | 1 | a0001c0001t0001g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.293+3482C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399657 | |||||||
| chr5:95399829 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.293+3654C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399829 | |||||||
| chr5:95399963 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.293+3788C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399963 | |||||||
| chr5:95400156 | C | A | 10 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0002g0129 others(7): Show |
10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+3981C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400156 | |||||||
| chr5:95400156 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.293+3981C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400156 | |||||||
| chr5:95400157 | G | T | 1 | a0008c0010t0001g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.293+3982G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400157 | |||||||
| chr5:95400246 | G | T | 1 | a0001c0002t0001g0311 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.293+4071G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400246 | |||||||
| chr5:95400329 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.293+4154T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400329 | |||||||
| chr5:95400336 | G | C | 10 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0002g0129 others(7): Show |
10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+4161G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400336 | |||||||
| chr5:95400382 | G | A | 10 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0002g0129 others(7): Show |
10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+4207G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400382 | |||||||
| chr5:95400401 | C | CACAT | 4 | a0001c0001t0001g0120 a0001c0001t0001g0134 a0001c0001t0002g0119 others(1): Show |
4 | HG01069.hp2 HG01433.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.293+4258_293+4261d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400401 | ||||||
| chr5:95400401 | CACAT | C | 5 | a0001c0002t0001g0009 a0001c0002t0001g0308 a0001c0002t0001g0309 others(2): Show |
6 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.293+4258_293+4261d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400401 | ||||||
| chr5:95400433 | T | C | 1 | a0001c0001t0002g0307 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.293+4258T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400433 | |||||||
| chr5:95400433 | T | TACATACA others(3): Show |
1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.293+4261_293+4262i others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | ||||||
| chr5:95400433 | T | TACATACA others(7): Show |
1 | a0001c0002t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.293+4261_293+4262i others(16): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | ||||||
| chr5:95400433 | T | TACATACA others(15): Show |
7 | a0001c0002t0001g0128 a0001c0002t0001g0179 a0001c0002t0001g0184 others(4): Show |
7 | HG02451.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.293+4261_293+4262i others(24): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | ||||||
| chr5:95400433 | T | TACATACA others(17): Show |
1 | a0001c0002t0002g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.293+4261_293+4262i others(26): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | ||||||
| chr5:95400433 | T | TACATACA others(11): Show |
2 | a0001c0002t0001g0093 a0001c0002t0001g0191 |
2 | HG01109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.293+4261_293+4262i others(20): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | ||||||
| chr5:95400433 | T | TACATACA others(15): Show |
5 | a0001c0001t0002g0118 a0001c0002t0001g0180 a0001c0002t0001g0192 others(2): Show |
5 | HG02559.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+4261_293+4262i others(24): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | ||||||
| chr5:95400433 | T | TACATACA others(15): Show |
1 | a0001c0002t0001g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.293+4261_293+4262i others(24): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | ||||||
| chr5:95400433 | TAC | T | 9 | a0001c0001t0001g0085 a0001c0001t0001g0140 a0001c0001t0001g0141 others(6): Show |
9 | HG01255.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.293+4274_293+4275d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | ||||||
| chr5:95400435 | C | CAT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0123 a0001c0001t0001g0194 others(2): Show |
6 | HG01934.hp1 HG04115.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+4261_293+4262i others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400435 | ||||||
| chr5:95400435 | C | CATACAT | 156 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(153): Show |
161 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.293+4261_293+4262i others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400435 | ||||||
| chr5:95400435 | C | CATACATA others(3): Show |
10 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0144 others(7): Show |
11 | HG01192.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.293+4261_293+4262i others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400435 | ||||||
| chr5:95400435 | C | CATACATA others(11): Show |
1 | a0001c0002t0001g0001 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.293+4261_293+4262i others(20): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400435 | ||||||
| chr5:95400437 | C | T | 5 | a0001c0001t0001g0028 a0001c0002t0001g0014 a0001c0002t0001g0188 others(2): Show |
5 | HG00280.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+4262C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400437 | |||||||
| chr5:95400438 | A | G | 5 | a0001c0001t0002g0018 a0001c0001t0002g0129 a0001c0002t0002g0019 others(2): Show |
5 | HG01255.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.293+4263A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400438 | |||||||
| chr5:95400439 | C | CGT | 5 | a0001c0001t0001g0028 a0001c0002t0001g0014 a0001c0002t0001g0188 others(2): Show |
5 | HG00280.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+4264_293+4265i others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400439 | |||||||
| chr5:95400439 | C | T | 5 | a0001c0001t0002g0018 a0001c0001t0002g0129 a0001c0002t0002g0019 others(2): Show |
5 | HG01255.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.293+4264C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400439 | |||||||
| chr5:95400447 | C | T | 18 | a0001c0001t0002g0118 a0001c0002t0001g0017 a0001c0002t0001g0093 others(15): Show |
18 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.293+4272C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400447 | |||||||
| chr5:95400658 | T | A | 10 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0002g0129 others(7): Show |
10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+4483T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400658 | |||||||
| chr5:95400698 | T | G | 10 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0002g0129 others(7): Show |
10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+4523T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400698 | |||||||
| chr5:95400764 | G | A | 1 | a0001c0002t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.293+4589G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400764 | |||||||
| chr5:95400927 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.293+4752C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400927 | |||||||
| chr5:95400930 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.293+4755C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400930 | |||||||
| chr5:95401014 | T | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG01978.hp2 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.293+4839T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401014 | |||||||
| chr5:95401184 | T | C | 10 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0002g0129 others(7): Show |
10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+5009T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401184 | |||||||
| chr5:95401274 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.293+5099C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401274 | |||||||
| chr5:95401403 | C | T | 13 | a0001c0002t0001g0017 a0001c0002t0001g0093 a0001c0002t0001g0177 others(10): Show |
13 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.293+5228C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401403 | |||||||
| chr5:95401792 | C | T | 1 | a0001c0001t0002g0299 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.293+5617C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401792 | |||||||
| chr5:95401815 | G | T | 8 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0002t0001g0014 others(5): Show |
8 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.293+5640G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401815 | |||||||
| chr5:95401913 | A | G | 8 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0002t0001g0014 others(5): Show |
8 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.293+5738A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401913 | |||||||
| chr5:95401920 | G | A | 1 | a0001c0002t0001g0170 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.293+5745G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401920 | |||||||
| chr5:95402189 | T | C | 8 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0002t0001g0014 others(5): Show |
8 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.293+6014T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402189 | |||||||
| chr5:95402196 | G | A | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.293+6021G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402196 | |||||||
| chr5:95402212 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.293+6037A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402212 | |||||||
| chr5:95402696 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.293+6521G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402696 | |||||||
| chr5:95402707 | G | T | 6 | a0001c0002t0001g0014 a0001c0002t0001g0188 a0001c0002t0002g0019 others(3): Show |
6 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.293+6532G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402707 | |||||||
| chr5:95402744 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
180 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.293+6569A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402744 | |||||||
| chr5:95402824 | C | G | 4 | a0001c0001t0001g0133 a0001c0001t0002g0018 a0001c0001t0002g0129 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.293+6649C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402824 | |||||||
| chr5:95402852 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.293+6677G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402852 | |||||||
| chr5:95402867 | A | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.293+6692A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402867 | |||||||
| chr5:95402914 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.293+6739A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402914 | |||||||
| chr5:95403000 | G | A | 67 | a0001c0001t0002g0307 a0001c0002t0001g0003 a0001c0002t0001g0004 others(64): Show |
71 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.293+6825G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403000 | |||||||
| chr5:95403029 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.293+6854T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403029 | |||||||
| chr5:95403077 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0002g0015 others(2): Show |
6 | HG02698.hp2 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.293+6902G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403077 | |||||||
| chr5:95403148 | C | T | 70 | a0001c0001t0002g0110 a0001c0001t0002g0118 a0001c0001t0002g0307 others(67): Show |
74 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.293+6973C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403148 | |||||||
| chr5:95403243 | G | A | 78 | a0001c0001t0002g0110 a0001c0001t0002g0118 a0001c0001t0002g0307 others(75): Show |
82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.293+7068G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403243 | |||||||
| chr5:95403244 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.293+7069C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403244 | |||||||
| chr5:95403303 | T | C | 78 | a0001c0001t0002g0110 a0001c0001t0002g0118 a0001c0001t0002g0307 others(75): Show |
82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.293+7128T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403303 | |||||||
| chr5:95403329 | T | G | 3 | a0001c0002t0002g0019 a0001c0002t0002g0020 a0001c0002t0002g0025 |
3 | HG01255.hp2 HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.293+7154T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403329 | |||||||
| chr5:95403391 | A | G | 14 | a0001c0002t0001g0093 a0001c0002t0001g0101 a0001c0002t0001g0128 others(11): Show |
14 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.293+7216A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403391 | |||||||
| chr5:95403420 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.293+7245T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403420 | |||||||
| chr5:95403625 | T | G | 79 | a0001c0001t0001g0216 a0001c0001t0002g0110 a0001c0001t0002g0118 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.293+7450T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403625 | |||||||
| chr5:95403710 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.293+7535G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403710 | |||||||
| chr5:95403737 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.293+7562G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403737 | |||||||
| chr5:95403916 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.293+7741G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403916 | |||||||
| chr5:95403986 | C | T | 78 | a0001c0001t0002g0110 a0001c0001t0002g0118 a0001c0001t0002g0307 others(75): Show |
82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.293+7811C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403986 | |||||||
| chr5:95404071 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.293+7896A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404071 | |||||||
| chr5:95404074 | G | A | 79 | a0001c0001t0002g0068 a0001c0001t0002g0110 a0001c0001t0002g0118 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.293+7899G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404074 | |||||||
| chr5:95404104 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.293+7929G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404104 | |||||||
| chr5:95404110 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.293+7935T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404110 | |||||||
| chr5:95404148 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293+7973G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404148 | |||||||
| chr5:95404303 | G | T | 1 | a0001c0002t0002g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.293+8128G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404303 | |||||||
| chr5:95404311 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.293+8136C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404311 | |||||||
| chr5:95404410 | T | C | 1 | a0001c0002t0001g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.293+8235T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404410 | |||||||
| chr5:95404604 | T | C | 2 | a0001c0002t0002g0019 a0001c0002t0002g0025 |
2 | HG01255.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.293+8429T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404604 | |||||||
| chr5:95404612 | C | CT | 14 | a0001c0002t0001g0093 a0001c0002t0001g0101 a0001c0002t0001g0128 others(11): Show |
14 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.293+8445dupT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95404612 | ||||||
| chr5:95404621 | G | T | 78 | a0001c0001t0002g0110 a0001c0001t0002g0118 a0001c0001t0002g0307 others(75): Show |
82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.293+8446G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404621 | |||||||
| chr5:95405051 | G | A | 2 | a0001c0002t0001g0177 a0001c0002t0001g0191 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.293+8876G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405051 | |||||||
| chr5:95405102 | G | A | 1 | a0009c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.294-8845G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405102 | |||||||
