Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3074 |
| ensemblid | ENSG00000049860.14 |
| hgncid | 4879 |
| symbol | HEXB |
| name | hexosaminidase subunit beta |
| refseq_nuc | NM_000521.4 |
| refseq_prot | NP_000512.2 |
| ensembl_nuc | ENST00000261416.12 |
| ensembl_prot | ENSP00000261416.7 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 74685233 |
| end | 74721288 |
| strand | + |
| ver | v1.2 |
| region | chr5:74685233-74721288 |
| region5000 | chr5:74680233-74726288 |
| regionname0 | HEXB_chr5_74685233_74721288 |
| regionname5000 | HEXB_chr5_74680233_74726288 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 556 | 237 | 62 | 38 | 97 | 7 | 32 | 67 | HEXB_chr5_74680233_74726288 | HEXB | MELCG others(551): Show |
chr5 | 74680233 | 74726288 |
| a0002 | 0/0 | 556 | 89 | 28 | 18 | 30 | 4 | 9 | 26 | HEXB_chr5_74680233_74726288 | HEXB | MELCG others(551): Show |
chr5 | 74680233 | 74726288 |
| a0003 | 0/0 | 556 | 54 | 1 | 12 | 35 | 2 | 4 | 28 | HEXB_chr5_74680233_74726288 | HEXB | MELCG others(551): Show |
chr5 | 74680233 | 74726288 |
| a0004 | 1/0 | 556 | 5 | 0 | 2 | 0 | 1 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | MELCG others(551): Show |
chr5 | 74680233 | 74726288 |
| a0005 | 0/0 | 556 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | MELCG others(551): Show |
chr5 | 74680233 | 74726288 |
| a0006 | 0/0 | 556 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | MELCG others(551): Show |
chr5 | 74680233 | 74726288 |
| a0007 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | MELCG others(551): Show |
chr5 | 74680233 | 74726288 |
| a0008 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | MELCG others(551): Show |
chr5 | 74680233 | 74726288 |
| a0009 | 0/0 | 556 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | MELCG others(551): Show |
chr5 | 74680233 | 74726288 |
| a0010 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | MELCG others(551): Show |
chr5 | 74680233 | 74726288 |
| a0011 | 0/0 | 556 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | MELCG others(551): Show |
chr5 | 74680233 | 74726288 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1668 | 231 | 56 | 38 | 97 | 7 | 32 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0001c0004 | 0/0 | 1668 | 5 | 5 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0001c0010 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0002c0002 | 0/0 | 1668 | 89 | 28 | 18 | 30 | 4 | 9 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0003c0003 | 0/0 | 1668 | 54 | 1 | 12 | 35 | 2 | 4 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0004c0005 | 1/0 | 1668 | 5 | 0 | 2 | 0 | 1 | 1 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0005c0007 | 0/0 | 1668 | 3 | 2 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0006c0006 | 0/0 | 1668 | 3 | 2 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0007c0011 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0008c0009 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0009c0008 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0010c0013 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 | ||
| a0011c0012 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | ATGGA others(1663): Show |
chr5 | 74680233 | 74726288 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1812 | 224 | 55 | 38 | 94 | 6 | 30 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0001c0001t0002 | 0/0 | 1810 | 6 | 1 | 0 | 2 | 1 | 2 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1805): Show |
chr5 | 74680233 | 74726288 |
| a0001c0001t0003 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0001c0004t0001 | 0/0 | 1812 | 5 | 5 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0001c0010t0001 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0002c0002t0001 | 0/0 | 1812 | 81 | 28 | 18 | 23 | 4 | 8 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0002c0002t0002 | 0/0 | 1810 | 8 | 0 | 0 | 7 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1805): Show |
chr5 | 74680233 | 74726288 |
| a0003c0003t0001 | 0/0 | 1812 | 31 | 1 | 6 | 18 | 2 | 4 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0003c0003t0002 | 0/0 | 1810 | 23 | 0 | 6 | 17 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1805): Show |
chr5 | 74680233 | 74726288 |
| a0004c0005t0001 | 1/0 | 1812 | 5 | 0 | 2 | 0 | 1 | 1 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0005c0007t0001 | 0/0 | 1812 | 3 | 2 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0006c0006t0001 | 0/0 | 1812 | 3 | 2 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0007c0011t0001 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0008c0009t0001 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0009c0008t0001 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0010c0013t0001 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1807): Show |
chr5 | 74680233 | 74726288 |
| a0011c0012t0002 | 0/0 | 1810 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | AGACC others(1805): Show |
chr5 | 74680233 | 74726288 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0004t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0004t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0001c0010t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0007 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0003c0003t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0004c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0004c0005t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0004c0005t0001g0228 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0004c0005t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0005c0007t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0005c0007t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0005c0007t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0006c0006t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0006c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0006c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0007c0011t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0008c0009t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0009c0008t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0010c0013t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| a0011c0012t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0036 | EUR | GBR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00099 | hp2 | a0004 | c0005 | t0001 | g0033 | EUR | GBR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | GBR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0007 | EUR | FIN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0305 | EUR | FIN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00423 | hp1 | a0007 | c0011 | t0001 | g0185 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00423 | hp2 | a0003 | c0003 | t0001 | g0207 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00438 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0173 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0316 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00642 | hp1 | a0005 | c0007 | t0001 | g0057 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00673 | hp1 | a0003 | c0003 | t0002 | g0180 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0294 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0270 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0007 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00741 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01069 | hp2 | a0004 | c0005 | t0001 | g0246 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01071 | hp1 | a0004 | c0005 | t0001 | g0033 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0288 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0278 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01109 | hp2 | a0006 | c0006 | t0001 | g0043 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0280 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01175 | hp1 | a0003 | c0003 | t0002 | g0209 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0260 | AMR | PUR | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0307 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0007 | EUR | IBS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0285 | EUR | IBS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | IBS | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0284 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0188 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0179 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0269 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0183 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0301 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0267 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0309 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02055 | hp1 | a0005 | c0007 | t0001 | g0171 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02055 | hp2 | a0005 | c0007 | t0001 | g0055 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02071 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0175 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0200 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0210 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02155 | hp1 | a0008 | c0009 | t0001 | g0232 | EAS | CDX | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0264 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02273 | hp1 | a0003 | c0003 | t0002 | g0197 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0275 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02293 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02293 | hp2 | a0003 | c0003 | t0001 | g0204 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02300 | hp2 | a0003 | c0003 | t0002 | g0003 | AMR | PEL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0261 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0268 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0279 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0290 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0272 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0306 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02717 | hp2 | a0009 | c0008 | t0001 | g0051 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02818 | hp2 | a0001 | c0010 | t0001 | g0064 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03041 | hp2 | a0006 | c0006 | t0001 | g0046 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0315 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0313 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0211 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0310 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03490 | hp2 | a0003 | c0003 | t0001 | g0026 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0293 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0286 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0026 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03516 | hp2 | a0006 | c0006 | t0001 | g0044 | AFR | ESN | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | GWD | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0298 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0273 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0255 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03927 | hp1 | a0003 | c0003 | t0001 | g0190 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0265 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0266 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG04228 | hp2 | a0004 | c0005 | t0001 | g0032 | SAS | STU | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0277 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18747 | hp1 | a0010 | c0013 | t0001 | g0023 | EAS | CHB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18939 | hp2 | a0003 | c0003 | t0001 | g0184 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18942 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18944 | hp1 | a0003 | c0003 | t0002 | g0027 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18946 | hp1 | a0003 | c0003 | t0002 | g0205 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18950 | hp2 | a0003 | c0003 | t0001 | g0206 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18954 | hp1 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18963 | hp2 | a0011 | c0012 | t0002 | g0012 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0201 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18965 | hp1 | a0003 | c0003 | t0002 | g0176 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18966 | hp2 | a0003 | c0003 | t0002 | g0195 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18970 | hp2 | a0003 | c0003 | t0001 | g0202 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18971 | hp1 | a0003 | c0003 | t0001 | g0186 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18983 | hp1 | a0003 | c0003 | t0002 | g0196 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18986 | hp1 | a0003 | c0003 | t0002 | g0174 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18987 | hp1 | a0003 | c0003 | t0002 | g0177 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18994 | hp1 | a0003 | c0003 | t0002 | g0027 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18994 | hp2 | a0003 | c0003 | t0001 | g0189 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18999 | hp2 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19005 | hp1 | a0003 | c0003 | t0002 | g0193 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0308 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0282 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0311 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19056 | hp1 | a0003 | c0003 | t0002 | g0203 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0318 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19065 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0194 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19075 | hp1 | a0003 | c0003 | t0002 | g0192 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19076 | hp2 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19080 | hp1 | a0003 | c0003 | t0002 | g0187 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19087 | hp1 | a0003 | c0003 | t0002 | g0198 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19090 | hp1 | a0003 | c0003 | t0002 | g0181 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0283 | AFR | YRI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ASW | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ASW | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0292 | EUR | TSI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0166 | EUR | TSI | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0007 | SAS | GIH | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0281 | AFR | MSL | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | USA | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | USA | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA18955 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | USA | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0199 | AFR | USA | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0094 | REF | REF | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| homoSapiens | grch38p0 | a0004 | c0005 | t0001 | g0228 | REF | REF | HEXB_chr5_74680233_74726288 | HEXB | chr5 | 74680233 | 74726288 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74685445 | T | C | 10 | a0001 a0002 a0003 others(7): Show |
