Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22993 |
| ensemblid | ENSG00000113716.13 |
| hgncid | 28982 |
| symbol | HMGXB3 |
| name | HMG-box containing 3 |
| refseq_nuc | NM_014983.3 |
| refseq_prot | NP_055798.3 |
| ensembl_nuc | ENST00000502717.6 |
| ensembl_prot | ENSP00000421917.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 150000739 |
| end | 150053128 |
| strand | + |
| ver | v1.2 |
| region | chr5:150000739-150053128 |
| region5000 | chr5:149995739-150058128 |
| regionname0 | HMGXB3_chr5_150000739_150053128 |
| regionname5000 | HMGXB3_chr5_149995739_150058128 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1292 | 180 | 72 | 29 | 55 | 4 | 19 | 40 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0002 | 1/0 | 1292 | 99 | 0 | 17 | 60 | 3 | 18 | 52 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0003 | 0/0 | 1292 | 42 | 4 | 15 | 21 | 2 | 0 | 15 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0004 | 0/0 | 1292 | 33 | 8 | 5 | 16 | 0 | 4 | 14 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0005 | 0/0 | 1292 | 8 | 5 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0006 | 0/0 | 1292 | 4 | 1 | 1 | 1 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0007 | 0/0 | 1292 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDTSY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0008 | 0/0 | 1292 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0009 | 0/0 | 1292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0010 | 0/0 | 1292 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0011 | 0/0 | 1292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0012 | 0/0 | 1292 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0013 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0014 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0015 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0016 | 0/0 | 1292 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| a0017 | 0/0 | 1292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | MDASY others(1287): Show |
chr5 | 149995739 | 150058128 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3876 | 123 | 21 | 26 | 55 | 3 | 17 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0001c0003 | 0/0 | 3876 | 52 | 48 | 3 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0001c0017 | 0/0 | 3876 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0001c0018 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0001c0019 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0001c0021 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0001c0026 | 0/0 | 3876 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0002c0002 | 1/0 | 3876 | 96 | 0 | 16 | 58 | 3 | 18 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0002c0013 | 0/0 | 3876 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0002c0014 | 0/0 | 3876 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0002c0023 | 0/0 | 3876 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0003c0004 | 0/0 | 3876 | 39 | 4 | 15 | 18 | 2 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0003c0010 | 0/0 | 3876 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0004c0005 | 0/0 | 3876 | 28 | 8 | 1 | 16 | 0 | 3 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0004c0007 | 0/0 | 3876 | 5 | 0 | 4 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0005c0006 | 0/0 | 3876 | 8 | 5 | 3 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0006c0008 | 0/0 | 3876 | 4 | 1 | 1 | 1 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0007c0009 | 0/0 | 3876 | 3 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0008c0011 | 0/0 | 3876 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0009c0012 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0010c0015 | 0/0 | 3876 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0011c0016 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0012c0022 | 0/0 | 3876 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0013c0027 | 0/0 | 3876 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0014c0028 | 0/0 | 3876 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0015c0024 | 0/0 | 3876 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0016c0025 | 0/0 | 3876 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 | ||
| a0017c0020 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | ATGGA others(3871): Show |
chr5 | 149995739 | 150058128 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5258 | 61 | 10 | 9 | 35 | 0 | 7 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0001t0002 | 0/0 | 5258 | 5 | 0 | 1 | 2 | 0 | 2 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0001t0003 | 0/1 | 5258 | 43 | 4 | 12 | 15 | 3 | 8 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0001t0005 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0001t0006 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0001t0011 | 0/0 | 5258 | 4 | 4 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0001t0012 | 0/0 | 5258 | 2 | 0 | 1 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0001t0013 | 0/0 | 5258 | 2 | 1 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0001t0021 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0001t0026 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0001t0027 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0001t0029 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0003t0001 | 0/0 | 5258 | 9 | 9 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0003t0003 | 0/0 | 5258 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0003t0005 | 0/0 | 5258 | 25 | 22 | 3 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0003t0006 | 0/0 | 5258 | 7 | 6 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0003t0008 | 0/0 | 5258 | 6 | 6 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0003t0019 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0003t0020 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0003t0030 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0017t0003 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0018t0005 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0019t0005 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0021t0006 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0001c0026t0003 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0002t0001 | 0/0 | 5258 | 6 | 0 | 0 | 6 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0002t0002 | 1/0 | 5258 | 74 | 0 | 15 | 43 | 2 | 13 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0002t0003 | 0/0 | 5258 | 3 | 0 | 0 | 1 | 0 | 2 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0002t0005 | 0/0 | 5258 | 3 | 0 | 0 | 2 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0002t0010 | 0/0 | 5258 | 5 | 0 | 0 | 5 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0002t0015 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0002t0016 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0002t0022 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0002t0023 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0002t0025 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0013t0002 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0014t0002 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0002c0023t0014 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0003c0004t0004 | 0/0 | 5258 | 32 | 4 | 10 | 18 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0003c0004t0007 | 0/0 | 5258 | 6 | 0 | 4 | 0 | 2 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0003c0004t0017 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0003c0010t0004 | 0/0 | 5258 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0004c0005t0001 | 0/0 | 5258 | 25 | 6 | 0 | 16 | 0 | 3 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0004c0005t0002 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0004c0005t0005 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0004c0005t0015 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0004c0007t0002 | 0/0 | 5258 | 4 | 0 | 3 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0004c0007t0024 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0005c0006t0005 | 0/0 | 5258 | 3 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0005c0006t0009 | 0/0 | 5258 | 5 | 2 | 3 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0006c0008t0004 | 0/0 | 5258 | 3 | 1 | 1 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0006c0008t0018 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0007c0009t0004 | 0/0 | 5258 | 3 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0008c0011t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0008c0011t0005 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0009c0012t0028 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0010c0015t0005 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0011c0016t0003 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0012c0022t0003 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0013c0027t0001 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0014c0028t0002 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0015c0024t0014 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0016c0025t0002 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| a0017c0020t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | GATCC others(5253): Show |
chr5 | 149995739 | 150058128 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0012g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0012g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0013g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0021g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0026g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0027g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0001t0029g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0006g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0008g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0019g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0020g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0003t0030g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0017t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0018t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0019t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0021t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0001c0026t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0002 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0010g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0010g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0015g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0016g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0022g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0023g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0002t0025g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0013t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0014t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0002c0023t0014g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0007g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0007g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0007g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0007g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0007g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0004t0017g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0010t0004g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0003c0010t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0005t0015g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0007t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0007t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0007t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0007t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0004c0007t0024g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0005c0006t0005g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0005c0006t0009g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0005c0006t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0005c0006t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0006c0008t0004g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0006c0008t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0006c0008t0018g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0007c0009t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0007c0009t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0007c0009t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0008c0011t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0008c0011t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0009c0012t0028g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0010c0015t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0011c0016t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0012c0022t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0013c0027t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0014c0028t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0015c0024t0014g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0016c0025t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| a0017c0020t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0007 | g0130 | EUR | GBR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00099 | hp2 | a0001 | c0017 | t0003 | g0199 | EUR | GBR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0266 | EUR | GBR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0043 | EUR | GBR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00544 | hp1 | a0003 | c0010 | t0004 | g0124 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00597 | hp2 | a0003 | c0004 | t0004 | g0133 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00639 | hp1 | a0004 | c0007 | t0024 | g0260 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00673 | hp1 | a0003 | c0010 | t0004 | g0027 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00673 | hp2 | a0003 | c0004 | t0004 | g0310 | EAS | CHS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00735 | hp1 | a0003 | c0004 | t0007 | g0107 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00735 | hp2 | a0001 | c0003 | t0005 | g0273 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0096 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01069 | hp2 | a0005 | c0006 | t0009 | g0010 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01071 | hp1 | a0005 | c0006 | t0009 | g0010 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0097 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01106 | hp1 | a0004 | c0005 | t0002 | g0261 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01167 | hp1 | a0001 | c0001 | t0026 | g0200 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01167 | hp2 | a0003 | c0004 | t0007 | g0028 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0099 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01169 | hp1 | a0003 | c0004 | t0007 | g0028 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0052 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01243 | hp1 | a0003 | c0004 | t0017 | g0122 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01243 | hp2 | a0001 | c0003 | t0005 | g0135 | AMR | PUR | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01255 | hp1 | a0004 | c0007 | t0002 | g0263 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0022 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01346 | hp2 | a0002 | c0014 | t0002 | g0069 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01361 | hp1 | a0004 | c0007 | t0002 | g0262 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01433 | hp1 | a0004 | c0007 | t0002 | g0264 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01433 | hp2 | a0003 | c0004 | t0004 | g0001 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01496 | hp1 | a0005 | c0006 | t0009 | g0010 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01496 | hp2 | a0003 | c0004 | t0004 | g0117 | AMR | CLM | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01517 | hp1 | a0002 | c0002 | t0015 | g0098 | EUR | IBS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0166 | EUR | IBS | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01884 | hp1 | a0005 | c0006 | t0005 | g0009 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01884 | hp2 | a0001 | c0003 | t0006 | g0284 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01891 | hp1 | a0001 | c0003 | t0005 | g0267 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01934 | hp1 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01934 | hp2 | a0001 | c0001 | t0027 | g0165 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01943 | hp1 | a0001 | c0001 | t0012 | g0003 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0044 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01952 | hp2 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01978 | hp1 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01981 | hp1 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01981 | hp2 | a0001 | c0003 | t0005 | g0269 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01993 | hp1 | a0003 | c0004 | t0004 | g0110 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG01993 | hp2 | a0003 | c0004 | t0007 | g0131 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02004 | hp1 | a0006 | c0008 | t0004 | g0025 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02040 | hp2 | a0006 | c0008 | t0004 | g0120 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02055 | hp1 | a0001 | c0003 | t0020 | g0301 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02055 | hp2 | a0001 | c0003 | t0005 | g0144 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0219 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02074 | hp2 | a0004 | c0005 | t0001 | g0243 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02083 | hp2 | a0003 | c0004 | t0004 | g0111 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02132 | hp1 | a0003 | c0004 | t0004 | g0118 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02135 | hp2 | a0004 | c0005 | t0001 | g0247 | EAS | KHV | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02145 | hp1 | a0005 | c0006 | t0009 | g0102 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02145 | hp2 | a0001 | c0003 | t0008 | g0283 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02148 | hp1 | a0003 | c0004 | t0004 | g0116 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02257 | hp1 | a0001 | c0003 | t0005 | g0231 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02258 | hp1 | a0004 | c0005 | t0001 | g0234 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02258 | hp2 | a0001 | c0003 | t0005 | g0274 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02273 | hp2 | a0001 | c0001 | t0013 | g0228 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02280 | hp1 | a0001 | c0003 | t0005 | g0134 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02280 | hp2 | a0007 | c0009 | t0004 | g0126 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02293 | hp1 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02293 | hp2 | a0002 | c0002 | t0022 | g0095 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02300 | hp2 | a0003 | c0004 | t0004 | g0001 | AMR | PEL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02451 | hp2 | a0001 | c0003 | t0008 | g0280 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02572 | hp2 | a0001 | c0003 | t0006 | g0289 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02615 | hp1 | a0003 | c0004 | t0004 | g0121 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0141 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0307 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02622 | hp2 | a0001 | c0003 | t0005 | g0295 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02630 | hp1 | a0009 | c0012 | t0028 | g0309 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0015 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02647 | hp2 | a0001 | c0003 | t0005 | g0298 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02683 | hp2 | a0010 | c0015 | t0005 | g0105 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02717 | hp1 | a0005 | c0006 | t0005 | g0009 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02717 | hp2 | a0007 | c0009 | t0004 | g0123 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02735 | hp2 | a0001 | c0026 | t0003 | g0221 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02809 | hp1 | a0004 | c0005 | t0005 | g0238 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02809 | hp2 | a0001 | c0003 | t0005 | g0268 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02818 | hp1 | a0005 | c0006 | t0005 | g0009 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0308 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02886 | hp1 | a0001 | c0003 | t0030 | g0291 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0047 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02895 | hp1 | a0001 | c0003 | t0008 | g0276 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02896 | hp1 | a0008 | c0011 | t0005 | g0037 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02922 | hp1 | a0001 | c0003 | t0005 | g0029 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02922 | hp2 | a0001 | c0003 | t0005 | g0304 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02965 | hp1 | a0001 | c0003 | t0006 | g0288 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02965 | hp2 | a0001 | c0003 | t0005 | g0038 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02970 | hp1 | a0011 | c0016 | t0003 | g0226 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02976 | hp1 | a0001 | c0003 | t0005 | g0008 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02976 | hp2 | a0004 | c0005 | t0001 | g0236 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03041 | hp1 | a0001 | c0003 | t0005 | g0299 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0300 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0293 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03098 | hp2 | a0001 | c0018 | t0005 | g0136 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03130 | hp1 | a0001 | c0003 | t0003 | g0297 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03130 | hp2 | a0001 | c0003 | t0005 | g0145 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03139 | hp1 | a0003 | c0004 | t0004 | g0127 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03139 | hp2 | a0001 | c0003 | t0005 | g0272 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03195 | hp1 | a0001 | c0003 | t0005 | g0038 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03195 | hp2 | a0001 | c0003 | t0005 | g0030 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03209 | hp1 | a0001 | c0003 | t0006 | g0281 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03209 | hp2 | a0001 | c0001 | t0021 | g0015 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03225 | hp1 | a0001 | c0003 | t0005 | g0303 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03225 | hp2 | a0004 | c0005 | t0015 | g0239 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03239 | hp2 | a0002 | c0002 | t0023 | g0002 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03453 | hp1 | a0001 | c0003 | t0006 | g0292 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0286 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03486 | hp1 | a0001 | c0003 | t0008 | g0290 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03486 | hp2 | a0001 | c0021 | t0006 | g0282 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0215 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0056 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0089 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0055 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0296 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03516 | hp2 | a0001 | c0019 | t0005 | g0029 | AFR | ESN | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03540 | hp1 | a0007 | c0009 | t0004 | g0125 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03540 | hp2 | a0001 | c0003 | t0005 | g0306 | AFR | GWD | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0302 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03579 | hp2 | a0004 | c0005 | t0001 | g0257 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03654 | hp1 | a0004 | c0005 | t0001 | g0248 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03669 | hp1 | a0006 | c0008 | t0018 | g0119 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0064 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03704 | hp2 | a0004 | c0007 | t0002 | g0265 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03710 | hp1 | a0004 | c0005 | t0001 | g0242 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0050 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0137 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0227 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03927 | hp2 | a0002 | c0002 | t0003 | g0053 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03942 | hp1 | a0002 | c0002 | t0005 | g0061 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03942 | hp2 | a0002 | c0002 | t0025 | g0088 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0090 | SAS | BEB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG04199 | hp1 | a0012 | c0022 | t0003 | g0014 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0063 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG04204 | hp1 | a0004 | c0005 | t0001 | g0253 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0232 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0054 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0275 | SAS | STU | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18522 | hp1 | a0004 | c0005 | t0001 | g0235 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18522 | hp2 | a0003 | c0004 | t0004 | g0026 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | CHB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18906 | hp2 | a0001 | c0003 | t0008 | g0279 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18939 | hp2 | a0002 | c0002 | t0010 | g0091 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18946 | hp1 | a0004 | c0005 | t0001 | g0246 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18954 | hp2 | a0002 | c0002 | t0005 | g0051 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18956 | hp1 | a0013 | c0027 | t0001 | g0222 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18957 | hp1 | a0003 | c0004 | t0004 | g0108 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18961 | hp2 | a0003 | c0004 | t0004 | g0129 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18964 | hp2 | a0003 | c0010 | t0004 | g0027 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18965 | hp1 | a0004 | c0005 | t0001 | g0036 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18965 | hp2 | a0002 | c0002 | t0010 | g0005 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18968 | hp1 | a0004 | c0005 | t0001 | g0254 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18968 | hp2 | a0002 | c0002 | t0010 | g0005 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18969 | hp1 | a0004 | c0005 | t0001 | g0241 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18969 | hp2 | a0002 | c0002 | t0010 | g0005 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18971 | hp1 | a0003 | c0004 | t0004 | g0024 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18979 | hp1 | a0004 | c0005 | t0001 | g0255 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18982 | hp2 | a0003 | c0004 | t0004 | g0112 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18992 | hp1 | a0001 | c0001 | t0012 | g0205 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18995 | hp1 | a0004 | c0005 | t0001 | g0250 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18997 | hp1 | a0003 | c0004 | t0004 | g0113 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19000 | hp1 | a0003 | c0004 | t0004 | g0132 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19003 | hp1 | a0002 | c0002 | t0010 | g0005 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19005 | hp1 | a0004 | c0005 | t0001 | g0245 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19006 | hp2 | a0003 | c0004 | t0004 | g0106 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19007 | hp1 | a0004 | c0005 | t0001 | g0036 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19011 | hp2 | a0004 | c0005 | t0001 | g0252 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19012 | hp1 | a0003 | c0004 | t0004 | g0115 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19030 | hp2 | a0001 | c0003 | t0019 | g0271 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19063 | hp1 | a0004 | c0005 | t0001 | g0249 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19065 | hp1 | a0003 | c0004 | t0004 | g0012 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19066 | hp2 | a0002 | c0013 | t0002 | g0065 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19067 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19068 | hp2 | a0003 | c0004 | t0004 | g0024 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19074 | hp1 | a0014 | c0028 | t0002 | g0086 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19076 | hp1 | a0015 | c0024 | t0014 | g0082 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19076 | hp2 | a0004 | c0005 | t0001 | g0259 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19077 | hp2 | a0004 | c0005 | t0001 | g0240 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19079 | hp2 | a0003 | c0004 | t0004 | g0012 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19084 | hp1 | a0002 | c0002 | t0016 | g0092 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19084 | hp2 | a0003 | c0004 | t0004 | g0012 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19085 | hp1 | a0004 | c0005 | t0001 | g0244 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19086 | hp2 | a0003 | c0004 | t0004 | g0109 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19088 | hp1 | a0001 | c0001 | t0029 | g0013 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19088 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19089 | hp2 | a0003 | c0004 | t0004 | g0114 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19090 | hp2 | a0004 | c0005 | t0001 | g0251 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19091 | hp1 | a0002 | c0023 | t0014 | g0093 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19240 | hp1 | a0001 | c0003 | t0005 | g0270 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA19240 | hp2 | a0001 | c0003 | t0008 | g0285 | AFR | YRI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA20129 | hp1 | a0001 | c0003 | t0005 | g0030 | AFR | ASW | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA20129 | hp2 | a0003 | c0004 | t0004 | g0026 | AFR | ASW | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0070 | EUR | TSI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA20752 | hp2 | a0016 | c0025 | t0002 | g0002 | EUR | TSI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0014 | EUR | TSI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA20805 | hp2 | a0003 | c0004 | t0007 | g0128 | EUR | TSI | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA20905 | hp1 | a0001 | c0003 | t0006 | g0278 | SAS | GIH | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0193 | SAS | GIH | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02109 | hp2 | a0001 | c0003 | t0005 | g0008 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02486 | hp1 | a0005 | c0006 | t0009 | g0100 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02486 | hp2 | a0004 | c0005 | t0001 | g0256 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0305 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0217 | AFR | ACB | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03471 | hp1 | a0001 | c0003 | t0006 | g0287 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG06807 | hp1 | a0004 | c0005 | t0001 | g0237 | AFR | USA | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | USA | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0294 | AFR | USA | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA20300 | hp2 | a0006 | c0008 | t0004 | g0025 | AFR | USA | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA21309 | hp1 | a0017 | c0020 | t0001 | g0277 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| NA21309 | hp2 | a0008 | c0011 | t0001 | g0037 | AFR | LWK | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0220 | REF | REF | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0068 | REF | REF | HMGXB3_chr5_149995739_150058128 | HMGXB3 | chr5 | 149995739 | 150058128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:150004859 | G | A | 1 | a0007 | 3 | HG02280.hp2 HG02717.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.7G>A | p.Ala3Thr | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/20 | 450/5258 | 7/3879 | 3/1292 | chr5 | 150004859 | |||
| chr5:150006524 | G | T | 1 | a0014 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.189G>T | p.Glu63Asp | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/20 | 632/5258 | 189/3879 | 63/1292 | chr5 | 150006524 | |||
| chr5:150010226 | G | T | 1 | a0013 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.428G>T | p.Ser143Ile | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/20 | 871/5258 | 428/3879 | 143/1292 | chr5 | 150010226 | |||
| chr5:150010399 | G | A | 1 | a0009 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.601G>A | p.Val201Ile | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/20 | 1044/5258 | 601/3879 | 201/1292 | chr5 | 150010399 | |||
| chr5:150010585 | G | A | 3 | a0003 a0006 a0007 |
49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
missense_variant | MODERATE | c.787G>A | p.Val263Ile | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/20 | 1230/5258 | 787/3879 | 263/1292 | chr5 | 150010585 | |||
| chr5:150012282 | C | T | 1 | a0016 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.838C>T | p.Pro280Ser | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/20 | 1281/5258 | 838/3879 | 280/1292 | chr5 | 150012282 | |||
| chr5:150024616 | G | T | 1 | a0004 | 33 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(30): Show |
missense_variant | MODERATE | c.1396G>T | p.Val466Leu | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1839/5258 | 1396/3879 | 466/1292 | chr5 | 150024616 | |||
| chr5:150024631 | G | A | 1 | a0012 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.1411G>A | p.Glu471Lys | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1854/5258 | 1411/3879 | 471/1292 | chr5 | 150024631 | |||
| chr5:150024650 | G | T | 2 | a0008 a0017 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1430G>T | p.Ser477Ile | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1873/5258 | 1430/3879 | 477/1292 | chr5 | 150024650 | |||
| chr5:150026708 | C | T | 13 | a0001 a0003 a0004 others(10): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
missense_variant&splice_region_variant | MODERATE | c.1463C>T | p.Ala488Val | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 8/20 | 1906/5258 | 1463/3879 | 488/1292 | chr5 | 150026708 | |||
| chr5:150030756 | T | A | 1 | a0006 | 4 | HG02004.hp1 HG02040.hp2 HG03669.hp1 others(1): Show |
missense_variant | MODERATE | c.1750T>A | p.Ser584Thr | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/20 | 2193/5258 | 1750/3879 | 584/1292 | chr5 | 150030756 | |||
| chr5:150036931 | G | A | 1 | a0005 | 8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
missense_variant | MODERATE | c.2279G>A | p.Gly760Glu | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 12/20 | 2722/5258 | 2279/3879 | 760/1292 | chr5 | 150036931 | |||
| chr5:150037489 | A | G | 1 | a0008 | 2 | HG02896.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.2375A>G | p.His792Arg | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/20 | 2818/5258 | 2375/3879 | 792/1292 | chr5 | 150037489 | |||
| chr5:150051824 | C | T | 1 | a0015 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.3511C>T | p.Arg1171Cys | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 3954/5258 | 3511/3879 | 1171/1292 | chr5 | 150051824 | |||
| chr5:150051953 | G | A | 1 | a0010 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.3640G>A | p.Gly1214Ser | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 4083/5258 | 3640/3879 | 1214/1292 | chr5 | 150051953 | |||
| chr5:150052176 | C | G | 1 | a0011 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.3863C>G | p.Ala1288Gly | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 4306/5258 | 3863/3879 | 1288/1292 | chr5 | 150052176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:150010245 | A | G | 1 | a0001c0026 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.447A>G | p.Leu149Leu | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/20 | 890/5258 | 447/3879 | 149/1292 | chr5 | 150010245 | |||
| chr5:150018655 | C | T | 1 | a0003c0010 | 3 | HG00544.hp1 HG00673.hp1 NA18964.hp2 |
synonymous_variant | LOW | c.999C>T | p.Cys333Cys | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/20 | 1442/5258 | 999/3879 | 333/1292 | chr5 | 150018655 | |||
| chr5:150024411 | A | G | 2 | a0002c0023 a0015c0024 |
2 | NA19076.hp1 NA19091.hp1 |
synonymous_variant | LOW | c.1191A>G | p.Val397Val | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1634/5258 | 1191/3879 | 397/1292 | chr5 | 150024411 | |||
| chr5:150024483 | C | T | 1 | a0012c0022 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1263C>T | p.Ser421Ser | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1706/5258 | 1263/3879 | 421/1292 | chr5 | 150024483 | |||
| chr5:150024486 | T | C | 1 | a0002c0013 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.1266T>C | p.Asp422Asp | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1709/5258 | 1266/3879 | 422/1292 | chr5 | 150024486 | |||
| chr5:150024630 | C | T | 1 | a0001c0021 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1410C>T | p.Ser470Ser | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/20 | 1853/5258 | 1410/3879 | 470/1292 | chr5 | 150024630 | |||
| chr5:150026793 | C | T | 1 | a0001c0019 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1548C>T | p.Pro516Pro | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 8/20 | 1991/5258 | 1548/3879 | 516/1292 | chr5 | 150026793 | |||
| chr5:150026850 | G | T | 1 | a0004c0007 | 5 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(2): Show |
synonymous_variant | LOW | c.1605G>T | p.Leu535Leu | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 8/20 | 2048/5258 | 1605/3879 | 535/1292 | chr5 | 150026850 | |||
| chr5:150036887 | G | A | 1 | a0010c0015 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.2235G>A | p.Pro745Pro | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 12/20 | 2678/5258 | 2235/3879 | 745/1292 | chr5 | 150036887 | |||
| chr5:150041939 | A | G | 10 | a0001c0003 a0001c0018 a0001c0019 others(7): Show |
106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
synonymous_variant | LOW | c.2700A>G | p.Glu900Glu | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/20 | 3143/5258 | 2700/3879 | 900/1292 | chr5 | 150041939 | |||
| chr5:150048640 | A | G | 1 | a0010c0015 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.3156A>G | p.Pro1052Pro | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/20 | 3599/5258 | 3156/3879 | 1052/1292 | chr5 | 150048640 | |||
| chr5:150051835 | T | C | 1 | a0001c0018 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.3522T>C | p.His1174His | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 3965/5258 | 3522/3879 | 1174/1292 | chr5 | 150051835 | |||
| chr5:150052141 | A | G | 1 | a0001c0017 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.3828A>G | p.Thr1276Thr | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 4271/5258 | 3828/3879 | 1276/1292 | chr5 | 150052141 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:150000832 | T | G | 1 | a0002c0002t0016 | 1 | NA19084.hp1 | 5_prime_UTR_variant | MODIFIER | c.-350T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/20 | 4021 | chr5 | 150000832 | ||||||
| chr5:150000902 | C | T | 5 | a0001c0001t0006 a0001c0003t0006 a0001c0003t0008 others(2): Show |
16 | HG01884.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-280C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/20 | 3951 | chr5 | 150000902 | ||||||
| chr5:150000930 | G | A | 7 | a0003c0004t0004 a0003c0004t0007 a0003c0004t0017 others(4): Show |
49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
5_prime_UTR_variant | MODIFIER | c.-252G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/20 | 3923 | chr5 | 150000930 | ||||||
| chr5:150000990 | G | T | 1 | a0001c0001t0029 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-192G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/20 | 3863 | chr5 | 150000990 | ||||||
| chr5:150052206 | A | G | 1 | a0002c0002t0010 | 5 | NA18939.hp2 NA18965.hp2 NA18968.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*14A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 14 | chr5 | 150052206 | ||||||
| chr5:150052240 | G | A | 3 | a0001c0003t0019 a0001c0003t0020 a0003c0004t0017 |
3 | HG01243.hp1 HG02055.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*48G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 48 | chr5 | 150052240 | ||||||
| chr5:150052367 | T | C | 3 | a0001c0001t0011 a0001c0001t0021 a0001c0003t0030 |
6 | HG02615.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*175T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 175 | chr5 | 150052367 | ||||||
| chr5:150052374 | C | T | 1 | a0005c0006t0009 | 5 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*182C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 182 | chr5 | 150052374 | ||||||
| chr5:150052445 | G | A | 1 | a0001c0001t0021 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*253G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 253 | chr5 | 150052445 | ||||||
| chr5:150052476 | C | G | 51 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(48): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*284C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 284 | chr5 | 150052476 | ||||||
| chr5:150052477 | G | A | 13 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(10): Show |
