Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10329 |
| ensemblid | ENSG00000118600.13 |
| hgncid | 13530 |
| symbol | RXYLT1 |
| name | ribitol xylosyltransferase 1 |
| refseq_nuc | NM_014254.3 |
| refseq_prot | NP_055069.1 |
| ensembl_nuc | ENST00000261234.11 |
| ensembl_prot | ENSP00000261234.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 63779909 |
| end | 63809562 |
| strand | + |
| ver | v1.2 |
| region | chr12:63779909-63809562 |
| region5000 | chr12:63774909-63814562 |
| regionname0 | RXYLT1_chr12_63779909_63809562 |
| regionname5000 | RXYLT1_chr12_63774909_63814562 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 443 | 349 | 70 | 59 | 177 | 10 | 31 | 143 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | MRLTR others(438): Show |
chr12 | 63774909 | 63814562 |
| a0002 | 0/0 | 443 | 13 | 1 | 4 | 3 | 2 | 3 | 2 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | MRLTR others(438): Show |
chr12 | 63774909 | 63814562 |
| a0003 | 0/0 | 443 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | MRLTR others(438): Show |
chr12 | 63774909 | 63814562 |
| a0004 | 0/0 | 443 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | MRLTR others(438): Show |
chr12 | 63774909 | 63814562 |
| a0005 | 0/0 | 443 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | MRLTR others(438): Show |
chr12 | 63774909 | 63814562 |
| a0006 | 0/0 | 443 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | MRLTR others(438): Show |
chr12 | 63774909 | 63814562 |
| a0007 | 0/0 | 443 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | MRLTR others(438): Show |
chr12 | 63774909 | 63814562 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1329 | 346 | 68 | 59 | 177 | 10 | 30 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | ATGCG others(1324): Show |
chr12 | 63774909 | 63814562 | ||
| a0001c0005 | 0/0 | 1329 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | ATGCG others(1324): Show |
chr12 | 63774909 | 63814562 | ||
| a0001c0009 | 0/0 | 1329 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | ATGCG others(1324): Show |
chr12 | 63774909 | 63814562 | ||
| a0002c0002 | 0/0 | 1329 | 13 | 1 | 4 | 3 | 2 | 3 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | ATGCG others(1324): Show |
chr12 | 63774909 | 63814562 | ||
| a0003c0003 | 0/0 | 1329 | 4 | 4 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | ATGCG others(1324): Show |
chr12 | 63774909 | 63814562 | ||
| a0004c0004 | 0/0 | 1329 | 3 | 3 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | ATGCG others(1324): Show |
chr12 | 63774909 | 63814562 | ||
| a0005c0008 | 0/0 | 1329 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | ATGCG others(1324): Show |
chr12 | 63774909 | 63814562 | ||
| a0006c0006 | 0/0 | 1329 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | ATGCG others(1324): Show |
chr12 | 63774909 | 63814562 | ||
| a0007c0007 | 0/0 | 1329 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | ATGCG others(1324): Show |
chr12 | 63774909 | 63814562 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1854 | 248 | 48 | 43 | 125 | 6 | 24 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0001c0001t0002 | 0/0 | 1854 | 82 | 9 | 13 | 51 | 3 | 6 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0001c0001t0003 | 0/0 | 1852 | 6 | 3 | 1 | 1 | 1 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1847): Show |
chr12 | 63774909 | 63814562 |
| a0001c0001t0004 | 0/0 | 1854 | 4 | 2 | 2 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0001c0001t0006 | 0/0 | 1854 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0001c0001t0007 | 0/0 | 1854 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0001c0001t0008 | 0/0 | 1854 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0001c0001t0009 | 0/0 | 1854 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0001c0005t0003 | 0/0 | 1852 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1847): Show |
chr12 | 63774909 | 63814562 |
| a0001c0009t0001 | 0/0 | 1854 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0002c0002t0001 | 0/0 | 1854 | 13 | 1 | 4 | 3 | 2 | 3 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0003c0003t0005 | 0/0 | 1854 | 3 | 3 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0003c0003t0010 | 0/0 | 1854 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0004c0004t0001 | 0/0 | 1854 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0004c0004t0002 | 0/0 | 1854 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0005c0008t0001 | 0/0 | 1854 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0006c0006t0002 | 0/0 | 1854 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| a0007c0007t0001 | 0/0 | 1854 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | CTCTT others(1849): Show |
chr12 | 63774909 | 63814562 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 23 | 1 | 4 | 12 | 0 | 6 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0003 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0004 | 0/0 | 14 | 1 | 2 | 10 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0005 | 1/0 | 13 | 0 | 4 | 4 | 2 | 2 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0006 | 0/0 | 10 | 1 | 7 | 1 | 1 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0007 | 0/0 | 10 | 4 | 3 | 2 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0001 | 0/0 | 25 | 0 | 3 | 21 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0003g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0004g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0001t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0005t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0001c0009t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0002c0002t0001g0005 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0002c0002t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0002c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0002c0002t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0003c0003t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0003c0003t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0003c0003t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0004c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0004c0004t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0005c0008t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0006c0006t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| a0007c0007t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0047 | EUR | FIN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00558 | hp1 | a0005 | c0008 | t0001 | g0137 | EAS | CHS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0147 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0078 | AMR | PUR | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01255 | hp1 | a0006 | c0006 | t0002 | g0076 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02257 | hp2 | a0004 | c0004 | t0002 | g0035 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02451 | hp1 | a0003 | c0003 | t0010 | g0019 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0115 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0058 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0175 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03139 | hp2 | a0001 | c0005 | t0003 | g0024 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03195 | hp1 | a0003 | c0003 | t0005 | g0019 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03225 | hp1 | a0003 | c0003 | t0005 | g0019 | AFR | MSL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03453 | hp2 | a0004 | c0004 | t0002 | g0035 | AFR | MSL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0120 | AFR | ESN | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | BEB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03927 | hp1 | a0001 | c0009 | t0001 | g0139 | SAS | BEB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | STU | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18522 | hp1 | a0001 | c0005 | t0003 | g0024 | AFR | YRI | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | YRI | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0026 | AFR | YRI | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18988 | hp2 | a0007 | c0007 | t0001 | g0004 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | LWK | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19043 | hp1 | a0003 | c0003 | t0005 | g0080 | AFR | LWK | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | LWK | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ASW | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0156 | EUR | TSI | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0099 | EUR | TSI | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | TSI | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | GIH | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | USA | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0101 | REF | REF | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | RXYLT1_chr12_63774909_63814562 | RXYLT1 | chr12 | 63774909 | 63814562 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:63780027 | G | A | 1 | a0002 | 13 | HG00323.hp2 HG00741.hp1 HG01071.hp2 others(10): Show |
missense_variant | MODERATE | c.67G>A | p.Ala23Thr | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 1/6 | 119/1854 | 67/1332 | 23/443 | chr12 | 63780027 | |||
| chr12:63781033 | G | A | 1 | a0006 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.184G>A | p.Glu62Lys | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/6 | 236/1854 | 184/1332 | 62/443 | chr12 | 63781033 | |||
| chr12:63802131 | G | A | 1 | a0004 | 3 | HG02257.hp2 HG02970.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.469G>A | p.Val157Ile | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/6 | 521/1854 | 469/1332 | 157/443 | chr12 | 63802131 | |||
| chr12:63802257 | G | A | 1 | a0007 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.595G>A | p.Val199Ile | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/6 | 647/1854 | 595/1332 | 199/443 | chr12 | 63802257 | |||
| chr12:63808962 | C | T | 1 | a0005 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.1202C>T | p.Thr401Ile | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 6/6 | 1254/1854 | 1202/1332 | 401/443 | chr12 | 63808962 | |||
| chr12:63808986 | A | G | 1 | a0003 | 4 | HG02451.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.1226A>G | p.Glu409Gly | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 6/6 | 1278/1854 | 1226/1332 | 409/443 | chr12 | 63808986 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:63802265 | C | T | 1 | a0001c0009 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.603C>T | p.Leu201Leu | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/6 | 655/1854 | 603/1332 | 201/443 | chr12 | 63802265 | |||
| chr12:63805315 | G | A | 1 | a0001c0005 | 2 | HG03139.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.825G>A | p.Thr275Thr | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/6 | 877/1854 | 825/1332 | 275/443 | chr12 | 63805315 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:63779917 | G | A | 1 | a0001c0001t0008 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 1/6 | 44 | chr12 | 63779917 | ||||||
| chr12:63809110 | C | G | 9 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(6): Show |
98 | HG00438.hp2 HG01071.hp1 HG01099.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*18C>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 6/6 | 18 | chr12 | 63809110 | ||||||
| chr12:63809110 | CAT | C | 2 | a0001c0001t0003 a0001c0005t0003 |
8 | HG01081.hp2 HG02132.hp2 HG02970.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*19_*20delAT | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 6/6 | 19 | chr12 | 63809110 | ||||||
| chr12:63809194 | C | A | 2 | a0001c0001t0004 a0001c0001t0006 |
6 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*102C>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 6/6 | 102 | chr12 | 63809194 | ||||||
| chr12:63809299 | C | A | 4 | a0001c0001t0007 a0001c0001t0008 a0003c0003t0005 others(1): Show |
7 | HG02451.hp1 HG02886.hp1 HG03195.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*207C>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 6/6 | 207 | chr12 | 63809299 | ||||||
| chr12:63809420 | A | C | 1 | a0001c0001t0009 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*328A>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 6/6 | 328 | chr12 | 63809420 | ||||||
| chr12:63809431 | G | C | 1 | a0001c0001t0004 | 4 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*339G>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 6/6 | 339 | chr12 | 63809431 | ||||||
| chr12:63809464 | A | G | 1 | a0003c0003t0010 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*372A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 6/6 | 372 | chr12 | 63809464 | ||||||
| chr12:63809500 | T | G | 2 | a0001c0001t0007 a0001c0001t0008 |
3 | HG02886.hp1 NA18906.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*408T>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 6/6 | 408 | chr12 | 63809500 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:63780168 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.169+39C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 1/5 | chr12 | 63780168 | |||||||
| chr12:63780493 | A | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(28): Show |
76 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(73): Show |
intron_variant | MODIFIER | c.169+364A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 1/5 | chr12 | 63780493 | |||||||
| chr12:63780598 | T | G | 1 | a0001c0001t0002g0054 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.170-421T>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 1/5 | chr12 | 63780598 | |||||||
| chr12:63780900 | G | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(95): Show |
203 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.170-119G>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 1/5 | chr12 | 63780900 | |||||||
| chr12:63781448 | A | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
10 | HG01071.hp1 HG01167.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.325+274A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63781448 | |||||||
| chr12:63781798 | TAGAA | T | 2 | a0001c0001t0003g0024 a0001c0005t0003g0024 |
3 | HG03139.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.325+627_325+630del others(4): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 63781798 | ||||||
| chr12:63781946 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.325+772T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63781946 | |||||||