390 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(387): Show |
missense_variant | MODERATE | c.185T>C | p.Leu62Ser | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/14 | 213/1812 | 185/1671 | 62/556 | chr5 | 74685445 | |||
| chr5:74685474 | C | T | 1 | a0010 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.214C>T | p.Leu72Phe | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/14 | 242/1812 | 214/1671 | 72/556 | chr5 | 74685474 | |||
| chr5:74689390 | A | G | 2 | a0002 a0011 |
90 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(87): Show |
missense_variant | MODERATE | c.362A>G | p.Lys121Arg | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/14 | 390/1812 | 362/1671 | 121/556 | chr5 | 74689390 | |||
| chr5:74689411 | T | G | 1 | a0009 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.383T>G | p.Leu128Arg | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/14 | 411/1812 | 383/1671 | 128/556 | chr5 | 74689411 | |||
| chr5:74693642 | C | A | 1 | a0006 | 3 | HG01109.hp2 HG03041.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.449C>A | p.Thr150Asn | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/14 | 477/1812 | 449/1671 | 150/556 | chr5 | 74693642 | |||
| chr5:74697056 | A | G | 2 | a0003 a0007 |
55 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(52): Show |
missense_variant | MODERATE | c.619A>G | p.Ile207Val | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/14 | 647/1812 | 619/1671 | 207/556 | chr5 | 74697056 | |||
| chr5:74713558 | T | C | 1 | a0008 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.824T>C | p.Ile275Thr | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/14 | 852/1812 | 824/1671 | 275/556 | chr5 | 74713558 | |||
| chr5:74715674 | G | A | 1 | a0007 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.1066G>A | p.Val356Met | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/14 | 1094/1812 | 1066/1671 | 356/556 | chr5 | 74715674 | |||
| chr5:74718804 | C | T | 1 | a0011 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.1250C>T | p.Pro417Leu | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/14 | 1278/1812 | 1250/1671 | 417/556 | chr5 | 74718804 | |||
| chr5:74718812 | A | G | 1 | a0005 | 3 | HG00642.hp1 HG02055.hp1 HG02055.hp2 |
missense_variant | MODERATE | c.1258A>G | p.Ile420Val | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/14 | 1286/1812 | 1258/1671 | 420/556 | chr5 | 74718812 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74685536 | C | T | 1 | a0001c0004 | 5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
synonymous_variant | LOW | c.276C>T | p.Thr92Thr | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/14 | 304/1812 | 276/1671 | 92/556 | chr5 | 74685536 | |||
| chr5:74715659 | T | C | 1 | a0001c0010 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.1051T>C | p.Leu351Leu | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/14 | 1079/1812 | 1051/1671 | 351/556 | chr5 | 74715659 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74721255 | CTG | C | 4 | a0001c0001t0002 a0002c0002t0002 a0003c0003t0002 others(1): Show |
38 | HG00673.hp1 HG00741.hp1 HG01123.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*82_*83delGT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 14/14 | 82 | INFO_REALIGN_3_PRIME | chr5 | 74721255 | |||||
| chr5:74721282 | G | A | 1 | a0001c0001t0003 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*107G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 14/14 | 107 | chr5 | 74721282 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74685634 | C | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.299+75C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74685634 | |||||||
| chr5:74685837 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.299+278G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74685837 | |||||||
| chr5:74686133 | G | GTCAGTGG others(1): Show |
43 | a0001c0001t0001g0208 a0003c0003t0001g0002 a0003c0003t0001g0007 others(40): Show |
56 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.299+576_299+583dup others(8): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 74686133 | ||||||
| chr5:74686254 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.299+695A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686254 | |||||||
| chr5:74686500 | C | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.299+941C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686500 | |||||||
| chr5:74686524 | C | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.299+965C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686524 | |||||||
| chr5:74686550 | C | T | 11 | a0001c0001t0001g0040 a0001c0001t0001g0322 a0001c0001t0001g0323 others(8): Show |
12 | HG00741.hp2 HG01106.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.299+991C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686550 | |||||||
| chr5:74686682 | C | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.299+1123C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686682 | |||||||
| chr5:74686764 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.299+1205T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686764 | |||||||
| chr5:74686799 | T | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.299+1240T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686799 | |||||||
| chr5:74686802 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.299+1243A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686802 | |||||||
| chr5:74686867 | G | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.299+1308G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686867 | |||||||
| chr5:74686870 | T | C | 44 | a0001c0001t0001g0050 a0001c0001t0001g0208 a0003c0003t0001g0002 others(41): Show |
57 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.299+1311T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686870 | |||||||
| chr5:74686964 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.299+1405G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74686964 | |||||||
| chr5:74687014 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0212 |
3 | HG01891.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299+1455C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74687014 | |||||||
| chr5:74687140 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
242 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.299+1581T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74687140 | |||||||
| chr5:74687224 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.299+1665A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74687224 | |||||||
| chr5:74687301 | C | T | 1 | a0002c0002t0001g0321 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.299+1742C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74687301 | |||||||
| chr5:74687907 | G | T | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.300-1421G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74687907 | |||||||
| chr5:74688042 | T | G | 1 | a0009c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.300-1286T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688042 | |||||||
| chr5:74688102 | T | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0053 others(5): Show |
11 | HG00642.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.300-1226T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688102 | |||||||
| chr5:74688200 | T | C | 1 | a0002c0002t0002g0029 | 2 | NA19074.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.300-1128T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688200 | |||||||
| chr5:74688249 | A | AT | 188 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.300-1077dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 74688249 | ||||||
| chr5:74688328 | A | C | 1 | a0001c0001t0002g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.300-1000A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688328 | |||||||
| chr5:74688333 | G | C | 1 | a0001c0001t0002g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.300-995G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688333 | |||||||
| chr5:74688336 | C | CT | 181 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.300-979dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 74688336 | ||||||
| chr5:74688336 | C | CTTTTTTT others(105): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0212 |
3 | HG01891.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.300-985_300-984ins others(112): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 74688336 | ||||||
| chr5:74688353 | A | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0048 |
5 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-975A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688353 | |||||||
| chr5:74688363 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.300-965G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688363 | |||||||
| chr5:74688412 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.300-916G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688412 | |||||||
| chr5:74688421 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.300-907A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688421 | |||||||
| chr5:74688439 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
242 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.300-889G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688439 | |||||||
| chr5:74688589 | C | T | 1 | a0003c0003t0001g0210 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.300-739C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688589 | |||||||
| chr5:74688635 | A | G | 91 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(88): Show |
103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.300-693A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688635 | |||||||
| chr5:74688785 | C | T | 89 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.300-543C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688785 | |||||||
| chr5:74688818 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.300-510G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688818 | |||||||
| chr5:74688897 | T | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.300-431T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74688897 | |||||||
| chr5:74689052 | C | CA | 89 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.300-276_300-275ins others(1): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689052 | |||||||
| chr5:74689061 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.300-267A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689061 | |||||||
| chr5:74689088 | A | G | 89 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.300-240A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689088 | |||||||
| chr5:74689127 | C | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.300-201C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689127 | |||||||
| chr5:74689282 | T | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
6 | HG00140.hp2 HG00639.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.300-46T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689282 | |||||||
| chr5:74689296 | C | T | 89 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.300-32C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 1/13 | chr5 | 74689296 | |||||||
| chr5:74689532 | T | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 |
6 | HG02145.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+59T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74689532 | |||||||
| chr5:74689709 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
330 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.445+236T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74689709 | |||||||
| chr5:74689753 | A | C | 80 | a0002c0002t0001g0011 a0002c0002t0001g0034 a0002c0002t0001g0035 others(77): Show |
90 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.445+280A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74689753 | |||||||
| chr5:74689839 | T | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.445+366T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74689839 | |||||||
| chr5:74689972 | T | G | 1 | a0002c0002t0001g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+499T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74689972 | |||||||
| chr5:74690010 | CT | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(274): Show |
331 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.445+542delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690010 | ||||||
| chr5:74690040 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445+567G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690040 | |||||||
| chr5:74690085 | A | G | 89 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.445+612A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690085 | |||||||
| chr5:74690175 | T | C | 1 | a0009c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.445+702T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690175 | |||||||
| chr5:74690317 | A | G | 2 | a0001c0001t0001g0163 a0003c0003t0002g0209 |
2 | HG00323.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.445+844A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690317 | |||||||
| chr5:74690364 | T | C | 89 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.445+891T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690364 | |||||||
| chr5:74690375 | C | T | 89 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.445+902C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690375 | |||||||
| chr5:74690381 | G | A | 89 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
101 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.445+908G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690381 | |||||||
| chr5:74690471 | GA | G | 79 | a0002c0002t0001g0011 a0002c0002t0001g0034 a0002c0002t0001g0035 others(76): Show |
89 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.445+1001delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690471 | ||||||