59 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 285 | chr5 | 150052477 | ||||||
| chr5:150052504 | G | T | 39 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(36): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*312G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 312 | chr5 | 150052504 | ||||||
| chr5:150052571 | C | T | 1 | a0009c0012t0028 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*379C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 379 | chr5 | 150052571 | ||||||
| chr5:150052598 | C | G | 1 | a0004c0007t0024 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*406C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 406 | chr5 | 150052598 | ||||||
| chr5:150052701 | T | C | 1 | a0001c0001t0013 | 2 | HG02273.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*509T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 509 | chr5 | 150052701 | ||||||
| chr5:150052746 | C | T | 1 | a0001c0001t0026 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*554C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 554 | chr5 | 150052746 | ||||||
| chr5:150052894 | G | A | 1 | a0002c0002t0022 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*702G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 702 | chr5 | 150052894 | ||||||
| chr5:150053029 | T | C | 2 | a0002c0023t0014 a0015c0024t0014 |
2 | NA19076.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*837T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 837 | chr5 | 150053029 | ||||||
| chr5:150053050 | A | G | 4 | a0002c0002t0015 a0002c0002t0023 a0003c0004t0007 others(1): Show |
9 | HG00099.hp1 HG00735.hp1 HG01167.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*858A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 858 | chr5 | 150053050 | ||||||
| chr5:150053100 | C | G | 1 | a0001c0001t0027 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*908C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 20/20 | 908 | chr5 | 150053100 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:150001269 | A | G | 1 | a0003c0004t0004g0310 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-3+90A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001269 | |||||||
| chr5:150001448 | A | G | 1 | a0009c0012t0028g0309 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+269A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001448 | |||||||
| chr5:150001685 | G | T | 35 | a0001c0001t0006g0286 a0001c0003t0001g0008 a0001c0003t0001g0293 others(32): Show |
37 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.-3+506G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001685 | |||||||
| chr5:150001709 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-3+530T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001709 | |||||||
| chr5:150001845 | C | T | 1 | a0001c0001t0003g0275 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-3+666C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001845 | |||||||
| chr5:150001856 | A | T | 14 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(11): Show |
14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-3+677A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150001856 | |||||||
| chr5:150002026 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-3+847T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002026 | |||||||
| chr5:150002030 | C | G | 9 | a0001c0003t0005g0038 a0001c0003t0005g0267 a0001c0003t0005g0268 others(6): Show |
10 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+851C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002030 | |||||||
| chr5:150002259 | T | C | 4 | a0001c0001t0011g0015 a0001c0001t0011g0046 a0001c0001t0011g0047 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+1080T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002259 | |||||||
| chr5:150002372 | G | T | 1 | a0001c0001t0003g0266 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-3+1193G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002372 | |||||||
| chr5:150002375 | T | A | 3 | a0001c0003t0005g0267 a0001c0003t0005g0268 a0001c0003t0005g0269 |
3 | HG01891.hp1 HG01981.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-3+1196T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002375 | |||||||
| chr5:150002389 | A | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(138): Show |
154 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-3+1210A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002389 | |||||||
| chr5:150002430 | A | C | 14 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0011g0141 others(11): Show |
15 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+1251A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002430 | |||||||
| chr5:150002550 | C | T | 1 | a0009c0012t0028g0309 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+1371C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002550 | |||||||
| chr5:150002845 | G | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(103): Show |
118 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-3+1666G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002845 | |||||||
| chr5:150002954 | A | G | 4 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0139 others(1): Show |
4 | HG00597.hp1 HG03834.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+1775A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150002954 | |||||||
| chr5:150003170 | T | G | 1 | a0002c0002t0002g0041 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-2-1681T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003170 | |||||||
| chr5:150003268 | C | A | 3 | a0001c0001t0003g0146 a0001c0001t0003g0147 a0001c0001t0003g0148 |
3 | HG02148.hp2 HG02273.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-2-1583C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003268 | |||||||
| chr5:150003349 | G | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0011g0141 |
3 | HG02109.hp1 HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-2-1502G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003349 | |||||||
| chr5:150003482 | C | T | 4 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(1): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-1369C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003482 | |||||||
| chr5:150003578 | C | G | 6 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0134 others(3): Show |
7 | HG01243.hp2 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-1273C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003578 | |||||||
| chr5:150003619 | T | C | 1 | a0002c0002t0002g0042 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-2-1232T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003619 | |||||||
| chr5:150003634 | A | AT | 141 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(138): Show |
154 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-2-1208dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 150003634 | ||||||
| chr5:150003678 | A | T | 234 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(231): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-2-1173A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003678 | |||||||
| chr5:150003687 | T | C | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-2-1164T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003687 | |||||||
| chr5:150003743 | C | T | 3 | a0002c0002t0001g0104 a0002c0002t0002g0011 a0002c0002t0002g0103 |
5 | NA18941.hp1 NA18989.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-1108C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003743 | |||||||
| chr5:150003748 | G | A | 6 | a0004c0005t0001g0234 a0004c0005t0001g0235 a0004c0005t0001g0236 others(3): Show |
6 | HG02258.hp1 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-1103G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003748 | |||||||
| chr5:150003816 | C | T | 35 | a0001c0001t0006g0286 a0001c0003t0001g0008 a0001c0003t0001g0293 others(32): Show |
37 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.-2-1035C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003816 | |||||||
| chr5:150003893 | G | A | 2 | a0002c0002t0002g0043 a0002c0002t0002g0044 |
2 | HG00140.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.-2-958G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003893 | |||||||
| chr5:150003948 | AAAAAAC | A | 5 | a0001c0001t0001g0045 a0001c0001t0011g0015 a0001c0001t0011g0046 others(2): Show |
5 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-891_-2-886delCA others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 150003948 | ||||||
| chr5:150003953 | ACAAAAAC others(8): Show |
A | 1 | a0001c0001t0003g0193 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-2-887_-2-873delAA others(13): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 150003953 | ||||||
| chr5:150003977 | A | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0005c0006t0005g0009 others(3): Show |
11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-874A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003977 | |||||||
| chr5:150003993 | A | G | 6 | a0004c0005t0002g0261 a0004c0007t0002g0262 a0004c0007t0002g0263 others(3): Show |
6 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-858A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150003993 | |||||||
| chr5:150004011 | CT | C | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0003t0008g0276 others(7): Show |
10 | HG01169.hp2 HG02132.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-827delT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr5 | 150004011 | ||||||
| chr5:150004137 | G | A | 1 | a0001c0001t0003g0151 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-2-714G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004137 | |||||||
| chr5:150004213 | A | G | 56 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0011g0141 others(53): Show |
71 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-2-638A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004213 | |||||||
| chr5:150004308 | A | C | 91 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0006g0286 others(88): Show |
108 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.-2-543A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004308 | |||||||
| chr5:150004391 | G | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(242): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-2-460G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004391 | |||||||
| chr5:150004413 | A | G | 56 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0011g0141 others(53): Show |
71 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-2-438A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004413 | |||||||
| chr5:150004565 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0011g0015 a0001c0001t0011g0046 others(2): Show |
5 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-286C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004565 | |||||||
| chr5:150004590 | C | T | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-2-261C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004590 | |||||||
| chr5:150004591 | G | A | 5 | a0001c0001t0001g0045 a0001c0001t0011g0015 a0001c0001t0011g0046 others(2): Show |
5 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-260G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004591 | |||||||
| chr5:150004642 | T | C | 1 | a0003c0004t0004g0106 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-2-209T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004642 | |||||||
| chr5:150004648 | G | T | 3 | a0001c0003t0006g0292 a0001c0003t0008g0276 a0001c0003t0030g0291 |
3 | HG02886.hp1 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-2-203G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 1/19 | chr5 | 150004648 | |||||||
| chr5:150005047 | C | T | 10 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0052 others(7): Show |
14 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.137+58C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005047 | |||||||
| chr5:150005112 | G | A | 36 | a0003c0004t0004g0001 a0003c0004t0004g0012 a0003c0004t0004g0024 others(33): Show |
49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.137+123G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005112 | |||||||
| chr5:150005117 | A | G | 245 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(242): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.137+128A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005117 | |||||||
| chr5:150005162 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0033 others(7): Show |
12 | HG01346.hp1 HG01358.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.137+173C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005162 | |||||||
| chr5:150005254 | A | G | 1 | a0001c0001t0003g0233 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.137+265A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005254 | |||||||
| chr5:150005332 | G | T | 53 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(50): Show |
68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.137+343G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005332 | |||||||
| chr5:150005381 | C | T | 32 | a0001c0001t0006g0286 a0001c0003t0001g0008 a0001c0003t0001g0293 others(29): Show |
34 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.137+392C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005381 | |||||||
| chr5:150005468 | G | A | 53 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(50): Show |
68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.137+479G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005468 | |||||||
| chr5:150005539 | C | T | 20 | a0001c0001t0006g0286 a0001c0003t0001g0008 a0001c0003t0001g0293 others(17): Show |
22 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.137+550C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005539 | |||||||
| chr5:150005540 | G | A | 1 | a0003c0004t0004g0310 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.137+551G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005540 | |||||||
| chr5:150005598 | C | CAA | 16 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(13): Show |
18 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+624_137+625dup others(2): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 150005598 | ||||||
| chr5:150005598 | C | CAAA | 35 | a0001c0003t0005g0270 a0003c0004t0004g0001 a0003c0004t0004g0012 others(32): Show |
48 | HG00099.hp1 HG00544.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.137+623_137+625dup others(3): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr5 | 150005598 | ||||||
| chr5:150005610 | A | G | 37 | a0002c0002t0001g0020 a0002c0002t0001g0080 a0002c0002t0002g0007 others(34): Show |
46 | HG00597.hp1 HG01106.hp2 HG01952.hp1 others(43): Show |
intron_variant | MODIFIER | c.137+621A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005610 | |||||||
| chr5:150005634 | A | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(241): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.137+645A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005634 | |||||||
| chr5:150005660 | A | C | 1 | a0004c0005t0001g0259 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.137+671A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005660 | |||||||
| chr5:150005831 | C | T | 53 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(50): Show |
68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-642C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005831 | |||||||
| chr5:150005862 | G | A | 53 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(50): Show |
68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-611G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005862 | |||||||
| chr5:150005944 | A | G | 1 | a0001c0003t0008g0290 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.138-529A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150005944 | |||||||
| chr5:150006309 | T | G | 36 | a0003c0004t0004g0001 a0003c0004t0004g0012 a0003c0004t0004g0024 others(33): Show |
49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.138-164T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150006309 | |||||||
| chr5:150006353 | C | T | 2 | a0001c0001t0001g0230 a0001c0003t0005g0231 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.138-120C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 2/19 | chr5 | 150006353 | |||||||
| chr5:150006751 | G | C | 90 | a0001c0001t0006g0286 a0001c0003t0001g0008 a0001c0003t0001g0293 others(87): Show |
107 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.312+104G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150006751 | |||||||
| chr5:150006759 | G | A | 2 | a0001c0001t0001g0152 a0004c0005t0001g0234 |
2 | HG02129.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.312+112G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150006759 | |||||||
| chr5:150006843 | C | T | 2 | a0002c0002t0002g0021 a0002c0002t0002g0094 |
3 | NA18950.hp2 NA18982.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.312+196C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150006843 | |||||||
| chr5:150006913 | T | A | 1 | a0002c0002t0002g0072 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.312+266T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150006913 | |||||||
| chr5:150007153 | G | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(240): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.312+506G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007153 | |||||||
| chr5:150007223 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.312+576C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007223 | |||||||
| chr5:150007276 | C | T | 1 | a0001c0003t0005g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.312+629C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007276 | |||||||
| chr5:150007355 | C | G | 1 | a0001c0001t0003g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.312+708C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007355 | |||||||
| chr5:150007446 | A | C | 2 | a0005c0006t0009g0010 a0005c0006t0009g0102 |
4 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+799A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007446 | |||||||
| chr5:150007731 | T | C | 1 | a0001c0001t0003g0266 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.312+1084T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007731 | |||||||
| chr5:150007926 | A | G | 3 | a0001c0003t0006g0287 a0001c0003t0006g0288 a0001c0003t0006g0289 |
3 | HG02572.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.312+1279A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007926 | |||||||
| chr5:150007963 | G | A | 1 | a0003c0004t0007g0107 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.312+1316G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007963 | |||||||
| chr5:150007980 | C | A | 8 | a0002c0002t0002g0007 a0002c0002t0002g0019 a0002c0002t0002g0042 others(5): Show |
12 | HG01106.hp2 HG01952.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.312+1333C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150007980 | |||||||
| chr5:150008054 | T | TTC | 6 | a0001c0001t0011g0047 a0001c0001t0011g0141 a0001c0003t0005g0231 others(3): Show |
6 | HG00735.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+1408_312+1409d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008054 | ||||||
| chr5:150008055 | T | TCA | 12 | a0002c0002t0002g0019 a0002c0002t0002g0044 a0002c0002t0002g0052 others(9): Show |
13 | HG01168.hp2 HG01169.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.312+1451_312+1452d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | ||||||
| chr5:150008055 | T | TCTCA | 11 | a0001c0001t0001g0023 a0001c0001t0001g0143 a0001c0001t0011g0015 others(8): Show |
14 | HG01243.hp2 HG01993.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.312+1409_312+1410i others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | ||||||
| chr5:150008055 | T | TCTCACA | 12 | a0003c0004t0004g0127 a0003c0004t0004g0129 a0003c0004t0007g0028 others(9): Show |
14 | HG00099.hp1 HG00544.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.312+1409_312+1410i others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | ||||||
| chr5:150008055 | T | TCTCACAC others(1): Show |
3 | a0001c0001t0001g0142 a0003c0004t0004g0026 a0003c0004t0017g0122 |
4 | HG01243.hp1 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+1409_312+1410i others(10): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | ||||||
| chr5:150008055 | T | TCTCACAC others(3): Show |
1 | a0003c0004t0004g0121 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.312+1409_312+1410i others(12): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | ||||||
| chr5:150008055 | T | TCTCACAC others(5): Show |
1 | a0001c0001t0001g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.312+1409_312+1410i others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | ||||||
| chr5:150008055 | TCA | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0032 others(117): Show |
134 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.312+1451_312+1452d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | ||||||