| chr12:63782329 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.325+1155C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63782329 | |||||||
| chr12:63782448 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325+1274C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63782448 | |||||||
| chr12:63782455 | G | A | 1 | a0001c0001t0003g0099 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.325+1281G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63782455 | |||||||
| chr12:63782502 | C | A | 1 | a0001c0001t0002g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.325+1328C>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63782502 | |||||||
| chr12:63782575 | C | A | 1 | a0001c0001t0002g0056 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.325+1401C>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63782575 | |||||||
| chr12:63783173 | C | T | 1 | a0001c0001t0001g0053 | 2 | NA18954.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.326-1797C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63783173 | |||||||
| chr12:63783175 | C | T | 25 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0029 others(22): Show |
37 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.326-1795C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63783175 | |||||||
| chr12:63783198 | C | G | 1 | a0001c0001t0001g0180 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.326-1772C>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63783198 | |||||||
| chr12:63783289 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326-1681C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63783289 | |||||||
| chr12:63783338 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.326-1632G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63783338 | |||||||
| chr12:63783385 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.326-1585C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63783385 | |||||||
| chr12:63784183 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.326-787A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63784183 | |||||||
| chr12:63784248 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.326-722C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63784248 | |||||||
| chr12:63784314 | G | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(23): Show |
70 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(67): Show |
intron_variant | MODIFIER | c.326-656G>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63784314 | |||||||
| chr12:63784338 | T | C | 1 | a0001c0001t0001g0048 | 2 | HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.326-632T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63784338 | |||||||
| chr12:63784841 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0159 a0001c0001t0001g0160 |
5 | HG02602.hp1 HG02683.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.326-129C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 2/5 | chr12 | 63784841 | |||||||
| chr12:63785433 | C | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(28): Show |
76 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(73): Show |
intron_variant | MODIFIER | c.428+361C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63785433 | |||||||
| chr12:63785556 | A | T | 1 | a0001c0001t0001g0158 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.428+484A>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63785556 | |||||||
| chr12:63785964 | A | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
10 | HG01071.hp1 HG01167.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.428+892A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63785964 | |||||||
| chr12:63786089 | G | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0078 a0001c0001t0006g0079 |
5 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+1017G>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63786089 | |||||||
| chr12:63786298 | C | A | 1 | a0001c0001t0001g0158 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.428+1226C>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63786298 | |||||||
| chr12:63786392 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18747.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.428+1320C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63786392 | |||||||
| chr12:63786510 | C | G | 1 | a0002c0002t0001g0047 | 2 | HG00323.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.428+1438C>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63786510 | |||||||
| chr12:63786511 | T | TA | 32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(29): Show |
77 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(74): Show |
intron_variant | MODIFIER | c.428+1451dupA | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63786511 | ||||||
| chr12:63786635 | A | C | 1 | a0001c0001t0002g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.428+1563A>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63786635 | |||||||
| chr12:63786663 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.428+1591G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63786663 | |||||||
| chr12:63786832 | G | A | 7 | a0001c0001t0002g0057 a0001c0001t0007g0026 a0001c0001t0007g0058 others(4): Show |
8 | HG02451.hp1 HG02886.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.428+1760G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63786832 | |||||||
| chr12:63786855 | T | C | 59 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0029 others(56): Show |
117 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.428+1783T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63786855 | |||||||
| chr12:63786943 | G | A | 1 | a0001c0001t0002g0014 | 3 | NA18945.hp1 NA18978.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.428+1871G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63786943 | |||||||
| chr12:63787052 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0081 a0001c0001t0001g0082 |
5 | HG00408.hp1 HG00597.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+1980G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63787052 | |||||||
| chr12:63787093 | G | A | 5 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
10 | HG01071.hp1 HG01167.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.428+2021G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63787093 | |||||||
| chr12:63787108 | A | AG | 3 | a0003c0003t0005g0019 a0003c0003t0005g0080 a0003c0003t0010g0019 |
4 | HG02451.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+2037dupG | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63787108 | ||||||
| chr12:63787635 | G | GT | 5 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
10 | HG01071.hp1 HG01167.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.428+2573dupT | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63787635 | ||||||
| chr12:63787654 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(8): Show |
23 | HG01074.hp1 HG01081.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.428+2582G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63787654 | |||||||
| chr12:63787738 | T | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
10 | HG01071.hp1 HG01167.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.428+2666T>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63787738 | |||||||