| chr5:74690478 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.445+1005C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690478 | |||||||
| chr5:74690602 | C | T | 91 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(88): Show |
103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.445+1129C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690602 | |||||||
| chr5:74690603 | A | G | 91 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(88): Show |
103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.445+1130A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690603 | |||||||
| chr5:74690629 | G | C | 1 | a0002c0002t0001g0253 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.445+1156G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690629 | |||||||
| chr5:74690649 | CAAAA | C | 18 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0069 others(15): Show |
19 | HG01106.hp2 HG02015.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.445+1223_445+1226d others(6): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAA | C | 13 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(10): Show |
14 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.445+1222_445+1226d others(7): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0070 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.445+1217_445+1226d others(12): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
6 | HG02055.hp2 NA18982.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+1216_445+1226d others(13): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0056 a0001c0001t0002g0074 |
2 | HG03098.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.445+1215_445+1226d others(14): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
7 | HG00642.hp1 HG00673.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.445+1214_445+1226d others(15): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0078 |
2 | HG01257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.445+1213_445+1226d others(16): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.445+1210_445+1226d others(19): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG01109.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.445+1208_445+1226d others(21): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(13): Show |
C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
9 | HG02145.hp2 HG02602.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+1207_445+1226d others(22): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0001g0251 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.445+1206_445+1226d others(23): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(17): Show |
C | 2 | a0001c0001t0001g0080 a0009c0008t0001g0051 |
2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.445+1203_445+1226d others(26): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(18): Show |
C | 49 | a0001c0001t0001g0015 a0001c0001t0001g0081 a0001c0001t0001g0082 others(46): Show |
63 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.445+1202_445+1226d others(27): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(19): Show |
C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(96): Show |
120 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.445+1201_445+1226d others(28): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(20): Show |
C | 91 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(88): Show |
103 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.445+1200_445+1226d others(29): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(21): Show |
C | 8 | a0001c0001t0001g0045 a0002c0002t0001g0315 a0002c0002t0001g0316 others(5): Show |
8 | HG00639.hp1 HG02895.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.445+1199_445+1226d others(30): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(23): Show |
C | 1 | a0001c0001t0001g0252 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.445+1197_445+1226d others(32): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690649 | CAAAAAAA others(28): Show |
C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0212 |
3 | HG01891.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.445+1192_445+1226d others(37): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74690649 | ||||||
| chr5:74690698 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.445+1225A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690698 | |||||||
| chr5:74690781 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.445+1308G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690781 | |||||||
| chr5:74690805 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445+1332T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690805 | |||||||
| chr5:74690823 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(173): Show |
204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.445+1350A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690823 | |||||||
| chr5:74690928 | T | C | 1 | a0009c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.445+1455T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690928 | |||||||
| chr5:74690969 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.445+1496C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74690969 | |||||||
| chr5:74691001 | T | C | 81 | a0001c0001t0001g0170 a0002c0002t0001g0011 a0002c0002t0001g0034 others(78): Show |
91 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.445+1528T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691001 | |||||||
| chr5:74691136 | G | A | 1 | a0008c0009t0001g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.445+1663G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691136 | |||||||
| chr5:74691223 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(109): Show |
131 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.445+1750C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691223 | |||||||
| chr5:74691310 | C | T | 81 | a0001c0001t0001g0170 a0002c0002t0001g0011 a0002c0002t0001g0034 others(78): Show |
91 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.445+1837C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691310 | |||||||
| chr5:74691529 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0104 a0001c0001t0001g0152 |
6 | HG00408.hp2 HG00597.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+2056G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691529 | |||||||
| chr5:74691665 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.446-1974G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691665 | |||||||
| chr5:74691721 | A | G | 91 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(88): Show |
103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.446-1918A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691721 | |||||||
| chr5:74691783 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.446-1856A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691783 | |||||||
| chr5:74691817 | C | G | 1 | a0003c0003t0001g0204 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.446-1822C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691817 | |||||||
| chr5:74691950 | A | G | 146 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0028 others(143): Show |
178 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.446-1689A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691950 | |||||||
| chr5:74691972 | A | T | 2 | a0002c0002t0001g0039 a0002c0002t0001g0314 |
3 | NA18975.hp2 NA18988.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.446-1667A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74691972 | |||||||
| chr5:74691973 | GA | G | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(3): Show |
6 | HG01109.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.446-1662delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74691973 | ||||||
| chr5:74692082 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0212 |
3 | HG01891.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.446-1557G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692082 | |||||||
| chr5:74692323 | C | T | 3 | a0006c0006t0001g0043 a0006c0006t0001g0044 a0006c0006t0001g0046 |
3 | HG01109.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.446-1316C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692323 | |||||||
| chr5:74692334 | C | CA | 20 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0069 others(17): Show |
25 | HG01258.hp1 HG01884.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.446-1287dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74692334 | ||||||
| chr5:74692334 | CA | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
13 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.446-1287delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 74692334 | ||||||
| chr5:74692667 | T | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.446-972T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692667 | |||||||
| chr5:74692721 | G | A | 81 | a0001c0001t0001g0170 a0002c0002t0001g0011 a0002c0002t0001g0034 others(78): Show |
91 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.446-918G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692721 | |||||||
| chr5:74692863 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.446-776C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692863 | |||||||
| chr5:74692911 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.446-728G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692911 | |||||||
| chr5:74692990 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.446-649T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74692990 | |||||||
| chr5:74693013 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.446-626A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74693013 | |||||||
| chr5:74693194 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.446-445G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74693194 | |||||||
| chr5:74693302 | A | G | 91 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(88): Show |
103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.446-337A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74693302 | |||||||
| chr5:74693472 | C | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
332 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.446-167C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 2/13 | chr5 | 74693472 | |||||||
| chr5:74693731 | C | T | 5 | a0002c0002t0001g0038 a0002c0002t0001g0310 a0002c0002t0001g0311 others(2): Show |
6 | HG02895.hp2 HG02965.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.511+27C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693731 | |||||||
| chr5:74693752 | T | C | 2 | a0002c0002t0001g0258 a0002c0002t0001g0321 |
2 | NA18972.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.511+48T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693752 | |||||||
| chr5:74693855 | T | G | 1 | a0002c0002t0001g0034 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.511+151T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693855 | |||||||
| chr5:74693857 | C | T | 1 | a0002c0002t0001g0034 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.511+153C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693857 | |||||||
| chr5:74693859 | A | C | 1 | a0002c0002t0001g0034 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.511+155A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693859 | |||||||
| chr5:74693876 | G | A | 3 | a0001c0001t0001g0322 a0001c0001t0001g0324 a0001c0001t0001g0329 |
3 | HG02559.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.511+172G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693876 | |||||||
| chr5:74693929 | G | A | 1 | a0002c0002t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.511+225G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693929 | |||||||
| chr5:74693968 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.511+264G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693968 | |||||||
| chr5:74693980 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0212 |
3 | HG01891.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.511+276G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74693980 | |||||||
| chr5:74694069 | G | C | 80 | a0001c0001t0001g0170 a0002c0002t0001g0011 a0002c0002t0001g0034 others(77): Show |
90 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.511+365G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694069 | |||||||
| chr5:74694069 | G | T | 1 | a0002c0002t0001g0309 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.511+365G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694069 | |||||||
| chr5:74694105 | G | A | 43 | a0003c0003t0001g0002 a0003c0003t0001g0007 a0003c0003t0001g0026 others(40): Show |
56 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.511+401G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694105 | |||||||
| chr5:74694187 | A | G | 91 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(88): Show |
103 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.511+483A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694187 | |||||||
| chr5:74694694 | G | A | 3 | a0002c0002t0001g0260 a0002c0002t0001g0261 a0002c0002t0001g0262 |
3 | HG01243.hp2 HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.511+990G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694694 | |||||||
| chr5:74694733 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.511+1029G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694733 | |||||||
| chr5:74694752 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.511+1048G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694752 | |||||||
| chr5:74694810 | C | CA | 82 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(79): Show |
92 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.511+1116dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr5 | 74694810 | ||||||
| chr5:74694824 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511+1120G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694824 | |||||||
| chr5:74694839 | G | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+1135G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694839 | |||||||
| chr5:74694959 | A | G | 167 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(164): Show |
202 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.511+1255A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74694959 | |||||||
| chr5:74695050 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.511+1346C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695050 | |||||||
| chr5:74695180 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+1476G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695180 | |||||||