| chr5:150008055 | TCACA | T | 26 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0163 others(23): Show |
27 | HG00597.hp1 HG01256.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.312+1449_312+1452d others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | ||||||
| chr5:150008055 | TCACACA | T | 11 | a0001c0001t0001g0031 a0001c0001t0001g0157 a0001c0001t0001g0160 others(8): Show |
12 | HG01192.hp2 HG02074.hp2 HG03471.hp1 others(9): Show |
intron_variant | MODIFIER | c.312+1447_312+1452d others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | ||||||
| chr5:150008055 | TCACACAC others(3): Show |
T | 1 | a0002c0002t0002g0077 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.312+1443_312+1452d others(12): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | ||||||
| chr5:150008055 | TCACACAC others(7): Show |
T | 4 | a0001c0001t0001g0154 a0001c0001t0002g0153 a0001c0001t0002g0155 others(1): Show |
4 | HG01071.hp2 HG01891.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+1439_312+1452d others(16): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008055 | ||||||
| chr5:150008057 | A | T | 22 | a0001c0001t0013g0217 a0001c0003t0005g0029 a0001c0003t0005g0134 others(19): Show |
22 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.312+1410A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008057 | |||||||
| chr5:150008059 | A | T | 38 | a0001c0001t0003g0227 a0001c0001t0006g0286 a0001c0001t0013g0228 others(35): Show |
39 | HG01884.hp2 HG02135.hp2 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.312+1412A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008059 | |||||||
| chr5:150008061 | A | T | 10 | a0001c0003t0001g0300 a0001c0003t0006g0281 a0001c0003t0006g0288 others(7): Show |
10 | HG02055.hp1 HG02886.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+1414A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008061 | |||||||
| chr5:150008063 | A | T | 4 | a0001c0003t0006g0287 a0004c0005t0001g0235 a0004c0005t0001g0242 others(1): Show |
4 | HG02074.hp2 HG03471.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+1416A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008063 | |||||||
| chr5:150008094 | C | CACACAT | 9 | a0003c0004t0004g0024 a0003c0004t0004g0110 a0003c0004t0004g0111 others(6): Show |
10 | HG00597.hp2 HG00673.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+1452_312+1453i others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008094 | ||||||
| chr5:150008094 | C | CACAT | 9 | a0003c0004t0004g0001 a0003c0004t0004g0012 a0003c0004t0004g0106 others(6): Show |
18 | HG01433.hp2 HG01496.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.312+1450_312+1451i others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008094 | ||||||
| chr5:150008094 | C | T | 52 | a0001c0001t0001g0045 a0001c0001t0001g0142 a0001c0001t0001g0143 others(49): Show |
57 | HG00099.hp1 HG00544.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.312+1447C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008094 | |||||||
| chr5:150008099 | A | AC | 3 | a0002c0002t0002g0004 a0002c0002t0002g0018 a0015c0024t0014g0082 |
3 | HG02027.hp1 NA18998.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.312+1452_312+1453i others(3): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008099 | |||||||
| chr5:150008250 | A | C | 4 | a0005c0006t0005g0009 a0005c0006t0009g0010 a0005c0006t0009g0100 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1603A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008250 | |||||||
| chr5:150008254 | A | T | 2 | a0001c0001t0003g0216 a0011c0016t0003g0226 |
2 | HG01175.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.312+1607A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008254 | |||||||
| chr5:150008290 | A | AGTTCTT | 4 | a0005c0006t0005g0009 a0005c0006t0009g0010 a0005c0006t0009g0100 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1644_312+1645i others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | 150008290 | ||||||
| chr5:150008292 | G | A | 1 | a0001c0001t0011g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.312+1645G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008292 | |||||||
| chr5:150008295 | A | C | 4 | a0005c0006t0005g0009 a0005c0006t0009g0010 a0005c0006t0009g0100 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1648A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008295 | |||||||
| chr5:150008296 | G | T | 4 | a0005c0006t0005g0009 a0005c0006t0009g0010 a0005c0006t0009g0100 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1649G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008296 | |||||||
| chr5:150008297 | T | TGGCTA | 4 | a0005c0006t0005g0009 a0005c0006t0009g0010 a0005c0006t0009g0100 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+1650_312+1651i others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008297 | |||||||
| chr5:150008777 | C | T | 53 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(50): Show |
68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.313-1334C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008777 | |||||||
| chr5:150008905 | G | A | 1 | a0003c0004t0007g0131 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.313-1206G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008905 | |||||||
| chr5:150008962 | C | T | 1 | a0002c0002t0002g0215 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.313-1149C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150008962 | |||||||
| chr5:150009061 | T | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(138): Show |
154 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.313-1050T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009061 | |||||||
| chr5:150009301 | T | C | 36 | a0003c0004t0004g0001 a0003c0004t0004g0012 a0003c0004t0004g0024 others(33): Show |
49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.313-810T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009301 | |||||||
| chr5:150009370 | A | T | 1 | a0004c0005t0001g0256 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.313-741A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009370 | |||||||
| chr5:150009641 | T | C | 3 | a0001c0001t0001g0154 a0001c0001t0002g0153 a0001c0001t0002g0155 |
3 | HG01071.hp2 HG02683.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.313-470T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009641 | |||||||
| chr5:150009777 | G | A | 1 | a0002c0002t0002g0057 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.313-334G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009777 | |||||||
| chr5:150009814 | T | G | 4 | a0003c0004t0004g0001 a0003c0004t0004g0110 a0003c0004t0004g0116 others(1): Show |
10 | HG01433.hp2 HG01496.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.313-297T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009814 | |||||||
| chr5:150009902 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(137): Show |
153 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.313-209C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150009902 | |||||||
| chr5:150010010 | A | G | 36 | a0003c0004t0004g0001 a0003c0004t0004g0012 a0003c0004t0004g0024 others(33): Show |
49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.313-101A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150010010 | |||||||
| chr5:150010084 | C | T | 15 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(12): Show |
15 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.313-27C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150010084 | |||||||
| chr5:150010109 | A | C | 1 | a0001c0001t0003g0151 | 1 | NA18955.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.313-2A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 3/19 | chr5 | 150010109 | |||||||
| chr5:150010659 | G | C | 9 | a0001c0003t0005g0038 a0001c0003t0005g0267 a0001c0003t0005g0268 others(6): Show |
10 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.810+51G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150010659 | |||||||
| chr5:150010899 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.810+291C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150010899 | |||||||
| chr5:150010906 | A | G | 1 | a0003c0004t0004g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.810+298A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150010906 | |||||||
| chr5:150011109 | C | G | 6 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0134 others(3): Show |
7 | HG01243.hp2 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.810+501C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011109 | |||||||
| chr5:150011244 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.810+636G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011244 | |||||||
| chr5:150011245 | G | A | 3 | a0005c0006t0009g0010 a0005c0006t0009g0100 a0005c0006t0009g0102 |
5 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.810+637G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011245 | |||||||
| chr5:150011337 | G | A | 1 | a0002c0002t0002g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.810+729G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011337 | |||||||
| chr5:150011384 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(242): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.810+776T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011384 | |||||||
| chr5:150011459 | T | C | 1 | a0001c0001t0003g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.811-796T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011459 | |||||||
| chr5:150011594 | T | A | 1 | a0001c0003t0001g0302 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.811-661T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011594 | |||||||
| chr5:150011594 | T | G | 308 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(305): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.811-661T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011594 | |||||||
| chr5:150011603 | G | GT | 45 | a0001c0001t0006g0286 a0001c0003t0001g0008 a0001c0003t0001g0294 others(42): Show |
48 | HG00735.hp2 HG01884.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.811-652_811-651ins others(1): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011603 | |||||||
| chr5:150011604 | G | GT | 51 | a0001c0001t0001g0034 a0001c0001t0001g0150 a0001c0001t0001g0169 others(48): Show |
52 | HG00140.hp2 HG00621.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.811-634dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr5 | 150011604 | ||||||
| chr5:150011604 | G | T | 53 | a0001c0001t0006g0286 a0001c0003t0001g0008 a0001c0003t0001g0293 others(50): Show |
57 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(54): Show |
intron_variant | MODIFIER | c.811-651G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011604 | |||||||
| chr5:150011623 | A | T | 1 | a0001c0001t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.811-632A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011623 | |||||||
| chr5:150011667 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.811-588C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011667 | |||||||
| chr5:150011814 | G | A | 17 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(14): Show |
19 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.811-441G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011814 | |||||||
| chr5:150011822 | G | A | 1 | a0002c0002t0002g0215 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.811-433G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011822 | |||||||
| chr5:150011844 | T | A | 2 | a0002c0002t0002g0016 a0002c0002t0002g0058 |
3 | HG01257.hp2 HG01258.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.811-411T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011844 | |||||||
| chr5:150011907 | C | T | 1 | a0002c0002t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.811-348C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011907 | |||||||
| chr5:150011913 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.811-342C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150011913 | |||||||
| chr5:150012042 | T | G | 1 | a0009c0012t0028g0309 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.811-213T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150012042 | |||||||
| chr5:150012066 | C | T | 3 | a0001c0003t0005g0030 a0001c0003t0005g0135 a0001c0018t0005g0136 |
4 | HG01243.hp2 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-189C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150012066 | |||||||
| chr5:150012240 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.811-15C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 4/19 | chr5 | 150012240 | |||||||
| chr5:150012494 | G | C | 1 | a0002c0002t0003g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.909+141G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012494 | |||||||
| chr5:150012580 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.909+227A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012580 | |||||||
| chr5:150012655 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.909+302A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012655 | |||||||
| chr5:150012743 | C | T | 2 | a0004c0005t0001g0242 a0004c0005t0001g0243 |
2 | HG02074.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.909+390C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012743 | |||||||
| chr5:150012762 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0005c0006t0005g0009 others(3): Show |
11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+409C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012762 | |||||||
| chr5:150012814 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(137): Show |
153 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.909+461C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012814 | |||||||
| chr5:150012843 | T | C | 1 | a0007c0009t0004g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.909+490T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012843 | |||||||
| chr5:150012972 | T | C | 2 | a0002c0002t0002g0054 a0002c0002t0002g0059 |
2 | HG02698.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.909+619T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150012972 | |||||||
| chr5:150013353 | G | C | 6 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0134 others(3): Show |
7 | HG01243.hp2 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.909+1000G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013353 | |||||||
| chr5:150013407 | G | A | 1 | a0001c0003t0005g0267 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.909+1054G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013407 | |||||||
| chr5:150013443 | G | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(240): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.909+1090G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013443 | |||||||
| chr5:150013538 | A | G | 4 | a0002c0002t0002g0042 a0002c0002t0002g0073 a0002c0002t0002g0074 others(1): Show |
4 | NA18612.hp2 NA18942.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+1185A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013538 | |||||||
| chr5:150013657 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0210 |
2 | HG00621.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.909+1304A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013657 | |||||||
| chr5:150013756 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0101 |
3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.909+1403C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013756 | |||||||
| chr5:150013834 | A | G | 2 | a0001c0003t0001g0308 a0001c0003t0005g0299 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.909+1481A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013834 | |||||||
| chr5:150013842 | A | G | 2 | a0001c0003t0001g0308 a0001c0003t0005g0299 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.909+1489A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150013842 | |||||||
| chr5:150014061 | C | A | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.909+1708C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014061 | |||||||
| chr5:150014078 | G | T | 1 | a0003c0004t0004g0115 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.909+1725G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014078 | |||||||
| chr5:150014238 | A | G | 1 | a0003c0004t0007g0107 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.909+1885A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014238 | |||||||
| chr5:150014331 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | NA18999.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.909+1978C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014331 | |||||||
| chr5:150014559 | C | G | 1 | a0001c0001t0003g0207 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.909+2206C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014559 | |||||||
| chr5:150014740 | A | G | 4 | a0001c0001t0001g0206 a0001c0001t0003g0203 a0001c0001t0003g0204 others(1): Show |
4 | NA18991.hp1 NA18992.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+2387A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014740 | |||||||
| chr5:150014848 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.909+2495G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014848 | |||||||
| chr5:150014892 | A | G | 2 | a0001c0001t0003g0166 a0001c0001t0003g0167 |
2 | HG01256.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.909+2539A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014892 | |||||||
| chr5:150014910 | C | T | 1 | a0001c0003t0019g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.909+2557C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014910 | |||||||
| chr5:150014941 | G | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0005c0006t0005g0009 others(3): Show |
11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+2588G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150014941 | |||||||
| chr5:150015019 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.909+2666A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015019 | |||||||
| chr5:150015023 | C | T | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.909+2670C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015023 | |||||||
| chr5:150015095 | C | G | 2 | a0002c0002t0002g0043 a0002c0002t0002g0044 |
2 | HG00140.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.909+2742C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015095 | |||||||
| chr5:150015110 | C | T | 1 | a0004c0005t0001g0241 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.909+2757C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015110 | |||||||
| chr5:150015141 | C | A | 53 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(50): Show |
68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.909+2788C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015141 | |||||||
| chr5:150015253 | G | A | 1 | a0004c0005t0001g0246 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.909+2900G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015253 | |||||||
| chr5:150015278 | C | CTTTCT | 17 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(14): Show |
19 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.909+2944_909+2948d others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 150015278 | ||||||
| chr5:150015290 | T | C | 1 | a0001c0001t0003g0173 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.909+2937T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015290 | |||||||
| chr5:150015309 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(241): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.909+2956A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015309 | |||||||
| chr5:150015391 | C | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
151 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.909+3038C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015391 | |||||||
| chr5:150015402 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
151 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.909+3049A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015402 | |||||||
| chr5:150015504 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01109.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.910-3062T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015504 | |||||||
| chr5:150015578 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0009c0012t0028g0309 |
4 | HG02451.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-2988C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015578 | |||||||
| chr5:150015673 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0169 |
2 | HG03831.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.910-2893T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015673 | |||||||
| chr5:150015691 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
151 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.910-2875A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015691 | |||||||
