Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6050 |
| ensemblid | ENSG00000023191.17 |
| hgncid | 10074 |
| symbol | RNH1 |
| name | ribonuclease/angiogenin inhibitor 1 |
| refseq_nuc | NM_203387.3 |
| refseq_prot | NP_976321.1 |
| ensembl_nuc | ENST00000354420.7 |
| ensembl_prot | ENSP00000346402.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 494515 |
| end | 507242 |
| strand | - |
| ver | v1.2 |
| region | chr11:494515-507242 |
| region5000 | chr11:489515-512242 |
| regionname0 | RNH1_chr11_494515_507242 |
| regionname5000 | RNH1_chr11_489515_512242 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 461 | 336 | 85 | 48 | 150 | 14 | 39 | 107 | RNH1_chr11_489515_512242 | RNH1 | MSLDI others(456): Show |
chr11 | 489515 | 512242 |
| a0002 | 0/0 | 461 | 21 | 6 | 10 | 0 | 0 | 5 | 0 | RNH1_chr11_489515_512242 | RNH1 | MSLDI others(456): Show |
chr11 | 489515 | 512242 |
| a0003 | 0/1 | 456 | 20 | 0 | 16 | 0 | 2 | 1 | 0 | RNH1_chr11_489515_512242 | RNH1 | MSLDI others(451): Show |
chr11 | 489515 | 512242 |
| a0004 | 0/0 | 461 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | RNH1_chr11_489515_512242 | RNH1 | MSLDI others(456): Show |
chr11 | 489515 | 512242 |
| a0005 | 0/0 | 461 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | MSLDI others(456): Show |
chr11 | 489515 | 512242 |
| a0006 | 0/0 | 461 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | MSLDI others(456): Show |
chr11 | 489515 | 512242 |
| a0007 | 0/0 | 461 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | MSLDI others(456): Show |
chr11 | 489515 | 512242 |
| a0008 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | MSLDI others(456): Show |
chr11 | 489515 | 512242 |
| a0009 | 0/0 | 298 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | MSLDI others(293): Show |
chr11 | 489515 | 512242 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1383 | 227 | 37 | 38 | 113 | 9 | 30 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0001c0002 | 0/0 | 1383 | 84 | 31 | 10 | 31 | 5 | 7 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0001c0005 | 0/0 | 1383 | 18 | 17 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0001c0008 | 0/0 | 1383 | 2 | 0 | 0 | 2 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0001c0009 | 0/0 | 1383 | 2 | 0 | 0 | 0 | 0 | 2 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0001c0012 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0001c0015 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0001c0016 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0002c0003 | 0/0 | 1383 | 21 | 6 | 10 | 0 | 0 | 5 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0003c0004 | 0/1 | 1368 | 20 | 0 | 16 | 0 | 2 | 1 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1363): Show |
chr11 | 489515 | 512242 | ||
| a0004c0006 | 0/0 | 1383 | 3 | 0 | 2 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0005c0007 | 0/0 | 1383 | 3 | 3 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0006c0010 | 0/0 | 1383 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0007c0014 | 0/0 | 1383 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0008c0013 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 | ||
| a0009c0011 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | ATGAG others(1378): Show |
chr11 | 489515 | 512242 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1952 | 221 | 33 | 37 | 112 | 9 | 30 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0001t0004 | 0/0 | 1952 | 3 | 2 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0001t0005 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0001t0008 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0001t0009 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0002t0001 | 0/0 | 1952 | 3 | 0 | 1 | 0 | 2 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0002t0002 | 0/0 | 1952 | 80 | 30 | 9 | 31 | 3 | 7 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0002t0010 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0005t0001 | 0/0 | 1952 | 16 | 15 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0005t0002 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0005t0007 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0008t0002 | 0/0 | 1952 | 2 | 0 | 0 | 2 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0009t0001 | 0/0 | 1952 | 2 | 0 | 0 | 0 | 0 | 2 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0012t0001 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0015t0001 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0001c0016t0001 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0002c0003t0001 | 0/0 | 1952 | 21 | 6 | 10 | 0 | 0 | 5 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0003c0004t0003 | 0/1 | 1937 | 20 | 0 | 16 | 0 | 2 | 1 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1932): Show |
chr11 | 489515 | 512242 |
| a0004c0006t0002 | 0/0 | 1952 | 3 | 0 | 2 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0005c0007t0001 | 0/0 | 1952 | 3 | 3 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0006c0010t0006 | 0/0 | 1952 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0007c0014t0001 | 0/0 | 1952 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0008c0013t0001 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| a0009c0011t0002 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | GAACA others(1947): Show |