| chr5:95405138 | C | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.294-8809C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405138 | |||||||
| chr5:95405377 | A | T | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294-8570A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405377 | |||||||
| chr5:95405405 | A | G | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.294-8542A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405405 | |||||||
| chr5:95405600 | C | T | 78 | a0001c0001t0002g0110 a0001c0001t0002g0118 a0001c0001t0002g0307 others(75): Show |
82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.294-8347C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405600 | |||||||
| chr5:95405746 | G | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0102 others(11): Show |
14 | HG00738.hp1 HG00741.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.294-8201G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405746 | |||||||
| chr5:95405840 | G | A | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-8107G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405840 | |||||||
| chr5:95405964 | T | C | 79 | a0001c0001t0001g0216 a0001c0001t0002g0110 a0001c0001t0002g0118 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-7983T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405964 | |||||||
| chr5:95406012 | A | G | 6 | a0001c0002t0001g0177 a0001c0002t0001g0188 a0001c0002t0001g0191 others(3): Show |
6 | HG02055.hp1 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.294-7935A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406012 | |||||||
| chr5:95406037 | C | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
182 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.294-7910C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406037 | |||||||
| chr5:95406133 | A | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(255): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.294-7814A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406133 | |||||||
| chr5:95406269 | T | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(253): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.294-7678T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406269 | |||||||
| chr5:95406410 | A | C | 79 | a0001c0001t0001g0216 a0001c0001t0002g0110 a0001c0001t0002g0118 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-7537A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406410 | |||||||
| chr5:95406423 | G | C | 2 | a0001c0001t0002g0029 a0001c0001t0002g0030 |
2 | HG00733.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.294-7524G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406423 | |||||||
| chr5:95407012 | C | T | 2 | a0001c0001t0002g0110 a0001c0001t0002g0118 |
2 | HG01167.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.294-6935C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407012 | |||||||
| chr5:95407161 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.294-6786T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407161 | |||||||
| chr5:95407261 | T | TAC | 10 | a0001c0001t0001g0125 a0001c0001t0001g0133 a0001c0001t0001g0136 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.294-6655_294-6654d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407261 | ||||||
| chr5:95407261 | TAC | T | 10 | a0001c0001t0001g0163 a0001c0001t0001g0234 a0001c0001t0002g0029 others(7): Show |
10 | HG00733.hp1 HG01255.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.294-6655_294-6654d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407261 | ||||||
| chr5:95407261 | TACAC | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
179 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.294-6657_294-6654d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407261 | ||||||
| chr5:95407261 | TACACAC | T | 60 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(57): Show |
64 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.294-6659_294-6654d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407261 | ||||||
| chr5:95407261 | TACACACA others(1): Show |
T | 17 | a0001c0001t0001g0298 a0001c0001t0002g0110 a0001c0001t0002g0118 others(14): Show |
17 | HG00280.hp2 HG01167.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.294-6661_294-6654d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407261 | ||||||
| chr5:95407362 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294-6585G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407362 | |||||||
| chr5:95407391 | T | TAC | 8 | a0001c0001t0001g0133 a0001c0001t0001g0300 a0001c0001t0002g0018 others(5): Show |
8 | HG02486.hp1 HG02630.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.294-6539_294-6538d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407391 | ||||||
| chr5:95407391 | T | TACAC | 66 | a0001c0001t0001g0216 a0001c0001t0002g0307 a0001c0002t0001g0003 others(63): Show |
70 | HG00280.hp1 HG00438.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.294-6541_294-6538d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407391 | ||||||
| chr5:95407391 | T | TACACAC | 4 | a0001c0001t0002g0118 a0001c0002t0002g0019 a0001c0002t0002g0025 others(1): Show |
4 | HG01255.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.294-6543_294-6538d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407391 | ||||||
| chr5:95407391 | T | TACACACA others(3): Show |
1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-6547_294-6538d others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407391 | ||||||
| chr5:95407410 | G | A | 1 | a0001c0002t0002g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.294-6537G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407410 | |||||||
| chr5:95407412 | A | G | 4 | a0001c0001t0001g0216 a0001c0002t0001g0192 a0001c0002t0002g0023 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.294-6535A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407412 | |||||||
| chr5:95407420 | A | G | 1 | a0001c0002t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.294-6527A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407420 | |||||||
| chr5:95407425 | T | C | 78 | a0001c0001t0002g0110 a0001c0001t0002g0118 a0001c0001t0002g0307 others(75): Show |
82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.294-6522T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407425 | |||||||
| chr5:95407427 | C | T | 66 | a0001c0001t0002g0307 a0001c0002t0001g0003 a0001c0002t0001g0004 others(63): Show |
70 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.294-6520C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407427 | |||||||
| chr5:95407428 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0148 |
2 | NA18959.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.294-6519G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407428 | |||||||
| chr5:95407429 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
182 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.294-6518C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407429 | |||||||
| chr5:95407430 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.294-6517G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407430 | |||||||
| chr5:95407437 | A | C | 79 | a0001c0001t0001g0216 a0001c0001t0002g0110 a0001c0001t0002g0118 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-6510A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407437 | |||||||
| chr5:95407494 | A | G | 62 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(59): Show |
64 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.294-6453A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407494 | |||||||
| chr5:95407640 | T | G | 1 | a0001c0001t0001g0235 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.294-6307T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407640 | |||||||
| chr5:95407765 | C | T | 79 | a0001c0001t0001g0216 a0001c0001t0002g0110 a0001c0001t0002g0118 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-6182C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407765 | |||||||
| chr5:95407864 | C | T | 7 | a0001c0002t0001g0177 a0001c0002t0001g0188 a0001c0002t0001g0191 others(4): Show |
7 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.294-6083C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407864 | |||||||
| chr5:95408075 | T | TGA | 13 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0102 others(10): Show |
13 | HG00621.hp1 HG00738.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.294-5836_294-5835d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408075 | T | TGAGA | 67 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0033 others(64): Show |
70 | HG00544.hp1 HG00642.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.294-5838_294-5835d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408075 | T | TGAGAGA | 10 | a0001c0001t0002g0307 a0001c0002t0001g0053 a0001c0002t0001g0062 others(7): Show |
10 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.294-5840_294-5835d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408075 | T | TGAGAGAG others(1): Show |
6 | a0001c0001t0001g0133 a0001c0001t0001g0303 a0001c0001t0002g0018 others(3): Show |
6 | HG00597.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.294-5842_294-5835d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408075 | T | TGAGAGAG others(3): Show |
2 | a0001c0001t0002g0189 a0009c0011t0001g0097 |
2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.294-5844_294-5835d others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408075 | T | TGAGAGAG others(5): Show |
1 | a0001c0002t0001g0139 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.294-5846_294-5835d others(14): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408075 | T | TGAGAGAG others(7): Show |
1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-5848_294-5835d others(16): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408075 | T | TGAGAGAG others(9): Show |
2 | a0001c0001t0002g0129 a0001c0002t0001g0093 |
2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.294-5850_294-5835d others(18): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408075 | TGA | T | 22 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0130 others(19): Show |
22 | HG00438.hp1 HG00741.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.294-5836_294-5835d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408075 | TGAGA | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
172 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.294-5838_294-5835d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408075 | TGAGAGA | T | 6 | a0001c0001t0001g0061 a0001c0001t0001g0104 a0001c0001t0001g0205 others(3): Show |
6 | HG02572.hp2 HG03139.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.294-5840_294-5835d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408075 | TGAGAGAG others(1): Show |
T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0175 a0001c0001t0001g0264 others(7): Show |
13 | HG00140.hp2 HG00438.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.294-5842_294-5835d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | ||||||
| chr5:95408291 | T | A | 2 | a0002c0003t0001g0324 a0002c0003t0001g0325 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.294-5656T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408291 | |||||||
| chr5:95408338 | T | C | 79 | a0001c0001t0001g0216 a0001c0001t0002g0110 a0001c0001t0002g0118 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-5609T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408338 | |||||||
| chr5:95408537 | T | A | 79 | a0001c0001t0001g0216 a0001c0001t0002g0110 a0001c0001t0002g0118 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-5410T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408537 | |||||||
| chr5:95408646 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.294-5301C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408646 | |||||||
| chr5:95408784 | T | C | 2 | a0001c0002t0002g0019 a0001c0002t0002g0025 |
2 | HG01255.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.294-5163T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408784 | |||||||
| chr5:95408908 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.294-5039C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408908 | |||||||
| chr5:95408989 | A | G | 81 | a0001c0001t0001g0216 a0001c0001t0002g0110 a0001c0001t0002g0118 others(78): Show |
87 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.294-4958A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408989 | |||||||
| chr5:95409007 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.294-4940A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409007 | |||||||
| chr5:95409105 | T | A | 82 | a0001c0001t0001g0216 a0001c0001t0002g0110 a0001c0001t0002g0118 others(79): Show |
88 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.294-4842T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409105 | |||||||
| chr5:95409128 | T | C | 1 | a0001c0002t0002g0025 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.294-4819T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409128 | |||||||
| chr5:95409213 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(256): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.294-4734T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409213 | |||||||
| chr5:95409254 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.294-4693G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409254 | |||||||
| chr5:95409289 | T | G | 82 | a0001c0001t0001g0216 a0001c0001t0002g0110 a0001c0001t0002g0118 others(79): Show |
88 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.294-4658T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409289 | |||||||
| chr5:95409439 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.294-4508G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409439 | |||||||
| chr5:95409472 | T | TAAAGAAT others(146): Show |
1 | a0009c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.294-4461_294-4460i others(155): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | ||||||
| chr5:95409472 | T | TAAAGAAT others(145): Show |
2 | a0001c0001t0002g0110 a0001c0002t0002g0178 |
2 | HG01167.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.294-4461_294-4460i others(154): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | ||||||
| chr5:95409472 | T | TAAAGAAT others(146): Show |
24 | a0001c0001t0002g0118 a0001c0002t0001g0017 a0001c0002t0001g0044 others(21): Show |
24 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.294-4461_294-4460i others(155): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | ||||||
| chr5:95409472 | T | TAAAGAAT others(146): Show |
4 | a0001c0002t0001g0177 a0001c0002t0001g0191 a0001c0002t0002g0016 others(1): Show |
4 | HG02922.hp1 HG02922.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.294-4461_294-4460i others(155): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | ||||||
| chr5:95409472 | T | TAAAGAAT others(147): Show |
48 | a0001c0001t0001g0216 a0001c0001t0002g0307 a0001c0002t0001g0001 others(45): Show |
54 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.294-4461_294-4460i others(156): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | ||||||
| chr5:95409472 | T | TAAAGAAT others(148): Show |
3 | a0001c0002t0001g0055 a0001c0002t0001g0099 a0001c0002t0002g0334 |
3 | HG01433.hp2 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.294-4461_294-4460i others(157): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | ||||||
| chr5:95409632 | C | T | 2 | a0001c0002t0001g0043 a0001c0002t0001g0076 |
2 | HG01070.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.294-4315C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409632 | |||||||
| chr5:95409654 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.294-4293A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409654 | |||||||
| chr5:95409656 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.294-4291C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409656 | |||||||
| chr5:95409891 | T | C | 68 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(65): Show |
74 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.294-4056T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409891 | |||||||
| chr5:95409901 | G | A | 2 | a0001c0002t0002g0019 a0001c0002t0002g0025 |
2 | HG01255.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.294-4046G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409901 | |||||||
| chr5:95409943 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.294-4004G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409943 | |||||||
| chr5:95409991 | A | T | 3 | a0001c0002t0001g0192 a0001c0002t0002g0023 a0001c0002t0002g0024 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.294-3956A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409991 | |||||||