| chr5:150015797 | T | C | 1 | a0001c0021t0006g0282 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.910-2769T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150015797 | |||||||
| chr5:150016048 | T | A | 1 | a0001c0001t0003g0275 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.910-2518T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016048 | |||||||
| chr5:150016197 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0003g0158 |
3 | HG03491.hp1 HG03492.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.910-2369G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016197 | |||||||
| chr5:150016340 | C | CA | 7 | a0002c0002t0002g0055 a0002c0002t0002g0059 a0002c0002t0002g0060 others(4): Show |
7 | HG00438.hp2 HG01243.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-2205dupA | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 150016340 | ||||||
| chr5:150016340 | CA | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(119): Show |
138 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.910-2205delA | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 150016340 | ||||||
| chr5:150016340 | CAA | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0001c0001t0001g0154 others(10): Show |
14 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-2206_910-2205d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 150016340 | ||||||
| chr5:150016359 | AAAGG | A | 30 | a0002c0002t0001g0258 a0004c0005t0001g0036 a0004c0005t0001g0234 others(27): Show |
31 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.910-2205_910-2202d others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr5 | 150016359 | ||||||
| chr5:150016441 | T | C | 14 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(11): Show |
14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-2125T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016441 | |||||||
| chr5:150016503 | A | G | 9 | a0001c0001t0001g0045 a0001c0001t0001g0142 a0001c0001t0001g0143 others(6): Show |
9 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-2063A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016503 | |||||||
| chr5:150016564 | A | G | 1 | a0001c0003t0008g0290 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.910-2002A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016564 | |||||||
| chr5:150016596 | C | A | 205 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(202): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.910-1970C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016596 | |||||||
| chr5:150016952 | A | G | 90 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(87): Show |
107 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.910-1614A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016952 | |||||||
| chr5:150016971 | T | G | 90 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(87): Show |
107 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.910-1595T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150016971 | |||||||
| chr5:150017009 | G | A | 1 | a0001c0017t0003g0199 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.910-1557G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017009 | |||||||
| chr5:150017083 | C | T | 90 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(87): Show |
107 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.910-1483C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017083 | |||||||
| chr5:150017541 | C | G | 36 | a0003c0004t0004g0001 a0003c0004t0004g0012 a0003c0004t0004g0024 others(33): Show |
49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.910-1025C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017541 | |||||||
| chr5:150017624 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.910-942A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017624 | |||||||
| chr5:150017874 | C | T | 33 | a0002c0002t0001g0258 a0004c0005t0001g0036 a0004c0005t0001g0234 others(30): Show |
34 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.910-692C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017874 | |||||||
| chr5:150017896 | G | C | 1 | a0002c0002t0001g0080 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.910-670G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150017896 | |||||||
| chr5:150018008 | A | G | 12 | a0002c0002t0001g0004 a0002c0002t0001g0104 a0002c0002t0002g0004 others(9): Show |
18 | HG00438.hp2 HG00609.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.910-558A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018008 | |||||||
| chr5:150018057 | G | C | 4 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(1): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-509G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018057 | |||||||
| chr5:150018162 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.910-404G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018162 | |||||||
| chr5:150018261 | A | G | 1 | a0001c0003t0006g0288 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.910-305A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018261 | |||||||
| chr5:150018281 | T | C | 2 | a0004c0005t0001g0244 a0004c0005t0001g0246 |
2 | NA18946.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.910-285T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018281 | |||||||
| chr5:150018299 | A | G | 11 | a0001c0001t0001g0171 a0001c0001t0001g0224 a0001c0001t0002g0201 others(8): Show |
11 | HG00099.hp2 HG01069.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-267A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018299 | |||||||
| chr5:150018365 | C | T | 2 | a0003c0004t0007g0028 a0003c0004t0007g0130 |
3 | HG00099.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.910-201C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018365 | |||||||
| chr5:150018396 | A | C | 1 | a0017c0020t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.910-170A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 5/19 | chr5 | 150018396 | |||||||
| chr5:150018917 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(100): Show |
115 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1041+220A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150018917 | |||||||
| chr5:150018992 | C | T | 36 | a0003c0004t0004g0001 a0003c0004t0004g0012 a0003c0004t0004g0024 others(33): Show |
49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1041+295C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150018992 | |||||||
| chr5:150019026 | C | T | 1 | a0001c0001t0013g0228 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1041+329C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019026 | |||||||
| chr5:150019048 | A | C | 1 | a0003c0004t0004g0113 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1041+351A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019048 | |||||||
| chr5:150019058 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1041+361C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019058 | |||||||
| chr5:150019272 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1041+575C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019272 | |||||||
| chr5:150019279 | A | G | 17 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(14): Show |
19 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1041+582A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019279 | |||||||
| chr5:150019602 | G | A | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1041+905G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019602 | |||||||
| chr5:150019627 | C | G | 34 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(31): Show |
36 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1041+930C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019627 | |||||||
| chr5:150019679 | G | A | 1 | a0004c0007t0024g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1041+982G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019679 | |||||||
| chr5:150019733 | A | G | 37 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(34): Show |
39 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1041+1036A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019733 | |||||||
| chr5:150019767 | G | A | 36 | a0003c0004t0004g0001 a0003c0004t0004g0012 a0003c0004t0004g0024 others(33): Show |
49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1041+1070G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019767 | |||||||
| chr5:150019780 | T | A | 2 | a0001c0001t0013g0217 a0001c0001t0013g0228 |
2 | HG02273.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1041+1083T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019780 | |||||||
| chr5:150019884 | T | G | 1 | a0004c0005t0001g0244 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1041+1187T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150019884 | |||||||
| chr5:150020094 | G | A | 1 | a0001c0003t0006g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1041+1397G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020094 | |||||||
| chr5:150020191 | A | G | 1 | a0001c0003t0001g0294 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1041+1494A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020191 | |||||||
| chr5:150020405 | G | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(132): Show |
148 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1041+1708G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020405 | |||||||
| chr5:150020497 | C | G | 1 | a0001c0001t0001g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1041+1800C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020497 | |||||||
| chr5:150020587 | T | C | 1 | a0003c0004t0007g0131 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1041+1890T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020587 | |||||||
| chr5:150020718 | C | A | 1 | a0001c0001t0003g0233 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1041+2021C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020718 | |||||||
| chr5:150020746 | C | CT | 74 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0001c0001t0001g0214 others(71): Show |
82 | HG00621.hp2 HG00639.hp1 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.1041+2065dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150020746 | ||||||
| chr5:150020746 | C | CTTT | 31 | a0003c0004t0004g0001 a0003c0004t0004g0012 a0003c0004t0004g0024 others(28): Show |
43 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1041+2063_1041+206 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150020746 | ||||||
| chr5:150020746 | C | CTTTT | 21 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(18): Show |
24 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1041+2062_1041+206 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150020746 | ||||||
| chr5:150020907 | G | A | 35 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(32): Show |
37 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1041+2210G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020907 | |||||||
| chr5:150020963 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0101 |
3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1041+2266G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150020963 | |||||||
| chr5:150021025 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1041+2328T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021025 | |||||||
| chr5:150021155 | C | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(242): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1041+2458C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021155 | |||||||
| chr5:150021360 | A | G | 1 | a0001c0003t0008g0280 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1041+2663A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021360 | |||||||
| chr5:150021472 | T | C | 1 | a0017c0020t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1041+2775T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021472 | |||||||
| chr5:150021519 | A | G | 2 | a0008c0011t0001g0037 a0008c0011t0005g0037 |
2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1042-2743A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021519 | |||||||
| chr5:150021618 | G | A | 1 | a0002c0002t0005g0061 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1042-2644G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021618 | |||||||
| chr5:150021761 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1042-2501G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021761 | |||||||
| chr5:150021767 | A | T | 1 | a0004c0005t0015g0239 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1042-2495A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021767 | |||||||
| chr5:150021968 | C | G | 1 | a0001c0001t0003g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1042-2294C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150021968 | |||||||
| chr5:150022033 | T | C | 237 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(234): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1042-2229T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022033 | |||||||
| chr5:150022059 | T | TATG | 90 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(87): Show |
107 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.1042-2201_1042-220 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022059 | ||||||
| chr5:150022077 | ATTAT | A | 3 | a0008c0011t0001g0037 a0008c0011t0005g0037 a0017c0020t0001g0277 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1042-2182_1042-217 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022077 | ||||||
| chr5:150022211 | C | G | 6 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0134 others(3): Show |
7 | HG01243.hp2 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1042-2051C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022211 | |||||||
| chr5:150022275 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1042-1987C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022275 | |||||||
| chr5:150022348 | T | C | 1 | a0002c0002t0002g0073 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1042-1914T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022348 | |||||||
| chr5:150022550 | C | T | 36 | a0003c0004t0004g0001 a0003c0004t0004g0012 a0003c0004t0004g0024 others(33): Show |
49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1042-1712C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022550 | |||||||
| chr5:150022647 | G | A | 17 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(14): Show |
19 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1042-1615G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022647 | |||||||
| chr5:150022817 | C | CT | 144 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(141): Show |
162 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.1042-1426dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022817 | ||||||
| chr5:150022817 | C | CTT | 12 | a0001c0001t0001g0161 a0001c0001t0003g0197 a0001c0001t0011g0015 others(9): Show |
12 | HG01934.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1042-1427_1042-142 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022817 | ||||||
| chr5:150022817 | CT | C | 19 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(16): Show |
22 | HG01257.hp2 HG01258.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1042-1426delT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022817 | ||||||
| chr5:150022857 | G | A | 2 | a0001c0003t0006g0289 a0001c0021t0006g0282 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1042-1405G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022857 | |||||||
| chr5:150022885 | C | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(136): Show |
152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1042-1377C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022885 | |||||||
| chr5:150022901 | C | T | 1 | a0001c0003t0001g0294 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1042-1361C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022901 | |||||||
| chr5:150022927 | C | T | 1 | a0001c0003t0005g0267 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1042-1335C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150022927 | |||||||
| chr5:150022986 | A | AT | 10 | a0001c0003t0003g0297 a0001c0003t0008g0279 a0001c0003t0008g0285 others(7): Show |
11 | HG02027.hp1 HG02071.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.1042-1253dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022986 | ||||||
| chr5:150022986 | AT | A | 101 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0101 others(98): Show |
121 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.1042-1253delT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022986 | ||||||
| chr5:150022986 | ATTT | A | 6 | a0001c0001t0001g0195 a0001c0001t0001g0223 a0001c0001t0003g0170 others(3): Show |
6 | HG00738.hp2 HG01175.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042-1255_1042-125 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022986 | ||||||
| chr5:150022986 | ATTTT | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(96): Show |
110 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1042-1256_1042-125 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr5 | 150022986 | ||||||
| chr5:150023300 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0229 |
2 | NA18959.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1042-962C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023300 | |||||||
| chr5:150023342 | A | G | 87 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(84): Show |
104 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1042-920A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023342 | |||||||
| chr5:150023379 | A | G | 20 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(17): Show |
22 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1042-883A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023379 | |||||||
| chr5:150023395 | T | C | 2 | a0002c0023t0014g0093 a0015c0024t0014g0082 |
2 | NA19076.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1042-867T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023395 | |||||||
| chr5:150023537 | C | T | 81 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(78): Show |
97 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.1042-725C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023537 | |||||||
| chr5:150023538 | G | A | 138 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
151 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1042-724G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023538 | |||||||
| chr5:150023630 | G | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(240): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1042-632G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023630 | |||||||
| chr5:150023779 | T | A | 2 | a0003c0010t0004g0027 a0003c0010t0004g0124 |
3 | HG00544.hp1 HG00673.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1042-483T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023779 | |||||||
| chr5:150023965 | C | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(224): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1042-297C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150023965 | |||||||
| chr5:150024170 | A | C | 1 | a0001c0001t0001g0192 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1042-92A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 6/19 | chr5 | 150024170 | |||||||
| chr5:150024727 | G | A | 3 | a0008c0011t0001g0037 a0008c0011t0005g0037 a0017c0020t0001g0277 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1460+47G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150024727 | |||||||
| chr5:150024817 | C | T | 1 | a0003c0004t0004g0127 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1460+137C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150024817 | |||||||
| chr5:150024916 | A | G | 3 | a0004c0005t0001g0235 a0004c0005t0001g0236 a0004c0005t0005g0238 |
3 | HG02809.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1460+236A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150024916 | |||||||
| chr5:150025008 | T | G | 3 | a0007c0009t0004g0123 a0007c0009t0004g0125 a0007c0009t0004g0126 |
3 | HG02280.hp2 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1460+328T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025008 | |||||||
| chr5:150025178 | G | A | 1 | a0001c0001t0003g0218 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1460+498G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025178 | |||||||
| chr5:150025353 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0210 a0004c0005t0001g0257 |
3 | HG00621.hp1 HG03579.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1460+673A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025353 | |||||||
| chr5:150025373 | A | G | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1460+693A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025373 | |||||||
| chr5:150025420 | G | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(101): Show |
116 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1460+740G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025420 | |||||||