chr11 | 489515 | 512242 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 38 | 1 | 5 | 25 | 1 | 6 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0002 | 0/0 | 34 | 1 | 1 | 26 | 0 | 6 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0003 | 0/0 | 25 | 0 | 6 | 17 | 0 | 2 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0004g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0004 | 0/0 | 10 | 0 | 2 | 6 | 1 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0005 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0012 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0024 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0026 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0053 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0002t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0005t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0008t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0008t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0009t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0009t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0012t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0015t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0001c0016t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0002c0003t0001g0007 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0002c0003t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0002c0003t0001g0028 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0002c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0002c0003t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0002c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0002c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0002c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0031 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0032 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0033 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0003c0004t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0004c0006t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0004c0006t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0005c0007t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0005c0007t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0006c0010t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0007c0014t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0008c0013t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| a0009c0011t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00099 | hp2 | a0003 | c0004 | t0003 | g0165 | EUR | GBR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0128 | EUR | FIN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0025 | EUR | FIN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | FIN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00639 | hp2 | a0003 | c0004 | t0003 | g0160 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00733 | hp1 | a0003 | c0004 | t0003 | g0031 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0139 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG00741 | hp2 | a0003 | c0004 | t0003 | g0163 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01070 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01106 | hp2 | a0003 | c0004 | t0003 | g0059 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01109 | hp1 | a0006 | c0010 | t0006 | g0170 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01167 | hp2 | a0004 | c0006 | t0002 | g0050 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01169 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01169 | hp2 | a0004 | c0006 | t0002 | g0050 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01175 | hp2 | a0003 | c0004 | t0003 | g0167 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0144 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0028 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01257 | hp1 | a0003 | c0004 | t0003 | g0033 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0028 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01258 | hp2 | a0003 | c0004 | t0003 | g0033 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0018 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01346 | hp2 | a0003 | c0004 | t0003 | g0032 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0092 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01496 | hp1 | a0003 | c0004 | t0003 | g0161 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01515 | hp2 | a0003 | c0004 | t0003 | g0031 | EUR | IBS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0132 | EUR | IBS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0075 | EUR | IBS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0074 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01928 | hp2 | a0003 | c0004 | t0003 | g0032 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01934 | hp1 | a0003 | c0004 | t0003 | g0158 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01975 | hp1 | a0007 | c0014 | t0001 | g0090 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01975 | hp2 | a0003 | c0004 | t0003 | g0032 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01993 | hp2 | a0003 | c0004 | t0003 | g0031 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02015 | hp1 | a0001 | c0012 | t0001 | g0077 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02056 | hp2 | a0008 | c0013 | t0001 | g0089 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02074 | hp1 | a0001 | c0008 | t0002 | g0124 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02083 | hp2 | a0001 | c0016 | t0001 | g0108 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0174 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CDX | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0093 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02258 | hp2 | a0001 | c0005 | t0001 | g0086 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0148 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02293 | hp1 | a0003 | c0004 | t0003 | g0033 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02300 | hp1 | a0003 | c0004 | t0003 | g0166 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02300 | hp2 | a0003 | c0004 | t0003 | g0159 | AMR | PEL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0029 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02523 | hp2 | a0001 | c0001 | t0008 | g0098 | EAS | KHV | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02572 | hp1 | a0001 | c0005 | t0002 | g0169 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02602 | hp1 | a0003 | c0004 | t0003 | g0162 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0012 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02622 | hp1 | a0001 | c0005 | t0001 | g0030 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02630 | hp2 | a0001 | c0005 | t0001 | g0147 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02717 | hp1 | a0005 | c0007 | t0001 | g0043 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0018 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0025 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02895 | hp1 | a0005 | c0007 | t0001 | g0043 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02897 | hp1 | a0005 | c0007 | t0001 | g0138 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02922 | hp2 | a0001 | c0002 | t0010 | g0175 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02970 | hp1 | a0001 | c0005 | t0001 | g0156 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0053 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0018 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0030 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0052 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0121 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03239 | hp2 | a0001 | c0009 | t0001 | g0097 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0129 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0150 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0007 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03492 | hp1 | a0004 | c0006 | t0002 | g0133 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | ESN | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0018 | AFR | GWD | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0030 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03654 | hp2 | a0001 | c0009 | t0001 | g0061 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03688 | hp1 | a0002 | c0003 | t0001 | g0028 | SAS | STU | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | STU | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0045 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0151 | SAS | BEB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0045 | SAS | BEB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0113 | SAS | STU | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | STU | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0149 | AFR | YRI | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | YRI | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0145 | EAS | CHB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | YRI | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18957 | hp1 | a0001 | c0015 | t0001 | g0091 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18964 | hp2 | a0001 | c0008 | t0002 | g0127 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18967 | hp1 | a0009 | c0011 | t0002 | g0119 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0052 | AFR | LWK | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0141 | AFR | LWK | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | LWK | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19059 | hp1 | a0001 | c0005 | t0001 | g0106 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0137 | AFR | YRI | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0122 | AFR | ASW | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0146 | AFR | ASW | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | TSI | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0123 | SAS | GIH | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0073 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0029 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0140 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03471 | hp1 | a0001 | c0005 | t0001 | g0029 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG03471 | hp2 | a0001 | c0005 | t0007 | g0168 | AFR | MSL | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | USA | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0120 | AFR | LWK | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| homoSapiens | chm13v2 | a0003 | c0004 | t0003 | g0164 | REF | REF | RNH1_chr11_489515_512242 | RNH1 | chr11 | 489515 | 512242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:495007 | C | T | 1 | a0006 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1174G>A | p.Ala392Thr | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 10/11 | 1564/1952 | 1174/1386 | 392/461 | chr11 | 495007 | |||
| chr11:498023 | G | A | 1 | a0008 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.1075C>T | p.Arg359Trp | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/11 | 1465/1952 | 1075/1386 | 359/461 | chr11 | 498023 | |||
| chr11:498517 | T | C | 1 | a0009 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.896A>G | p.Glu299Gly | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 8/11 | 1286/1952 | 896/1386 | 299/461 | chr11 | 498517 | |||
| chr11:498518 | C | A | 1 | a0009 | 1 | NA18967.hp1 | stop_gained | HIGH | c.895G>T | p.Glu299* | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 8/11 | 1285/1952 | 895/1386 | 299/461 | chr11 | 498518 | |||