| chr5:95410129 | T | C | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-3818T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410129 | |||||||
| chr5:95410190 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.294-3757C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410190 | |||||||
| chr5:95410255 | T | C | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-3692T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410255 | |||||||
| chr5:95410312 | A | G | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-3635A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410312 | |||||||
| chr5:95410476 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294-3471C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410476 | |||||||
| chr5:95410561 | G | T | 2 | a0001c0002t0002g0019 a0001c0002t0002g0025 |
2 | HG01255.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.294-3386G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410561 | |||||||
| chr5:95410699 | G | A | 1 | a0001c0002t0001g0100 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.294-3248G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410699 | |||||||
| chr5:95410809 | G | A | 69 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(66): Show |
75 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.294-3138G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410809 | |||||||
| chr5:95410815 | A | G | 1 | a0001c0001t0001g0006 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.294-3132A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410815 | |||||||
| chr5:95411192 | A | T | 1 | a0001c0001t0002g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.294-2755A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411192 | |||||||
| chr5:95411234 | C | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-2713C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411234 | |||||||
| chr5:95411283 | A | G | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-2664A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411283 | |||||||
| chr5:95411386 | CAT | C | 67 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(64): Show |
73 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.294-2557_294-2556d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95411386 | ||||||
| chr5:95411462 | C | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-2485C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411462 | |||||||
| chr5:95411570 | A | G | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-2377A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411570 | |||||||
| chr5:95411616 | T | C | 4 | a0001c0002t0001g0128 a0001c0002t0001g0179 a0001c0002t0002g0127 others(1): Show |
4 | HG02451.hp2 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.294-2331T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411616 | |||||||
| chr5:95411685 | G | A | 1 | a0001c0002t0001g0311 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.294-2262G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411685 | |||||||
| chr5:95411732 | T | C | 1 | a0001c0001t0002g0269 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.294-2215T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411732 | |||||||
| chr5:95411948 | C | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1999C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411948 | |||||||
| chr5:95412029 | G | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1918G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412029 | |||||||
| chr5:95412085 | T | G | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-1862T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412085 | |||||||
| chr5:95412144 | C | CT | 75 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(72): Show |
81 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.294-1793dupT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95412144 | ||||||
| chr5:95412162 | G | A | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1785G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412162 | |||||||
| chr5:95412214 | C | T | 1 | a0001c0002t0002g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.294-1733C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412214 | |||||||
| chr5:95412260 | A | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1687A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412260 | |||||||
| chr5:95412352 | A | C | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1595A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412352 | |||||||
| chr5:95412476 | T | C | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1471T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412476 | |||||||
| chr5:95412648 | A | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1299A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412648 | |||||||
| chr5:95412656 | A | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1291A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412656 | |||||||
| chr5:95412850 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-1097C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412850 | |||||||
| chr5:95412903 | A | G | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1044A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412903 | |||||||
| chr5:95412958 | A | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-989A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412958 | |||||||
| chr5:95413174 | C | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-773C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413174 | |||||||
| chr5:95413185 | A | G | 7 | a0001c0002t0001g0092 a0001c0002t0001g0177 a0001c0002t0001g0188 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.294-762A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413185 | |||||||
| chr5:95413207 | C | G | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-740C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413207 | |||||||
| chr5:95413240 | T | A | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-707T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413240 | |||||||
| chr5:95413264 | A | C | 3 | a0001c0001t0001g0262 a0005c0006t0001g0263 a0005c0006t0001g0313 |
3 | HG00741.hp2 HG01123.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.294-683A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413264 | |||||||
| chr5:95413300 | A | T | 265 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(262): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.294-647A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413300 | |||||||
| chr5:95413307 | G | A | 1 | a0002c0003t0001g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.294-640G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413307 | |||||||
| chr5:95413459 | G | A | 4 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0301 others(1): Show |
4 | NA18953.hp2 NA18964.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.294-488G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413459 | |||||||
| chr5:95413464 | A | T | 2 | a0001c0002t0002g0019 a0001c0002t0002g0025 |
2 | HG01255.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.294-483A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413464 | |||||||
| chr5:95413513 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.294-434T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413513 | |||||||
| chr5:95413584 | T | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(37): Show |
43 | HG00140.hp2 HG00738.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.294-363T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413584 | |||||||
| chr5:95413607 | T | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
193 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.294-340T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413607 | |||||||
| chr5:95413718 | G | C | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-229G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413718 | |||||||
| chr5:95413910 | T | C | 10 | a0001c0001t0001g0233 a0001c0001t0001g0236 a0001c0001t0001g0327 others(7): Show |
10 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.294-37T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413910 | |||||||
| chr5:95414199 | C | CT | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+14dupT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 95414199 | ||||||
| chr5:95414265 | C | G | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+75C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414265 | |||||||
| chr5:95414405 | A | G | 6 | a0001c0001t0001g0316 a0001c0001t0001g0318 a0001c0001t0002g0315 others(3): Show |
6 | HG01243.hp2 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.537+215A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414405 | |||||||
| chr5:95414528 | T | A | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+338T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414528 | |||||||
| chr5:95414589 | A | G | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+399A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414589 | |||||||
| chr5:95414595 | G | A | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+405G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414595 | |||||||
| chr5:95414634 | C | T | 1 | a0009c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.537+444C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414634 | |||||||
| chr5:95414739 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.537+549G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414739 | |||||||
| chr5:95414741 | G | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+551G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414741 | |||||||
| chr5:95415054 | T | A | 264 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.537+864T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415054 | |||||||
| chr5:95415063 | T | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.537+873T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415063 | |||||||
| chr5:95415065 | A | T | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.537+875A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415065 | |||||||
| chr5:95415068 | G | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.537+878G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415068 | |||||||
| chr5:95415069 | C | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.537+879C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415069 | |||||||
| chr5:95415190 | G | C | 1 | a0009c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.537+1000G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415190 | |||||||
| chr5:95415429 | A | G | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+1239A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415429 | |||||||
| chr5:95415463 | A | C | 1 | a0001c0001t0001g0208 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.537+1273A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415463 | |||||||
| chr5:95415658 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.537+1468C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415658 | |||||||
| chr5:95415689 | G | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(177): Show |
186 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.537+1499G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415689 | |||||||
| chr5:95415784 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.537+1594A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415784 | |||||||
| chr5:95415785 | T | C | 78 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(75): Show |
84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+1595T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415785 | |||||||
| chr5:95415843 | C | T | 2 | a0001c0002t0001g0188 a0001c0002t0002g0187 |
2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.537+1653C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415843 | |||||||
| chr5:95415922 | G | A | 1 | a0009c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.537+1732G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415922 | |||||||
| chr5:95416237 | C | A | 1 | a0001c0002t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.537+2047C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95416237 | |||||||
| chr5:95416255 | C | A | 2 | a0001c0002t0001g0188 a0001c0002t0002g0187 |
2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.537+2065C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95416255 | |||||||
| chr5:95416525 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.537+2335T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95416525 | |||||||
| chr5:95416805 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.537+2615G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95416805 | |||||||
| chr5:95417092 | C | T | 71 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(68): Show |
71 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.537+2902C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417092 | |||||||
| chr5:95417189 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0335 |
2 | NA18942.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.537+2999G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417189 | |||||||
| chr5:95417312 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.538-2972T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417312 | |||||||
| chr5:95417599 | C | T | 71 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(68): Show |
71 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.538-2685C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417599 | |||||||
| chr5:95417600 | G | A | 1 | a0009c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.538-2684G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417600 | |||||||
| chr5:95417711 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
189 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.538-2573T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417711 | |||||||
| chr5:95417834 | T | C | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.538-2450T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417834 | |||||||
| chr5:95418087 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0129 a0001c0001t0002g0189 |
3 | HG02486.hp1 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.538-2197G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418087 | |||||||
| chr5:95418140 | C | T | 1 | a0001c0002t0001g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.538-2144C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418140 | |||||||
| chr5:95418475 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.538-1809A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418475 | |||||||
| chr5:95418501 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.538-1783C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418501 | |||||||
| chr5:95418676 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.538-1608C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418676 | |||||||
| chr5:95418989 | A | G | 52 | a0001c0001t0001g0134 a0001c0001t0001g0215 a0001c0002t0001g0001 others(49): Show |
58 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.538-1295A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418989 | |||||||
| chr5:95419026 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.538-1258T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419026 | |||||||
| chr5:95419467 | A | G | 4 | a0001c0001t0001g0133 a0001c0001t0002g0018 a0001c0001t0002g0129 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.538-817A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419467 | |||||||
| chr5:95419525 | A | T | 81 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(78): Show |
81 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.538-759A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419525 | |||||||
| chr5:95419557 | C | T | 82 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(79): Show |
82 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.538-727C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419557 | |||||||
| chr5:95419603 | C | A | 5 | a0001c0002t0001g0180 a0001c0002t0001g0184 a0001c0002t0001g0185 others(2): Show |
5 | HG02818.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-681C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419603 | |||||||
| chr5:95419648 | T | A | 82 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(79): Show |
82 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.538-636T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419648 | |||||||
| chr5:95419675 | T | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0328 a0001c0001t0002g0329 |
3 | HG03654.hp2 HG03710.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.538-609T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419675 | |||||||
