Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6003 |
| ensemblid | ENSG00000127074.15 |
| hgncid | 9995 |
| symbol | RGS13 |
| name | regulator of G protein signaling 13 |
| refseq_nuc | NM_002927.5 |
| refseq_prot | NP_002918.1 |
| ensembl_nuc | ENST00000391995.7 |
| ensembl_prot | ENSP00000375853.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 192636147 |
| end | 192660311 |
| strand | + |
| ver | v1.2 |
| region | chr1:192636147-192660311 |
| region5000 | chr1:192631147-192665311 |
| regionname0 | RGS13_chr1_192636147_192660311 |
| regionname5000 | RGS13_chr1_192631147_192665311 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 159 | 395 | 83 | 61 | 191 | 14 | 44 | 146 | RGS13_chr1_192631147_192665311 | RGS13 | MSRRN others(154): Show |
chr1 | 192631147 | 192665311 |
| a0002 | 0/0 | 159 | 13 | 0 | 6 | 7 | 0 | 0 | 6 | RGS13_chr1_192631147_192665311 | RGS13 | MSRQN others(154): Show |
chr1 | 192631147 | 192665311 |
| a0003 | 0/0 | 159 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | MSRRN others(154): Show |
chr1 | 192631147 | 192665311 |
| a0004 | 0/0 | 159 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | MSRRN others(154): Show |
chr1 | 192631147 | 192665311 |
| a0005 | 0/0 | 159 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | MSRRN others(154): Show |
chr1 | 192631147 | 192665311 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 477 | 383 | 80 | 57 | 191 | 12 | 41 | RGS13_chr1_192631147_192665311 | RGS13 | ATGAG others(472): Show |
chr1 | 192631147 | 192665311 | ||
| a0001c0003 | 0/0 | 477 | 11 | 2 | 4 | 0 | 2 | 3 | RGS13_chr1_192631147_192665311 | RGS13 | ATGAG others(472): Show |
chr1 | 192631147 | 192665311 | ||
| a0001c0007 | 0/0 | 477 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATGAG others(472): Show |
chr1 | 192631147 | 192665311 | ||
| a0002c0002 | 0/0 | 477 | 13 | 0 | 6 | 7 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATGAG others(472): Show |
chr1 | 192631147 | 192665311 | ||
| a0003c0004 | 0/0 | 477 | 9 | 9 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATGAG others(472): Show |
chr1 | 192631147 | 192665311 | ||
| a0004c0005 | 0/0 | 477 | 2 | 2 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATGAG others(472): Show |
chr1 | 192631147 | 192665311 | ||
| a0005c0006 | 0/0 | 477 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATGAG others(472): Show |
chr1 | 192631147 | 192665311 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1554 | 175 | 56 | 33 | 58 | 5 | 21 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0001c0001t0002 | 0/0 | 1554 | 164 | 6 | 20 | 113 | 7 | 18 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0001c0001t0003 | 0/0 | 1554 | 31 | 9 | 1 | 19 | 0 | 2 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0001c0001t0006 | 0/0 | 1554 | 9 | 9 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0001c0001t0007 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0001c0001t0008 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0001c0001t0010 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0001c0001t0011 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0001c0003t0005 | 0/0 | 1554 | 10 | 2 | 3 | 0 | 2 | 3 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0001c0003t0009 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0001c0007t0001 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0002c0002t0004 | 0/0 | 1554 | 13 | 0 | 6 | 7 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0003c0004t0001 | 0/0 | 1554 | 8 | 8 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0003c0004t0006 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0004c0005t0001 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| a0005c0006t0002 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | ATACT others(1549): Show |
chr1 | 192631147 | 192665311 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 30 | 5 | 12 | 10 | 1 | 2 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0009 | 0/0 | 7 | 2 | 4 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0011 | 0/0 | 7 | 0 | 5 | 0 | 0 | 2 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0017 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0022 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0072 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0001 | 0/0 | 59 | 2 | 8 | 40 | 4 | 5 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0004 | 0/0 | 12 | 0 | 5 | 6 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0006 | 0/0 | 9 | 1 | 2 | 6 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0010 | 0/0 | 7 | 0 | 0 | 4 | 1 | 2 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0003 | 0/0 | 15 | 1 | 0 | 13 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0006g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0008g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0010g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0001t0011g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0003t0005g0008 | 0/0 | 8 | 0 | 3 | 0 | 2 | 3 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0003t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0003t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0003t0009g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0001c0007t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0002c0002t0004g0005 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0002c0002t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0002c0002t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0002c0002t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0003c0004t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0003c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0003c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0003c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0003c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0003c0004t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0003c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0003c0004t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0004c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0004c0005t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| a0005c0006t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | GBR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | FIN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0096 | EUR | FIN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0184 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01081 | hp2 | a0001 | c0003 | t0009 | g0094 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01106 | hp1 | a0002 | c0002 | t0004 | g0005 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01257 | hp2 | a0001 | c0003 | t0005 | g0008 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01258 | hp1 | a0001 | c0003 | t0005 | g0008 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01261 | hp2 | a0002 | c0002 | t0004 | g0005 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01358 | hp1 | a0002 | c0002 | t0004 | g0005 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0101 | EUR | IBS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01516 | hp2 | a0001 | c0003 | t0005 | g0008 | EUR | IBS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01517 | hp1 | a0001 | c0003 | t0005 | g0008 | EUR | IBS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01891 | hp2 | a0003 | c0004 | t0006 | g0061 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01928 | hp2 | a0001 | c0001 | t0007 | g0182 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01978 | hp1 | a0005 | c0006 | t0002 | g0097 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01993 | hp1 | a0002 | c0002 | t0004 | g0146 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01993 | hp2 | a0002 | c0002 | t0004 | g0145 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02004 | hp1 | a0001 | c0001 | t0010 | g0091 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02129 | hp1 | a0002 | c0002 | t0004 | g0005 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CDX | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CDX | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02258 | hp2 | a0001 | c0003 | t0005 | g0070 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02293 | hp2 | a0002 | c0002 | t0004 | g0144 | AMR | PEL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02451 | hp2 | a0003 | c0004 | t0001 | g0043 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0158 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02698 | hp2 | a0001 | c0003 | t0005 | g0008 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02809 | hp2 | a0003 | c0004 | t0001 | g0153 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02818 | hp2 | a0004 | c0005 | t0001 | g0179 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0065 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0170 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02976 | hp2 | a0003 | c0004 | t0001 | g0056 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03098 | hp1 | a0001 | c0007 | t0001 | g0068 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03209 | hp1 | a0003 | c0004 | t0001 | g0137 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03225 | hp2 | a0003 | c0004 | t0001 | g0043 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03486 | hp2 | a0003 | c0004 | t0001 | g0083 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03491 | hp1 | a0001 | c0003 | t0005 | g0008 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03492 | hp1 | a0001 | c0003 | t0005 | g0008 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0066 | AFR | GWD | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | STU | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | BEB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | STU | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | STU | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0139 | SAS | STU | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | CHB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18992 | hp1 | a0002 | c0002 | t0004 | g0005 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18994 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19004 | hp2 | a0002 | c0002 | t0004 | g0005 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19011 | hp2 | a0002 | c0002 | t0004 | g0005 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19059 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19064 | hp2 | a0002 | c0002 | t0004 | g0005 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19070 | hp2 | a0002 | c0002 | t0004 | g0005 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19087 | hp1 | a0002 | c0002 | t0004 | g0005 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | GIH | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG01123 | hp2 | a0001 | c0003 | t0005 | g0008 | AMR | CLM | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02109 | hp1 | a0001 | c0003 | t0005 | g0150 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02486 | hp2 | a0004 | c0005 | t0001 | g0053 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | ACB | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | USA | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | USA | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | USA | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | LWK | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0177 | REF | REF | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0072 | REF | REF | RGS13_chr1_192631147_192665311 | RGS13 | chr1 | 192631147 | 192665311 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:192637590 | G | T | 2 | a0001 a0003 |