| chr11:498785 | T | C | 1 | a0007 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.763A>G | p.Ser255Gly | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 7/11 | 1153/1952 | 763/1386 | 255/461 | chr11 | 498785 | |||
| chr11:498911 | A | G | 1 | a0005 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.637T>C | p.Ser213Pro | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 7/11 | 1027/1952 | 637/1386 | 213/461 | chr11 | 498911 | |||
| chr11:499066 | C | T | 1 | a0004 | 3 | HG01167.hp2 HG01169.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.563G>A | p.Arg188His | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 6/11 | 953/1952 | 563/1386 | 188/461 | chr11 | 499066 | |||
| chr11:499120 | G | A | 1 | a0002 | 21 | HG00639.hp1 HG00735.hp1 HG01070.hp2 others(18): Show |
missense_variant | MODERATE | c.509C>T | p.Pro170Leu | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 6/11 | 899/1952 | 509/1386 | 170/461 | chr11 | 499120 | |||
| chr11:502129 | ACTGGATG others(8): Show |
A | 1 | a0003 | 19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
conservative_inframe_deletion | MODERATE | c.19_33delAGCCTGGACA others(5): Show |
p.Ser7_Gln11del | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/11 | 423/1952 | 19/1386 | 7/461 | chr11 | 502129 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:494942 | G | C | 7 | a0001c0002 a0001c0005 a0003c0004 others(4): Show |
127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
synonymous_variant | LOW | c.1239C>G | p.Ala413Ala | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 10/11 | 1629/1952 | 1239/1386 | 413/461 | chr11 | 494942 | |||
| chr11:495008 | G | A | 1 | a0001c0012 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.1173C>T | p.Ala391Ala | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 10/11 | 1563/1952 | 1173/1386 | 391/461 | chr11 | 495008 | |||
| chr11:498516 | C | T | 1 | a0009c0011 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.897G>A | p.Glu299Glu | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 8/11 | 1287/1952 | 897/1386 | 299/461 | chr11 | 498516 | |||
| chr11:498809 | G | A | 1 | a0001c0015 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.739C>T | p.Leu247Leu | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 7/11 | 1129/1952 | 739/1386 | 247/461 | chr11 | 498809 | |||
| chr11:499059 | C | T | 5 | a0001c0002 a0001c0008 a0004c0006 others(2): Show |
91 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
synonymous_variant | LOW | c.570G>A | p.Leu190Leu | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 6/11 | 960/1952 | 570/1386 | 190/461 | chr11 | 499059 | |||
| chr11:499071 | G | A | 1 | a0001c0016 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.558C>T | p.Gly186Gly | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 6/11 | 948/1952 | 558/1386 | 186/461 | chr11 | 499071 | |||
| chr11:500540 | G | A | 1 | a0001c0009 | 2 | HG03239.hp2 HG03654.hp2 |
synonymous_variant | LOW | c.216C>T | p.Gly72Gly | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/11 | 606/1952 | 216/1386 | 72/461 | chr11 | 500540 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:494567 | A | G | 1 | a0001c0001t0005 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*124T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 11/11 | 124 | chr11 | 494567 | ||||||
| chr11:494637 | C | A | 1 | a0001c0001t0004 | 3 | HG01433.hp1 HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*54G>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 11/11 | 54 | chr11 | 494637 | ||||||
| chr11:494662 | G | A | 1 | a0003c0004t0003 | 19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*29C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 11/11 | 29 | chr11 | 494662 | ||||||
| chr11:494690 | C | T | 1 | a0001c0005t0007 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 11/11 | 1 | chr11 | 494690 | ||||||
| chr11:502204 | A | G | 1 | a0006c0010t0006 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/11 | 42 | chr11 | 502204 | ||||||
| chr11:502217 | C | T | 9 | a0001c0002t0002 a0001c0002t0010 a0001c0005t0002 others(6): Show |
109 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-55G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/11 | 55 | chr11 | 502217 | ||||||
| chr11:502218 | G | A | 1 | a0001c0001t0008 | 1 | HG02523.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-56C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/11 | chr11 | 502218 | |||||||
| chr11:504867 | G | C | 1 | a0001c0001t0009 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-131C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/11 | 2705 | chr11 | 504867 | ||||||
| chr11:504872 | A | C | 1 | a0001c0001t0005 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-136T>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/11 | 2710 | chr11 | 504872 | ||||||
| chr11:507152 | A | C | 1 | a0001c0001t0005 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-300T>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/11 | 4990 | chr11 | 507152 | ||||||
| chr11:507153 | G | C | 1 | a0001c0002t0010 | 1 | HG02922.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-301C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/11 | chr11 | 507153 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:494873 | G | A | 2 | a0003c0004t0003g0031 a0003c0004t0003g0059 |
4 | HG00733.hp1 HG01106.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1298+10C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 10/10 | chr11 | 494873 | |||||||
| chr11:495057 | G | T | 21 | a0001c0005t0001g0029 a0001c0005t0001g0137 a0001c0005t0001g0146 others(18): Show |
29 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.1128-4C>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495057 | |||||||