| chr12:63787837 | G | C | 27 | a0001c0001t0001g0071 a0001c0001t0002g0001 a0001c0001t0002g0008 others(24): Show |
66 | HG00438.hp2 HG01099.hp1 HG01123.hp1 others(63): Show |
intron_variant | MODIFIER | c.428+2765G>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63787837 | |||||||
| chr12:63787868 | G | C | 2 | a0001c0001t0002g0017 a0001c0001t0002g0077 |
4 | HG02145.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+2796G>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63787868 | |||||||
| chr12:63788356 | T | A | 2 | a0001c0001t0001g0176 a0004c0004t0001g0175 |
2 | HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.428+3284T>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63788356 | |||||||
| chr12:63788419 | T | C | 2 | a0001c0001t0002g0017 a0001c0001t0002g0077 |
4 | HG02145.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+3347T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63788419 | |||||||
| chr12:63788505 | A | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
7 | HG01361.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+3433A>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63788505 | |||||||
| chr12:63788567 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.428+3495A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63788567 | |||||||
| chr12:63788751 | C | A | 1 | a0001c0001t0002g0059 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.428+3679C>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63788751 | |||||||
| chr12:63788929 | C | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG00544.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.428+3857C>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63788929 | |||||||
| chr12:63788982 | T | C | 1 | a0001c0001t0001g0038 | 2 | HG01106.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.428+3910T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63788982 | |||||||
| chr12:63789236 | G | C | 27 | a0001c0001t0001g0071 a0001c0001t0002g0001 a0001c0001t0002g0008 others(24): Show |
66 | HG00438.hp2 HG01099.hp1 HG01123.hp1 others(63): Show |
intron_variant | MODIFIER | c.428+4164G>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789236 | |||||||
| chr12:63789374 | A | T | 1 | a0002c0002t0001g0156 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.428+4302A>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789374 | |||||||
| chr12:63789390 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.428+4318C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789390 | |||||||
| chr12:63789421 | G | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0155 |
3 | HG01109.hp2 HG01123.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.428+4349G>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789421 | |||||||
| chr12:63789517 | A | G | 27 | a0001c0001t0001g0071 a0001c0001t0002g0001 a0001c0001t0002g0008 others(24): Show |
66 | HG00438.hp2 HG01099.hp1 HG01123.hp1 others(63): Show |
intron_variant | MODIFIER | c.428+4445A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789517 | |||||||
| chr12:63789537 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.428+4465A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789537 | |||||||
| chr12:63789654 | A | G | 3 | a0001c0001t0007g0026 a0001c0001t0007g0058 a0001c0001t0008g0026 |
3 | HG02886.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.428+4582A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789654 | |||||||
| chr12:63789674 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.428+4602C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789674 | |||||||
| chr12:63789693 | A | G | 4 | a0001c0001t0002g0012 a0001c0001t0002g0034 a0001c0001t0002g0097 others(1): Show |
8 | HG01071.hp1 HG01167.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.428+4621A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789693 | |||||||
| chr12:63789769 | G | A | 27 | a0001c0001t0001g0071 a0001c0001t0002g0001 a0001c0001t0002g0008 others(24): Show |
66 | HG00438.hp2 HG01099.hp1 HG01123.hp1 others(63): Show |
intron_variant | MODIFIER | c.428+4697G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789769 | |||||||
| chr12:63789818 | C | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(92): Show |
198 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.428+4746C>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789818 | |||||||
| chr12:63789923 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.428+4851G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63789923 | |||||||
| chr12:63790056 | A | G | 1 | a0001c0001t0003g0153 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.428+4984A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63790056 | |||||||
| chr12:63790172 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.428+5100T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63790172 | |||||||
| chr12:63790260 | A | G | 1 | a0006c0006t0002g0076 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.428+5188A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63790260 | |||||||
| chr12:63790698 | A | C | 1 | a0001c0001t0002g0075 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.428+5626A>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63790698 | |||||||
| chr12:63790711 | C | T | 3 | a0003c0003t0005g0019 a0003c0003t0005g0080 a0003c0003t0010g0019 |
4 | HG02451.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+5639C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63790711 | |||||||
| chr12:63790883 | A | C | 50 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0029 others(47): Show |
100 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.428+5811A>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63790883 | |||||||
| chr12:63791488 | A | C | 1 | a0001c0001t0001g0152 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.428+6416A>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63791488 | |||||||
| chr12:63791614 | G | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(91): Show |
197 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.428+6542G>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63791614 | |||||||
| chr12:63791674 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0151 |
3 | HG02280.hp2 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.428+6602A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63791674 | |||||||
| chr12:63791754 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.428+6682C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63791754 | |||||||
| chr12:63791889 | A | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
10 | HG01071.hp1 HG01167.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.428+6817A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63791889 | |||||||
| chr12:63791998 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.428+6926C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63791998 | |||||||
| chr12:63792031 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0087 |
5 | HG00544.hp2 HG02135.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+6959A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63792031 | |||||||
| chr12:63792080 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.428+7008A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63792080 | |||||||