| chr5:74695201 | C | CT | 31 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0048 others(28): Show |
33 | HG00733.hp1 HG01243.hp1 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.512-1472dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr5 | 74695201 | ||||||
| chr5:74695201 | CT | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
16 | HG00673.hp2 HG01257.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.512-1472delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr5 | 74695201 | ||||||
| chr5:74695234 | T | C | 85 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(82): Show |
98 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.512-1459T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695234 | |||||||
| chr5:74695243 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.512-1450G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695243 | |||||||
| chr5:74695360 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(106): Show |
128 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.512-1333C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695360 | |||||||
| chr5:74695399 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.512-1294T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695399 | |||||||
| chr5:74695418 | T | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 |
6 | HG02145.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.512-1275T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695418 | |||||||
| chr5:74695483 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.512-1210G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695483 | |||||||
| chr5:74695579 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.512-1114G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695579 | |||||||
| chr5:74695814 | C | A | 2 | a0002c0002t0001g0310 a0002c0002t0001g0311 |
2 | HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.512-879C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695814 | |||||||
| chr5:74695839 | T | TA | 185 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(182): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.512-837dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr5 | 74695839 | ||||||
| chr5:74695898 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.512-795G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695898 | |||||||
| chr5:74695973 | T | C | 1 | a0003c0003t0001g0179 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.512-720T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74695973 | |||||||
| chr5:74696204 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.512-489A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74696204 | |||||||
| chr5:74696387 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.512-306T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74696387 | |||||||
| chr5:74696574 | A | G | 1 | a0002c0002t0001g0037 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.512-119A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74696574 | |||||||
| chr5:74696581 | T | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(161): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.512-112T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 3/13 | chr5 | 74696581 | |||||||
| chr5:74696784 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(270): Show |
324 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.558+45G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 4/13 | chr5 | 74696784 | |||||||
| chr5:74696978 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.559-18A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 4/13 | chr5 | 74696978 | |||||||
| chr5:74697387 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0068 others(5): Show |
9 | HG04184.hp2 NA18948.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+281C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697387 | |||||||
| chr5:74697454 | G | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
12 | HG00673.hp2 HG01257.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.669+348G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697454 | |||||||
| chr5:74697483 | T | C | 1 | a0009c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+377T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697483 | |||||||
| chr5:74697505 | C | T | 1 | a0002c0002t0001g0254 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.669+399C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697505 | |||||||
| chr5:74697594 | C | T | 1 | a0002c0002t0001g0301 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.669+488C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697594 | |||||||
| chr5:74697595 | G | A | 42 | a0003c0003t0001g0002 a0003c0003t0001g0007 a0003c0003t0001g0026 others(39): Show |
55 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.669+489G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697595 | |||||||
| chr5:74697727 | C | CA | 183 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.669+640dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74697727 | ||||||
| chr5:74697727 | C | CAA | 19 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0042 others(16): Show |
20 | HG00673.hp1 HG02055.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.669+639_669+640dup others(2): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74697727 | ||||||
| chr5:74697727 | CA | C | 71 | a0002c0002t0001g0011 a0002c0002t0001g0035 a0002c0002t0001g0036 others(68): Show |
80 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.669+640delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74697727 | ||||||
| chr5:74697843 | G | A | 1 | a0003c0003t0002g0181 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.669+737G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697843 | |||||||
| chr5:74697868 | T | G | 9 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+762T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697868 | |||||||
| chr5:74697953 | T | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0058 |
2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.669+847T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697953 | |||||||
| chr5:74697975 | C | T | 1 | a0009c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+869C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74697975 | |||||||
| chr5:74698046 | A | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(272): Show |
326 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.669+940A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698046 | |||||||
| chr5:74698055 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 |
6 | HG02145.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+949A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698055 | |||||||
| chr5:74698108 | G | A | 44 | a0002c0002t0001g0011 a0002c0002t0001g0034 a0002c0002t0001g0035 others(41): Show |
50 | HG00735.hp2 HG01081.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.669+1002G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698108 | |||||||
| chr5:74698139 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.669+1033G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698139 | |||||||
| chr5:74698146 | C | T | 3 | a0002c0002t0001g0038 a0002c0002t0001g0312 a0002c0002t0001g0313 |
4 | HG02895.hp2 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+1040C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698146 | |||||||
| chr5:74698178 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.669+1072A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698178 | |||||||
| chr5:74698218 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.669+1112C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698218 | |||||||
| chr5:74698239 | A | G | 53 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(50): Show |
61 | HG00733.hp1 HG00735.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.669+1133A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698239 | |||||||
| chr5:74698393 | A | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+1287A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698393 | |||||||
| chr5:74698395 | TA | T | 20 | a0002c0002t0001g0011 a0002c0002t0001g0034 a0002c0002t0001g0037 others(17): Show |
25 | HG01081.hp2 HG01167.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.669+1290delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698395 | |||||||
| chr5:74698396 | A | AT | 3 | a0003c0003t0001g0007 a0003c0003t0001g0026 a0003c0003t0002g0209 |
7 | HG00280.hp2 HG00738.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.669+1299dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74698396 | ||||||
| chr5:74698396 | A | T | 69 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0040 others(66): Show |
76 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.669+1290A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698396 | |||||||
| chr5:74698396 | AT | A | 23 | a0002c0002t0001g0035 a0002c0002t0001g0253 a0002c0002t0001g0258 others(20): Show |
24 | HG00735.hp2 HG01243.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.669+1299delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74698396 | ||||||
| chr5:74698399 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0236 a0009c0008t0001g0051 |
3 | HG02015.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.669+1293T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698399 | |||||||
| chr5:74698400 | T | A | 2 | a0002c0002t0001g0260 a0002c0002t0001g0267 |
2 | HG01243.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.669+1294T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698400 | |||||||
| chr5:74698431 | C | T | 3 | a0002c0002t0001g0277 a0002c0002t0001g0283 a0002c0002t0001g0284 |
3 | HG01884.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.669+1325C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698431 | |||||||
| chr5:74698436 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.669+1330G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698436 | |||||||
| chr5:74698454 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.669+1348C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698454 | |||||||
| chr5:74698468 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+1362T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698468 | |||||||
| chr5:74698477 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.669+1371C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698477 | |||||||
| chr5:74698485 | G | A | 44 | a0002c0002t0001g0011 a0002c0002t0001g0034 a0002c0002t0001g0035 others(41): Show |
50 | HG00735.hp2 HG01081.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.669+1379G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698485 | |||||||
| chr5:74698508 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0048 |
5 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+1402C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698508 | |||||||
| chr5:74698641 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0076 others(6): Show |
11 | HG00673.hp2 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+1535C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698641 | |||||||
| chr5:74698868 | T | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0068 others(8): Show |
12 | HG00438.hp1 HG03239.hp2 HG04184.hp2 others(9): Show |
intron_variant | MODIFIER | c.669+1762T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74698868 | |||||||
| chr5:74699270 | A | C | 1 | a0001c0001t0001g0150 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+2164A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699270 | |||||||
| chr5:74699271 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+2165C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699271 | |||||||
| chr5:74699289 | T | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0114 |
2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.669+2183T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699289 | |||||||
| chr5:74699317 | A | G | 1 | a0001c0001t0001g0327 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.669+2211A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699317 | |||||||
| chr5:74699357 | C | G | 1 | a0002c0002t0001g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.669+2251C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699357 | |||||||
| chr5:74699369 | AGTTCAAG others(725): Show |
A | 1 | a0001c0001t0001g0230 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.669+2272_669+3003d others(2): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74699369 | ||||||
| chr5:74699400 | G | C | 1 | a0003c0003t0001g0204 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.669+2294G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699400 | |||||||
| chr5:74699417 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.669+2311G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699417 | |||||||
| chr5:74699418 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.669+2312G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699418 | |||||||
| chr5:74699482 | TCAGGCTG others(1426): Show |
T | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+2404_669+3836d others(2): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74699482 | ||||||
| chr5:74699516 | T | C | 12 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(9): Show |
13 | HG00741.hp2 HG01106.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.669+2410T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699516 | |||||||
| chr5:74699552 | G | A | 12 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(9): Show |
13 | HG00741.hp2 HG01106.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.669+2446G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699552 | |||||||
| chr5:74699794 | A | G | 34 | a0001c0001t0001g0006 a0001c0001t0001g0104 a0001c0001t0001g0107 others(31): Show |
44 | HG00408.hp2 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.669+2688A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74699794 | |||||||
| chr5:74699947 | C | CT | 274 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
327 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.669+2849dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74699947 | ||||||
| chr5:74700001 | C | CT | 10 | a0001c0001t0001g0009 a0001c0001t0001g0071 a0001c0001t0001g0072 others(7): Show |
10 | HG00140.hp1 HG00735.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.669+2920dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | ||||||
| chr5:74700001 | CT | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0059 others(19): Show |
26 | HG00408.hp2 HG00558.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.669+2920delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | ||||||