| chr5:95419690 | G | A | 2 | a0001c0001t0001g0251 a0001c0001t0001g0312 |
2 | HG01496.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.538-594G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419690 | |||||||
| chr5:95419699 | C | A | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.538-585C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419699 | |||||||
| chr5:95419773 | C | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.538-511C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419773 | |||||||
| chr5:95419804 | A | G | 82 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(79): Show |
82 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.538-480A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419804 | |||||||
| chr5:95419834 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.538-450T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419834 | |||||||
| chr5:95419857 | T | G | 2 | a0001c0001t0001g0133 a0001c0002t0001g0017 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.538-427T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419857 | |||||||
| chr5:95419882 | T | G | 1 | a0001c0002t0001g0098 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.538-402T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419882 | |||||||
| chr5:95419932 | T | C | 82 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(79): Show |
82 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.538-352T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419932 | |||||||
| chr5:95420005 | T | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.538-279T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95420005 | |||||||
| chr5:95420097 | TCAAA | T | 82 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(79): Show |
82 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.538-185_538-182del others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 95420097 | ||||||
| chr5:95420103 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.538-181C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95420103 | |||||||
| chr5:95420512 | C | A | 10 | a0001c0002t0001g0179 a0001c0002t0001g0184 a0001c0002t0001g0185 others(7): Show |
10 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.656+110C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420512 | |||||||
| chr5:95420557 | C | G | 77 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(74): Show |
77 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.656+155C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420557 | |||||||
| chr5:95420567 | C | T | 1 | a0003c0007t0001g0149 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.656+165C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420567 | |||||||
| chr5:95420574 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656+172G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420574 | |||||||
| chr5:95420574 | G | C | 88 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(85): Show |
88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.656+172G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420574 | |||||||
| chr5:95420593 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0321 |
3 | HG02698.hp1 HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.656+191G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420593 | |||||||
| chr5:95420647 | T | C | 87 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(84): Show |
87 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.656+245T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420647 | |||||||
| chr5:95420648 | G | A | 87 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(84): Show |
87 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.656+246G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420648 | |||||||
| chr5:95420660 | G | A | 138 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(135): Show |
144 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.656+258G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420660 | |||||||
| chr5:95420678 | A | G | 87 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(84): Show |
87 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.656+276A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420678 | |||||||
| chr5:95420700 | C | A | 88 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(85): Show |
88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.656+298C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420700 | |||||||
| chr5:95420716 | CAT | C | 88 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(85): Show |
88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.656+317_656+318del others(2): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95420716 | ||||||
| chr5:95420732 | G | T | 88 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(85): Show |
88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.656+330G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420732 | |||||||
| chr5:95420792 | A | G | 88 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(85): Show |
88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.656+390A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420792 | |||||||
| chr5:95420846 | T | C | 3 | a0001c0002t0001g0093 a0001c0002t0001g0101 a0001c0002t0002g0019 |
3 | HG01109.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.656+444T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420846 | |||||||
| chr5:95420906 | A | G | 91 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.656+504A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420906 | |||||||
| chr5:95420976 | C | A | 54 | a0001c0001t0001g0215 a0001c0001t0002g0131 a0001c0002t0001g0001 others(51): Show |
60 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.656+574C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420976 | |||||||
| chr5:95421039 | T | C | 110 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(107): Show |
110 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.656+637T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421039 | |||||||
| chr5:95421074 | C | G | 1 | a0001c0002t0002g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.656+672C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421074 | |||||||
| chr5:95421232 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.656+830C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421232 | |||||||
| chr5:95421486 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656+1084G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421486 | |||||||
| chr5:95421495 | T | C | 2 | a0001c0002t0001g0188 a0001c0002t0002g0187 |
2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.656+1093T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421495 | |||||||
| chr5:95421554 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.656+1152T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421554 | |||||||
| chr5:95421606 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(110): Show |
116 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.656+1204T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421606 | |||||||
| chr5:95421625 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0273 |
3 | HG00673.hp2 HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.656+1223G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421625 | |||||||
| chr5:95421678 | C | CA | 226 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
239 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.656+1283dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95421678 | ||||||
| chr5:95421785 | A | T | 3 | a0001c0002t0001g0004 a0001c0002t0001g0083 a0001c0002t0001g0084 |
4 | NA18984.hp2 NA19004.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+1383A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421785 | |||||||
| chr5:95421796 | A | T | 3 | a0001c0001t0001g0117 a0001c0001t0002g0078 a0001c0001t0002g0122 |
3 | HG02258.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.656+1394A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421796 | |||||||
| chr5:95421980 | A | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(72): Show |
76 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.656+1578A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421980 | |||||||
| chr5:95422062 | A | G | 67 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(64): Show |
68 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.656+1660A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422062 | |||||||
| chr5:95422093 | C | T | 63 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(60): Show |
64 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.656+1691C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422093 | |||||||
| chr5:95422122 | T | C | 4 | a0001c0001t0001g0133 a0001c0001t0002g0018 a0001c0001t0002g0129 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+1720T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422122 | |||||||
| chr5:95422138 | GGAAAGAC others(2): Show |
G | 61 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(58): Show |
62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+1746_656+1754d others(11): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95422138 | ||||||
| chr5:95422174 | A | G | 61 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(58): Show |
62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+1772A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422174 | |||||||
| chr5:95422204 | G | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(75): Show |
87 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.656+1802G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422204 | |||||||
| chr5:95422224 | G | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.656+1822G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422224 | |||||||
| chr5:95422235 | A | T | 61 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(58): Show |
62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+1833A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422235 | |||||||
| chr5:95422456 | A | G | 14 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0075 others(11): Show |
14 | HG00741.hp2 HG01074.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.656+2054A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422456 | |||||||
| chr5:95422500 | C | T | 61 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(58): Show |
62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+2098C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422500 | |||||||
| chr5:95422514 | G | A | 61 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(58): Show |
62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+2112G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422514 | |||||||
| chr5:95422557 | ACTGCAGC others(2): Show |
A | 80 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(77): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.656+2160_656+2168d others(11): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95422557 | ||||||
| chr5:95422656 | A | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(56): Show |
60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.656+2254A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422656 | |||||||
| chr5:95422680 | T | A | 3 | a0001c0001t0001g0316 a0001c0001t0001g0318 a0001c0001t0002g0315 |
3 | HG02818.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.656+2278T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422680 | |||||||
| chr5:95422761 | T | G | 44 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(41): Show |
44 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.656+2359T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422761 | |||||||
| chr5:95422864 | C | T | 1 | a0001c0001t0002g0253 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.656+2462C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422864 | |||||||
| chr5:95422881 | T | A | 59 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(56): Show |
60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.656+2479T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422881 | |||||||
| chr5:95422948 | A | G | 5 | a0001c0001t0001g0133 a0001c0001t0002g0018 a0001c0001t0002g0129 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.656+2546A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422948 | |||||||
| chr5:95422998 | C | G | 100 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(97): Show |
101 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.656+2596C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422998 | |||||||
| chr5:95423070 | T | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(56): Show |
60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.656+2668T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95423070 | |||||||
| chr5:95423148 | A | ATTAAG | 59 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(56): Show |
60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.656+2748_656+2749i others(7): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423148 | ||||||
| chr5:95423371 | C | G | 61 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(58): Show |
63 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.656+2969C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95423371 | |||||||
| chr5:95423547 | T | TA | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(5): Show |
8 | HG02258.hp1 HG06807.hp2 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.656+3166dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423547 | ||||||
| chr5:95423547 | T | TAA | 37 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(34): Show |
37 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.656+3165_656+3166d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423547 | ||||||
| chr5:95423547 | TA | T | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(79): Show |
91 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.656+3166delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423547 | ||||||
| chr5:95423547 | TAAAAA | T | 54 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(51): Show |
55 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.656+3162_656+3166d others(7): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423547 | ||||||
| chr5:95423547 | TAAAAAAA others(5): Show |
T | 1 | a0001c0002t0001g0042 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.656+3155_656+3166d others(14): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423547 | ||||||
| chr5:95423862 | T | C | 59 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(56): Show |
60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.656+3460T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95423862 | |||||||
| chr5:95423933 | G | A | 1 | a0001c0002t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.656+3531G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95423933 | |||||||
| chr5:95424013 | G | A | 24 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0028 others(21): Show |
24 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.656+3611G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424013 | |||||||
| chr5:95424098 | G | A | 60 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(57): Show |
61 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.656+3696G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424098 | |||||||
| chr5:95424155 | T | C | 2 | a0001c0002t0001g0128 a0001c0002t0002g0127 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.656+3753T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424155 | |||||||
| chr5:95424206 | A | G | 1 | a0001c0002t0002g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.656+3804A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424206 | |||||||
| chr5:95424331 | A | T | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656+3929A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424331 | |||||||
| chr5:95424448 | T | TA | 74 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0026 others(71): Show |
76 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.656+4063dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95424448 | ||||||
| chr5:95424448 | TA | T | 63 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(60): Show |
64 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.656+4063delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95424448 | ||||||
| chr5:95424472 | C | G | 2 | a0006c0005t0002g0218 a0006c0005t0002g0219 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.656+4070C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424472 | |||||||
| chr5:95424509 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.657-4094G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424509 | |||||||