| chr12:63792255 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.428+7183T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63792255 | |||||||
| chr12:63792459 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.428+7387A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63792459 | |||||||
| chr12:63792514 | T | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01361.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.428+7442T>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63792514 | |||||||
| chr12:63792572 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.428+7500C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63792572 | |||||||
| chr12:63793109 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.428+8037C>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63793109 | |||||||
| chr12:63793323 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG00558.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.428+8251G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63793323 | |||||||
| chr12:63793613 | G | C | 1 | a0001c0001t0002g0061 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.429-8478G>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63793613 | |||||||
| chr12:63793690 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.429-8401G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63793690 | |||||||
| chr12:63793696 | T | C | 3 | a0001c0001t0007g0026 a0001c0001t0007g0058 a0001c0001t0008g0026 |
3 | HG02886.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-8395T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63793696 | |||||||
| chr12:63793957 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.429-8134C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63793957 | |||||||
| chr12:63794423 | T | A | 1 | a0001c0001t0001g0114 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.429-7668T>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63794423 | |||||||
| chr12:63794533 | C | T | 5 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
10 | HG01071.hp1 HG01167.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.429-7558C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63794533 | |||||||
| chr12:63794590 | T | C | 1 | a0001c0001t0001g0045 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.429-7501T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63794590 | |||||||
| chr12:63794670 | T | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(87): Show |
192 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.429-7421T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63794670 | |||||||
| chr12:63794827 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.429-7264G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63794827 | |||||||
| chr12:63794848 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(83): Show |
184 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.429-7243C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63794848 | |||||||
| chr12:63794873 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.429-7218C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63794873 | |||||||
| chr12:63794940 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG00544.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.429-7151G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63794940 | |||||||
| chr12:63795285 | A | AAAG | 28 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0001g0118 others(25): Show |
68 | HG00438.hp2 HG01099.hp1 HG01123.hp1 others(65): Show |
intron_variant | MODIFIER | c.429-6781_429-6779d others(5): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63795285 | ||||||
| chr12:63795285 | A | G | 7 | a0001c0001t0002g0057 a0002c0002t0001g0022 a0002c0002t0001g0047 others(4): Show |
10 | HG00323.hp2 HG00741.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-6806A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63795285 | |||||||
| chr12:63795332 | C | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0097 others(1): Show |
8 | HG01071.hp1 HG01167.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.429-6759C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63795332 | |||||||
| chr12:63795447 | T | A | 6 | a0001c0001t0002g0055 a0001c0001t0004g0018 a0001c0001t0004g0078 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.429-6644T>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63795447 | |||||||
| chr12:63795453 | C | T | 6 | a0001c0001t0002g0055 a0001c0001t0004g0018 a0001c0001t0004g0078 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.429-6638C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63795453 | |||||||
| chr12:63795554 | G | A | 1 | a0001c0001t0002g0015 | 3 | NA18952.hp2 NA18957.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.429-6537G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63795554 | |||||||
| chr12:63795577 | C | CA | 10 | a0001c0001t0001g0040 a0001c0001t0001g0118 a0001c0001t0001g0121 others(7): Show |
13 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.429-6496dupA | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63795577 | ||||||
| chr12:63795577 | CA | C | 5 | a0001c0001t0001g0051 a0001c0001t0001g0108 a0001c0001t0001g0144 others(2): Show |
6 | HG00323.hp1 HG01099.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-6496delA | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63795577 | ||||||
| chr12:63795770 | G | C | 1 | a0001c0001t0002g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.429-6321G>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63795770 | |||||||
| chr12:63796220 | C | G | 1 | a0001c0001t0002g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.429-5871C>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63796220 | |||||||
| chr12:63796395 | T | C | 6 | a0001c0001t0007g0026 a0001c0001t0007g0058 a0001c0001t0008g0026 others(3): Show |
7 | HG02451.hp1 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.429-5696T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63796395 | |||||||
| chr12:63796438 | A | G | 21 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0030 others(18): Show |
31 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.429-5653A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63796438 | |||||||
| chr12:63796704 | A | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0169 a0001c0001t0001g0172 |
5 | NA18945.hp2 NA18981.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.429-5387A>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63796704 | |||||||
| chr12:63796870 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.429-5221T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63796870 | |||||||
| chr12:63796963 | C | CT | 11 | a0001c0001t0001g0044 a0001c0001t0001g0121 a0001c0001t0001g0142 others(8): Show |
13 | HG02132.hp1 HG03654.hp1 HG04199.hp1 others(10): Show |
intron_variant | MODIFIER | c.429-5110dupT | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63796963 | ||||||
| chr12:63796963 | CT | C | 13 | a0001c0001t0001g0123 a0001c0001t0001g0166 a0001c0001t0002g0012 others(10): Show |
21 | HG01071.hp1 HG01109.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.429-5110delT | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63796963 | ||||||
| chr12:63796969 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.429-5122T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63796969 | |||||||