| chr5:74700001 | CTT | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(194): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.669+2919_669+2920d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | ||||||
| chr5:74700001 | CTTT | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0053 others(8): Show |
14 | HG00323.hp1 HG00558.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.669+2918_669+2920d others(5): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | ||||||
| chr5:74700001 | CTTTT | C | 10 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(7): Show |
11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+2917_669+2920d others(6): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | ||||||
| chr5:74700001 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0101 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.669+2908_669+2920d others(15): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74700001 | ||||||
| chr5:74700070 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.669+2964A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700070 | |||||||
| chr5:74700109 | C | T | 1 | a0002c0002t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.669+3003C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700109 | |||||||
| chr5:74700146 | A | G | 1 | a0002c0002t0001g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.669+3040A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700146 | |||||||
| chr5:74700163 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+3057C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700163 | |||||||
| chr5:74700164 | A | C | 1 | a0001c0001t0001g0150 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+3058A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700164 | |||||||
| chr5:74700165 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+3059C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700165 | |||||||
| chr5:74700285 | G | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0002c0002t0001g0281 others(2): Show |
7 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.669+3179G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700285 | |||||||
| chr5:74700582 | G | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(221): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.669+3476G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700582 | |||||||
| chr5:74700723 | T | C | 3 | a0005c0007t0001g0055 a0005c0007t0001g0057 a0005c0007t0001g0171 |
3 | HG00642.hp1 HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.669+3617T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700723 | |||||||
| chr5:74700729 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0223 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.669+3623C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700729 | |||||||
| chr5:74700771 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.669+3665G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700771 | |||||||
| chr5:74700818 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.669+3712C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700818 | |||||||
| chr5:74700999 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(176): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.669+3893T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74700999 | |||||||
| chr5:74701050 | A | AT | 9 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0106 others(6): Show |
14 | HG00733.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.669+3958dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74701050 | ||||||
| chr5:74701050 | AT | A | 8 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0153 others(5): Show |
8 | HG01069.hp2 HG01169.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.669+3958delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74701050 | ||||||
| chr5:74701108 | C | T | 2 | a0003c0003t0001g0190 a0003c0003t0001g0207 |
2 | HG00423.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.669+4002C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701108 | |||||||
| chr5:74701120 | C | T | 10 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(7): Show |
11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+4014C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701120 | |||||||
| chr5:74701500 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.670-3719A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701500 | |||||||
| chr5:74701699 | A | T | 31 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(28): Show |
35 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.670-3520A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701699 | |||||||
| chr5:74701747 | A | G | 1 | a0003c0003t0001g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.670-3472A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701747 | |||||||
| chr5:74701793 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.670-3426C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701793 | |||||||
| chr5:74701904 | G | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0098 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.670-3315G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701904 | |||||||
| chr5:74701939 | C | T | 2 | a0002c0002t0001g0277 a0002c0002t0001g0284 |
2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.670-3280C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74701939 | |||||||
| chr5:74702032 | C | A | 1 | a0003c0003t0001g0184 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.670-3187C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702032 | |||||||
| chr5:74702061 | C | A | 20 | a0001c0001t0001g0052 a0001c0001t0001g0071 a0001c0001t0001g0072 others(17): Show |
25 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.670-3158C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702061 | |||||||
| chr5:74702063 | T | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0006c0006t0001g0046 |
3 | HG03041.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.670-3156T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702063 | |||||||
| chr5:74702067 | C | CT | 14 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0100 others(11): Show |
14 | HG01109.hp1 HG01175.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-3123dupT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | ||||||
| chr5:74702067 | CT | C | 16 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0077 others(13): Show |
17 | HG00558.hp1 HG01975.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.670-3123delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | ||||||
| chr5:74702067 | CTT | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(60): Show |
73 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.670-3124_670-3123d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | ||||||
| chr5:74702067 | CTTT | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(170): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.670-3125_670-3123d others(5): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | ||||||
| chr5:74702067 | CTTTT | C | 24 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0040 others(21): Show |
27 | HG00597.hp1 HG00639.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.670-3126_670-3123d others(6): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | ||||||
| chr5:74702067 | CTTTTT | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0002c0002t0001g0281 others(1): Show |
6 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-3127_670-3123d others(7): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74702067 | ||||||
| chr5:74702109 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.670-3110C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702109 | |||||||
| chr5:74702117 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-3102C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702117 | |||||||
| chr5:74702148 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(206): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.670-3071G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702148 | |||||||
| chr5:74702239 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.670-2980T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702239 | |||||||
| chr5:74702241 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0002c0002t0001g0281 others(2): Show |
7 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-2978G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702241 | |||||||
| chr5:74702305 | C | T | 1 | a0003c0003t0002g0197 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.670-2914C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702305 | |||||||
| chr5:74702325 | G | A | 30 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(27): Show |
33 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.670-2894G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702325 | |||||||
| chr5:74702369 | C | T | 7 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0105 others(4): Show |
7 | HG00673.hp2 NA18940.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-2850C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702369 | |||||||
| chr5:74702670 | G | T | 1 | a0001c0010t0001g0064 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.670-2549G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702670 | |||||||
| chr5:74702726 | C | T | 1 | a0002c0002t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.670-2493C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702726 | |||||||
| chr5:74702883 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.670-2336G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702883 | |||||||
| chr5:74702896 | G | T | 34 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0001c0001t0002g0074 others(31): Show |
41 | HG00673.hp1 HG00741.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.670-2323G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74702896 | |||||||
| chr5:74703044 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.670-2175C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703044 | |||||||
| chr5:74703055 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.670-2164C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703055 | |||||||
| chr5:74703077 | T | G | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.670-2142T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703077 | |||||||
| chr5:74703149 | C | T | 30 | a0001c0001t0002g0074 a0001c0001t0002g0096 a0001c0001t0002g0142 others(27): Show |
37 | HG00673.hp1 HG00741.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.670-2070C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703149 | |||||||
| chr5:74703214 | A | G | 34 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0001c0001t0002g0074 others(31): Show |
41 | HG00673.hp1 HG00741.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.670-2005A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703214 | |||||||
| chr5:74703235 | G | T | 1 | a0001c0010t0001g0064 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.670-1984G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703235 | |||||||
| chr5:74703380 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.670-1839T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703380 | |||||||
| chr5:74703401 | C | T | 3 | a0001c0001t0001g0149 a0002c0002t0001g0292 a0003c0003t0002g0209 |
3 | HG01175.hp1 HG01346.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.670-1818C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703401 | |||||||
| chr5:74703535 | G | C | 2 | a0002c0002t0001g0254 a0002c0002t0001g0302 |
2 | HG00621.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.670-1684G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703535 | |||||||
| chr5:74703606 | T | C | 2 | a0002c0002t0001g0261 a0002c0002t0001g0315 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.670-1613T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703606 | |||||||
| chr5:74703607 | A | G | 62 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(59): Show |
69 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.670-1612A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703607 | |||||||
| chr5:74703614 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.670-1605C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703614 | |||||||
| chr5:74703616 | A | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.670-1603A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703616 | |||||||
| chr5:74703807 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0006c0006t0001g0046 |
3 | HG03041.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.670-1412C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703807 | |||||||
| chr5:74703817 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.670-1402G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703817 | |||||||
| chr5:74703957 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.670-1262A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703957 | |||||||
| chr5:74703969 | G | A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(7): Show |
11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-1250G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703969 | |||||||
| chr5:74703975 | G | A | 2 | a0002c0002t0001g0258 a0002c0002t0001g0321 |
2 | NA18972.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.670-1244G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74703975 | |||||||
| chr5:74704006 | G | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.670-1213G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704006 | |||||||
| chr5:74704013 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0155 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.670-1206C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704013 | |||||||
| chr5:74704042 | A | G | 10 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(7): Show |
11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-1177A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704042 | |||||||
| chr5:74704259 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(180): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.670-960C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704259 | |||||||
| chr5:74704260 | C | A | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.670-959C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704260 | |||||||
| chr5:74704305 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.670-914C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704305 | |||||||
| chr5:74704370 | G | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.670-849G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704370 | |||||||