10 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(7): Show |
splice_region_variant | LOW | c.-115G>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 2/7 | chr1 | 192637590 | |||||||
| chr1:192644345 | G | A | 1 | a0002 | 13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
missense_variant | MODERATE | c.11G>A | p.Arg4Gln | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/7 | 297/1554 | 11/480 | 4/159 | chr1 | 192644345 | |||
| chr1:192658207 | C | T | 1 | a0004 | 2 | HG02486.hp2 HG02818.hp2 |
missense_variant | MODERATE | c.134C>T | p.Pro45Leu | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/7 | 420/1554 | 134/480 | 45/159 | chr1 | 192658207 | |||
| chr1:192659432 | T | C | 1 | a0005 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.389T>C | p.Met130Thr | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 7/7 | 675/1554 | 389/480 | 130/159 | chr1 | 192659432 | |||
| chr1:192659493 | G | C | 1 | a0003 | 9 | HG01891.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
missense_variant | MODERATE | c.450G>C | p.Leu150Phe | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 7/7 | 736/1554 | 450/480 | 150/159 | chr1 | 192659493 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:192658208 | A | C | 1 | a0001c0007 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.135A>C | p.Pro45Pro | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/7 | 421/1554 | 135/480 | 45/159 | chr1 | 192658208 | |||
| chr1:192658301 | G | A | 1 | a0001c0003 | 11 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(8): Show |
synonymous_variant | LOW | c.228G>A | p.Arg76Arg | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/7 | 514/1554 | 228/480 | 76/159 | chr1 | 192658301 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:192636195 | C | T | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(2): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
5_prime_UTR_variant | MODIFIER | c.-238C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/7 | 8140 | chr1 | 192636195 | ||||||
| chr1:192637657 | C | G | 2 | a0001c0001t0003 a0002c0002t0004 |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
5_prime_UTR_variant | MODIFIER | c.-48C>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 2/7 | 6678 | chr1 | 192637657 | ||||||
| chr1:192659601 | A | G | 1 | a0001c0001t0011 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 7/7 | 78 | chr1 | 192659601 | ||||||
| chr1:192659935 | C | A | 2 | a0001c0003t0005 a0001c0003t0009 |
11 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*412C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 7/7 | 412 | chr1 | 192659935 | ||||||
| chr1:192660195 | T | C | 2 | a0001c0001t0007 a0002c0002t0004 |
14 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*672T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 7/7 | 672 | chr1 | 192660195 | ||||||
| chr1:192660249 | A | T | 2 | a0001c0001t0008 a0001c0001t0010 |
2 | HG01081.hp1 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*726A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 7/7 | 726 | chr1 | 192660249 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:192636377 | C | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(66): Show |
172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.-116+60C>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192636377 | |||||||
| chr1:192636457 | A | G | 1 | a0001c0001t0002g0136 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-116+140A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192636457 | |||||||
| chr1:192636463 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
9 | HG02451.hp1 HG02922.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-116+146A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192636463 | |||||||
| chr1:192636477 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-116+160G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192636477 | |||||||
| chr1:192636586 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-116+269T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192636586 | |||||||
| chr1:192636643 | C | A | 1 | a0003c0004t0001g0137 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-116+326C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192636643 | |||||||
| chr1:192636714 | C | CA | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-116+397_-116+398i others(3): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192636714 | |||||||
| chr1:192636776 | A | T | 1 | a0001c0001t0003g0147 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-116+459A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192636776 | |||||||
| chr1:192636953 | TAAAG | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-115-633_-115-630d others(6): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 192636953 | ||||||
| chr1:192637370 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-115-220T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192637370 | |||||||
| chr1:192637462 | C | T | 1 | a0001c0001t0002g0130 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-115-128C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192637462 | |||||||
| chr1:192637487 | A | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(10): Show |
36 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-115-103A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192637487 | |||||||
| chr1:192637552 | T | C | 12 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(9): Show |
31 | HG00438.hp2 HG01109.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.-115-38T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192637552 | |||||||
| chr1:192637557 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0131 |
5 | HG02965.hp2 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-115-33T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 1/6 | chr1 | 192637557 | |||||||
| chr1:192637714 | G | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-45+54G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 2/6 | chr1 | 192637714 | |||||||
| chr1:192637744 | T | C | 1 | a0001c0001t0002g0051 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-45+84T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 2/6 | chr1 | 192637744 | |||||||
| chr1:192637954 | C | G | 1 | a0001c0001t0002g0129 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-44-210C>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 2/6 | chr1 | 192637954 | |||||||
| chr1:192637988 | G | A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-44-176G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 2/6 | chr1 | 192637988 | |||||||
| chr1:192638015 | T | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
3 | HG00609.hp2 HG02080.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-44-149T>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 2/6 | chr1 | 192638015 | |||||||
| chr1:192638116 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44-48C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 2/6 | chr1 | 192638116 | |||||||
| chr1:192638151 | C | A | 1 | a0001c0001t0003g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-44-13C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 2/6 | chr1 | 192638151 | |||||||
| chr1:192638261 | T | G | 11 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(8): Show |
18 | HG01074.hp1 HG01884.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-5+58T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638261 | |||||||
| chr1:192638408 | A | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-5+205A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638408 | |||||||
| chr1:192638428 | T | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-5+225T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638428 | |||||||
| chr1:192638457 | G | A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-5+254G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638457 | |||||||
| chr1:192638545 | G | A | 11 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(8): Show |
18 | HG01074.hp1 HG01884.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-5+342G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638545 | |||||||
| chr1:192638715 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-5+512T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638715 | |||||||
| chr1:192638724 | C | T | 1 | a0001c0001t0003g0042 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-5+521C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638724 | |||||||
| chr1:192638769 | A | T | 1 | a0001c0001t0002g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-5+566A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638769 | |||||||
| chr1:192638785 | C | T | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0136 |
3 | HG02040.hp2 HG02083.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-5+582C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638785 | |||||||
| chr1:192638796 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-5+593C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638796 | |||||||
| chr1:192638828 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-5+625T>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638828 | |||||||
| chr1:192638963 | A | G | 1 | a0004c0005t0001g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-5+760A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192638963 | |||||||
| chr1:192639309 | T | C | 1 | a0001c0001t0002g0031 | 2 | NA18978.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-5+1106T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192639309 | |||||||
| chr1:192639328 | C | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-5+1125C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192639328 | |||||||
| chr1:192639356 | A | AC | 70 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(67): Show |
173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-5+1155dupC | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192639356 | ||||||
| chr1:192639362 | T | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(67): Show |
173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-5+1159T>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192639362 | |||||||
| chr1:192639364 | G | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(67): Show |
173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-5+1161G>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192639364 | |||||||
| chr1:192639489 | G | T | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5+1286G>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192639489 | |||||||
| chr1:192639551 | G | T | 1 | a0001c0001t0002g0124 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-5+1348G>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192639551 | |||||||
| chr1:192639756 | C | A | 12 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(9): Show |
14 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-5+1553C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192639756 | |||||||
| chr1:192639821 | G | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-5+1618G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192639821 | |||||||
| chr1:192639851 | C | A | 1 | a0004c0005t0001g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-5+1648C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192639851 | |||||||