| chr12:63797027 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0100 a0001c0001t0001g0124 others(4): Show |
8 | HG00280.hp2 HG00323.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.429-5064G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63797027 | |||||||
| chr12:63797049 | C | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0161 |
2 | HG02083.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.429-5042C>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63797049 | |||||||
| chr12:63797087 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.429-5004C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63797087 | |||||||
| chr12:63797206 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.429-4885C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63797206 | |||||||
| chr12:63797302 | T | TAAGAATA others(305): Show |
2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.429-4779_429-4778i others(314): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63797302 | ||||||
| chr12:63797332 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | NA18941.hp1 NA18966.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.429-4759G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63797332 | |||||||
| chr12:63797551 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
6 | HG01361.hp2 HG01884.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.429-4540A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63797551 | |||||||
| chr12:63797599 | T | C | 2 | a0001c0001t0002g0017 a0001c0001t0002g0077 |
4 | HG02145.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-4492T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63797599 | |||||||
| chr12:63797616 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(21): Show |
63 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(60): Show |
intron_variant | MODIFIER | c.429-4475C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63797616 | |||||||
| chr12:63797927 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.429-4164G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63797927 | |||||||
| chr12:63798137 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.429-3954C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63798137 | |||||||
| chr12:63798443 | A | G | 3 | a0003c0003t0005g0019 a0003c0003t0005g0080 a0003c0003t0010g0019 |
4 | HG02451.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-3648A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63798443 | |||||||
| chr12:63798694 | T | C | 2 | a0001c0001t0002g0017 a0001c0001t0002g0077 |
4 | HG02145.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-3397T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63798694 | |||||||
| chr12:63798886 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.429-3205T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63798886 | |||||||
| chr12:63798993 | C | T | 3 | a0001c0001t0007g0026 a0001c0001t0007g0058 a0001c0001t0008g0026 |
3 | HG02886.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-3098C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63798993 | |||||||
| chr12:63799066 | C | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0077 |
4 | HG02145.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-3025C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799066 | |||||||
| chr12:63799070 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.429-3021G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799070 | |||||||
| chr12:63799137 | C | G | 1 | a0001c0001t0002g0070 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.429-2954C>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799137 | |||||||
| chr12:63799139 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0145 |
3 | HG02109.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.429-2952G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799139 | |||||||
| chr12:63799220 | C | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0077 |
4 | HG02145.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.429-2871C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799220 | |||||||
| chr12:63799283 | T | C | 3 | a0001c0001t0007g0026 a0001c0001t0007g0058 a0001c0001t0008g0026 |
3 | HG02886.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-2808T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799283 | |||||||
| chr12:63799298 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.429-2793T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799298 | |||||||
| chr12:63799302 | C | CT | 5 | a0001c0001t0001g0154 a0001c0001t0002g0012 a0001c0001t0002g0033 others(2): Show |
10 | HG01071.hp1 HG01257.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-2767dupT | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63799302 | ||||||
| chr12:63799302 | CT | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.429-2767delT | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63799302 | ||||||
| chr12:63799302 | CTT | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(27): Show |
68 | HG00438.hp2 HG01123.hp1 HG01255.hp1 others(65): Show |
intron_variant | MODIFIER | c.429-2768_429-2767d others(4): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63799302 | ||||||
| chr12:63799328 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.429-2763A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799328 | |||||||
| chr12:63799365 | C | T | 1 | a0001c0001t0002g0027 | 2 | HG03831.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.429-2726C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799365 | |||||||
| chr12:63799399 | G | C | 6 | a0001c0001t0002g0055 a0001c0001t0004g0018 a0001c0001t0004g0078 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.429-2692G>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799399 | |||||||
| chr12:63799529 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.429-2562G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799529 | |||||||
| chr12:63799548 | A | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0021 others(26): Show |
62 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.429-2543A>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799548 | |||||||
| chr12:63799579 | C | G | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.429-2512C>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799579 | |||||||
| chr12:63799814 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.429-2277A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799814 | |||||||
| chr12:63799876 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.429-2215C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63799876 | |||||||
| chr12:63800142 | A | G | 4 | a0001c0001t0004g0018 a0001c0001t0004g0078 a0001c0001t0006g0079 others(1): Show |
6 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-1949A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63800142 | |||||||
| chr12:63800533 | A | G | 3 | a0001c0001t0007g0026 a0001c0001t0007g0058 a0001c0001t0008g0026 |
3 | HG02886.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429-1558A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63800533 | |||||||
| chr12:63800834 | T | C | 1 | a0002c0002t0001g0146 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.429-1257T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63800834 | |||||||