| chr5:74704443 | A | G | 2 | a0001c0001t0001g0023 a0010c0013t0001g0023 |
2 | HG00642.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.670-776A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704443 | |||||||
| chr5:74704529 | C | T | 6 | a0001c0001t0001g0326 a0001c0001t0001g0331 a0002c0002t0001g0038 others(3): Show |
7 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-690C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704529 | |||||||
| chr5:74704574 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.670-645G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704574 | |||||||
| chr5:74704802 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.670-417T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704802 | |||||||
| chr5:74704812 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.670-407C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704812 | |||||||
| chr5:74704868 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.670-351G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704868 | |||||||
| chr5:74704945 | A | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-274A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | chr5 | 74704945 | |||||||
| chr5:74705091 | C | CA | 61 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(58): Show |
71 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.670-107dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74705091 | ||||||
| chr5:74705091 | CA | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(191): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.670-107delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74705091 | ||||||
| chr5:74705091 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0095 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.670-118_670-107del others(12): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr5 | 74705091 | ||||||
| chr5:74705535 | A | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0131 |
2 | HG01074.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.771+215A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705535 | |||||||
| chr5:74705540 | A | G | 12 | a0001c0001t0001g0075 a0001c0001t0001g0237 a0001c0001t0001g0242 others(9): Show |
12 | HG01928.hp2 HG01943.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.771+220A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705540 | |||||||
| chr5:74705656 | C | A | 6 | a0002c0002t0001g0035 a0002c0002t0001g0263 a0002c0002t0001g0267 others(3): Show |
7 | HG01361.hp1 HG01496.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+336C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705656 | |||||||
| chr5:74705757 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(8): Show |
14 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.771+437A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705757 | |||||||
| chr5:74705792 | T | C | 20 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0106 others(17): Show |
22 | HG00597.hp1 HG00735.hp2 HG02148.hp1 others(19): Show |
intron_variant | MODIFIER | c.771+472T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705792 | |||||||
| chr5:74705874 | G | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+554G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705874 | |||||||
| chr5:74705929 | A | C | 1 | a0003c0003t0002g0196 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.771+609A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74705929 | |||||||
| chr5:74706152 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.771+832G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706152 | |||||||
| chr5:74706351 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.771+1031G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706351 | |||||||
| chr5:74706416 | T | C | 1 | a0002c0002t0001g0275 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.771+1096T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706416 | |||||||
| chr5:74706443 | C | T | 4 | a0001c0001t0001g0090 a0001c0001t0001g0143 a0001c0001t0001g0236 others(1): Show |
4 | HG00558.hp1 HG02015.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+1123C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706443 | |||||||
| chr5:74706447 | G | A | 3 | a0005c0007t0001g0055 a0005c0007t0001g0057 a0005c0007t0001g0171 |
3 | HG00642.hp1 HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.771+1127G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706447 | |||||||
| chr5:74706472 | G | A | 12 | a0001c0001t0001g0076 a0001c0001t0001g0084 a0001c0001t0001g0088 others(9): Show |
12 | HG00673.hp2 HG02056.hp2 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.771+1152G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706472 | |||||||
| chr5:74706473 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.771+1153C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706473 | |||||||
| chr5:74706474 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.771+1154G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706474 | |||||||
| chr5:74706489 | G | C | 10 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(7): Show |
11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+1169G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706489 | |||||||
| chr5:74706506 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(204): Show |
247 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.771+1186G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706506 | |||||||
| chr5:74706569 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(241): Show |
288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.771+1249G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706569 | |||||||
| chr5:74706578 | G | A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(7): Show |
11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+1258G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706578 | |||||||
| chr5:74706610 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.771+1290G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706610 | |||||||
| chr5:74706613 | G | A | 48 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(45): Show |
54 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.771+1293G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706613 | |||||||
| chr5:74706653 | C | A | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.771+1333C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706653 | |||||||
| chr5:74706689 | G | C | 38 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(35): Show |
43 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.771+1369G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706689 | |||||||
| chr5:74706732 | C | T | 1 | a0003c0003t0001g0173 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.771+1412C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706732 | |||||||
| chr5:74706791 | G | A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(7): Show |
11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+1471G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706791 | |||||||
| chr5:74706832 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(203): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.771+1512G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706832 | |||||||
| chr5:74706979 | C | T | 38 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(35): Show |
43 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.771+1659C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74706979 | |||||||
| chr5:74707106 | C | T | 34 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(31): Show |
37 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.771+1786C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707106 | |||||||
| chr5:74707129 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.771+1809T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707129 | |||||||
| chr5:74707131 | C | T | 1 | a0003c0003t0002g0195 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.771+1811C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707131 | |||||||
| chr5:74707133 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.771+1813C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707133 | |||||||
| chr5:74707169 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.771+1849C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707169 | |||||||
| chr5:74707171 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.771+1851C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707171 | |||||||
| chr5:74707175 | C | T | 1 | a0002c0002t0001g0253 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.771+1855C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707175 | |||||||
| chr5:74707276 | C | A | 1 | a0002c0002t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.771+1956C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707276 | |||||||
| chr5:74707306 | A | C | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.771+1986A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707306 | |||||||
| chr5:74707360 | C | T | 1 | a0003c0003t0001g0201 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.771+2040C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707360 | |||||||
| chr5:74707439 | G | A | 1 | a0002c0002t0001g0309 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.771+2119G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707439 | |||||||
| chr5:74707454 | T | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(45): Show |
54 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.771+2134T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707454 | |||||||
| chr5:74707754 | A | C | 1 | a0001c0001t0001g0229 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.771+2434A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707754 | |||||||
| chr5:74707822 | CTGAAAG | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.771+2512_771+2517d others(8): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 74707822 | ||||||
| chr5:74707838 | C | T | 5 | a0001c0001t0001g0100 a0001c0001t0001g0325 a0002c0002t0001g0037 others(2): Show |
6 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.771+2518C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707838 | |||||||
| chr5:74707863 | T | G | 3 | a0005c0007t0001g0055 a0005c0007t0001g0057 a0005c0007t0001g0171 |
3 | HG00642.hp1 HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.771+2543T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707863 | |||||||
| chr5:74707966 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.771+2646G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74707966 | |||||||
| chr5:74708057 | A | T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0113 others(2): Show |
5 | HG00438.hp1 HG00735.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+2737A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708057 | |||||||
| chr5:74708093 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.771+2773C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708093 | |||||||
| chr5:74708201 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | NA18982.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.771+2881G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708201 | |||||||
| chr5:74708325 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0002c0002t0001g0281 others(2): Show |
7 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+3005G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708325 | |||||||
| chr5:74708387 | A | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.771+3067A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708387 | |||||||
| chr5:74708526 | G | A | 22 | a0001c0001t0001g0052 a0001c0001t0001g0071 a0001c0001t0001g0072 others(19): Show |
27 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.771+3206G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708526 | |||||||
| chr5:74708532 | G | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.771+3212G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708532 | |||||||
| chr5:74708577 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.771+3257T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708577 | |||||||
| chr5:74708626 | T | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.771+3306T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708626 | |||||||
| chr5:74708704 | C | T | 1 | a0002c0002t0001g0274 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.771+3384C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708704 | |||||||
| chr5:74708722 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.771+3402A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708722 | |||||||
| chr5:74708734 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.771+3414A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708734 | |||||||
| chr5:74708792 | C | A | 1 | a0002c0002t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.771+3472C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708792 | |||||||
| chr5:74708883 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.771+3563C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74708883 | |||||||
| chr5:74709153 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.771+3833C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709153 | |||||||
| chr5:74709190 | T | C | 2 | a0001c0001t0001g0126 a0003c0003t0001g0206 |
2 | NA18612.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.771+3870T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709190 | |||||||
| chr5:74709328 | C | CA | 5 | a0003c0003t0001g0189 a0003c0003t0002g0027 a0003c0003t0002g0174 others(2): Show |
6 | NA18944.hp1 NA18986.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.771+4010dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 74709328 | ||||||
| chr5:74709367 | A | T | 1 | a0001c0001t0001g0015 | 2 | NA18954.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.771+4047A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709367 | |||||||
| chr5:74709481 | T | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0006c0006t0001g0046 |
3 | HG03041.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.772-4025T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709481 | |||||||
| chr5:74709533 | G | T | 1 | a0001c0001t0001g0239 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.772-3973G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709533 | |||||||
| chr5:74709554 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.772-3952A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709554 | |||||||
| chr5:74709654 | C | T | 23 | a0001c0001t0001g0052 a0001c0001t0001g0071 a0001c0001t0001g0072 others(20): Show |