| chr1:192640001 | C | T | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5+1798C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640001 | |||||||
| chr1:192640038 | T | C | 2 | a0001c0001t0001g0149 a0001c0003t0005g0150 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-5+1835T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640038 | |||||||
| chr1:192640126 | A | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(131): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.-5+1923A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640126 | |||||||
| chr1:192640138 | T | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(67): Show |
173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-5+1935T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640138 | |||||||
| chr1:192640177 | A | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-5+1974A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640177 | |||||||
| chr1:192640263 | A | C | 1 | a0001c0001t0002g0123 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-5+2060A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640263 | |||||||
| chr1:192640438 | C | A | 5 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0003c0004t0001g0043 others(2): Show |
6 | HG01884.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+2235C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640438 | |||||||
| chr1:192640504 | A | T | 1 | a0001c0001t0002g0122 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-5+2301A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640504 | |||||||
| chr1:192640505 | G | T | 1 | a0001c0001t0002g0122 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-5+2302G>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640505 | |||||||
| chr1:192640515 | A | G | 64 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(61): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.-5+2312A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640515 | |||||||
| chr1:192640562 | A | G | 5 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0003c0004t0001g0043 others(2): Show |
6 | HG01884.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+2359A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640562 | |||||||
| chr1:192640668 | GTCCTCCT others(59): Show |
G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(48): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.-5+2468_-5+2533del others(66): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192640668 | ||||||
| chr1:192640773 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-5+2570C>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640773 | |||||||
| chr1:192640773 | C | T | 1 | a0001c0001t0002g0136 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-5+2570C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640773 | |||||||
| chr1:192640823 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-5+2620C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640823 | |||||||
| chr1:192640833 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(44): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-5+2630G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640833 | |||||||
| chr1:192640860 | G | A | 1 | a0001c0001t0002g0088 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-5+2657G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640860 | |||||||
| chr1:192640908 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0131 |
5 | HG02965.hp2 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+2705T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640908 | |||||||
| chr1:192640931 | T | C | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5+2728T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192640931 | |||||||
| chr1:192641005 | G | A | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5+2802G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641005 | |||||||
| chr1:192641009 | G | C | 1 | a0001c0001t0001g0030 | 2 | HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-5+2806G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641009 | |||||||
| chr1:192641077 | C | G | 1 | a0001c0001t0002g0121 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-5+2874C>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641077 | |||||||
| chr1:192641129 | G | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-5+2926G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641129 | |||||||
| chr1:192641190 | AAAAAAGA others(43): Show |
A | 1 | a0001c0001t0003g0143 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-5+2991_-5+3040del others(50): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641190 | ||||||
| chr1:192641190 | AAAAAAGA others(73): Show |
A | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5+2991_-4-3058del others(80): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641190 | ||||||
| chr1:192641194 | A | G | 11 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(8): Show |
28 | HG01109.hp2 HG02027.hp1 HG02559.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5+2991A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641194 | |||||||
| chr1:192641195 | AGAAAAAA others(51): Show |
A | 4 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(1): Show |
5 | HG01109.hp2 HG02896.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+2993_-5+3050del others(58): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641195 | |||||||
| chr1:192641196 | G | A | 10 | a0001c0001t0003g0003 a0001c0001t0003g0040 a0001c0001t0003g0041 others(7): Show |
23 | HG02027.hp1 HG02559.hp2 HG02615.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+2993G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641196 | |||||||
| chr1:192641198 | AAAAAGGA others(53): Show |
A | 1 | a0001c0001t0003g0028 | 2 | HG00438.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.-5+2999_-5+3058del others(60): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641198 | ||||||
| chr1:192641200 | A | G | 10 | a0001c0001t0003g0003 a0001c0001t0003g0040 a0001c0001t0003g0041 others(7): Show |
23 | HG02027.hp1 HG02559.hp2 HG02615.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+2997A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641200 | |||||||
| chr1:192641203 | GGAAAGAA others(1): Show |
G | 19 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0010 others(16): Show |
37 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.-5+3011_-5+3018del others(8): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641203 | ||||||
| chr1:192641203 | GGAAAGAA others(47): Show |
G | 1 | a0001c0001t0003g0003 | 2 | NA18971.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-5+3019_-4-3056del others(54): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641203 | ||||||
| chr1:192641208 | GAAAGAAA others(39): Show |
G | 2 | a0001c0001t0003g0003 a0001c0001t0003g0147 |
2 | NA18999.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-5+3019_-5+3064del others(46): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641208 | ||||||
| chr1:192641210 | AAGAAAGA others(5): Show |
A | 13 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(10): Show |
27 | HG00423.hp2 HG00438.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-5+3019_-5+3030del others(12): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641210 | ||||||
| chr1:192641212 | GAAAGAAA others(35): Show |
G | 5 | a0001c0001t0003g0003 a0001c0001t0003g0040 a0001c0001t0003g0041 others(2): Show |
10 | HG02630.hp1 HG02886.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.-5+3019_-5+3060del others(42): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641212 | ||||||
| chr1:192641214 | A | G | 46 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(43): Show |
103 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-5+3011A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641214 | |||||||
| chr1:192641216 | GAAAGAGA others(31): Show |
G | 4 | a0001c0001t0003g0003 a0001c0001t0003g0042 a0001c0001t0003g0138 others(1): Show |
7 | HG02027.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+3019_-5+3056del others(38): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641216 | ||||||
| chr1:192641220 | GAGAGAAA others(27): Show |
G | 1 | a0001c0001t0003g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-5+3019_-5+3052del others(34): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641220 | ||||||
| chr1:192641222 | G | A | 47 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(44): Show |
105 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-5+3019G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641222 | |||||||
| chr1:192641222 | G | GAGAA | 6 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0148 others(3): Show |
6 | HG00558.hp2 HG01981.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+3041_-5+3044dup others(4): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641222 | ||||||
| chr1:192641222 | G | GAGAAAGA others(1): Show |
7 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
9 | HG02717.hp1 HG03130.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5+3037_-5+3044dup others(8): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641222 | ||||||
| chr1:192641222 | GAGAA | G | 15 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0054 others(12): Show |
19 | HG01074.hp1 HG01123.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-5+3041_-5+3044del others(4): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641222 | ||||||
| chr1:192641226 | A | G | 13 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(10): Show |
27 | HG00423.hp2 HG00438.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-5+3023A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641226 | |||||||
| chr1:192641228 | GAAAGAAA others(10): Show |
G | 1 | a0001c0001t0002g0004 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-5+3037_-5+3053del others(17): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641228 | ||||||
| chr1:192641229 | AAAG | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0033 a0001c0001t0002g0052 |
4 | HG01168.hp2 HG01169.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+3029_-5+3031del others(3): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641229 | ||||||
| chr1:192641232 | G | GA | 27 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(24): Show |
55 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-5+3032dupA | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641232 | ||||||
| chr1:192641232 | GAAAGAAA others(6): Show |
G | 2 | a0001c0001t0002g0001 a0001c0001t0002g0090 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-5+3041_-5+3053del others(13): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641232 | ||||||
| chr1:192641233 | AAAG | A | 21 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0014 others(18): Show |
40 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-5+3033_-5+3035del others(3): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641233 | ||||||
| chr1:192641233 | AAAGAAAG others(18): Show |
A | 1 | a0001c0001t0002g0004 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-5+3033_-5+3057del others(25): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641233 | ||||||
| chr1:192641236 | G | GA | 2 | a0001c0001t0001g0020 a0001c0001t0001g0085 |
3 | NA18939.hp1 NA18961.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-5+3036dupA | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641236 | ||||||