| chr11:495074 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0114 others(1): Show |
6 | HG01884.hp2 HG02630.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1128-21C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495074 | |||||||
| chr11:495098 | A | G | 2 | a0001c0002t0002g0024 a0001c0002t0002g0122 |
4 | HG00642.hp1 HG00642.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-45T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495098 | |||||||
| chr11:495103 | A | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0023 others(87): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1128-50T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495103 | |||||||
| chr11:495139 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1128-86C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495139 | |||||||
| chr11:495140 | A | G | 4 | a0001c0002t0002g0047 a0001c0002t0002g0118 a0001c0002t0002g0142 others(1): Show |
5 | NA18939.hp1 NA18951.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1128-87T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495140 | |||||||
| chr11:495141 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1128-88G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495141 | |||||||
| chr11:495283 | T | C | 12 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(9): Show |
18 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1128-230A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495283 | |||||||
| chr11:495298 | A | G | 2 | a0003c0004t0003g0031 a0003c0004t0003g0059 |
4 | HG00733.hp1 HG01106.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-245T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495298 | |||||||
| chr11:495335 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1128-282G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495335 | |||||||
| chr11:495365 | G | A | 1 | a0001c0005t0007g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1128-312C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495365 | |||||||
| chr11:495396 | A | C | 1 | a0001c0005t0001g0106 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1128-343T>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495396 | |||||||
| chr11:495441 | G | A | 1 | a0001c0002t0002g0123 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1128-388C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495441 | |||||||
| chr11:495479 | C | A | 1 | a0001c0002t0002g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1128-426G>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495479 | |||||||
| chr11:495501 | G | A | 4 | a0001c0002t0002g0005 a0001c0002t0002g0073 a0001c0002t0002g0116 others(1): Show |
12 | HG01074.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1128-448C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495501 | |||||||
| chr11:495605 | C | A | 1 | a0001c0002t0002g0048 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1128-552G>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495605 | |||||||
| chr11:495699 | A | C | 11 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(8): Show |
17 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.1128-646T>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495699 | |||||||
| chr11:495733 | G | A | 1 | a0006c0010t0006g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1128-680C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495733 | |||||||
| chr11:495804 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1128-751G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495804 | |||||||
| chr11:495825 | C | T | 14 | a0001c0002t0002g0012 a0001c0002t0002g0019 a0001c0002t0002g0024 others(11): Show |
26 | HG00597.hp1 HG00609.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1128-772G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495825 | |||||||
| chr11:495892 | C | G | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1128-839G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 495892 | |||||||
| chr11:496050 | TC | T | 11 | a0003c0004t0003g0032 a0003c0004t0003g0033 a0003c0004t0003g0158 others(8): Show |
15 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1128-998delG | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496050 | |||||||
| chr11:496073 | C | G | 52 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0088 others(49): Show |
99 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1128-1020G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496073 | |||||||
| chr11:496100 | G | GA | 8 | a0001c0002t0002g0012 a0001c0002t0002g0019 a0001c0002t0002g0035 others(5): Show |
16 | HG00597.hp1 HG00609.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1128-1048dupT | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496100 | |||||||
| chr11:496116 | G | A | 50 | a0001c0001t0001g0042 a0001c0001t0001g0130 a0001c0001t0001g0134 others(47): Show |
96 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1128-1063C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496116 | |||||||
| chr11:496193 | T | G | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1128-1140A>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496193 | |||||||
| chr11:496207 | AAG | A | 1 | a0002c0003t0001g0018 | 4 | HG01346.hp1 HG02717.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1128-1156_1128-115 others(6): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496207 | |||||||
| chr11:496326 | T | C | 1 | a0001c0002t0010g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1128-1273A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496326 | |||||||
| chr11:496407 | C | T | 1 | a0002c0003t0001g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1128-1354G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496407 | |||||||