| chr12:63800864 | T | A | 1 | a0001c0001t0001g0134 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.429-1227T>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63800864 | |||||||
| chr12:63800920 | C | CA | 14 | a0001c0001t0001g0045 a0001c0001t0001g0112 a0001c0001t0001g0121 others(11): Show |
16 | HG00558.hp2 HG02451.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.429-1157dupA | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63800920 | ||||||
| chr12:63801033 | A | C | 4 | a0001c0001t0004g0018 a0001c0001t0004g0078 a0001c0001t0006g0079 others(1): Show |
6 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-1058A>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63801033 | |||||||
| chr12:63801249 | CT | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0103 others(6): Show |
20 | HG01081.hp1 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.429-835delT | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 63801249 | ||||||
| chr12:63801310 | C | T | 5 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
10 | HG01071.hp1 HG01167.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.429-781C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63801310 | |||||||
| chr12:63801428 | A | C | 6 | a0001c0001t0007g0026 a0001c0001t0007g0058 a0001c0001t0008g0026 others(3): Show |
7 | HG02451.hp1 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.429-663A>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63801428 | |||||||
| chr12:63801635 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(25): Show |
73 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(70): Show |
intron_variant | MODIFIER | c.429-456C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63801635 | |||||||
| chr12:63801802 | A | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(25): Show |
73 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(70): Show |
intron_variant | MODIFIER | c.429-289A>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 3/5 | chr12 | 63801802 | |||||||
| chr12:63802504 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.743+99G>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63802504 | |||||||
| chr12:63802613 | A | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0077 |
4 | HG02145.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+208A>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63802613 | |||||||
| chr12:63802642 | A | G | 2 | a0001c0001t0002g0055 a0004c0004t0002g0035 |
3 | HG01243.hp1 HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.743+237A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63802642 | |||||||
| chr12:63803003 | T | TAAA | 6 | a0001c0001t0007g0026 a0001c0001t0007g0058 a0001c0001t0008g0026 others(3): Show |
7 | HG02451.hp1 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.743+610_743+612dup others(3): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 63803003 | ||||||
| chr12:63803181 | C | CA | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(67): Show |
159 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(156): Show |
intron_variant | MODIFIER | c.743+806dupA | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 63803181 | ||||||
| chr12:63803181 | C | CAA | 19 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(16): Show |
35 | HG00438.hp1 HG00438.hp2 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.743+805_743+806dup others(2): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 63803181 | ||||||
| chr12:63803181 | CA | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0031 others(17): Show |
32 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.743+806delA | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 63803181 | ||||||
| chr12:63803181 | CAA | C | 5 | a0001c0001t0001g0083 a0001c0001t0001g0176 a0001c0001t0002g0055 others(2): Show |
8 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.743+805_743+806del others(2): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 63803181 | ||||||
| chr12:63803181 | CAAA | C | 6 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0034 others(3): Show |
12 | HG01071.hp1 HG01257.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+804_743+806del others(3): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 63803181 | ||||||
| chr12:63803181 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0170 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.743+795_743+806del others(12): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 63803181 | ||||||
| chr12:63803181 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0002g0069 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.743+789_743+806del others(18): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 63803181 | ||||||
| chr12:63803269 | T | C | 1 | a0001c0009t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.743+864T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63803269 | |||||||
| chr12:63803349 | TG | T | 5 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
10 | HG01071.hp1 HG01167.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.743+945delG | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63803349 | |||||||
| chr12:63803466 | A | G | 1 | a0001c0001t0006g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.743+1061A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63803466 | |||||||
| chr12:63803542 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.743+1137G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63803542 | |||||||
| chr12:63803753 | ATGT | A | 5 | a0001c0001t0002g0055 a0001c0001t0004g0018 a0001c0001t0004g0078 others(2): Show |
8 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.743+1354_743+1356d others(5): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 63803753 | ||||||
| chr12:63803781 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.743+1376T>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63803781 | |||||||
| chr12:63803851 | C | CT | 23 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0050 others(20): Show |
27 | HG01099.hp1 HG01106.hp2 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.744-1363dupT | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 63803851 | ||||||
| chr12:63803851 | CT | C | 5 | a0001c0001t0001g0130 a0001c0001t0002g0034 a0001c0001t0002g0055 others(2): Show |
6 | HG01243.hp1 HG01257.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-1363delT | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 63803851 | ||||||
| chr12:63803959 | T | C | 27 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(24): Show |
66 | HG00438.hp2 HG01099.hp1 HG01123.hp1 others(63): Show |
intron_variant | MODIFIER | c.744-1275T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63803959 | |||||||
| chr12:63804000 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(23): Show |
70 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(67): Show |
intron_variant | MODIFIER | c.744-1234G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63804000 | |||||||
| chr12:63804017 | C | A | 1 | a0005c0008t0001g0137 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.744-1217C>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63804017 | |||||||
| chr12:63804060 | C | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(25): Show |