| chr5:95424745 | C | A | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.657-3858C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424745 | |||||||
| chr5:95424787 | C | CTTATTAG others(3): Show |
62 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(59): Show |
63 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.657-3810_657-3809i others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95424787 | ||||||
| chr5:95424952 | A | G | 2 | a0001c0002t0001g0092 a0001c0002t0002g0019 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.657-3651A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424952 | |||||||
| chr5:95425100 | G | A | 306 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(303): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.657-3503G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425100 | |||||||
| chr5:95425105 | A | G | 61 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(58): Show |
62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.657-3498A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425105 | |||||||
| chr5:95425146 | C | T | 55 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(52): Show |
56 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.657-3457C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425146 | |||||||
| chr5:95425174 | C | CA | 43 | a0001c0001t0001g0027 a0001c0001t0001g0115 a0001c0001t0001g0116 others(40): Show |
43 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.657-3416dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95425174 | ||||||
| chr5:95425631 | G | A | 59 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(56): Show |
60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.657-2972G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425631 | |||||||
| chr5:95425631 | G | C | 1 | a0001c0001t0001g0266 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.657-2972G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425631 | |||||||
| chr5:95425632 | A | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(56): Show |
60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.657-2971A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425632 | |||||||
| chr5:95425839 | ATATC | A | 5 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0316 others(2): Show |
5 | HG02630.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-2761_657-2758d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95425839 | ||||||
| chr5:95425997 | T | A | 59 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(56): Show |
60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.657-2606T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425997 | |||||||
| chr5:95426088 | CTG | C | 8 | a0001c0001t0001g0298 a0001c0002t0001g0001 a0001c0002t0001g0009 others(5): Show |
11 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-2509_657-2508d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426088 | ||||||
| chr5:95426092 | G | GTA | 10 | a0001c0001t0001g0196 a0001c0001t0001g0264 a0001c0002t0001g0004 others(7): Show |
11 | HG00280.hp2 HG00735.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-2510_657-2509i others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426092 | ||||||
| chr5:95426092 | G | GTATA | 5 | a0001c0001t0001g0151 a0001c0001t0001g0209 a0001c0002t0001g0128 others(2): Show |
5 | HG00733.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-2510_657-2509i others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426092 | ||||||
| chr5:95426092 | G | GTATATAT others(3): Show |
1 | a0001c0002t0002g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.657-2510_657-2509i others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426092 | ||||||
| chr5:95426092 | GTGTA | G | 3 | a0001c0001t0001g0274 a0001c0002t0001g0076 a0001c0002t0001g0138 |
3 | HG01070.hp2 HG02293.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.657-2509_657-2506d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426092 | ||||||
| chr5:95426092 | GTGTATA | G | 4 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0002g0243 others(1): Show |
4 | NA18948.hp2 NA18973.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-2509_657-2504d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426092 | ||||||
| chr5:95426094 | G | A | 52 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0058 others(49): Show |
55 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.657-2509G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426094 | |||||||
| chr5:95426094 | G | GTA | 37 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0038 others(34): Show |
38 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.657-2481_657-2480d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTATA | 38 | a0001c0001t0001g0008 a0001c0001t0001g0086 a0001c0001t0001g0088 others(35): Show |
39 | HG00621.hp2 HG01099.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.657-2483_657-2480d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTATATA | 26 | a0001c0001t0001g0075 a0001c0001t0001g0087 a0001c0001t0001g0104 others(23): Show |
26 | HG01069.hp1 HG01071.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.657-2485_657-2480d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTATATAT others(1): Show |
10 | a0001c0001t0001g0117 a0001c0001t0001g0208 a0001c0001t0001g0328 others(7): Show |
10 | HG01243.hp2 HG01358.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.657-2487_657-2480d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTATATAT others(3): Show |
6 | a0001c0001t0001g0027 a0001c0001t0001g0262 a0001c0001t0002g0091 others(3): Show |
6 | HG00741.hp2 HG01123.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.657-2489_657-2480d others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.657-2491_657-2480d others(14): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0147 a0001c0002t0002g0178 |
2 | HG02622.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.657-2493_657-2480d others(16): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTATATAT others(9): Show |
6 | a0001c0001t0001g0273 a0001c0001t0001g0284 a0001c0001t0002g0121 others(3): Show |
6 | HG01074.hp1 HG02523.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-2495_657-2480d others(18): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTATATAT others(11): Show |
1 | a0001c0001t0002g0319 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.657-2497_657-2480d others(20): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTATATAT others(13): Show |
1 | a0001c0001t0002g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.657-2499_657-2480d others(22): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTATATAT others(15): Show |
2 | a0001c0001t0001g0012 a0001c0001t0002g0114 |
3 | HG00673.hp2 HG02071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.657-2501_657-2480d others(24): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTGTATAT others(11): Show |
1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.657-2508_657-2507i others(20): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | G | GTGTATAT others(17): Show |
1 | a0001c0001t0002g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.657-2508_657-2507i others(26): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | GTA | G | 31 | a0001c0001t0001g0005 a0001c0001t0001g0059 a0001c0001t0001g0060 others(28): Show |
32 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.657-2481_657-2480d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | GTATA | G | 3 | a0001c0001t0001g0133 a0001c0001t0001g0321 a0001c0001t0002g0189 |
3 | HG02630.hp2 HG02698.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.657-2483_657-2480d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426094 | GTATATA | G | 7 | a0001c0001t0001g0116 a0001c0001t0001g0124 a0001c0001t0001g0198 others(4): Show |
7 | HG01496.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-2485_657-2480d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | ||||||
| chr5:95426096 | A | G | 7 | a0001c0001t0001g0181 a0001c0001t0001g0215 a0001c0001t0002g0203 others(4): Show |
9 | HG00438.hp2 HG02155.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.657-2507A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426096 | |||||||
| chr5:95426098 | A | G | 1 | a0001c0001t0002g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.657-2505A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426098 | |||||||
| chr5:95426100 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.657-2503A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426100 | |||||||
| chr5:95426116 | ATATATAT others(1): Show |
A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0031 others(33): Show |
37 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.657-2484_657-2477d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426116 | ||||||
| chr5:95426118 | ATATATG | A | 16 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0036 others(13): Show |
16 | HG00738.hp1 HG00741.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.657-2482_657-2477d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426118 | ||||||
| chr5:95426122 | ATG | A | 3 | a0001c0001t0001g0028 a0001c0001t0002g0131 a0001c0001t0002g0203 |
3 | HG02165.hp1 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.657-2479_657-2478d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426122 | ||||||
| chr5:95426124 | G | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0026 others(98): Show |
109 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.657-2479G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426124 | |||||||
| chr5:95426125 | T | C | 8 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0305 others(5): Show |
11 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-2478T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426125 | |||||||
| chr5:95426483 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.657-2120T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426483 | |||||||
| chr5:95426524 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0145 a0001c0002t0001g0053 others(5): Show |
9 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.657-2079G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426524 | |||||||
| chr5:95426602 | C | A | 196 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(193): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.657-2001C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426602 | |||||||
| chr5:95426747 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.657-1856G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426747 | |||||||
| chr5:95426819 | C | T | 1 | a0001c0001t0002g0317 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.657-1784C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426819 | |||||||
| chr5:95426831 | G | A | 28 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0124 others(25): Show |
28 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.657-1772G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426831 | |||||||
| chr5:95426862 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.657-1741G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426862 | |||||||
| chr5:95426890 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.657-1713T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426890 | |||||||
| chr5:95426914 | T | C | 2 | a0001c0002t0001g0001 a0001c0002t0001g0305 |
4 | HG01192.hp1 HG02683.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-1689T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426914 | |||||||
| chr5:95426919 | C | G | 5 | a0001c0001t0001g0135 a0001c0001t0001g0148 a0001c0001t0002g0285 others(2): Show |
7 | HG01192.hp1 HG02040.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-1684C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426919 | |||||||
| chr5:95426920 | A | G | 5 | a0001c0001t0001g0135 a0001c0001t0001g0148 a0001c0001t0002g0285 others(2): Show |
7 | HG01192.hp1 HG02040.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-1683A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426920 | |||||||
| chr5:95426921 | T | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0148 a0001c0001t0002g0285 others(2): Show |
7 | HG01192.hp1 HG02040.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-1682T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426921 | |||||||
| chr5:95426933 | T | C | 73 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(70): Show |
75 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.657-1670T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426933 | |||||||
| chr5:95426938 | A | C | 70 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(67): Show |
72 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.657-1665A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426938 | |||||||
| chr5:95426948 | G | C | 1 | a0001c0002t0001g0009 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.657-1655G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426948 | |||||||
| chr5:95426954 | C | T | 4 | a0001c0002t0001g0043 a0001c0002t0001g0062 a0001c0002t0001g0076 others(1): Show |
4 | HG01069.hp2 HG01070.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-1649C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426954 | |||||||
| chr5:95426970 | A | G | 2 | a0001c0002t0001g0177 a0001c0002t0001g0191 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.657-1633A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426970 | |||||||
| chr5:95426973 | T | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0314 a0001c0001t0002g0072 others(3): Show |
6 | NA18957.hp1 NA18960.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.657-1630T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426973 | |||||||
| chr5:95427003 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0002g0237 a0001c0002t0001g0308 |
3 | HG03579.hp2 HG04184.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.657-1600T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427003 | |||||||
| chr5:95427003 | T | G | 1 | a0001c0001t0001g0314 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.657-1600T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427003 | |||||||
| chr5:95427005 | T | C | 1 | a0001c0001t0001g0314 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.657-1598T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427005 | |||||||
| chr5:95427015 | C | G | 1 | a0001c0002t0001g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.657-1588C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427015 | |||||||
| chr5:95427030 | T | C | 2 | a0001c0001t0002g0040 a0001c0002t0002g0173 |
2 | HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.657-1573T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427030 | |||||||
| chr5:95427055 | AAG | A | 39 | a0001c0001t0001g0028 a0001c0001t0001g0102 a0001c0001t0001g0104 others(36): Show |
39 | HG01106.hp2 HG01109.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.657-1546_657-1545d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95427055 | ||||||
| chr5:95427057 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.657-1546G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427057 | |||||||
| chr5:95427062 | G | A | 40 | a0001c0001t0001g0028 a0001c0001t0001g0102 a0001c0001t0001g0104 others(37): Show |
40 | HG01106.hp2 HG01109.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.657-1541G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427062 | |||||||
| chr5:95427112 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0259 a0001c0001t0001g0289 |
3 | HG01496.hp1 HG02273.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.657-1491C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427112 | |||||||
| chr5:95427223 | A | G | 1 | a0001c0002t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.657-1380A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427223 | |||||||
| chr5:95427278 | A | G | 2 | a0001c0002t0001g0177 a0001c0002t0001g0191 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.657-1325A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427278 | |||||||
| chr5:95427290 | A | G | 4 | a0001c0001t0001g0133 a0001c0001t0002g0091 a0001c0001t0002g0223 others(1): Show |
4 | HG01891.hp1 HG02630.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-1313A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427290 | |||||||
| chr5:95427411 | A | C | 1 | a0001c0001t0001g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.657-1192A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427411 | |||||||
| chr5:95427440 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.657-1163C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427440 | |||||||
| chr5:95427476 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.657-1127A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427476 | |||||||