| chr11:496444 | C | T | 1 | a0004c0006t0002g0133 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1128-1391G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496444 | |||||||
| chr11:496465 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1128-1412G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496465 | |||||||
| chr11:496472 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1128-1419T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496472 | |||||||
| chr11:496541 | C | T | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1127+1430G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496541 | |||||||
| chr11:496542 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0076 others(1): Show |
8 | HG02135.hp1 NA18951.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.1127+1429C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496542 | |||||||
| chr11:496626 | A | G | 65 | a0001c0001t0001g0027 a0001c0001t0009g0140 a0001c0002t0001g0075 others(62): Show |
120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1127+1345T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496626 | |||||||
| chr11:496637 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1127+1334G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496637 | |||||||
| chr11:496698 | A | G | 1 | a0002c0003t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1127+1273T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496698 | |||||||
| chr11:496767 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1127+1204G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496767 | |||||||
| chr11:496802 | G | A | 1 | a0001c0001t0008g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1127+1169C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496802 | |||||||
| chr11:496924 | G | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
260 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.1127+1047C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496924 | |||||||
| chr11:496942 | A | G | 8 | a0001c0001t0001g0111 a0001c0005t0001g0029 a0001c0005t0001g0137 others(5): Show |
10 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1127+1029T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496942 | |||||||
| chr11:496990 | A | C | 1 | a0001c0002t0002g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1127+981T>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 496990 | |||||||
| chr11:497039 | C | T | 12 | a0001c0002t0001g0075 a0001c0002t0001g0131 a0001c0002t0001g0132 others(9): Show |
24 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.1127+932G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497039 | |||||||
| chr11:497133 | ACACT | A | 11 | a0003c0004t0003g0032 a0003c0004t0003g0033 a0003c0004t0003g0158 others(8): Show |
15 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1127+834_1127+837d others(6): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497133 | |||||||
| chr11:497151 | A | G | 22 | a0001c0002t0002g0123 a0001c0005t0001g0029 a0001c0005t0001g0137 others(19): Show |
30 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1127+820T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497151 | |||||||
| chr11:497177 | ACACGGAC others(27): Show |
A | 1 | a0006c0010t0006g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1127+760_1127+793d others(36): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497177 | |||||||
| chr11:497201 | ACCCATGT others(15): Show |
A | 2 | a0001c0005t0002g0169 a0001c0005t0007g0168 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1127+748_1127+769d others(24): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497201 | |||||||
| chr11:497211 | T | TCACA | 67 | a0001c0002t0001g0075 a0001c0002t0001g0131 a0001c0002t0001g0132 others(64): Show |
120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1127+759_1127+760i others(6): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497211 | |||||||
| chr11:497215 | G | A | 1 | a0001c0002t0002g0015 | 4 | HG00544.hp1 NA19009.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+756C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497215 | |||||||
| chr11:497217 | A | ACTCTCGC others(31): Show |
1 | a0001c0002t0002g0121 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1127+753_1127+754i others(40): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497217 | |||||||
| chr11:497249 | A | G | 8 | a0001c0005t0001g0029 a0001c0005t0001g0137 a0001c0005t0001g0146 others(5): Show |
10 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1127+722T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497249 | |||||||
| chr11:497255 | A | C | 8 | a0001c0005t0001g0029 a0001c0005t0001g0137 a0001c0005t0001g0146 others(5): Show |
10 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1127+716T>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497255 | |||||||
| chr11:497266 | T | TGTGCTCA others(65): Show |
13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1127+633_1127+704d others(74): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497266 | |||||||
| chr11:497266 | T | TGTGCTCA others(27): Show |
8 | a0001c0005t0001g0029 a0001c0005t0001g0137 a0001c0005t0001g0146 others(5): Show |
10 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1127+704_1127+705i others(36): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497266 | |||||||
| chr11:497351 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1127+620C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497351 | |||||||
| chr11:497359 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0023 others(104): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1127+612T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497359 | |||||||