28 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.772-3852C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709654 | |||||||
| chr5:74709715 | T | A | 2 | a0003c0003t0002g0176 a0003c0003t0002g0177 |
2 | NA18965.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.772-3791T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709715 | |||||||
| chr5:74709757 | A | G | 4 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0244 others(1): Show |
4 | NA18972.hp1 NA18975.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.772-3749A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709757 | |||||||
| chr5:74709841 | C | T | 1 | a0003c0003t0002g0194 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.772-3665C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709841 | |||||||
| chr5:74709862 | G | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0098 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.772-3644G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709862 | |||||||
| chr5:74709936 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.772-3570A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709936 | |||||||
| chr5:74709945 | G | A | 1 | a0001c0001t0002g0167 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.772-3561G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709945 | |||||||
| chr5:74709967 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.772-3539G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74709967 | |||||||
| chr5:74709987 | AAGAGAAT others(3): Show |
A | 21 | a0001c0001t0001g0052 a0001c0001t0001g0072 a0001c0001t0001g0077 others(18): Show |
26 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.772-3515_772-3506d others(12): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 74709987 | ||||||
| chr5:74710034 | C | G | 1 | a0001c0001t0001g0229 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.772-3472C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710034 | |||||||
| chr5:74710038 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0002c0002t0001g0281 others(2): Show |
7 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-3468A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710038 | |||||||
| chr5:74710117 | G | A | 1 | a0001c0010t0001g0064 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.772-3389G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710117 | |||||||
| chr5:74710122 | C | G | 123 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(120): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.772-3384C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710122 | |||||||
| chr5:74710136 | C | T | 20 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0106 others(17): Show |
22 | HG00597.hp1 HG00735.hp2 HG02148.hp1 others(19): Show |
intron_variant | MODIFIER | c.772-3370C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710136 | |||||||
| chr5:74710240 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.772-3266C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710240 | |||||||
| chr5:74710282 | A | G | 112 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(109): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.772-3224A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710282 | |||||||
| chr5:74710298 | A | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(61): Show |
77 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.772-3208A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710298 | |||||||
| chr5:74710319 | C | A | 123 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(120): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.772-3187C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710319 | |||||||
| chr5:74710341 | G | T | 35 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(32): Show |
40 | HG00140.hp2 HG00280.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.772-3165G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710341 | |||||||
| chr5:74710359 | TC | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(40): Show |
51 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.772-3144delC | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 74710359 | ||||||
| chr5:74710420 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(40): Show |
51 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.772-3086G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710420 | |||||||
| chr5:74710518 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-2988T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710518 | |||||||
| chr5:74710519 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-2987G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710519 | |||||||
| chr5:74710524 | T | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-2982T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710524 | |||||||
| chr5:74710543 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.772-2963T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710543 | |||||||
| chr5:74710636 | C | T | 21 | a0001c0001t0001g0052 a0001c0001t0001g0072 a0001c0001t0001g0077 others(18): Show |
26 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.772-2870C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710636 | |||||||
| chr5:74710788 | T | C | 29 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(26): Show |
32 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.772-2718T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710788 | |||||||
| chr5:74710794 | C | G | 1 | a0003c0003t0001g0201 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.772-2712C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710794 | |||||||
| chr5:74710860 | C | G | 1 | a0001c0001t0001g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.772-2646C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710860 | |||||||
| chr5:74710967 | A | G | 112 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(109): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.772-2539A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74710967 | |||||||
| chr5:74711016 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.772-2490G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711016 | |||||||
| chr5:74711049 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.772-2457A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711049 | |||||||
| chr5:74711051 | T | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(45): Show |
54 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.772-2455T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711051 | |||||||
| chr5:74711070 | C | T | 1 | a0005c0007t0001g0055 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.772-2436C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711070 | |||||||
| chr5:74711108 | C | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0077 |
2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.772-2398C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711108 | |||||||
| chr5:74711126 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0006c0006t0001g0046 |
3 | HG03041.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.772-2380C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711126 | |||||||
| chr5:74711151 | G | C | 1 | a0002c0002t0001g0294 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.772-2355G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711151 | |||||||
| chr5:74711273 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.772-2233C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711273 | |||||||
| chr5:74711664 | A | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(62): Show |
78 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.772-1842A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711664 | |||||||
| chr5:74711692 | A | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-1814A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711692 | |||||||
| chr5:74711702 | G | A | 2 | a0001c0001t0001g0225 a0003c0003t0001g0199 |
2 | HG01975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.772-1804G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711702 | |||||||
| chr5:74711713 | G | GAGCGATG others(33): Show |
3 | a0003c0003t0002g0027 a0003c0003t0002g0174 a0003c0003t0002g0192 |
4 | NA18944.hp1 NA18986.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.772-1793_772-1792i others(42): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711713 | |||||||
| chr5:74711714 | C | A | 3 | a0003c0003t0002g0027 a0003c0003t0002g0174 a0003c0003t0002g0192 |
4 | NA18944.hp1 NA18986.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.772-1792C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711714 | |||||||
| chr5:74711728 | A | T | 1 | a0002c0002t0001g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.772-1778A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711728 | |||||||
| chr5:74711739 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.772-1767A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711739 | |||||||
| chr5:74711750 | T | G | 33 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(30): Show |
36 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.772-1756T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711750 | |||||||
| chr5:74711799 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
11 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-1707G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711799 | |||||||
| chr5:74711964 | G | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(61): Show |
77 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.772-1542G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711964 | |||||||
| chr5:74711994 | T | C | 1 | a0003c0003t0002g0193 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.772-1512T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74711994 | |||||||
| chr5:74712175 | A | G | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(122): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.772-1331A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712175 | |||||||
| chr5:74712234 | G | C | 1 | a0002c0002t0001g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.772-1272G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712234 | |||||||
| chr5:74712372 | T | G | 1 | a0006c0006t0001g0044 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.772-1134T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712372 | |||||||
| chr5:74712433 | T | TA | 61 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(58): Show |
74 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.772-1071dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 74712433 | ||||||
| chr5:74712435 | AT | A | 46 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0017 others(43): Show |
54 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.772-1070delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712435 | |||||||
| chr5:74712436 | T | A | 80 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0028 others(77): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.772-1070T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712436 | |||||||
| chr5:74712461 | T | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(64): Show |
80 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.772-1045T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712461 | |||||||
| chr5:74712585 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.772-921T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712585 | |||||||
| chr5:74712586 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.772-920T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712586 | |||||||
| chr5:74712588 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.772-918T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712588 | |||||||
| chr5:74712601 | T | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(110): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.772-905T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712601 | |||||||
| chr5:74712691 | C | T | 3 | a0001c0004t0001g0008 a0001c0004t0001g0211 a0002c0002t0001g0300 |
6 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.772-815C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712691 | |||||||
| chr5:74712694 | C | T | 2 | a0002c0002t0001g0266 a0002c0002t0001g0273 |
2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.772-812C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712694 | |||||||
| chr5:74712698 | C | T | 113 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(110): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.772-808C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712698 | |||||||
| chr5:74712849 | C | T | 3 | a0001c0004t0001g0008 a0001c0004t0001g0211 a0002c0002t0001g0300 |
6 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.772-657C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712849 | |||||||
| chr5:74712938 | A | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(62): Show |
78 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.772-568A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74712938 | |||||||
| chr5:74713119 | G | A | 65 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(62): Show |
78 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.772-387G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713119 | |||||||
| chr5:74713196 | G | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(8): Show |
14 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.772-310G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713196 | |||||||
| chr5:74713254 | C | A | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.772-252C>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713254 | |||||||
| chr5:74713374 | T | G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0113 others(2): Show |
5 | HG00438.hp1 HG00735.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-132T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713374 | |||||||
| chr5:74713467 | C | T | 9 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(6): Show |
10 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.772-39C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713467 | |||||||
| chr5:74713502 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0059 others(5): Show |
10 | HG00639.hp2 HG01074.hp2 HG01169.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.772-4A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 6/13 | chr5 | 74713502 | |||||||
| chr5:74713733 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.901+98G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74713733 | |||||||
| chr5:74713944 | G | T | 4 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0244 others(1): Show |