| chr1:192641236 | G | GAAAGA | 16 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0030 others(13): Show |
20 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-5+3036_-5+3040dup others(5): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641236 | ||||||
| chr1:192641236 | GAAAGAAA others(2): Show |
G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0046 others(2): Show |
6 | HG01256.hp1 HG01258.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+3054_-5+3062del others(9): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641236 | ||||||
| chr1:192641238 | AAGAAAGA others(61): Show |
A | 1 | a0001c0001t0003g0142 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-5+3037_-4-3024del others(68): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641238 | ||||||
| chr1:192641240 | GAAAGA | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0022 others(3): Show |
10 | HG00280.hp1 HG00544.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5+3045_-5+3049del others(5): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641240 | ||||||
| chr1:192641240 | GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0002g0001 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-5+3045_-5+3058del others(14): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641240 | ||||||
| chr1:192641241 | AAAGAAAA others(18): Show |
A | 1 | a0001c0001t0006g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-5+3041_-4-3063del others(25): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641241 | ||||||
| chr1:192641244 | G | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): Show |
48 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.-5+3041G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641244 | |||||||
| chr1:192641244 | GA | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(52): Show |
121 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-5+3045delA | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641244 | ||||||
| chr1:192641244 | GAAAAGAA others(3): Show |
G | 2 | a0001c0001t0001g0156 a0001c0001t0002g0114 |
2 | NA18522.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-5+3045_-5+3054del others(10): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641244 | ||||||
| chr1:192641245 | A | AAAG | 12 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(9): Show |
12 | HG00741.hp1 HG01243.hp2 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.-5+3044_-5+3045ins others(3): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641245 | ||||||
| chr1:192641245 | A | AAAGAAAA others(1): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0157 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+3044_-5+3045ins others(8): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641245 | ||||||
| chr1:192641245 | A | AAAGAAAG others(5): Show |
1 | a0001c0001t0001g0002 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-5+3044_-5+3045ins others(12): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641245 | ||||||
| chr1:192641245 | A | AAAGAAAG others(8): Show |
1 | a0001c0001t0001g0168 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-5+3044_-5+3045ins others(15): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641245 | ||||||
| chr1:192641245 | A | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): Show |
48 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.-5+3042A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641245 | |||||||
| chr1:192641245 | AAAAGAAA others(10): Show |
A | 1 | a0001c0003t0005g0008 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-5+3054_-4-3058del others(17): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641245 | ||||||
| chr1:192641248 | A | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0155 others(3): Show |
7 | HG00423.hp1 HG01074.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5+3045A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641248 | |||||||
| chr1:192641249 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0155 others(4): Show |
8 | HG00423.hp1 HG01074.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5+3046G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641249 | |||||||
| chr1:192641249 | GAAAGA | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0020 others(9): Show |
17 | HG00423.hp2 HG00741.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.-5+3054_-5+3058del others(5): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641249 | ||||||
| chr1:192641250 | A | G | 1 | a0001c0001t0003g0143 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-5+3047A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641250 | |||||||
| chr1:192641253 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(15): Show |
31 | HG00323.hp2 HG00408.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.-5+3050G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641253 | |||||||
| chr1:192641253 | GA | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(78): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-5+3054delA | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641253 | ||||||
| chr1:192641254 | A | AAAAG | 6 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0071 others(3): Show |
6 | HG02258.hp2 HG03098.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-3025_-4-3022dup others(4): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641254 | ||||||
| chr1:192641254 | A | AAAAGAAA others(1): Show |
6 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0073 others(3): Show |
6 | HG01256.hp2 HG02280.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-3029_-4-3022dup others(8): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641254 | ||||||
| chr1:192641254 | A | AAAAGAAA others(5): Show |
1 | a0001c0001t0001g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-4-3033_-4-3022dup others(12): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641254 | ||||||
| chr1:192641254 | A | AAAG | 32 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(29): Show |
46 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5+3053_-5+3054ins others(3): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641254 | ||||||
| chr1:192641254 | A | AAAGAAAG | 8 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(5): Show |
10 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5+3053_-5+3054ins others(7): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641254 | ||||||
| chr1:192641254 | A | AAAGAAAG others(4): Show |
2 | a0001c0001t0001g0149 a0003c0004t0001g0083 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-5+3053_-5+3054ins others(11): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641254 | ||||||
| chr1:192641254 | A | AAAGAAAG others(8): Show |
1 | a0001c0001t0001g0016 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-5+3053_-5+3054ins others(15): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641254 | ||||||
| chr1:192641254 | A | G | 19 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(16): Show |
33 | HG00323.hp2 HG00408.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-5+3051A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641254 | |||||||
| chr1:192641254 | AAAAG | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0019 others(12): Show |
19 | HG00597.hp1 HG01074.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-4-3025_-4-3022del others(4): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641254 | ||||||
| chr1:192641254 | AAAAGAAA others(1): Show |
A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0135 |
4 | HG01981.hp1 HG02273.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-3029_-4-3022del others(8): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641254 | ||||||
| chr1:192641257 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0175 |
2 | HG02148.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-5+3054A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641257 | |||||||
| chr1:192641258 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0175 |
2 | HG02148.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-5+3055G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641258 | |||||||
| chr1:192641261 | A | G | 4 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(1): Show |
5 | HG01109.hp2 HG02896.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+3058A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641261 | |||||||
| chr1:192641265 | A | G | 2 | a0001c0001t0002g0039 a0001c0001t0003g0028 |
3 | HG00438.hp2 HG02071.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-5+3062A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641265 | |||||||
| chr1:192641276 | AAG | A | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-4-3053_-4-3052del others(2): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641276 | ||||||
| chr1:192641285 | A | G | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-4-3046A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641285 | |||||||
| chr1:192641304 | AAG | A | 56 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0010 others(53): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-4-3025_-4-3024del others(2): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641304 | ||||||
| chr1:192641306 | G | GAA | 13 | a0001c0001t0002g0006 a0001c0001t0002g0035 a0001c0001t0002g0036 others(10): Show |
25 | HG00621.hp2 HG01109.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.-4-3022_-4-3021dup others(2): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641306 | ||||||
| chr1:192641306 | GA | G | 3 | a0001c0001t0002g0119 a0001c0001t0003g0028 a0001c0001t0003g0147 |
5 | HG00438.hp2 HG02071.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-3021delA | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641306 | ||||||
| chr1:192641320 | G | A | 1 | a0001c0001t0002g0114 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-4-3011G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641320 | |||||||
| chr1:192641322 | G | A | 1 | a0001c0001t0002g0114 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-4-3009G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641322 | |||||||
| chr1:192641359 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-4-2972G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641359 | |||||||
| chr1:192641359 | G | T | 2 | a0001c0001t0001g0154 a0004c0005t0001g0179 |
2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-4-2972G>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641359 | |||||||
| chr1:192641753 | T | C | 11 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(8): Show |
18 | HG01074.hp1 HG01884.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-4-2578T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641753 | |||||||
| chr1:192641772 | G | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-4-2559G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641772 | |||||||
| chr1:192641781 | A | AT | 3 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0087 |
7 | NA18942.hp1 NA18945.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4-2542dupT | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192641781 | ||||||
| chr1:192641907 | A | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-4-2424A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641907 | |||||||
| chr1:192641987 | T | A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-4-2344T>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192641987 | |||||||
| chr1:192642047 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-4-2284G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642047 | |||||||