| chr5:150025504 | AT | A | 20 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0101 others(17): Show |
23 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1460+834delT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 150025504 | ||||||
| chr5:150025504 | ATT | A | 53 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(50): Show |
68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1460+833_1460+834d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 150025504 | ||||||
| chr5:150025630 | C | CG | 26 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0001c0003t0001g0008 others(23): Show |
33 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.1460+951dupG | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 150025630 | ||||||
| chr5:150025730 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1461-976G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025730 | |||||||
| chr5:150025931 | T | C | 1 | a0004c0005t0001g0247 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1461-775T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150025931 | |||||||
| chr5:150026032 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0101 |
3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1461-674G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026032 | |||||||
| chr5:150026037 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1461-669A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026037 | |||||||
| chr5:150026051 | T | C | 2 | a0002c0002t0005g0061 a0004c0005t0001g0237 |
2 | HG03942.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1461-655T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026051 | |||||||
| chr5:150026065 | T | C | 1 | a0004c0005t0001g0237 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1461-641T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026065 | |||||||
| chr5:150026138 | C | CT | 67 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(64): Show |
82 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1461-561dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr5 | 150026138 | ||||||
| chr5:150026324 | G | A | 1 | a0001c0003t0005g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1461-382G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026324 | |||||||
| chr5:150026606 | C | T | 2 | a0008c0011t0001g0037 a0008c0011t0005g0037 |
2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1461-100C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026606 | |||||||
| chr5:150026647 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1461-59G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 7/19 | chr5 | 150026647 | |||||||
| chr5:150027170 | G | T | 225 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(222): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1734+53G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027170 | |||||||
| chr5:150027440 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1734+323T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027440 | |||||||
| chr5:150027553 | A | AT | 18 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0001c0001t0001g0149 others(15): Show |
19 | HG00673.hp2 HG01433.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1734+450dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150027553 | ||||||
| chr5:150027631 | A | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0005c0006t0005g0009 others(3): Show |
11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1734+514A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027631 | |||||||
| chr5:150027730 | G | A | 1 | a0006c0008t0018g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1734+613G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027730 | |||||||
| chr5:150027873 | A | G | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1734+756A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027873 | |||||||
| chr5:150027958 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1734+841A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150027958 | |||||||
| chr5:150028047 | C | T | 20 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(17): Show |
22 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1734+930C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028047 | |||||||
| chr5:150028213 | G | C | 1 | a0004c0007t0002g0265 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1734+1096G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028213 | |||||||
| chr5:150028354 | T | G | 1 | a0017c0020t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1734+1237T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028354 | |||||||
| chr5:150028408 | T | TTA | 4 | a0001c0001t0003g0178 a0001c0001t0003g0179 a0001c0003t0030g0291 others(1): Show |
4 | HG01106.hp1 HG02886.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734+1305_1734+130 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028408 | ||||||
| chr5:150028426 | A | G | 2 | a0003c0010t0004g0027 a0003c0010t0004g0124 |
3 | HG00544.hp1 HG00673.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1734+1309A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028426 | |||||||
| chr5:150028437 | T | C | 1 | a0001c0001t0003g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1734+1320T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028437 | |||||||
| chr5:150028450 | A | G | 1 | a0002c0002t0002g0004 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1734+1333A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028450 | |||||||
| chr5:150028495 | ATATG | A | 5 | a0001c0003t0005g0144 a0001c0003t0005g0272 a0003c0004t0004g0026 others(2): Show |
6 | HG01243.hp1 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1734+1388_1734+139 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028495 | ||||||
| chr5:150028501 | A | ATGTGTGT others(3): Show |
1 | a0004c0005t0001g0240 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1734+1387_1734+138 others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028501 | ||||||
| chr5:150028501 | A | ATGTGTGT others(5): Show |
2 | a0004c0005t0001g0235 a0004c0005t0001g0236 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1734+1387_1734+138 others(16): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028501 | ||||||
| chr5:150028501 | A | G | 8 | a0001c0001t0001g0150 a0001c0001t0001g0189 a0001c0001t0001g0190 others(5): Show |
8 | HG01256.hp1 HG02683.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1734+1384A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028501 | |||||||
| chr5:150028501 | ATGTATG | A | 30 | a0001c0003t0001g0307 a0001c0003t0005g0145 a0001c0003t0006g0284 others(27): Show |
35 | HG00099.hp1 HG00597.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1734+1388_1734+139 others(10): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028501 | ||||||
| chr5:150028501 | ATGTATGT others(1): Show |
A | 40 | a0001c0003t0001g0008 a0001c0003t0001g0294 a0001c0003t0001g0300 others(37): Show |
50 | HG00544.hp1 HG00673.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.1734+1388_1734+139 others(12): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028501 | ||||||
| chr5:150028501 | ATGTATGT others(3): Show |
A | 3 | a0001c0003t0001g0293 a0001c0003t0005g0134 a0001c0003t0008g0283 |
3 | HG02145.hp2 HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1734+1388_1734+139 others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028501 | ||||||
| chr5:150028503 | GTA | G | 5 | a0001c0001t0001g0230 a0001c0003t0005g0038 a0001c0003t0005g0270 others(2): Show |
6 | HG00735.hp2 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1734+1388_1734+138 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028503 | ||||||
| chr5:150028505 | A | ATG | 6 | a0002c0002t0001g0020 a0002c0002t0002g0041 a0002c0002t0002g0059 others(3): Show |
7 | HG02071.hp1 HG02698.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.1734+1424_1734+142 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028505 | ||||||
| chr5:150028505 | A | ATGTGTG | 4 | a0001c0001t0011g0015 a0001c0001t0011g0046 a0001c0001t0011g0047 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734+1420_1734+142 others(10): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028505 | ||||||
| chr5:150028505 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(143): Show |
159 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1734+1388A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028505 | |||||||
| chr5:150028505 | ATG | A | 3 | a0002c0002t0002g0064 a0002c0002t0002g0078 a0002c0002t0023g0002 |
3 | HG03239.hp2 HG03669.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1734+1424_1734+142 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028505 | ||||||
| chr5:150028505 | ATGTGTGT others(5): Show |
A | 2 | a0008c0011t0001g0037 a0008c0011t0005g0037 |
2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1734+1414_1734+142 others(16): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028505 | ||||||
| chr5:150028527 | G | A | 1 | a0001c0003t0019g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1734+1410G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028527 | |||||||
| chr5:150028529 | G | A | 1 | a0001c0003t0019g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1734+1412G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028529 | |||||||
| chr5:150028531 | G | A | 3 | a0001c0003t0005g0267 a0001c0003t0005g0268 a0001c0003t0019g0271 |
3 | HG01891.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1734+1414G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028531 | |||||||
| chr5:150028533 | G | A | 8 | a0001c0003t0005g0038 a0001c0003t0005g0267 a0001c0003t0005g0268 others(5): Show |
9 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1734+1416G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028533 | |||||||
| chr5:150028535 | G | A | 11 | a0001c0003t0005g0038 a0001c0003t0005g0144 a0001c0003t0005g0145 others(8): Show |
12 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1734+1418G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028535 | |||||||
| chr5:150028537 | G | A | 12 | a0001c0001t0002g0201 a0001c0003t0005g0038 a0001c0003t0005g0144 others(9): Show |
13 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1734+1420G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028537 | |||||||
| chr5:150028539 | G | A | 22 | a0001c0001t0001g0101 a0001c0001t0001g0180 a0001c0001t0002g0201 others(19): Show |
24 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1734+1422G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028539 | |||||||
| chr5:150028541 | G | A | 50 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0101 others(47): Show |
59 | HG00597.hp2 HG00673.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.1734+1424G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028541 | |||||||
| chr5:150028541 | G | GTGTA | 3 | a0001c0001t0001g0154 a0001c0001t0001g0184 a0001c0001t0003g0204 |
3 | HG02683.hp1 NA18948.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | ||||||
| chr5:150028541 | G | GTGTGTA | 5 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0191 others(2): Show |
6 | HG02896.hp2 HG02897.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(10): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | ||||||
| chr5:150028541 | G | GTGTGTGT others(1): Show |
5 | a0001c0001t0001g0040 a0001c0001t0001g0163 a0004c0005t0001g0237 others(2): Show |
5 | HG02080.hp1 HG06807.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(12): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | ||||||
| chr5:150028541 | G | GTGTGTGT others(3): Show |
10 | a0004c0005t0001g0036 a0004c0005t0001g0241 a0004c0005t0001g0244 others(7): Show |
11 | HG00639.hp1 HG01361.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | ||||||
| chr5:150028541 | G | GTGTGTGT others(3): Show |
5 | a0001c0001t0003g0198 a0004c0005t0001g0234 a0004c0005t0001g0253 others(2): Show |
5 | HG02258.hp1 HG02698.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | ||||||
| chr5:150028541 | G | GTGTGTGT others(5): Show |
5 | a0004c0005t0001g0252 a0004c0005t0001g0255 a0004c0005t0002g0261 others(2): Show |
5 | HG01106.hp1 HG01255.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.1734+1425_1734+142 others(16): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028541 | ||||||
| chr5:150028543 | A | G | 51 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0033 others(48): Show |
59 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1734+1426A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028543 | |||||||
| chr5:150028545 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0006g0286 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1734+1428A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028545 | |||||||
| chr5:150028555 | ATATATTT others(3): Show |
A | 4 | a0001c0003t0006g0284 a0001c0003t0006g0292 a0001c0003t0008g0276 others(1): Show |
4 | HG01884.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+1440_1734+144 others(14): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028555 | ||||||
| chr5:150028557 | ATATTTTT others(1): Show |
A | 29 | a0001c0003t0001g0008 a0001c0003t0001g0294 a0001c0003t0001g0300 others(26): Show |
31 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1734+1442_1734+144 others(12): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028557 | ||||||
| chr5:150028559 | A | AT | 8 | a0001c0001t0011g0015 a0001c0001t0011g0046 a0001c0001t0011g0047 others(5): Show |
8 | HG02293.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1734+1461dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028559 | ||||||
| chr5:150028559 | A | ATAT | 7 | a0001c0001t0001g0045 a0001c0001t0003g0003 a0001c0001t0006g0286 others(4): Show |
7 | HG01167.hp1 HG03453.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1734+1443_1734+144 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028559 | ||||||
| chr5:150028559 | A | T | 10 | a0001c0003t0005g0030 a0001c0003t0005g0134 a0001c0003t0005g0135 others(7): Show |
14 | HG01243.hp2 HG02280.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.1734+1442A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028559 | |||||||
| chr5:150028559 | AT | A | 41 | a0001c0001t0001g0180 a0001c0001t0003g0146 a0001c0001t0003g0275 others(38): Show |
53 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1734+1461delT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028559 | ||||||
| chr5:150028559 | ATTT | A | 9 | a0003c0004t0004g0026 a0003c0004t0004g0121 a0003c0004t0007g0028 others(6): Show |
11 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1734+1459_1734+146 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150028559 | ||||||
| chr5:150028560 | T | TA | 46 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0040 others(43): Show |
51 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.1734+1443_1734+144 others(5): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028560 | |||||||
| chr5:150028560 | T | TATA | 51 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0001t0001g0150 others(48): Show |
56 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1734+1443_1734+144 others(7): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028560 | |||||||
| chr5:150028560 | T | TATATA | 32 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0033 others(29): Show |
37 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1734+1443_1734+144 others(9): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028560 | |||||||
| chr5:150028560 | T | TATATATA | 3 | a0004c0005t0001g0242 a0004c0005t0001g0243 a0004c0005t0001g0245 |
3 | HG02074.hp2 HG03710.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1734+1443_1734+144 others(11): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028560 | |||||||
| chr5:150028561 | T | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0101 others(19): Show |
24 | HG01106.hp1 HG01243.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1734+1444T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028561 | |||||||
| chr5:150028562 | T | A | 63 | a0001c0001t0001g0224 a0001c0001t0003g0035 a0001c0001t0011g0141 others(60): Show |
79 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1734+1445T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028562 | |||||||
| chr5:150028563 | T | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0001c0003t0005g0144 others(5): Show |
9 | HG01106.hp1 HG02055.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1734+1446T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028563 | |||||||
| chr5:150028564 | T | A | 16 | a0002c0002t0002g0089 a0003c0004t0004g0118 a0004c0005t0001g0036 others(13): Show |
17 | HG02074.hp2 HG02132.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1734+1447T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028564 | |||||||
| chr5:150028565 | T | A | 2 | a0001c0003t0001g0293 a0004c0005t0001g0259 |
2 | HG03098.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1734+1448T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028565 | |||||||
| chr5:150028566 | T | A | 1 | a0004c0005t0001g0252 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1734+1449T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028566 | |||||||
| chr5:150028584 | A | G | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1734+1467A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028584 | |||||||
| chr5:150028615 | G | A | 2 | a0008c0011t0001g0037 a0008c0011t0005g0037 |
2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1734+1498G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028615 | |||||||
| chr5:150028694 | G | A | 1 | a0001c0021t0006g0282 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1734+1577G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028694 | |||||||
| chr5:150028714 | G | C | 2 | a0002c0002t0002g0016 a0002c0002t0002g0058 |
3 | HG01257.hp2 HG01258.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.1734+1597G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150028714 | |||||||
| chr5:150029009 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0184 a0001c0001t0003g0151 |
4 | NA18948.hp2 NA18950.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-1732C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029009 | |||||||
| chr5:150029018 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(102): Show |
117 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1735-1723A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029018 | |||||||
| chr5:150029133 | T | A | 1 | a0002c0002t0002g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1735-1608T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029133 | |||||||
| chr5:150029330 | G | GT | 118 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0101 others(115): Show |
139 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.1735-1395dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150029330 | ||||||
| chr5:150029366 | G | A | 52 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(49): Show |
67 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.1735-1375G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029366 | |||||||
| chr5:150029731 | C | T | 239 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(236): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1735-1010C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029731 | |||||||
| chr5:150029901 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0005c0006t0005g0009 others(3): Show |
11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1735-840G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029901 | |||||||
| chr5:150029974 | T | C | 1 | a0001c0001t0003g0167 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1735-767T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029974 | |||||||
| chr5:150029994 | T | C | 1 | a0001c0003t0001g0300 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1735-747T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150029994 | |||||||
| chr5:150030134 | TTTTC | T | 86 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(83): Show |
103 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.1735-599_1735-596d others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr5 | 150030134 | ||||||
| chr5:150030210 | T | A | 89 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(86): Show |
106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1735-531T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150030210 | |||||||
| chr5:150030579 | T | C | 1 | a0001c0001t0003g0178 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1735-162T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150030579 | |||||||
| chr5:150030590 | T | G | 89 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(86): Show |
106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1735-151T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150030590 | |||||||
| chr5:150030669 | C | T | 3 | a0008c0011t0001g0037 a0008c0011t0005g0037 a0017c0020t0001g0277 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1735-72C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150030669 | |||||||