| chr5:95427563 | A | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0316 a0001c0002t0001g0092 |
3 | HG01884.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.657-1040A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427563 | |||||||
| chr5:95427988 | C | T | 4 | a0001c0001t0001g0236 a0001c0001t0001g0327 a0001c0002t0001g0177 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-615C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427988 | |||||||
| chr5:95428198 | A | C | 4 | a0001c0001t0001g0236 a0001c0001t0001g0327 a0001c0002t0001g0177 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-405A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428198 | |||||||
| chr5:95428302 | A | G | 30 | a0001c0001t0001g0071 a0001c0001t0001g0125 a0001c0001t0001g0142 others(27): Show |
30 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.657-301A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428302 | |||||||
| chr5:95428305 | A | G | 2 | a0001c0001t0002g0068 a0001c0002t0002g0173 |
2 | HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.657-298A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428305 | |||||||
| chr5:95428463 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.657-140T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428463 | |||||||
| chr5:95428488 | T | C | 5 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0327 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-115T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428488 | |||||||
| chr5:95428516 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.657-87G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428516 | |||||||
| chr5:95428584 | A | G | 15 | a0001c0001t0001g0152 a0001c0001t0002g0030 a0001c0001t0002g0091 others(12): Show |
15 | HG00733.hp1 HG01167.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.657-19A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428584 | |||||||
| chr5:95429134 | C | T | 5 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0327 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+402C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429134 | |||||||
| chr5:95429151 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.786+419C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429151 | |||||||
| chr5:95429371 | T | A | 1 | a0001c0001t0001g0316 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.786+639T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429371 | |||||||
| chr5:95429650 | C | T | 7 | a0001c0001t0001g0125 a0001c0001t0001g0181 a0001c0001t0001g0236 others(4): Show |
7 | HG01884.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+918C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429650 | |||||||
| chr5:95429657 | A | G | 8 | a0001c0001t0001g0117 a0001c0001t0002g0282 a0001c0002t0002g0054 others(5): Show |
8 | HG00642.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+925A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429657 | |||||||
| chr5:95429675 | T | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0181 a0001c0001t0001g0236 others(4): Show |
7 | HG01884.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+943T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429675 | |||||||
| chr5:95429898 | G | C | 75 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0034 others(72): Show |
79 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.786+1166G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429898 | |||||||
| chr5:95429910 | T | C | 5 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0248 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+1178T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429910 | |||||||
| chr5:95430034 | A | G | 44 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0152 others(41): Show |
44 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.786+1302A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430034 | |||||||
| chr5:95430220 | G | A | 1 | a0001c0002t0002g0173 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.786+1488G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430220 | |||||||
| chr5:95430277 | T | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0181 a0001c0001t0001g0236 others(4): Show |
7 | HG01884.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+1545T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430277 | |||||||
| chr5:95430292 | G | A | 1 | a0001c0002t0001g0310 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.786+1560G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430292 | |||||||
| chr5:95430328 | A | G | 2 | a0001c0001t0001g0155 a0004c0004t0001g0063 |
2 | HG00735.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.786+1596A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430328 | |||||||
| chr5:95430383 | G | GTA | 222 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(219): Show |
229 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.786+1662_786+1663d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95430383 | ||||||
| chr5:95430383 | G | GTATA | 16 | a0001c0001t0001g0125 a0001c0001t0001g0181 a0001c0001t0001g0236 others(13): Show |
16 | HG01884.hp2 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.786+1660_786+1663d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95430383 | ||||||
| chr5:95430422 | T | G | 1 | a0001c0002t0001g0224 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.786+1690T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430422 | |||||||
| chr5:95430436 | TA | T | 39 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0036 others(36): Show |
39 | HG00544.hp1 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.786+1716delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95430436 | ||||||
| chr5:95430436 | TAA | T | 39 | a0001c0001t0001g0130 a0001c0001t0001g0152 a0001c0001t0002g0030 others(36): Show |
39 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.786+1715_786+1716d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95430436 | ||||||
| chr5:95430544 | G | C | 16 | a0001c0001t0001g0133 a0001c0001t0002g0018 a0001c0001t0002g0109 others(13): Show |
16 | HG02040.hp1 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.786+1812G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430544 | |||||||
| chr5:95430572 | A | G | 2 | a0001c0001t0002g0068 a0001c0002t0002g0173 |
2 | HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.786+1840A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430572 | |||||||
| chr5:95430618 | A | G | 27 | a0001c0001t0002g0015 a0001c0001t0002g0029 a0001c0001t0002g0037 others(24): Show |
27 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.786+1886A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430618 | |||||||
| chr5:95430640 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.786+1908C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430640 | |||||||
| chr5:95430649 | T | C | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.786+1917T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430649 | |||||||
| chr5:95430664 | C | A | 1 | a0001c0001t0002g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.786+1932C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430664 | |||||||
| chr5:95430858 | C | T | 31 | a0001c0001t0002g0015 a0001c0001t0002g0029 a0001c0001t0002g0037 others(28): Show |
31 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.786+2126C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430858 | |||||||
| chr5:95430947 | G | C | 5 | a0001c0001t0001g0104 a0001c0001t0001g0233 a0001c0002t0001g0128 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+2215G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430947 | |||||||
| chr5:95431072 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.786+2340T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431072 | |||||||
| chr5:95431135 | T | C | 5 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0327 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+2403T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431135 | |||||||
| chr5:95431580 | T | C | 31 | a0001c0001t0002g0015 a0001c0001t0002g0029 a0001c0001t0002g0037 others(28): Show |
31 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.786+2848T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431580 | |||||||
| chr5:95431587 | T | A | 2 | a0003c0007t0001g0149 a0003c0007t0001g0212 |
2 | NA18981.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.786+2855T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431587 | |||||||
| chr5:95431641 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0255 |
2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.786+2909G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431641 | |||||||
| chr5:95431653 | A | T | 4 | a0001c0001t0001g0204 a0001c0001t0001g0301 a0001c0002t0001g0010 others(1): Show |
5 | NA18953.hp2 NA18983.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+2921A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431653 | |||||||
| chr5:95431752 | C | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.786+3020C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431752 | |||||||
| chr5:95431769 | A | G | 8 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0120 others(5): Show |
8 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+3037A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431769 | |||||||
| chr5:95431830 | T | G | 1 | a0001c0001t0002g0320 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.786+3098T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431830 | |||||||
| chr5:95431900 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0074 |
2 | HG00544.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.786+3168C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431900 | |||||||
| chr5:95431936 | C | G | 1 | a0001c0001t0002g0285 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.786+3204C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431936 | |||||||
| chr5:95432027 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.786+3295T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432027 | |||||||
| chr5:95432045 | T | C | 1 | a0001c0001t0002g0137 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.786+3313T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432045 | |||||||
| chr5:95432127 | C | T | 16 | a0001c0001t0001g0133 a0001c0001t0002g0018 a0001c0001t0002g0109 others(13): Show |
16 | HG02040.hp1 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.786+3395C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432127 | |||||||
| chr5:95432219 | T | C | 2 | a0001c0001t0001g0199 a0001c0002t0001g0093 |
2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.786+3487T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432219 | |||||||
| chr5:95432346 | C | G | 100 | a0001c0001t0001g0104 a0001c0001t0001g0125 a0001c0001t0001g0130 others(97): Show |
100 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.786+3614C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432346 | |||||||
| chr5:95432387 | T | C | 101 | a0001c0001t0001g0104 a0001c0001t0001g0125 a0001c0001t0001g0130 others(98): Show |
101 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.786+3655T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432387 | |||||||
| chr5:95432457 | T | C | 1 | a0001c0001t0002g0276 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.786+3725T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432457 | |||||||
| chr5:95432645 | GA | G | 5 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0248 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3921delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95432645 | ||||||
| chr5:95432845 | T | C | 2 | a0001c0001t0001g0133 a0001c0002t0001g0017 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.787-3955T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432845 | |||||||
| chr5:95433112 | A | G | 5 | a0001c0001t0002g0018 a0001c0001t0002g0122 a0001c0001t0002g0237 others(2): Show |
5 | HG02040.hp1 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-3688A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433112 | |||||||
| chr5:95433261 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0256 |
2 | NA18955.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.787-3539G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433261 | |||||||
| chr5:95433261 | G | GA | 84 | a0001c0001t0001g0104 a0001c0001t0001g0125 a0001c0001t0001g0130 others(81): Show |
84 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.787-3539_787-3538i others(3): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433261 | |||||||
| chr5:95433419 | C | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0233 a0001c0002t0001g0128 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-3381C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433419 | |||||||
| chr5:95433455 | T | C | 33 | a0001c0001t0001g0125 a0001c0001t0001g0316 a0001c0001t0002g0015 others(30): Show |
33 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.787-3345T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433455 | |||||||
| chr5:95433528 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0233 a0001c0002t0001g0128 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-3272G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433528 | |||||||
| chr5:95433669 | A | G | 1 | a0001c0001t0001g0328 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.787-3131A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433669 | |||||||
| chr5:95433899 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.787-2901C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433899 | |||||||
| chr5:95434018 | A | G | 49 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0181 others(46): Show |
49 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.787-2782A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434018 | |||||||
| chr5:95434041 | A | G | 35 | a0001c0001t0001g0125 a0001c0001t0001g0316 a0001c0001t0002g0015 others(32): Show |
35 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.787-2759A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434041 | |||||||
| chr5:95434165 | A | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0264 |
2 | HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.787-2635A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434165 | |||||||
| chr5:95434447 | C | T | 9 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0118 others(6): Show |
9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-2353C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434447 | |||||||
| chr5:95434514 | T | C | 2 | a0001c0001t0002g0068 a0001c0002t0002g0173 |
2 | HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.787-2286T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434514 | |||||||
| chr5:95434616 | CT | C | 5 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0327 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-2180delT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95434616 | ||||||
| chr5:95434641 | C | T | 4 | a0001c0001t0002g0131 a0001c0001t0002g0223 a0001c0001t0002g0320 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-2159C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434641 | |||||||
| chr5:95434805 | C | T | 9 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0118 others(6): Show |
9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-1995C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434805 | |||||||
| chr5:95434854 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.787-1946T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434854 | |||||||
| chr5:95434875 | C | T | 4 | a0001c0001t0002g0015 a0001c0001t0002g0106 a0001c0001t0002g0255 others(1): Show |
4 | HG03654.hp1 HG03927.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-1925C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434875 | |||||||
| chr5:95435094 | C | T | 9 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0118 others(6): Show |
9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-1706C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435094 | |||||||
| chr5:95435134 | G | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.787-1666G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435134 | |||||||
| chr5:95435168 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.787-1632T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435168 | |||||||
| chr5:95435234 | T | C | 4 | a0001c0001t0001g0236 a0001c0001t0001g0327 a0001c0002t0001g0177 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-1566T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435234 | |||||||
| chr5:95435297 | G | T | 1 | a0001c0001t0002g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.787-1503G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435297 | |||||||