| chr1:192642048 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-4-2283C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642048 | |||||||
| chr1:192642112 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-4-2219C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642112 | |||||||
| chr1:192642145 | T | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-4-2186T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642145 | |||||||
| chr1:192642168 | C | T | 67 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0002g0001 others(64): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.-4-2163C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642168 | |||||||
| chr1:192642182 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0131 |
5 | HG02965.hp2 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-2149C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642182 | |||||||
| chr1:192642217 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0148 others(17): Show |
53 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.-4-2114G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642217 | |||||||
| chr1:192642225 | T | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-4-2106T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642225 | |||||||
| chr1:192642239 | T | C | 12 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(9): Show |
31 | HG00438.hp2 HG01109.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.-4-2092T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642239 | |||||||
| chr1:192642322 | C | CT | 69 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0154 others(66): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-4-1992dupT | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192642322 | ||||||
| chr1:192642322 | CTT | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-4-1993_-4-1992del others(2): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192642322 | ||||||
| chr1:192642346 | A | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-4-1985A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642346 | |||||||
| chr1:192642390 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-4-1941C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642390 | |||||||
| chr1:192642422 | A | T | 1 | a0001c0001t0002g0124 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-4-1909A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642422 | |||||||
| chr1:192642489 | T | A | 65 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(62): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.-4-1842T>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642489 | |||||||
| chr1:192642602 | T | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-4-1729T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642602 | |||||||
| chr1:192642644 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-4-1687C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642644 | |||||||
| chr1:192642839 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0060 |
4 | HG01884.hp2 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-1492A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642839 | |||||||
| chr1:192642895 | T | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-4-1436T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642895 | |||||||
| chr1:192642983 | C | T | 2 | a0001c0001t0001g0149 a0001c0003t0005g0150 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-4-1348C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192642983 | |||||||
| chr1:192643102 | C | T | 1 | a0001c0001t0002g0112 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-4-1229C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643102 | |||||||
| chr1:192643264 | A | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(130): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-4-1067A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643264 | |||||||
| chr1:192643264 | A | T | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0136 |
3 | HG02040.hp2 HG02083.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-4-1067A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643264 | |||||||
| chr1:192643363 | C | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-4-968C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643363 | |||||||
| chr1:192643455 | T | TCA | 67 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0002g0001 others(64): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.-4-876_-4-875insCA | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643455 | |||||||
| chr1:192643511 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-4-820T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643511 | |||||||
| chr1:192643544 | AC | A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(13): Show |
44 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-4-784delC | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192643544 | ||||||
| chr1:192643581 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0169 |
3 | HG00280.hp1 NA19000.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-4-750T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643581 | |||||||
| chr1:192643663 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-4-668A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643663 | |||||||
| chr1:192643695 | G | A | 91 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(88): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-4-636G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643695 | |||||||
| chr1:192643721 | T | G | 109 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(106): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-4-610T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643721 | |||||||
| chr1:192643933 | A | T | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-4-398A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643933 | |||||||
| chr1:192643946 | C | G | 1 | a0001c0001t0002g0111 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-4-385C>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643946 | |||||||
| chr1:192643954 | A | AAAAAAT | 3 | a0001c0001t0002g0032 a0001c0001t0002g0115 a0001c0001t0010g0091 |
4 | HG01361.hp2 HG02004.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-362_-4-357dupAA others(4): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 192643954 | ||||||
| chr1:192643987 | A | C | 8 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
9 | HG02451.hp1 HG02451.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-344A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192643987 | |||||||
| chr1:192644015 | G | A | 17 | a0001c0001t0003g0003 a0001c0001t0003g0028 a0001c0001t0003g0040 others(14): Show |
45 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.-4-316G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192644015 | |||||||
| chr1:192644148 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-4-183T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192644148 | |||||||
| chr1:192644190 | C | T | 19 | a0001c0001t0001g0082 a0001c0001t0001g0168 a0001c0001t0002g0120 others(16): Show |
47 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.-4-141C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192644190 | |||||||
| chr1:192644248 | A | G | 19 | a0001c0001t0001g0082 a0001c0001t0001g0168 a0001c0001t0002g0120 others(16): Show |
47 | HG00438.hp2 HG01106.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.-4-83A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 3/6 | chr1 | 192644248 | |||||||
| chr1:192644531 | T | C | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+132T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644531 | |||||||
| chr1:192644637 | G | C | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+238G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644637 | |||||||
| chr1:192644730 | C | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG02451.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.65+331C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644730 | |||||||
| chr1:192644768 | G | A | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+369G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644768 | |||||||
| chr1:192644900 | G | A | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+501G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644900 | |||||||
| chr1:192644931 | A | T | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+532A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644931 | |||||||
| chr1:192644932 | A | C | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+533A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644932 | |||||||
| chr1:192644934 | A | C | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+535A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644934 | |||||||
| chr1:192644935 | G | C | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+536G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644935 | |||||||
| chr1:192644936 | T | TG | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+537_65+538insG | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644936 | |||||||
| chr1:192644937 | T | A | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+538T>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644937 | |||||||
| chr1:192644938 | G | A | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+539G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192644938 | |||||||
| chr1:192645067 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.65+668A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192645067 | |||||||
| chr1:192645118 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.65+719G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192645118 | |||||||
| chr1:192645158 | T | C | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+759T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192645158 | |||||||
| chr1:192645213 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.65+814G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192645213 | |||||||
| chr1:192645363 | A | G | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+964A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192645363 | |||||||
| chr1:192645370 | T | G | 4 | a0001c0001t0003g0042 a0001c0001t0003g0138 a0001c0001t0003g0140 others(1): Show |
5 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.65+971T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192645370 | |||||||
| chr1:192645457 | C | T | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+1058C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192645457 | |||||||
| chr1:192645621 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0112 a0001c0001t0002g0119 others(1): Show |
6 | HG02083.hp2 HG02165.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.65+1222C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192645621 | |||||||
| chr1:192645731 | TTG | T | 15 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(12): Show |
25 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.65+1335_65+1336del others(2): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 192645731 | ||||||
| chr1:192645744 | C | CA | 4 | a0001c0001t0003g0042 a0001c0001t0003g0138 a0001c0001t0003g0140 others(1): Show |
5 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.65+1353dupA | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 192645744 | ||||||