| chr5:150030721 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1735-20T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 9/19 | chr5 | 150030721 | |||||||
| chr5:150030925 | G | A | 2 | a0001c0001t0002g0153 a0001c0001t0002g0155 |
2 | HG01071.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1833+86G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150030925 | |||||||
| chr5:150030956 | A | C | 56 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(53): Show |
73 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1833+117A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150030956 | |||||||
| chr5:150030977 | AAGAT | A | 3 | a0008c0011t0001g0037 a0008c0011t0005g0037 a0017c0020t0001g0277 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1833+139_1833+142d others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150030977 | |||||||
| chr5:150031180 | C | A | 5 | a0001c0001t0003g0181 a0001c0001t0003g0196 a0001c0001t0003g0207 others(2): Show |
5 | HG00639.hp2 HG01109.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1833+341C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031180 | |||||||
| chr5:150031301 | C | G | 1 | a0003c0010t0004g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1833+462C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031301 | |||||||
| chr5:150031339 | C | A | 9 | a0001c0003t0005g0038 a0001c0003t0005g0267 a0001c0003t0005g0268 others(6): Show |
10 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1833+500C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031339 | |||||||
| chr5:150031349 | G | C | 5 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(2): Show |
7 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1833+510G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031349 | |||||||
| chr5:150031417 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1833+578G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031417 | |||||||
| chr5:150031470 | A | G | 10 | a0001c0001t0001g0045 a0001c0001t0001g0142 a0001c0001t0001g0143 others(7): Show |
10 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1833+631A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031470 | |||||||
| chr5:150031609 | G | C | 2 | a0008c0011t0001g0037 a0008c0011t0005g0037 |
2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1833+770G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150031609 | |||||||
| chr5:150032038 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1834-416T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150032038 | |||||||
| chr5:150032088 | TTTGTCTT others(16): Show |
T | 2 | a0001c0003t0005g0303 a0001c0003t0005g0304 |
2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1834-364_1834-342d others(25): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr5 | 150032088 | ||||||
| chr5:150032260 | C | T | 1 | a0001c0001t0003g0218 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1834-194C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150032260 | |||||||
| chr5:150032387 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1834-67T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150032387 | |||||||
| chr5:150032425 | A | G | 1 | a0001c0001t0003g0233 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1834-29A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 10/19 | chr5 | 150032425 | |||||||
| chr5:150032668 | G | A | 1 | a0004c0005t0001g0245 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1983+65G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150032668 | |||||||
| chr5:150032747 | A | T | 1 | a0017c0020t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1983+144A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150032747 | |||||||
| chr5:150032808 | A | G | 1 | a0002c0002t0002g0070 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1983+205A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150032808 | |||||||
| chr5:150032884 | A | G | 37 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(34): Show |
39 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1983+281A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150032884 | |||||||
| chr5:150032982 | G | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(239): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1983+379G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150032982 | |||||||
| chr5:150033215 | A | G | 54 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(51): Show |
69 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1983+612A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033215 | |||||||
| chr5:150033292 | G | A | 18 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(15): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1983+689G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033292 | |||||||
| chr5:150033368 | G | A | 4 | a0001c0001t0011g0015 a0001c0001t0011g0046 a0001c0001t0011g0047 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1983+765G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033368 | |||||||
| chr5:150033553 | C | T | 1 | a0002c0014t0002g0069 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1983+950C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033553 | |||||||
| chr5:150033598 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0101 |
3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1983+995G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033598 | |||||||
| chr5:150033623 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(241): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1983+1020A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033623 | |||||||
| chr5:150033878 | G | T | 54 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(51): Show |
69 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1983+1275G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150033878 | |||||||
| chr5:150034047 | T | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(136): Show |
152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1983+1444T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034047 | |||||||
| chr5:150034096 | T | C | 91 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(88): Show |
108 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1983+1493T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034096 | |||||||
| chr5:150034435 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1983+1832G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034435 | |||||||
| chr5:150034446 | C | T | 1 | a0001c0003t0019g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1983+1843C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034446 | |||||||
| chr5:150034453 | C | T | 1 | a0002c0002t0003g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1983+1850C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034453 | |||||||
| chr5:150034454 | G | A | 54 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(51): Show |
69 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1983+1851G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034454 | |||||||
| chr5:150034455 | C | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0142 a0001c0001t0001g0143 others(6): Show |
9 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1983+1852C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034455 | |||||||
| chr5:150034481 | T | C | 1 | a0001c0003t0005g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1983+1878T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034481 | |||||||
| chr5:150034512 | C | T | 20 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(17): Show |
22 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1983+1909C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034512 | |||||||
| chr5:150034678 | A | G | 2 | a0001c0003t0006g0287 a0001c0003t0006g0288 |
2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1984-1958A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034678 | |||||||
| chr5:150034732 | T | C | 3 | a0002c0002t0001g0104 a0002c0002t0002g0011 a0002c0002t0002g0103 |
5 | NA18941.hp1 NA18989.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.1984-1904T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034732 | |||||||
| chr5:150034812 | A | T | 1 | a0001c0003t0006g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1984-1824A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034812 | |||||||
| chr5:150034859 | G | T | 3 | a0001c0003t0005g0029 a0001c0003t0005g0134 a0001c0019t0005g0029 |
3 | HG02280.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1984-1777G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150034859 | |||||||
| chr5:150035009 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0006g0286 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1984-1627G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035009 | |||||||
| chr5:150035048 | C | T | 2 | a0001c0003t0003g0296 a0001c0003t0003g0297 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1984-1588C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035048 | |||||||
| chr5:150035076 | G | T | 2 | a0001c0003t0006g0289 a0001c0021t0006g0282 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1984-1560G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035076 | |||||||
| chr5:150035089 | A | G | 36 | a0003c0004t0004g0001 a0003c0004t0004g0012 a0003c0004t0004g0024 others(33): Show |
49 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1984-1547A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035089 | |||||||
| chr5:150035107 | C | T | 1 | a0001c0003t0019g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1984-1529C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035107 | |||||||
| chr5:150035176 | G | A | 6 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0134 others(3): Show |
7 | HG01243.hp2 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1984-1460G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035176 | |||||||
| chr5:150035336 | A | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(237): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1984-1300A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035336 | |||||||
| chr5:150035382 | T | C | 2 | a0001c0001t0005g0219 a0013c0027t0001g0222 |
2 | HG02074.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1984-1254T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035382 | |||||||
| chr5:150035446 | G | A | 12 | a0001c0003t0005g0038 a0001c0003t0005g0144 a0001c0003t0005g0145 others(9): Show |
13 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1984-1190G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035446 | |||||||
| chr5:150035532 | A | G | 54 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(51): Show |
69 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1984-1104A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035532 | |||||||
| chr5:150035646 | T | A | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1984-990T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035646 | |||||||
| chr5:150035656 | G | A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(206): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1984-980G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035656 | |||||||
| chr5:150035683 | G | T | 4 | a0001c0001t0011g0015 a0001c0001t0011g0046 a0001c0001t0011g0047 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1984-953G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035683 | |||||||
| chr5:150035838 | A | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(137): Show |
153 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1984-798A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035838 | |||||||
| chr5:150035995 | A | G | 91 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(88): Show |
108 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1984-641A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150035995 | |||||||
| chr5:150036042 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1984-594A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 11/19 | chr5 | 150036042 | |||||||
| chr5:150036967 | A | T | 1 | a0002c0002t0002g0057 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2285+30A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 12/19 | chr5 | 150036967 | |||||||
| chr5:150037575 | G | T | 55 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(52): Show |
70 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.2413+48G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150037575 | |||||||
| chr5:150037980 | C | T | 2 | a0002c0002t0002g0049 a0002c0002t0002g0050 |
2 | HG02132.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2413+453C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150037980 | |||||||
| chr5:150037989 | C | T | 89 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(86): Show |
106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.2413+462C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150037989 | |||||||
| chr5:150038190 | C | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0005c0006t0005g0009 others(3): Show |
11 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.2413+663C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150038190 | |||||||
| chr5:150038268 | T | G | 4 | a0001c0001t0011g0015 a0001c0001t0011g0046 a0001c0001t0011g0047 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2413+741T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150038268 | |||||||
| chr5:150038563 | A | G | 92 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(89): Show |
109 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.2413+1036A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150038563 | |||||||
| chr5:150038761 | G | A | 1 | a0001c0001t0003g0168 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2413+1234G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150038761 | |||||||
| chr5:150038849 | A | G | 4 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(1): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2413+1322A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150038849 | |||||||
| chr5:150039135 | G | T | 1 | a0003c0004t0004g0310 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2413+1608G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039135 | |||||||
| chr5:150039453 | G | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0142 a0001c0001t0001g0143 others(6): Show |
9 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2414-1295G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039453 | |||||||
| chr5:150039487 | G | A | 2 | a0001c0003t0006g0289 a0001c0021t0006g0282 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2414-1261G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039487 | |||||||
| chr5:150039625 | T | C | 89 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(86): Show |
106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.2414-1123T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039625 | |||||||
| chr5:150039713 | A | C | 2 | a0001c0003t0005g0272 a0001c0003t0005g0274 |
2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2414-1035A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039713 | |||||||
| chr5:150039734 | C | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(241): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.2414-1014C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039734 | |||||||
| chr5:150039759 | C | CTT | 92 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(89): Show |
109 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.2414-986_2414-985d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | 150039759 | ||||||
| chr5:150039784 | A | G | 4 | a0003c0004t0004g0001 a0003c0004t0004g0110 a0003c0004t0004g0116 others(1): Show |
10 | HG01433.hp2 HG01496.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.2414-964A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039784 | |||||||
| chr5:150039846 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0101 |
3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2414-902C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039846 | |||||||
| chr5:150039863 | C | T | 20 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(17): Show |
22 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2414-885C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150039863 | |||||||
| chr5:150040028 | C | T | 14 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(11): Show |
14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2414-720C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040028 | |||||||
| chr5:150040172 | G | A | 3 | a0008c0011t0001g0037 a0008c0011t0005g0037 a0017c0020t0001g0277 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2414-576G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040172 | |||||||
| chr5:150040222 | A | G | 2 | a0007c0009t0004g0123 a0007c0009t0004g0126 |
2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2414-526A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040222 | |||||||
| chr5:150040229 | G | A | 56 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(53): Show |
71 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2414-519G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040229 | |||||||
| chr5:150040257 | A | T | 3 | a0008c0011t0001g0037 a0008c0011t0005g0037 a0017c0020t0001g0277 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2414-491A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040257 | |||||||
| chr5:150040428 | C | T | 89 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(86): Show |
106 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.2414-320C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040428 | |||||||
| chr5:150040584 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2414-164C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040584 | |||||||
| chr5:150040595 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2414-153C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040595 | |||||||
| chr5:150040600 | A | G | 18 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0038 others(15): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2414-148A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040600 | |||||||
| chr5:150040617 | A | C | 12 | a0001c0003t0005g0038 a0001c0003t0005g0144 a0001c0003t0005g0145 others(9): Show |
13 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.2414-131A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040617 | |||||||
| chr5:150040742 | C | T | 4 | a0003c0004t0004g0024 a0003c0004t0004g0109 a0003c0004t0004g0113 others(1): Show |
5 | NA18971.hp1 NA18997.hp1 NA19012.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2414-6C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 13/19 | chr5 | 150040742 | |||||||
| chr5:150040928 | G | A | 1 | a0001c0003t0005g0273 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2545+49G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150040928 | |||||||
| chr5:150040990 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2545+111A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150040990 | |||||||
| chr5:150040996 | A | C | 2 | a0002c0002t0002g0021 a0002c0002t0002g0085 |
3 | NA18950.hp2 NA18982.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2545+117A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150040996 | |||||||
| chr5:150041126 | C | A | 1 | a0003c0004t0004g0111 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2545+247C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041126 | |||||||
| chr5:150041135 | G | T | 69 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(66): Show |
84 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2545+256G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041135 | |||||||
| chr5:150041153 | C | T | 12 | a0001c0003t0005g0038 a0001c0003t0005g0144 a0001c0003t0005g0145 others(9): Show |
13 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.2545+274C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041153 | |||||||
| chr5:150041154 | C | G | 1 | a0003c0004t0007g0107 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2545+275C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041154 | |||||||
| chr5:150041187 | C | T | 1 | a0002c0002t0002g0139 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2545+308C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041187 | |||||||
| chr5:150041434 | G | A | 3 | a0008c0011t0001g0037 a0008c0011t0005g0037 a0017c0020t0001g0277 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2546-351G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041434 | |||||||
| chr5:150041548 | G | A | 2 | a0001c0003t0001g0302 a0001c0003t0001g0305 |
2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2546-237G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041548 | |||||||
| chr5:150041603 | T | C | 1 | a0002c0002t0002g0075 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2546-182T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 14/19 | chr5 | 150041603 | |||||||
| chr5:150041990 | G | T | 1 | a0001c0001t0002g0211 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2730+21G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150041990 | |||||||