| chr5:95435406 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.787-1394T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435406 | |||||||
| chr5:95436020 | G | A | 1 | a0001c0002t0002g0334 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.787-780G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436020 | |||||||
| chr5:95436103 | T | C | 2 | a0001c0001t0002g0317 a0001c0001t0002g0319 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.787-697T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436103 | |||||||
| chr5:95436308 | A | T | 31 | a0001c0001t0002g0015 a0001c0001t0002g0029 a0001c0001t0002g0037 others(28): Show |
31 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.787-492A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436308 | |||||||
| chr5:95436427 | C | T | 1 | a0001c0002t0001g0076 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.787-373C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436427 | |||||||
| chr5:95436718 | G | A | 5 | a0001c0001t0002g0015 a0001c0001t0002g0091 a0001c0001t0002g0106 others(2): Show |
5 | HG03225.hp2 HG03654.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-82G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436718 | |||||||
| chr5:95436791 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0316 |
2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.787-9T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436791 | |||||||
| chr5:95436908 | TA | T | 4 | a0001c0001t0002g0015 a0001c0001t0002g0106 a0001c0001t0002g0255 others(1): Show |
4 | HG03654.hp1 HG03927.hp1 HG04204.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.893+4delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95436908 | ||||||
| chr5:95436990 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.893+84C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95436990 | |||||||
| chr5:95437084 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.893+178A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437084 | |||||||
| chr5:95437346 | T | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0142 a0001c0001t0001g0235 |
3 | HG02602.hp2 HG02738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.893+440T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437346 | |||||||
| chr5:95437445 | C | T | 43 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0233 others(40): Show |
43 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.893+539C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437445 | |||||||
| chr5:95437499 | G | A | 44 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0233 others(41): Show |
44 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.893+593G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437499 | |||||||
| chr5:95437777 | TC | T | 4 | a0001c0001t0001g0133 a0001c0002t0001g0017 a0001c0002t0002g0023 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.893+872delC | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437777 | |||||||
| chr5:95437778 | C | T | 96 | a0001c0001t0001g0104 a0001c0001t0001g0125 a0001c0001t0001g0130 others(93): Show |
96 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.893+872C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437778 | |||||||
| chr5:95437880 | A | C | 60 | a0001c0001t0001g0104 a0001c0001t0001g0125 a0001c0001t0001g0130 others(57): Show |
60 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.893+974A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437880 | |||||||
| chr5:95438008 | T | C | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0002g0257 |
3 | NA18948.hp2 NA18960.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.893+1102T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438008 | |||||||
| chr5:95438057 | C | T | 1 | a0001c0002t0001g0310 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.893+1151C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438057 | |||||||
| chr5:95438058 | G | A | 44 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0233 others(41): Show |
44 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.893+1152G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438058 | |||||||
| chr5:95438109 | C | A | 14 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0327 others(11): Show |
14 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.893+1203C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438109 | |||||||
| chr5:95438194 | T | C | 100 | a0001c0001t0001g0104 a0001c0001t0001g0125 a0001c0001t0001g0130 others(97): Show |
100 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.893+1288T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438194 | |||||||
| chr5:95438319 | G | A | 5 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0327 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+1413G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438319 | |||||||
| chr5:95438363 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.893+1457T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438363 | |||||||
| chr5:95438470 | A | C | 1 | a0001c0001t0002g0285 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.893+1564A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438470 | |||||||
| chr5:95438498 | G | A | 44 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0233 others(41): Show |
44 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.893+1592G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438498 | |||||||
| chr5:95438629 | G | A | 1 | a0001c0002t0002g0173 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.893+1723G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438629 | |||||||
| chr5:95438752 | C | T | 1 | a0002c0003t0001g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.893+1846C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438752 | |||||||
| chr5:95438785 | T | TA | 11 | a0001c0001t0001g0033 a0001c0001t0001g0069 a0001c0001t0001g0133 others(8): Show |
11 | HG00738.hp2 HG01109.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.893+1895dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95438785 | ||||||
| chr5:95438785 | TA | T | 89 | a0001c0001t0001g0104 a0001c0001t0001g0125 a0001c0001t0001g0130 others(86): Show |
89 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.893+1895delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95438785 | ||||||
| chr5:95438797 | A | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG00738.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.893+1891A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438797 | |||||||
| chr5:95438798 | A | C | 1 | a0001c0001t0001g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.893+1892A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438798 | |||||||
| chr5:95439215 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0322 |
2 | HG01106.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.893+2309G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439215 | |||||||
| chr5:95439232 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.893+2326A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439232 | |||||||
| chr5:95439236 | G | GTA | 77 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0035 others(74): Show |
82 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.893+2358_893+2359d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATA | 51 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0059 others(48): Show |
54 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.893+2356_893+2359d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATA | 27 | a0001c0001t0001g0012 a0001c0001t0001g0065 a0001c0001t0001g0113 others(24): Show |
28 | HG00140.hp2 HG00438.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.893+2354_893+2359d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(1): Show |
21 | a0001c0001t0001g0002 a0001c0001t0001g0080 a0001c0001t0001g0086 others(18): Show |
22 | HG00280.hp1 HG00280.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.893+2352_893+2359d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(3): Show |
13 | a0001c0001t0001g0033 a0001c0001t0001g0087 a0001c0001t0001g0266 others(10): Show |
13 | HG00733.hp2 HG01109.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.893+2350_893+2359d others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(5): Show |
11 | a0001c0001t0001g0067 a0001c0001t0001g0096 a0001c0001t0001g0157 others(8): Show |
11 | HG01069.hp2 HG01070.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.893+2348_893+2359d others(14): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(7): Show |
10 | a0001c0001t0001g0291 a0001c0001t0002g0119 a0001c0001t0002g0269 others(7): Show |
10 | HG00140.hp1 HG01099.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.893+2346_893+2359d others(16): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(9): Show |
7 | a0001c0001t0001g0133 a0001c0001t0001g0258 a0001c0001t0001g0270 others(4): Show |
7 | HG02071.hp2 HG02257.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.893+2344_893+2359d others(18): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(11): Show |
8 | a0001c0001t0001g0104 a0001c0001t0001g0233 a0001c0001t0001g0261 others(5): Show |
8 | HG01074.hp1 HG01081.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.893+2342_893+2359d others(20): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(13): Show |
7 | a0001c0001t0002g0029 a0001c0001t0002g0118 a0001c0001t0002g0211 others(4): Show |
7 | HG01255.hp1 HG03041.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.893+2340_893+2359d others(22): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(15): Show |
6 | a0001c0001t0001g0075 a0001c0001t0002g0091 a0001c0001t0002g0112 others(3): Show |
6 | HG01934.hp2 HG03130.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.893+2338_893+2359d others(24): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(17): Show |
5 | a0001c0001t0002g0015 a0001c0001t0002g0106 a0001c0001t0002g0137 others(2): Show |
5 | HG00544.hp1 HG01361.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.893+2336_893+2359d others(26): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(19): Show |
2 | a0001c0001t0002g0285 a0001c0001t0002g0319 |
2 | HG02040.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.893+2334_893+2359d others(28): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(21): Show |
1 | a0001c0001t0002g0276 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.893+2332_893+2359d others(30): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTATATAT others(41): Show |
1 | a0001c0001t0002g0255 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.893+2359_893+2360i others(50): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTGTATAT others(9): Show |
1 | a0001c0001t0002g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.893+2331_893+2332i others(18): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | G | GTGTATAT others(13): Show |
1 | a0001c0001t0002g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.893+2331_893+2332i others(22): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | GTA | G | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0028 others(12): Show |
15 | HG00741.hp1 HG01109.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.893+2358_893+2359d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | GTATATAT others(3): Show |
G | 5 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0327 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+2350_893+2359d others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | GTATATAT others(5): Show |
G | 1 | a0001c0002t0002g0094 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.893+2348_893+2359d others(14): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | GTATATAT others(7): Show |
G | 12 | a0001c0001t0002g0037 a0001c0001t0002g0072 a0001c0001t0002g0201 others(9): Show |
12 | HG00597.hp2 HG02165.hp1 NA18960.hp2 others(9): Show |
intron_variant | MODIFIER | c.893+2346_893+2359d others(16): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439236 | GTATATAT others(9): Show |
G | 1 | a0001c0001t0002g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.893+2344_893+2359d others(18): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | ||||||
| chr5:95439321 | G | A | 5 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0248 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.893+2415G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439321 | |||||||
| chr5:95439526 | T | C | 4 | a0001c0001t0001g0113 a0001c0001t0001g0154 a0001c0001t0001g0220 others(1): Show |
4 | HG01943.hp2 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.893+2620T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439526 | |||||||
| chr5:95439594 | GTAAGACA others(8): Show |
G | 84 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 others(81): Show |
87 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.893+2690_893+2704d others(17): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439594 | ||||||
| chr5:95439595 | T | G | 1 | a0001c0002t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.893+2689T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439595 | |||||||
| chr5:95439607 | AT | A | 49 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0181 others(46): Show |
49 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.893+2711delT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439607 | ||||||
| chr5:95439610 | T | A | 1 | a0001c0002t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.893+2704T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439610 | |||||||
| chr5:95439954 | G | A | 2 | a0001c0001t0001g0006 a0002c0003t0001g0050 |
3 | HG01256.hp1 HG01258.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.893+3048G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439954 | |||||||
| chr5:95440110 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.893+3204A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95440110 | |||||||
| chr5:95440170 | CA | C | 49 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0181 others(46): Show |
49 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.893+3266delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95440170 | ||||||
| chr5:95440303 | T | C | 2 | a0001c0001t0001g0208 a0001c0002t0001g0032 |
2 | NA18966.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.893+3397T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95440303 | |||||||
| chr5:95440452 | T | C | 9 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0118 others(6): Show |
9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.893+3546T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95440452 | |||||||
| chr5:95440719 | T | C | 7 | a0001c0001t0001g0133 a0001c0001t0002g0018 a0001c0001t0002g0122 others(4): Show |
7 | HG02040.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.893+3813T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95440719 | |||||||
| chr5:95440808 | T | C | 1 | a0001c0001t0002g0329 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.893+3902T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95440808 | |||||||
| chr5:95440962 | GAA | G | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0116 others(4): Show |
7 | HG00738.hp1 HG01496.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.893+4060_893+4061d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95440962 | ||||||
| chr5:95441212 | C | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0233 a0001c0002t0001g0128 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+4306C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441212 | |||||||
| chr5:95441291 | C | T | 5 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0327 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+4385C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441291 | |||||||
| chr5:95441297 | G | A | 79 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 others(76): Show |
82 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.893+4391G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441297 | |||||||
| chr5:95441342 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0233 a0001c0002t0001g0128 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+4436G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441342 | |||||||
| chr5:95441373 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0233 a0001c0002t0001g0128 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+4467A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441373 | |||||||
| chr5:95441378 | G | C | 1 | a0001c0002t0001g0042 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.893+4472G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441378 | |||||||
| chr5:95441429 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.893+4523C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441429 | |||||||