| chr1:192645901 | T | C | 1 | a0001c0001t0002g0093 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.65+1502T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192645901 | |||||||
| chr1:192645935 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.65+1536C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192645935 | |||||||
| chr1:192646000 | C | G | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.65+1601C>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192646000 | |||||||
| chr1:192646092 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.65+1693G>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192646092 | |||||||
| chr1:192646201 | T | C | 2 | a0001c0001t0002g0025 a0001c0001t0002g0035 |
5 | HG00621.hp2 NA18942.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.66-1725T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192646201 | |||||||
| chr1:192646296 | T | C | 1 | a0001c0001t0006g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.66-1630T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192646296 | |||||||
| chr1:192646479 | T | C | 15 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(12): Show |
25 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.66-1447T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192646479 | |||||||
| chr1:192646789 | T | C | 44 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(41): Show |
74 | HG01081.hp2 HG01106.hp1 HG01109.hp2 others(71): Show |
intron_variant | MODIFIER | c.66-1137T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192646789 | |||||||
| chr1:192646844 | T | C | 7 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
8 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.66-1082T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192646844 | |||||||
| chr1:192647007 | T | G | 1 | a0001c0001t0002g0095 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.66-919T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647007 | |||||||
| chr1:192647058 | C | A | 2 | a0001c0003t0005g0008 a0001c0003t0009g0094 |
9 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.66-868C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647058 | |||||||
| chr1:192647065 | G | A | 14 | a0001c0001t0001g0149 a0001c0003t0005g0008 a0001c0003t0009g0094 others(11): Show |
31 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.66-861G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647065 | |||||||
| chr1:192647180 | G | T | 1 | a0002c0002t0004g0146 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.66-746G>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647180 | |||||||
| chr1:192647277 | T | C | 1 | a0001c0001t0001g0046 | 2 | NA19063.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.66-649T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647277 | |||||||
| chr1:192647434 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.66-492A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647434 | |||||||
| chr1:192647448 | C | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG02451.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.66-478C>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647448 | |||||||
| chr1:192647483 | G | A | 14 | a0001c0001t0001g0149 a0001c0003t0005g0008 a0001c0003t0009g0094 others(11): Show |
31 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.66-443G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647483 | |||||||
| chr1:192647550 | A | C | 131 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(128): Show |
279 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.66-376A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647550 | |||||||
| chr1:192647565 | A | G | 2 | a0001c0001t0001g0149 a0001c0007t0001g0068 |
2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.66-361A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647565 | |||||||
| chr1:192647599 | A | C | 1 | a0001c0001t0001g0174 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.66-327A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647599 | |||||||
| chr1:192647615 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.66-311A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647615 | |||||||
| chr1:192647890 | T | C | 1 | a0001c0001t0003g0028 | 3 | HG00438.hp2 HG02071.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.66-36T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 4/6 | chr1 | 192647890 | |||||||
| chr1:192648416 | A | G | 5 | a0001c0001t0001g0156 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+429A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192648416 | |||||||
| chr1:192648471 | G | A | 2 | a0001c0003t0005g0008 a0001c0003t0009g0094 |
9 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+484G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192648471 | |||||||
| chr1:192648513 | G | A | 14 | a0001c0001t0001g0149 a0001c0003t0005g0008 a0001c0003t0009g0094 others(11): Show |
31 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.127+526G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192648513 | |||||||
| chr1:192648672 | G | GT | 4 | a0001c0001t0003g0042 a0001c0001t0003g0138 a0001c0001t0003g0140 others(1): Show |
5 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+693dupT | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 192648672 | ||||||
| chr1:192648863 | C | A | 1 | a0001c0001t0002g0033 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.127+876C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192648863 | |||||||
| chr1:192648898 | G | C | 57 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(54): Show |
104 | HG00280.hp1 HG00544.hp2 HG01081.hp2 others(101): Show |
intron_variant | MODIFIER | c.127+911G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192648898 | |||||||
| chr1:192649020 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.127+1033C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649020 | |||||||
| chr1:192649052 | T | C | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(38): Show |
69 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(66): Show |
intron_variant | MODIFIER | c.127+1065T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649052 | |||||||
| chr1:192649056 | T | A | 1 | a0004c0005t0001g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.127+1069T>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649056 | |||||||
| chr1:192649170 | G | A | 11 | a0001c0001t0001g0149 a0001c0001t0001g0161 a0001c0003t0005g0008 others(8): Show |
19 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.127+1183G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649170 | |||||||
| chr1:192649177 | G | C | 14 | a0001c0001t0001g0149 a0001c0003t0005g0008 a0001c0003t0009g0094 others(11): Show |
31 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.127+1190G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649177 | |||||||
| chr1:192649262 | C | A | 1 | a0001c0001t0003g0040 | 2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.127+1275C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649262 | |||||||
| chr1:192649264 | G | A | 43 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(40): Show |
73 | HG01081.hp2 HG01106.hp1 HG01109.hp2 others(70): Show |
intron_variant | MODIFIER | c.127+1277G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649264 | |||||||
| chr1:192649283 | T | G | 14 | a0001c0001t0001g0149 a0001c0003t0005g0008 a0001c0003t0009g0094 others(11): Show |
31 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.127+1296T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649283 | |||||||
| chr1:192649524 | T | C | 5 | a0001c0001t0001g0156 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+1537T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649524 | |||||||
| chr1:192649547 | A | G | 5 | a0001c0001t0001g0156 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+1560A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649547 | |||||||
| chr1:192649594 | G | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG02451.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.127+1607G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649594 | |||||||
| chr1:192649655 | A | C | 26 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(23): Show |
44 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(41): Show |
intron_variant | MODIFIER | c.127+1668A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649655 | |||||||
| chr1:192649701 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.127+1714C>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649701 | |||||||
| chr1:192649766 | C | T | 12 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(9): Show |
13 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.127+1779C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192649766 | |||||||
| chr1:192650097 | T | C | 10 | a0001c0001t0001g0149 a0001c0003t0005g0008 a0001c0003t0009g0094 others(7): Show |
18 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.127+2110T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650097 | |||||||
| chr1:192650120 | T | A | 14 | a0001c0001t0001g0149 a0001c0003t0005g0008 a0001c0003t0009g0094 others(11): Show |
31 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.127+2133T>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650120 | |||||||
| chr1:192650123 | A | C | 14 | a0001c0001t0001g0149 a0001c0003t0005g0008 a0001c0003t0009g0094 others(11): Show |
31 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.127+2136A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650123 | |||||||
| chr1:192650321 | G | A | 4 | a0001c0001t0003g0042 a0001c0001t0003g0138 a0001c0001t0003g0140 others(1): Show |
5 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+2334G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650321 | |||||||
| chr1:192650391 | A | G | 15 | a0001c0001t0001g0082 a0001c0001t0001g0149 a0001c0003t0005g0008 others(12): Show |
32 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.127+2404A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650391 | |||||||
| chr1:192650429 | G | C | 15 | a0001c0001t0001g0082 a0001c0001t0001g0149 a0001c0003t0005g0008 others(12): Show |
32 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.127+2442G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650429 | |||||||
| chr1:192650453 | C | A | 15 | a0001c0001t0001g0082 a0001c0001t0001g0149 a0001c0003t0005g0008 others(12): Show |
32 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.127+2466C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650453 | |||||||
| chr1:192650478 | G | A | 2 | a0001c0003t0005g0008 a0001c0003t0009g0094 |
9 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+2491G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650478 | |||||||
| chr1:192650585 | T | C | 15 | a0001c0001t0001g0082 a0001c0001t0001g0149 a0001c0003t0005g0008 others(12): Show |
32 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.127+2598T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650585 | |||||||
| chr1:192650726 | A | G | 15 | a0001c0001t0001g0082 a0001c0001t0001g0149 a0001c0003t0005g0008 others(12): Show |
32 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.127+2739A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650726 | |||||||
| chr1:192650826 | AT | A | 15 | a0001c0001t0001g0082 a0001c0001t0001g0149 a0001c0003t0005g0008 others(12): Show |
32 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.127+2847delT | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 192650826 | ||||||