| chr5:150042002 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0225 |
2 | NA18946.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2730+33C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042002 | |||||||
| chr5:150042003 | G | A | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
3 | NA18954.hp1 NA18983.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2730+34G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042003 | |||||||
| chr5:150042024 | C | T | 2 | a0008c0011t0001g0037 a0008c0011t0005g0037 |
2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2730+55C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042024 | |||||||
| chr5:150042224 | T | C | 1 | a0001c0003t0008g0283 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2730+255T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042224 | |||||||
| chr5:150042271 | T | C | 3 | a0002c0002t0002g0007 a0002c0002t0002g0019 a0002c0002t0003g0076 |
7 | HG01106.hp2 HG01952.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.2730+302T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042271 | |||||||
| chr5:150042284 | T | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(136): Show |
152 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.2730+315T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042284 | |||||||
| chr5:150042852 | A | C | 1 | a0001c0001t0003g0218 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2730+883A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042852 | |||||||
| chr5:150042964 | A | G | 32 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(29): Show |
34 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.2730+995A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150042964 | |||||||
| chr5:150043040 | G | C | 138 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(135): Show |
151 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.2730+1071G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043040 | |||||||
| chr5:150043095 | C | G | 5 | a0001c0003t0005g0295 a0001c0003t0005g0298 a0001c0003t0005g0303 others(2): Show |
5 | HG02622.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2730+1126C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043095 | |||||||
| chr5:150043099 | A | G | 1 | a0017c0020t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2730+1130A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043099 | |||||||
| chr5:150043107 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2730+1138G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043107 | |||||||
| chr5:150043173 | G | A | 4 | a0002c0002t0002g0042 a0002c0002t0002g0073 a0002c0002t0002g0074 others(1): Show |
4 | NA18612.hp2 NA18942.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.2730+1204G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043173 | |||||||
| chr5:150043306 | ACACT | A | 31 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(28): Show |
33 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.2730+1341_2730+134 others(8): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr5 | 150043306 | ||||||
| chr5:150043423 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2730+1454G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043423 | |||||||
| chr5:150043636 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(98): Show |
113 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2730+1667C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043636 | |||||||
| chr5:150043817 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0101 |
3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2731-1649A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043817 | |||||||
| chr5:150043876 | C | T | 1 | a0001c0001t0003g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2731-1590C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043876 | |||||||
| chr5:150043893 | C | T | 3 | a0008c0011t0001g0037 a0008c0011t0005g0037 a0017c0020t0001g0277 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2731-1573C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150043893 | |||||||
| chr5:150044101 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2731-1365C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044101 | |||||||
| chr5:150044276 | G | A | 14 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(11): Show |
14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2731-1190G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044276 | |||||||
| chr5:150044447 | GGT | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0101 |
3 | HG02451.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2731-1017_2731-101 others(6): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr5 | 150044447 | ||||||
| chr5:150044476 | G | A | 1 | a0001c0003t0005g0270 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2731-990G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044476 | |||||||
| chr5:150044524 | C | T | 2 | a0004c0005t0001g0249 a0004c0005t0001g0255 |
2 | NA18979.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2731-942C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044524 | |||||||
| chr5:150044659 | C | T | 14 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(11): Show |
14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2731-807C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044659 | |||||||
| chr5:150044740 | A | G | 1 | a0002c0002t0002g0017 | 2 | NA18971.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.2731-726A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044740 | |||||||
| chr5:150044819 | T | G | 3 | a0008c0011t0001g0037 a0008c0011t0005g0037 a0017c0020t0001g0277 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2731-647T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044819 | |||||||
| chr5:150044866 | A | G | 3 | a0008c0011t0001g0037 a0008c0011t0005g0037 a0017c0020t0001g0277 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2731-600A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044866 | |||||||
| chr5:150044945 | C | T | 33 | a0001c0001t0001g0154 a0004c0005t0001g0036 a0004c0005t0001g0234 others(30): Show |
34 | HG00639.hp1 HG01106.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.2731-521C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150044945 | |||||||
| chr5:150045403 | G | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(239): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.2731-63G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150045403 | |||||||
| chr5:150045445 | T | A | 3 | a0002c0002t0001g0020 a0002c0002t0002g0079 a0014c0028t0002g0086 |
4 | NA18973.hp1 NA19007.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2731-21T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 15/19 | chr5 | 150045445 | |||||||
| chr5:150045915 | G | A | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2950+230G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150045915 | |||||||
| chr5:150045966 | C | T | 1 | a0001c0021t0006g0282 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2950+281C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150045966 | |||||||
| chr5:150046225 | C | T | 72 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(69): Show |
87 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.2950+540C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046225 | |||||||
| chr5:150046277 | G | A | 1 | a0002c0002t0002g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2950+592G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046277 | |||||||
| chr5:150046322 | A | G | 9 | a0001c0001t0001g0045 a0001c0001t0001g0142 a0001c0001t0001g0143 others(6): Show |
9 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2950+637A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046322 | |||||||
| chr5:150046340 | C | T | 69 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(66): Show |
84 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2950+655C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046340 | |||||||
| chr5:150046483 | T | C | 1 | a0007c0009t0004g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2950+798T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046483 | |||||||
| chr5:150046629 | G | A | 3 | a0001c0003t0006g0292 a0001c0003t0008g0276 a0001c0003t0030g0291 |
3 | HG02886.hp1 HG02895.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2950+944G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046629 | |||||||
| chr5:150046744 | G | A | 37 | a0002c0014t0002g0069 a0003c0004t0004g0001 a0003c0004t0004g0012 others(34): Show |
50 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2951-880G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046744 | |||||||
| chr5:150046767 | G | A | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2951-857G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046767 | |||||||
| chr5:150046799 | G | A | 2 | a0008c0011t0001g0037 a0008c0011t0005g0037 |
2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2951-825G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046799 | |||||||
| chr5:150046807 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2951-817G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046807 | |||||||
| chr5:150046891 | C | CT | 20 | a0001c0001t0003g0197 a0001c0003t0001g0008 a0001c0003t0001g0293 others(17): Show |
22 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2951-721dupT | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr5 | 150046891 | ||||||
| chr5:150046891 | C | CTT | 14 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(11): Show |
14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2951-722_2951-721d others(4): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr5 | 150046891 | ||||||
| chr5:150046908 | C | T | 1 | a0004c0005t0001g0254 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2951-716C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046908 | |||||||
| chr5:150046977 | C | T | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2951-647C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150046977 | |||||||
| chr5:150047024 | A | G | 1 | a0017c0020t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2951-600A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047024 | |||||||
| chr5:150047033 | C | T | 8 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0006g0286 others(5): Show |
8 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2951-591C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047033 | |||||||
| chr5:150047044 | C | A | 1 | a0001c0001t0001g0180 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2951-580C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047044 | |||||||
| chr5:150047185 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2951-439C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047185 | |||||||
| chr5:150047387 | T | G | 4 | a0001c0001t0011g0015 a0001c0001t0011g0046 a0001c0001t0011g0047 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2951-237T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047387 | |||||||
| chr5:150047403 | A | G | 310 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(307): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.2951-221A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047403 | |||||||
| chr5:150047420 | C | G | 1 | a0002c0002t0003g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2951-204C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047420 | |||||||
| chr5:150047505 | A | G | 1 | a0003c0004t0007g0028 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2951-119A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 16/19 | chr5 | 150047505 | |||||||
| chr5:150047972 | G | A | 1 | a0002c0002t0003g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3084+215G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150047972 | |||||||
| chr5:150047980 | G | A | 91 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(88): Show |
108 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.3084+223G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150047980 | |||||||
| chr5:150048179 | A | C | 1 | a0003c0004t0004g0118 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3085-390A>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150048179 | |||||||
| chr5:150048187 | A | G | 1 | a0002c0002t0002g0138 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3085-382A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150048187 | |||||||
| chr5:150048400 | T | TTGCTTAC others(9): Show |
88 | a0001c0003t0001g0008 a0001c0003t0001g0293 a0001c0003t0001g0294 others(85): Show |
105 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.3085-168_3085-153d others(18): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr5 | 150048400 | ||||||
| chr5:150048533 | C | T | 14 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(11): Show |
14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3085-36C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150048533 | |||||||
| chr5:150048541 | T | C | 1 | a0013c0027t0001g0222 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3085-28T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 17/19 | chr5 | 150048541 | |||||||
| chr5:150048768 | G | A | 1 | a0004c0005t0001g0257 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3201+83G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048768 | |||||||
| chr5:150048768 | G | T | 3 | a0007c0009t0004g0123 a0007c0009t0004g0125 a0007c0009t0004g0126 |
3 | HG02280.hp2 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3201+83G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048768 | |||||||
| chr5:150048799 | C | T | 1 | a0001c0001t0026g0200 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3201+114C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048799 | |||||||
| chr5:150048817 | G | A | 1 | a0001c0003t0019g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3201+132G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048817 | |||||||
| chr5:150048832 | C | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(243): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.3201+147C>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048832 | |||||||
| chr5:150048835 | G | A | 14 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(11): Show |
14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3201+150G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048835 | |||||||
| chr5:150048861 | G | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(210): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.3201+176G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048861 | |||||||
| chr5:150048968 | G | A | 11 | a0001c0003t0005g0038 a0001c0003t0005g0144 a0001c0003t0005g0145 others(8): Show |
12 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.3201+283G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048968 | |||||||
| chr5:150048970 | A | G | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3201+285A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150048970 | |||||||
| chr5:150049002 | T | C | 1 | a0002c0002t0002g0073 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3201+317T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049002 | |||||||
| chr5:150049299 | G | A | 1 | a0001c0003t0005g0030 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3201+614G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049299 | |||||||
| chr5:150049327 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(245): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.3201+642A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049327 | |||||||
| chr5:150049410 | A | AC | 142 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(139): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.3201+734dupC | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 150049410 | ||||||
| chr5:150049575 | C | T | 4 | a0005c0006t0005g0009 a0005c0006t0009g0010 a0005c0006t0009g0100 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.3202-677C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049575 | |||||||
| chr5:150049646 | C | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(153): Show |
174 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.3202-606C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049646 | |||||||
| chr5:150049693 | T | C | 14 | a0001c0003t0001g0300 a0001c0003t0001g0302 a0001c0003t0001g0305 others(11): Show |
14 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3202-559T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049693 | |||||||
| chr5:150049726 | TGTGGAAT others(21): Show |
T | 1 | a0017c0020t0001g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3202-520_3202-493d others(30): Show |
HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr5 | 150049726 | ||||||
| chr5:150049777 | A | G | 8 | a0001c0001t0001g0045 a0001c0001t0006g0286 a0001c0001t0011g0015 others(5): Show |
8 | HG02630.hp2 HG02886.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3202-475A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049777 | |||||||
| chr5:150049976 | G | C | 1 | a0010c0015t0005g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3202-276G>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150049976 | |||||||
| chr5:150050170 | G | A | 18 | a0001c0001t0001g0045 a0001c0003t0001g0008 a0001c0003t0001g0293 others(15): Show |
20 | HG02109.hp2 HG02145.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.3202-82G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 18/19 | chr5 | 150050170 | |||||||
| chr5:150050527 | G | A | 5 | a0002c0002t0001g0080 a0002c0002t0005g0005 a0002c0002t0005g0051 others(2): Show |
8 | NA18939.hp2 NA18954.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.3411+66G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150050527 | |||||||
| chr5:150050762 | T | G | 33 | a0001c0001t0001g0045 a0001c0003t0001g0008 a0001c0003t0001g0293 others(30): Show |
35 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.3411+301T>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150050762 | |||||||
| chr5:150050773 | G | T | 3 | a0008c0011t0001g0037 a0008c0011t0005g0037 a0017c0020t0001g0277 |
3 | HG02896.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3411+312G>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150050773 | |||||||
| chr5:150050928 | A | G | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
3 | NA18954.hp1 NA18983.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.3411+467A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150050928 | |||||||
| chr5:150051071 | C | T | 36 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0134 others(33): Show |
49 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.3411+610C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051071 | |||||||
| chr5:150051094 | A | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(104): Show |
119 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.3412-631A>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051094 | |||||||
| chr5:150051352 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(109): Show |
124 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.3412-373T>C | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051352 | |||||||
| chr5:150051445 | C | A | 31 | a0001c0003t0006g0278 a0003c0004t0004g0001 a0003c0004t0004g0012 others(28): Show |
43 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3412-280C>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051445 | |||||||
| chr5:150051462 | C | T | 135 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0101 others(132): Show |
159 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.3412-263C>T | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051462 | |||||||
| chr5:150051487 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3412-238G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051487 | |||||||
| chr5:150051606 | A | G | 7 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0134 others(4): Show |
8 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3412-119A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051606 | |||||||
| chr5:150051615 | T | A | 51 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0154 others(48): Show |
53 | HG00735.hp2 HG01891.hp1 HG01981.hp2 others(50): Show |
intron_variant | MODIFIER | c.3412-110T>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051615 | |||||||
| chr5:150051630 | A | G | 7 | a0001c0003t0005g0029 a0001c0003t0005g0030 a0001c0003t0005g0134 others(4): Show |
8 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3412-95A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051630 | |||||||
| chr5:150051660 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(237): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.3412-65G>A | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051660 | |||||||
| chr5:150051696 | A | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(238): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.3412-29A>G | HMGXB3 | ENSG00000113716.13 | transcript | ENST00000502717.6 | protein_coding | 19/19 | chr5 | 150051696 |