| chr5:95441442 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.893+4536G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441442 | |||||||
| chr5:95441493 | C | T | 26 | a0001c0001t0002g0029 a0001c0001t0002g0037 a0001c0001t0002g0040 others(23): Show |
26 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.893+4587C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441493 | |||||||
| chr5:95441507 | T | G | 2 | a0001c0001t0001g0153 a0007c0009t0001g0166 |
2 | HG04184.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.893+4601T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441507 | |||||||
| chr5:95441541 | C | T | 3 | a0001c0001t0002g0029 a0001c0001t0002g0040 a0001c0002t0002g0052 |
3 | HG01081.hp1 HG02257.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.893+4635C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441541 | |||||||
| chr5:95441838 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
8 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.894-4724A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441838 | |||||||
| chr5:95441842 | T | C | 9 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0118 others(6): Show |
9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.894-4720T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441842 | |||||||
| chr5:95441914 | T | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0095 a0001c0001t0001g0115 others(3): Show |
7 | HG00280.hp2 HG01074.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.894-4648T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441914 | |||||||
| chr5:95441975 | AG | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
8 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.894-4586delG | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441975 | |||||||
| chr5:95442100 | A | T | 1 | a0001c0002t0002g0323 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.894-4462A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442100 | |||||||
| chr5:95442262 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.894-4300T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442262 | |||||||
| chr5:95442331 | C | CAGAAATA others(2): Show |
3 | a0001c0002t0002g0025 a0003c0008t0002g0288 a0004c0004t0002g0064 |
3 | HG01255.hp1 HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.894-4229_894-4221d others(11): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95442331 | ||||||
| chr5:95442392 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.894-4170T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442392 | |||||||
| chr5:95442433 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.894-4129C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442433 | |||||||
| chr5:95442452 | C | A | 1 | a0001c0001t0001g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.894-4110C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442452 | |||||||
| chr5:95442611 | AC | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0233 a0001c0002t0001g0128 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-3950delC | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442611 | |||||||
| chr5:95442999 | T | C | 9 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0118 others(6): Show |
9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.894-3563T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442999 | |||||||
| chr5:95443071 | C | T | 177 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
179 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.894-3491C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95443071 | |||||||
| chr5:95443114 | T | C | 177 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
179 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.894-3448T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95443114 | |||||||
| chr5:95443236 | C | T | 59 | a0001c0001t0001g0130 a0001c0001t0002g0015 a0001c0001t0002g0018 others(56): Show |
59 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.894-3326C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95443236 | |||||||
| chr5:95443638 | GA | G | 83 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 others(80): Show |
86 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.894-2919delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95443638 | ||||||
| chr5:95444091 | A | T | 1 | a0001c0002t0001g0004 | 2 | NA18984.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.894-2471A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444091 | |||||||
| chr5:95444151 | T | G | 1 | a0001c0001t0001g0227 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.894-2411T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444151 | |||||||
| chr5:95444163 | C | T | 4 | a0001c0001t0001g0236 a0001c0001t0001g0327 a0001c0002t0001g0177 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.894-2399C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444163 | |||||||
| chr5:95444412 | A | T | 1 | a0001c0001t0002g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.894-2150A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444412 | |||||||
| chr5:95444599 | T | A | 1 | a0001c0001t0002g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.894-1963T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444599 | |||||||
| chr5:95444633 | C | T | 4 | a0001c0001t0001g0236 a0001c0001t0001g0327 a0001c0002t0001g0177 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.894-1929C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444633 | |||||||
| chr5:95444645 | C | T | 1 | a0005c0006t0001g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.894-1917C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444645 | |||||||
| chr5:95444685 | T | C | 5 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0327 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-1877T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444685 | |||||||
| chr5:95444711 | G | A | 1 | a0009c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.894-1851G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444711 | |||||||
| chr5:95444774 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.894-1788T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444774 | |||||||
| chr5:95445167 | T | C | 9 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0118 others(6): Show |
9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.894-1395T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445167 | |||||||
| chr5:95445263 | C | G | 9 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0118 others(6): Show |
9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.894-1299C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445263 | |||||||
| chr5:95445569 | T | A | 5 | a0001c0001t0001g0096 a0001c0001t0001g0144 a0001c0002t0001g0043 others(2): Show |
5 | HG01070.hp2 HG01192.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-993T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445569 | |||||||
| chr5:95445590 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.894-972A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445590 | |||||||
| chr5:95445647 | C | T | 5 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0327 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-915C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445647 | |||||||
| chr5:95445657 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.894-905A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445657 | |||||||
| chr5:95445903 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.894-659G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445903 | |||||||
| chr5:95446790 | G | A | 2 | a0002c0003t0001g0045 a0002c0003t0001g0089 |
2 | HG00733.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1029+93G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446790 | |||||||
| chr5:95446793 | A | G | 1 | a0001c0001t0002g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1029+96A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446793 | |||||||
| chr5:95446812 | C | CT | 62 | a0001c0001t0001g0133 a0001c0001t0002g0015 a0001c0001t0002g0018 others(59): Show |
62 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.1029+127dupT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 95446812 | ||||||
| chr5:95446948 | T | TA | 5 | a0001c0001t0002g0110 a0001c0001t0002g0246 a0001c0001t0002g0247 others(2): Show |
5 | HG01167.hp1 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029+251_1029+252i others(3): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446948 | |||||||
| chr5:95446949 | T | A | 6 | a0001c0001t0002g0110 a0001c0001t0002g0246 a0001c0001t0002g0247 others(3): Show |
6 | HG01167.hp1 HG02040.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1029+252T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446949 | |||||||
| chr5:95446949 | T | TA | 34 | a0001c0001t0002g0018 a0001c0001t0002g0030 a0001c0001t0002g0057 others(31): Show |
34 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1029+252_1029+253i others(3): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446949 | |||||||
| chr5:95446949 | T | TAA | 5 | a0001c0001t0002g0111 a0001c0001t0002g0119 a0001c0001t0002g0126 others(2): Show |
5 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1029+252_1029+253i others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446949 | |||||||
| chr5:95446950 | T | A | 45 | a0001c0001t0002g0018 a0001c0001t0002g0030 a0001c0001t0002g0057 others(42): Show |
45 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1029+253T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446950 | |||||||
| chr5:95446950 | T | TA | 14 | a0001c0001t0002g0015 a0001c0001t0002g0091 a0001c0001t0002g0106 others(11): Show |
14 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1029+253_1029+254i others(3): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446950 | |||||||
| chr5:95446951 | T | A | 77 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(74): Show |
77 | HG00642.hp1 HG00733.hp1 HG01074.hp1 others(74): Show |
intron_variant | MODIFIER | c.1029+254T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446951 | |||||||
| chr5:95446951 | TA | T | 7 | a0001c0001t0001g0135 a0001c0001t0001g0141 a0001c0001t0001g0154 others(4): Show |
7 | HG01516.hp2 HG01943.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1029+267delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 95446951 | ||||||
| chr5:95446952 | A | T | 31 | a0001c0001t0001g0133 a0001c0001t0001g0162 a0001c0001t0001g0181 others(28): Show |
31 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.1029+255A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446952 | |||||||
| chr5:95446953 | A | T | 2 | a0001c0001t0001g0133 a0001c0002t0001g0017 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1029+256A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446953 | |||||||
| chr5:95447095 | T | A | 1 | a0001c0001t0001g0330 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1029+398T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447095 | |||||||
| chr5:95447171 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0233 others(2): Show |
5 | HG02572.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029+474G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447171 | |||||||
| chr5:95447471 | A | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(103): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1029+774A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447471 | |||||||
| chr5:95447485 | G | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0293 a0001c0001t0001g0304 others(1): Show |
4 | NA18947.hp2 NA18949.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1030-784G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447485 | |||||||
| chr5:95447720 | G | A | 1 | a0001c0001t0001g0335 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1030-549G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447720 | |||||||
| chr5:95447887 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1030-382C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447887 | |||||||
| chr5:95447916 | C | T | 99 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0133 others(96): Show |
99 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.1030-353C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447916 | |||||||
| chr5:95447917 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1030-352G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447917 | |||||||
| chr5:95447918 | A | C | 1 | a0001c0001t0002g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1030-351A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447918 | |||||||
| chr5:95448172 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1030-97C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95448172 | |||||||
| chr5:95448635 | C | A | 1 | a0001c0002t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1225+171C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95448635 | |||||||
| chr5:95448693 | A | AT | 8 | a0001c0001t0001g0198 a0001c0001t0001g0208 a0001c0001t0001g0242 others(5): Show |
8 | HG01358.hp1 HG02738.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1225+250dupT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 95448693 | ||||||
| chr5:95448693 | AT | A | 40 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0176 others(37): Show |
40 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1225+250delT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 95448693 | ||||||
| chr5:95448714 | T | A | 5 | a0001c0001t0002g0109 a0001c0001t0002g0114 a0001c0001t0002g0248 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225+250T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95448714 | |||||||
| chr5:95448858 | C | T | 5 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0327 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+394C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95448858 | |||||||
| chr5:95448922 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0036 others(2): Show |
5 | HG00741.hp1 HG01243.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+458G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95448922 | |||||||
| chr5:95449161 | T | C | 1 | a0001c0001t0002g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1225+697T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449161 | |||||||
| chr5:95449188 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0233 others(2): Show |
5 | HG02572.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+724A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449188 | |||||||
| chr5:95449480 | C | T | 87 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0029 others(84): Show |
87 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.1226-669C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449480 | |||||||
| chr5:95449655 | G | T | 5 | a0001c0001t0002g0015 a0001c0001t0002g0091 a0001c0001t0002g0106 others(2): Show |
5 | HG03225.hp2 HG03654.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1226-494G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449655 | |||||||
| chr5:95449697 | T | C | 94 | a0001c0001t0001g0133 a0001c0001t0001g0181 a0001c0001t0001g0236 others(91): Show |
94 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1226-452T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449697 | |||||||
| chr5:95449807 | C | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0225 |
3 | NA18961.hp1 NA19007.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1226-342C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449807 | |||||||
| chr5:95449834 | T | A | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1226-315T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449834 | |||||||
| chr5:95449835 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1226-314C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449835 | |||||||
| chr5:95449861 | T | G | 1 | a0001c0001t0001g0280 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1226-288T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449861 | |||||||
| chr5:95449943 | T | C | 191 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(188): Show |
195 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(192): Show |
intron_variant | MODIFIER | c.1226-206T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449943 | |||||||
| chr5:95450039 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1226-110G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95450039 | |||||||
| chr5:95450070 | G | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | HG00738.hp2 HG01975.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-79G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95450070 | |||||||
| chr5:95450071 | G | C | 1 | a0001c0001t0002g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1226-78G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95450071 |