| chr1:192650836 | T | A | 12 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(9): Show |
13 | HG02109.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.127+2849T>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650836 | |||||||
| chr1:192650897 | C | T | 10 | a0001c0001t0001g0082 a0001c0003t0005g0008 a0001c0003t0009g0094 others(7): Show |
26 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.127+2910C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650897 | |||||||
| chr1:192650905 | G | C | 3 | a0001c0001t0002g0026 a0001c0001t0002g0037 a0001c0001t0002g0098 |
6 | HG00673.hp1 HG02135.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+2918G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650905 | |||||||
| chr1:192650921 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.127+2934G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650921 | |||||||
| chr1:192650997 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG02451.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.127+3010A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192650997 | |||||||
| chr1:192651008 | C | T | 14 | a0001c0001t0001g0082 a0001c0003t0005g0008 a0001c0003t0009g0094 others(11): Show |
31 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.127+3021C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651008 | |||||||
| chr1:192651015 | G | A | 14 | a0001c0001t0001g0082 a0001c0003t0005g0008 a0001c0003t0009g0094 others(11): Show |
31 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.127+3028G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651015 | |||||||
| chr1:192651030 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.127+3043G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651030 | |||||||
| chr1:192651036 | G | A | 2 | a0001c0003t0005g0008 a0001c0003t0009g0094 |
9 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+3049G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651036 | |||||||
| chr1:192651236 | A | G | 19 | a0001c0001t0001g0082 a0001c0001t0003g0042 a0001c0001t0003g0138 others(16): Show |
37 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.127+3249A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651236 | |||||||
| chr1:192651266 | C | A | 19 | a0001c0001t0001g0082 a0001c0001t0003g0042 a0001c0001t0003g0138 others(16): Show |
37 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.127+3279C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651266 | |||||||
| chr1:192651323 | A | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(166): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.127+3336A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651323 | |||||||
| chr1:192651323 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.127+3336A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651323 | |||||||
| chr1:192651353 | A | G | 14 | a0001c0001t0001g0082 a0001c0003t0005g0008 a0001c0003t0009g0094 others(11): Show |
31 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.127+3366A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651353 | |||||||
| chr1:192651445 | C | T | 31 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(28): Show |
57 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.127+3458C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651445 | |||||||
| chr1:192651471 | T | TC | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(38): Show |
70 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(67): Show |
intron_variant | MODIFIER | c.127+3484_127+3485i others(3): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651471 | |||||||
| chr1:192651554 | G | A | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.127+3567G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651554 | |||||||
| chr1:192651560 | A | G | 5 | a0001c0001t0002g0014 a0001c0001t0002g0031 a0001c0001t0002g0110 others(2): Show |
10 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+3573A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651560 | |||||||
| chr1:192651586 | C | T | 38 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0080 others(35): Show |
110 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.127+3599C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651586 | |||||||
| chr1:192651599 | C | CAAAGTAG others(9): Show |
2 | a0001c0001t0001g0168 a0001c0001t0003g0040 |
3 | HG01109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.127+3622_127+3637d others(18): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 192651599 | ||||||
| chr1:192651727 | GT | G | 4 | a0002c0002t0004g0005 a0002c0002t0004g0144 a0002c0002t0004g0145 others(1): Show |
13 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.127+3742delT | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 192651727 | ||||||
| chr1:192651758 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.127+3771G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651758 | |||||||
| chr1:192651920 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.127+3933G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651920 | |||||||
| chr1:192651959 | T | C | 3 | a0001c0001t0003g0042 a0001c0001t0003g0138 a0001c0001t0003g0140 |
4 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+3972T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651959 | |||||||
| chr1:192651969 | G | A | 3 | a0001c0001t0003g0042 a0001c0001t0003g0138 a0001c0001t0003g0140 |
4 | HG02615.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+3982G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651969 | |||||||
| chr1:192651980 | T | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(63): Show |
161 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.127+3993T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192651980 | |||||||
| chr1:192652216 | C | T | 2 | a0001c0003t0005g0070 a0001c0003t0005g0150 |
2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.127+4229C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652216 | |||||||
| chr1:192652385 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.127+4398T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652385 | |||||||
| chr1:192652444 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.127+4457C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652444 | |||||||
| chr1:192652450 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(90): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.127+4463C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652450 | |||||||
| chr1:192652508 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.127+4521A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652508 | |||||||
| chr1:192652570 | G | A | 8 | a0003c0004t0001g0043 a0003c0004t0001g0056 a0003c0004t0001g0083 others(5): Show |
9 | HG01891.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+4583G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652570 | |||||||
| chr1:192652602 | A | AT | 9 | a0001c0001t0007g0182 a0001c0003t0005g0008 a0001c0003t0005g0070 others(6): Show |
25 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.127+4625dupT | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 192652602 | ||||||
| chr1:192652602 | A | ATT | 4 | a0001c0001t0002g0014 a0001c0001t0002g0110 a0001c0001t0002g0117 others(1): Show |
8 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+4624_127+4625d others(4): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 192652602 | ||||||
| chr1:192652604 | T | C | 2 | a0001c0001t0006g0062 a0001c0001t0006g0063 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.127+4617T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652604 | |||||||
| chr1:192652606 | T | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(58): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.127+4619T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652606 | |||||||
| chr1:192652651 | A | T | 1 | a0002c0002t0004g0144 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.127+4664A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652651 | |||||||
| chr1:192652665 | C | G | 13 | a0001c0001t0002g0014 a0001c0001t0002g0110 a0001c0001t0002g0117 others(10): Show |
33 | HG00408.hp1 HG00558.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.127+4678C>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652665 | |||||||
| chr1:192652727 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
217 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.127+4740C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652727 | |||||||
| chr1:192652797 | TG | T | 4 | a0001c0003t0005g0008 a0001c0003t0005g0070 a0001c0003t0005g0150 others(1): Show |
11 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+4811delG | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652797 | |||||||
| chr1:192652802 | T | C | 1 | a0001c0001t0001g0047 | 2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.127+4815T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652802 | |||||||
| chr1:192652809 | A | G | 8 | a0001c0001t0002g0014 a0001c0001t0002g0110 a0001c0001t0002g0117 others(5): Show |
19 | HG00408.hp1 HG00558.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.127+4822A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192652809 | |||||||
| chr1:192653022 | G | A | 8 | a0003c0004t0001g0043 a0003c0004t0001g0056 a0003c0004t0001g0083 others(5): Show |
9 | HG01891.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+5035G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192653022 | |||||||
| chr1:192653049 | T | C | 2 | a0004c0005t0001g0053 a0004c0005t0001g0179 |
2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.127+5062T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192653049 | |||||||
| chr1:192653307 | A | G | 5 | a0001c0001t0007g0182 a0002c0002t0004g0005 a0002c0002t0004g0144 others(2): Show |
14 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.128-4894A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192653307 | |||||||
| chr1:192653515 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.128-4686A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192653515 | |||||||
| chr1:192653637 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.128-4564T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192653637 | |||||||
| chr1:192653666 | T | C | 27 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(24): Show |
45 | HG00408.hp1 HG00558.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.128-4535T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192653666 | |||||||
| chr1:192653691 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.128-4510G>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192653691 | |||||||
| chr1:192653886 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.128-4315C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192653886 | |||||||
| chr1:192653958 | G | C | 1 | a0001c0001t0002g0102 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.128-4243G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192653958 | |||||||
| chr1:192653974 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.128-4227G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192653974 | |||||||
| chr1:192654020 | G | T | 3 | a0001c0001t0001g0134 a0001c0001t0006g0023 a0001c0001t0006g0067 |
5 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-4181G>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192654020 | |||||||