| chr11:497387 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0065 others(2): Show |
10 | HG00741.hp1 HG01358.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1127+584C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497387 | |||||||
| chr11:497397 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0095 |
3 | HG00741.hp1 HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1127+574C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497397 | |||||||
| chr11:497433 | T | TCTCTCGC others(27): Show |
2 | a0001c0002t0002g0118 a0001c0002t0002g0142 |
2 | NA19072.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1127+504_1127+537d others(36): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497433 | |||||||
| chr11:497464 | C | CCCTCTCG others(17): Show |
1 | a0009c0011t0002g0119 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1127+506_1127+507i others(26): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497464 | |||||||
| chr11:497466 | C | G | 1 | a0009c0011t0002g0119 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1127+505G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497466 | |||||||
| chr11:497467 | CCT | C | 2 | a0001c0001t0001g0027 a0001c0001t0009g0140 |
4 | HG02486.hp2 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1127+502_1127+503d others(4): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497467 | |||||||
| chr11:497469 | T | C | 1 | a0009c0011t0002g0119 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1127+502A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497469 | |||||||
| chr11:497474 | C | G | 1 | a0001c0002t0002g0126 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1127+497G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497474 | |||||||
| chr11:497569 | A | ACC | 2 | a0001c0002t0002g0024 a0001c0002t0002g0122 |
4 | HG00642.hp1 HG00642.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+401_1127+402i others(4): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497569 | |||||||
| chr11:497571 | A | ACT | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(145): Show |
311 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.1127+399_1127+400i others(4): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497571 | |||||||
| chr11:497571 | A | T | 2 | a0001c0002t0002g0024 a0001c0002t0002g0122 |
4 | HG00642.hp1 HG00642.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+400T>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497571 | |||||||
| chr11:497580 | T | A | 1 | a0009c0011t0002g0119 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1127+391A>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497580 | |||||||
| chr11:497588 | C | G | 4 | a0001c0002t0002g0005 a0001c0002t0002g0073 a0001c0002t0002g0116 others(1): Show |
12 | HG01074.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1127+383G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497588 | |||||||
| chr11:497603 | T | G | 2 | a0003c0004t0003g0031 a0003c0004t0003g0059 |
4 | HG00733.hp1 HG01106.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+368A>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497603 | |||||||
| chr11:497641 | ACT | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0114 others(1): Show |
6 | HG01884.hp2 HG02630.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1127+328_1127+329d others(4): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497641 | |||||||
| chr11:497647 | G | GCTCA | 21 | a0001c0005t0001g0029 a0001c0005t0001g0137 a0001c0005t0001g0146 others(18): Show |
29 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.1127+323_1127+324i others(6): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497647 | |||||||
| chr11:497672 | CGTGCTCA others(19): Show |
C | 2 | a0002c0003t0001g0007 a0002c0003t0001g0092 |
7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127+273_1127+298d others(28): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497672 | |||||||
| chr11:497731 | ACACGGAC others(13): Show |
A | 1 | a0001c0002t0002g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1127+220_1127+239d others(22): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497731 | |||||||
| chr11:497745 | GCTCA | G | 13 | a0001c0001t0001g0027 a0001c0001t0009g0140 a0003c0004t0003g0032 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1127+222_1127+225d others(6): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497745 | |||||||
| chr11:497764 | C | T | 2 | a0001c0001t0001g0037 a0001c0005t0001g0086 |
3 | HG01943.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1127+207G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497764 | |||||||
| chr11:497777 | ACT | A | 14 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0067 others(11): Show |
21 | HG02109.hp2 HG02135.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1127+192_1127+193d others(4): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497777 | |||||||
| chr11:497784 | C | T | 16 | a0001c0001t0001g0130 a0001c0002t0001g0075 a0001c0002t0001g0132 others(13): Show |
35 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1127+187G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497784 | |||||||
| chr11:497785 | A | G | 70 | a0001c0001t0001g0130 a0001c0002t0001g0075 a0001c0002t0001g0131 others(67): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1127+186T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497785 | |||||||
| chr11:497793 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG01175.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1127+178C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497793 | |||||||
| chr11:497812 | CAT | C | 3 | a0001c0001t0001g0109 a0001c0005t0001g0148 a0006c0010t0006g0170 |