73 | HG01168.hp2 HG01257.hp1 HG01258.hp1 others(70): Show |
intron_variant | MODIFIER | c.744-1174C>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63804060 | |||||||
| chr12:63804608 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.744-626G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63804608 | |||||||
| chr12:63804654 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.744-580A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63804654 | |||||||
| chr12:63804659 | T | C | 2 | a0001c0001t0002g0017 a0001c0001t0002g0077 |
4 | HG02145.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.744-575T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63804659 | |||||||
| chr12:63804741 | T | A | 1 | a0001c0001t0001g0021 | 3 | HG02965.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.744-493T>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63804741 | |||||||
| chr12:63804938 | T | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
10 | HG01071.hp1 HG01167.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.744-296T>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63804938 | |||||||
| chr12:63804950 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0122 a0001c0001t0001g0163 |
4 | HG02615.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.744-284C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63804950 | |||||||
| chr12:63805016 | G | A | 3 | a0003c0003t0005g0019 a0003c0003t0005g0080 a0003c0003t0010g0019 |
4 | HG02451.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.744-218G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 4/5 | chr12 | 63805016 | |||||||
| chr12:63805533 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.914+129T>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63805533 | |||||||
| chr12:63805849 | A | C | 1 | a0001c0001t0002g0066 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.914+445A>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63805849 | |||||||
| chr12:63805967 | G | A | 6 | a0001c0001t0007g0026 a0001c0001t0007g0058 a0001c0001t0008g0026 others(3): Show |
7 | HG02451.hp1 HG02886.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.914+563G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63805967 | |||||||
| chr12:63806073 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.914+669G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63806073 | |||||||
| chr12:63806364 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.914+960A>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63806364 | |||||||
| chr12:63806503 | C | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0077 |
4 | HG02145.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.914+1099C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63806503 | |||||||
| chr12:63806722 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.914+1318T>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63806722 | |||||||
| chr12:63806726 | C | A | 1 | a0001c0001t0001g0167 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.914+1322C>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63806726 | |||||||
| chr12:63806734 | TAATC | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0078 a0001c0001t0006g0079 |
5 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.914+1331_914+1334d others(6): Show |
RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63806734 | |||||||
| chr12:63806771 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.914+1367C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63806771 | |||||||
| chr12:63806803 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.914+1399C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63806803 | |||||||
| chr12:63806820 | C | A | 1 | a0001c0001t0002g0057 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.914+1416C>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63806820 | |||||||
| chr12:63806912 | A | G | 3 | a0001c0001t0007g0026 a0001c0001t0007g0058 a0001c0001t0008g0026 |
3 | HG02886.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.914+1508A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63806912 | |||||||
| chr12:63807011 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.914+1607T>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807011 | |||||||
| chr12:63807086 | A | G | 1 | a0005c0008t0001g0137 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.915-1589A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807086 | |||||||
| chr12:63807290 | A | G | 6 | a0001c0001t0002g0055 a0001c0001t0004g0018 a0001c0001t0004g0078 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.915-1385A>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807290 | |||||||
| chr12:63807365 | G | A | 1 | a0004c0004t0001g0175 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.915-1310G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807365 | |||||||
| chr12:63807420 | T | C | 1 | a0001c0001t0007g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.915-1255T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807420 | |||||||
| chr12:63807491 | C | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0065 |
2 | NA18989.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.915-1184C>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807491 | |||||||
| chr12:63807708 | G | A | 3 | a0003c0003t0005g0019 a0003c0003t0005g0080 a0003c0003t0010g0019 |
4 | HG02451.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.915-967G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807708 | |||||||
| chr12:63807721 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.915-954C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807721 | |||||||
| chr12:63807722 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.915-953G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807722 | |||||||
| chr12:63807798 | G | A | 20 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0030 others(17): Show |
30 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.915-877G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807798 | |||||||
| chr12:63807805 | C | T | 1 | a0001c0001t0002g0014 | 3 | NA18945.hp1 NA18978.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.915-870C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807805 | |||||||
| chr12:63807898 | C | T | 26 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(23): Show |
65 | HG00438.hp2 HG01099.hp1 HG01123.hp1 others(62): Show |
intron_variant | MODIFIER | c.915-777C>T | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807898 | |||||||
| chr12:63807997 | T | G | 1 | a0001c0001t0006g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.915-678T>G | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63807997 | |||||||
| chr12:63808279 | T | C | 24 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(21): Show |
63 | HG00438.hp2 HG01099.hp1 HG01123.hp1 others(60): Show |
intron_variant | MODIFIER | c.915-396T>C | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63808279 | |||||||
| chr12:63808453 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(23): Show |
65 | HG00438.hp2 HG01099.hp1 HG01123.hp1 others(62): Show |
intron_variant | MODIFIER | c.915-222G>A | RXYLT1 | ENSG00000118600.13 | transcript | ENST00000261234.11 | protein_coding | 5/5 | chr12 | 63808453 |