| chr1:192654154 | A | G | 1 | a0001c0001t0006g0064 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.128-4047A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192654154 | |||||||
| chr1:192654259 | A | G | 1 | a0001c0001t0001g0017 | 5 | HG00099.hp1 HG01069.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-3942A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192654259 | |||||||
| chr1:192654284 | C | A | 2 | a0001c0001t0001g0172 a0001c0001t0002g0103 |
2 | NA18967.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.128-3917C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192654284 | |||||||
| chr1:192654408 | TATA | T | 4 | a0001c0001t0002g0014 a0001c0001t0002g0110 a0001c0001t0002g0117 others(1): Show |
8 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-3789_128-3787d others(5): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 192654408 | ||||||
| chr1:192654456 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.128-3745A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192654456 | |||||||
| chr1:192655002 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0002g0100 |
6 | NA18942.hp1 NA18945.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-3199T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192655002 | |||||||
| chr1:192655141 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.128-3060T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192655141 | |||||||
| chr1:192655172 | C | T | 5 | a0001c0001t0007g0182 a0002c0002t0004g0005 a0002c0002t0004g0144 others(2): Show |
14 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.128-3029C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192655172 | |||||||
| chr1:192655643 | T | C | 1 | a0001c0001t0002g0104 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.128-2558T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192655643 | |||||||
| chr1:192655902 | G | C | 62 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0047 others(59): Show |
159 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.128-2299G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192655902 | |||||||
| chr1:192656092 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.128-2109C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192656092 | |||||||
| chr1:192656230 | G | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0077 others(8): Show |
21 | HG01243.hp2 HG01361.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.128-1971G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192656230 | |||||||
| chr1:192656284 | C | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(2): Show |
9 | HG02258.hp1 HG02622.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.128-1917C>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192656284 | |||||||
| chr1:192656345 | GT | G | 6 | a0001c0001t0001g0015 a0001c0001t0002g0004 a0001c0001t0002g0033 others(3): Show |
7 | HG01167.hp1 HG01167.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-1843delT | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 192656345 | ||||||
| chr1:192656345 | GTTT | G | 4 | a0001c0003t0005g0008 a0001c0003t0005g0070 a0001c0003t0005g0150 others(1): Show |
11 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.128-1845_128-1843d others(5): Show |
RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 192656345 | ||||||
| chr1:192656346 | T | G | 5 | a0001c0001t0007g0182 a0002c0002t0004g0005 a0002c0002t0004g0144 others(2): Show |
14 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.128-1855T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192656346 | |||||||
| chr1:192656348 | T | G | 1 | a0001c0001t0002g0112 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.128-1853T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192656348 | |||||||
| chr1:192656356 | T | A | 12 | a0001c0001t0001g0059 a0001c0001t0001g0076 a0001c0001t0001g0156 others(9): Show |
13 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.128-1845T>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192656356 | |||||||
| chr1:192656400 | C | A | 77 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0020 others(74): Show |
186 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.128-1801C>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192656400 | |||||||
| chr1:192656458 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.128-1743C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192656458 | |||||||
| chr1:192656663 | G | A | 4 | a0001c0003t0005g0008 a0001c0003t0005g0070 a0001c0003t0005g0150 others(1): Show |
11 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.128-1538G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192656663 | |||||||
| chr1:192656771 | C | T | 4 | a0001c0003t0005g0008 a0001c0003t0005g0070 a0001c0003t0005g0150 others(1): Show |
11 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.128-1430C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192656771 | |||||||
| chr1:192656837 | G | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0105 |
3 | HG03688.hp1 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.128-1364G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192656837 | |||||||
| chr1:192657302 | C | CA | 86 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0020 others(83): Show |
197 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.128-890dupA | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 192657302 | ||||||
| chr1:192657342 | C | T | 5 | a0001c0001t0007g0182 a0002c0002t0004g0005 a0002c0002t0004g0144 others(2): Show |
14 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.128-859C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657342 | |||||||
| chr1:192657358 | A | G | 2 | a0001c0001t0002g0098 a0001c0001t0002g0127 |
2 | HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.128-843A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657358 | |||||||
| chr1:192657594 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.128-607C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657594 | |||||||
| chr1:192657631 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(3): Show |
10 | HG02258.hp1 HG02622.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-570T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657631 | |||||||
| chr1:192657689 | T | C | 1 | a0001c0001t0003g0147 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.128-512T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657689 | |||||||
| chr1:192657696 | A | G | 119 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0020 others(116): Show |
255 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.128-505A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657696 | |||||||
| chr1:192657705 | G | A | 1 | a0001c0001t0006g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.128-496G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657705 | |||||||
| chr1:192657713 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.128-488C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657713 | |||||||
| chr1:192657726 | A | C | 79 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0020 others(76): Show |
188 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.128-475A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657726 | |||||||
| chr1:192657764 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.128-437T>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657764 | |||||||
| chr1:192657773 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.128-428C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657773 | |||||||
| chr1:192657865 | C | T | 4 | a0001c0003t0005g0008 a0001c0003t0005g0070 a0001c0003t0005g0150 others(1): Show |
11 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.128-336C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657865 | |||||||
| chr1:192657994 | T | C | 40 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(37): Show |
67 | HG00408.hp1 HG00558.hp1 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.128-207T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192657994 | |||||||
| chr1:192658059 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.128-142T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192658059 | |||||||
| chr1:192658075 | G | C | 1 | a0001c0007t0001g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.128-126G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192658075 | |||||||
| chr1:192658156 | T | C | 36 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(33): Show |
56 | HG00408.hp1 HG00558.hp1 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.128-45T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 5/6 | chr1 | 192658156 | |||||||
| chr1:192658409 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.294+42C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192658409 | |||||||
| chr1:192658440 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0168 |
2 | HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.294+73A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192658440 | |||||||
| chr1:192658574 | T | C | 4 | a0001c0003t0005g0008 a0001c0003t0005g0070 a0001c0003t0005g0150 others(1): Show |
11 | HG01081.hp2 HG01123.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.294+207T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192658574 | |||||||
| chr1:192658630 | G | A | 39 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0055 others(36): Show |
66 | HG00408.hp1 HG00558.hp1 HG01081.hp2 others(63): Show |
intron_variant | MODIFIER | c.294+263G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192658630 | |||||||
| chr1:192658757 | A | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0110 a0001c0001t0002g0117 |
7 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+390A>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192658757 | |||||||
| chr1:192658822 | A | G | 75 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0020 others(72): Show |
180 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.294+455A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192658822 | |||||||
| chr1:192658850 | T | C | 2 | a0001c0001t0008g0184 a0001c0001t0010g0091 |
2 | HG01081.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.294+483T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192658850 | |||||||
| chr1:192658852 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.294+485G>A | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192658852 | |||||||
| chr1:192658863 | G | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0057 a0001c0001t0001g0073 others(1): Show |
6 | HG02451.hp1 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-475G>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192658863 | |||||||
| chr1:192658867 | A | C | 2 | a0001c0001t0006g0062 a0001c0001t0006g0063 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.295-471A>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192658867 | |||||||
| chr1:192658930 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.295-408C>T | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192658930 | |||||||
| chr1:192659024 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.295-314A>G | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192659024 | |||||||
| chr1:192659156 | T | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0002g0032 others(4): Show |
14 | HG01361.hp2 HG03490.hp1 HG03492.hp2 others(11): Show |
intron_variant | MODIFIER | c.295-182T>C | RGS13 | ENSG00000127074.15 | transcript | ENST00000391995.7 | protein_coding | 6/6 | chr1 | 192659156 |