4 | NA18972.hp1 NA18975.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.901+309G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74713944 | |||||||
| chr5:74714027 | G | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0006c0006t0001g0046 |
3 | HG03041.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.901+392G>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714027 | |||||||
| chr5:74714110 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.901+475T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714110 | |||||||
| chr5:74714183 | T | C | 1 | a0003c0003t0002g0203 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.901+548T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714183 | |||||||
| chr5:74714277 | C | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0050 a0001c0001t0001g0063 others(6): Show |
10 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.901+642C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714277 | |||||||
| chr5:74714625 | T | C | 1 | a0003c0003t0002g0195 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.902-885T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714625 | |||||||
| chr5:74714801 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.902-709G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714801 | |||||||
| chr5:74714934 | C | T | 3 | a0001c0004t0001g0008 a0001c0004t0001g0211 a0002c0002t0001g0300 |
6 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.902-576C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74714934 | |||||||
| chr5:74715108 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.902-402G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74715108 | |||||||
| chr5:74715242 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.902-268A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | chr5 | 74715242 | |||||||
| chr5:74715459 | CT | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(61): Show |
77 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.902-48delT | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr5 | 74715459 | ||||||
| chr5:74715716 | T | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(71): Show |
90 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1082+26T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | chr5 | 74715716 | |||||||
| chr5:74715716 | T | TA | 6 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0048 others(3): Show |
9 | HG00733.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1082+40dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 74715716 | ||||||
| chr5:74715991 | T | G | 48 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(45): Show |
54 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1082+301T>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | chr5 | 74715991 | |||||||
| chr5:74716016 | C | CA | 33 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0065 others(30): Show |
35 | HG00423.hp1 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1082+351dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 74716016 | ||||||
| chr5:74716016 | CA | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0028 others(43): Show |
58 | HG00741.hp1 HG01123.hp1 HG01175.hp1 others(55): Show |
intron_variant | MODIFIER | c.1082+351delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 74716016 | ||||||
| chr5:74716016 | CAA | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0056 a0001c0001t0001g0069 others(13): Show |
17 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.1082+350_1082+351d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 74716016 | ||||||
| chr5:74716016 | CAAA | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(56): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1082+349_1082+351d others(5): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 74716016 | ||||||
| chr5:74716027 | AAAAAAAA others(8): Show |
A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0083 a0001c0001t0001g0102 others(1): Show |
5 | HG01081.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1082+338_1082+352d others(17): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | chr5 | 74716027 | |||||||
| chr5:74716040 | AAT | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0025 others(28): Show |
35 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1082+351_1082+352d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | chr5 | 74716040 | |||||||
| chr5:74716044 | G | T | 1 | a0001c0001t0001g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1082+354G>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 8/13 | chr5 | 74716044 | |||||||
| chr5:74716734 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1169+61G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74716734 | |||||||
| chr5:74716762 | T | A | 4 | a0002c0002t0001g0261 a0002c0002t0001g0262 a0002c0002t0001g0315 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169+89T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74716762 | |||||||
| chr5:74716915 | C | T | 1 | a0003c0003t0001g0007 | 4 | HG00280.hp2 HG00738.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1169+242C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74716915 | |||||||
| chr5:74716918 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1169+245G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74716918 | |||||||
| chr5:74717017 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1169+344C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717017 | |||||||
| chr5:74717066 | T | A | 1 | a0006c0006t0001g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1169+393T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717066 | |||||||
| chr5:74717086 | C | T | 1 | a0003c0003t0001g0186 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1169+413C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717086 | |||||||
| chr5:74717246 | G | A | 1 | a0002c0002t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1169+573G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717246 | |||||||
| chr5:74717414 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0002c0002t0001g0281 others(2): Show |
7 | HG00733.hp1 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1169+741C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717414 | |||||||
| chr5:74717428 | C | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(42): Show |
53 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1169+755C>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717428 | |||||||
| chr5:74717450 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1169+777G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717450 | |||||||
| chr5:74717477 | C | CAT | 53 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0032 others(50): Show |
60 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1170-796_1170-795d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | ||||||
| chr5:74717477 | C | CATAT | 24 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0042 others(21): Show |
30 | HG01257.hp1 HG01258.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.1170-798_1170-795d others(6): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | ||||||
| chr5:74717477 | C | CATATAT | 5 | a0001c0001t0001g0100 a0001c0001t0001g0325 a0002c0002t0001g0037 others(2): Show |
6 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170-800_1170-795d others(8): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | ||||||
| chr5:74717477 | C | CATATATA others(1): Show |
41 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(38): Show |
47 | HG00140.hp2 HG00280.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1170-802_1170-795d others(10): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | ||||||
| chr5:74717477 | C | CATATATA others(3): Show |
2 | a0001c0001t0001g0170 a0002c0002t0001g0260 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1170-804_1170-795d others(12): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | ||||||
| chr5:74717477 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0091 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1170-806_1170-795d others(14): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | ||||||
| chr5:74717477 | CAT | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0053 others(8): Show |
15 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1170-796_1170-795d others(4): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717477 | ||||||
| chr5:74717670 | T | TA | 3 | a0001c0001t0001g0108 a0001c0001t0001g0164 a0002c0002t0001g0011 |
5 | HG02809.hp1 HG03041.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170-612dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr5 | 74717670 | ||||||
| chr5:74717714 | G | A | 1 | a0002c0002t0001g0288 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1170-577G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717714 | |||||||
| chr5:74717782 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1170-509C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717782 | |||||||
| chr5:74717786 | A | G | 253 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(250): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1170-505A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 9/13 | chr5 | 74717786 | |||||||
| chr5:74718418 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1242+55T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 10/13 | chr5 | 74718418 | |||||||
| chr5:74718717 | T | C | 1 | a0003c0003t0002g0198 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1243-80T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 10/13 | chr5 | 74718717 | |||||||
| chr5:74719187 | A | G | 1 | a0002c0002t0001g0320 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1417+216A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719187 | |||||||
| chr5:74719200 | T | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(42): Show |
53 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1417+229T>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719200 | |||||||
| chr5:74719341 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1417+370C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719341 | |||||||
| chr5:74719409 | A | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(42): Show |
53 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1417+438A>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719409 | |||||||
| chr5:74719525 | A | C | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(148): Show |
176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1417+554A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719525 | |||||||
| chr5:74719622 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1417+651C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719622 | |||||||
| chr5:74719709 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1418-719C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719709 | |||||||
| chr5:74719815 | A | G | 10 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(7): Show |
11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1418-613A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719815 | |||||||
| chr5:74719876 | G | A | 1 | a0001c0001t0001g0021 | 2 | NA18944.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1418-552G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719876 | |||||||
| chr5:74719897 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1418-531C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719897 | |||||||
| chr5:74719940 | C | CA | 50 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0031 others(47): Show |
59 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1418-473dupA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 74719940 | ||||||
| chr5:74719940 | CA | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(7): Show |
13 | HG01943.hp2 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1418-473delA | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 74719940 | ||||||
| chr5:74719954 | A | AAAAC | 49 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(46): Show |
54 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1418-473_1418-472i others(6): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 74719954 | ||||||
| chr5:74719954 | A | AAAC | 19 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0042 others(16): Show |
22 | HG00642.hp1 HG00733.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1418-473_1418-472i others(5): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr5 | 74719954 | ||||||
| chr5:74719954 | A | AC | 4 | a0001c0001t0001g0079 a0002c0002t0001g0289 a0002c0002t0001g0290 others(1): Show |
4 | HG02602.hp1 HG02602.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1418-474_1418-473i others(3): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74719954 | |||||||
| chr5:74720032 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1418-396C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74720032 | |||||||
| chr5:74720157 | C | T | 1 | a0009c0008t0001g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1418-271C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74720157 | |||||||
| chr5:74720165 | C | T | 1 | a0002c0002t0001g0039 | 2 | NA18988.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1418-263C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74720165 | |||||||
| chr5:74720231 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1418-197A>G | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74720231 | |||||||
| chr5:74720235 | T | A | 3 | a0005c0007t0001g0055 a0005c0007t0001g0057 a0005c0007t0001g0171 |
3 | HG00642.hp1 HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1418-193T>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 11/13 | chr5 | 74720235 | |||||||
| chr5:74720619 | G | A | 4 | a0002c0002t0002g0029 a0002c0002t0002g0297 a0002c0002t0002g0298 others(1): Show |
5 | HG03704.hp2 NA18962.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1509-24G>A | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 12/13 | chr5 | 74720619 | |||||||
| chr5:74721041 | AATATCAA others(21): Show |
A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0222 a0001c0001t0001g0238 others(7): Show |
11 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1614-63_1614-36del others(28): Show |
HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr5 | 74721041 | ||||||
| chr5:74721052 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1614-66A>C | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 13/13 | chr5 | 74721052 | |||||||
| chr5:74721074 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1614-44C>T | HEXB | ENSG00000049860.14 | transcript | ENST00000261416.12 | protein_coding | 13/13 | chr5 | 74721074 |