3 | HG01109.hp1 HG02280.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1127+157_1127+158d others(4): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497812 | |||||||
| chr11:497880 | TCACA | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0001g0084 |
5 | HG00733.hp2 HG01099.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1127+87_1127+90del others(4): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497880 | |||||||
| chr11:497899 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1127+72G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 9/10 | chr11 | 497899 | |||||||
| chr11:498250 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.957-109T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 8/10 | chr11 | 498250 | |||||||
| chr11:498383 | C | T | 45 | a0001c0002t0001g0075 a0001c0002t0001g0131 a0001c0002t0001g0132 others(42): Show |
90 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.956+74G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 8/10 | chr11 | 498383 | |||||||
| chr11:498402 | G | T | 8 | a0001c0005t0001g0029 a0001c0005t0001g0137 a0001c0005t0001g0146 others(5): Show |
10 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.956+55C>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 8/10 | chr11 | 498402 | |||||||
| chr11:498442 | G | A | 21 | a0001c0005t0001g0029 a0001c0005t0001g0137 a0001c0005t0001g0146 others(18): Show |
29 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.956+15C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 8/10 | chr11 | 498442 | |||||||
| chr11:498654 | T | C | 1 | a0009c0011t0002g0119 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.786-27A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 7/10 | chr11 | 498654 | |||||||
| chr11:498975 | CT | C | 10 | a0001c0001t0004g0036 a0001c0001t0004g0069 a0001c0005t0001g0029 others(7): Show |
13 | HG01433.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.614+39delA | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 6/10 | chr11 | 498975 | |||||||
| chr11:498976 | T | C | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.614+39A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 6/10 | chr11 | 498976 | |||||||
| chr11:498996 | C | A | 3 | a0001c0002t0002g0118 a0001c0002t0002g0142 a0009c0011t0002g0119 |
3 | NA18967.hp1 NA19072.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.614+19G>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 6/10 | chr11 | 498996 | |||||||
| chr11:499195 | A | G | 8 | a0001c0005t0001g0029 a0001c0005t0001g0137 a0001c0005t0001g0146 others(5): Show |
10 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.444-10T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499195 | |||||||
| chr11:499201 | G | A | 8 | a0001c0005t0001g0029 a0001c0005t0001g0137 a0001c0005t0001g0146 others(5): Show |
10 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.444-16C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499201 | |||||||
| chr11:499288 | T | TCTC | 21 | a0001c0005t0001g0029 a0001c0005t0001g0137 a0001c0005t0001g0146 others(18): Show |
29 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.444-104_444-103ins others(3): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499288 | |||||||
| chr11:499296 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.444-111C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499296 | |||||||
| chr11:499390 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.444-205G>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499390 | |||||||
| chr11:499412 | G | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0001g0084 |
5 | HG00733.hp2 HG01099.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.444-227C>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499412 | |||||||
| chr11:499498 | C | T | 1 | a0006c0010t0006g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.444-313G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499498 | |||||||
| chr11:499544 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.443+285C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499544 | |||||||
| chr11:499547 | A | C | 50 | a0001c0001t0001g0105 a0001c0002t0001g0075 a0001c0002t0001g0131 others(47): Show |
98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.443+282T>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499547 | |||||||
| chr11:499583 | G | A | 48 | a0001c0002t0001g0075 a0001c0002t0001g0131 a0001c0002t0001g0132 others(45): Show |
96 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.443+246C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499583 | |||||||
| chr11:499638 | C | CCCCAGCA others(116): Show |
1 | a0001c0002t0002g0116 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.443+190_443+191ins others(123): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499638 | |||||||
| chr11:499638 | CCCCAGCA others(34): Show |
C | 8 | a0001c0005t0001g0029 a0001c0005t0001g0137 a0001c0005t0001g0146 others(5): Show |
10 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.443+150_443+190del others(41): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499638 | |||||||
| chr11:499653 | G | C | 1 | a0001c0001t0001g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.443+176C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499653 | |||||||
| chr11:499655 | GAGGAGAG others(34): Show |
G | 2 | a0001c0001t0001g0115 a0001c0005t0001g0030 |
4 | HG02622.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+133_443+173del others(41): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499655 | |||||||
| chr11:499694 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.443+135C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499694 | |||||||
| chr11:499782 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.443+47C>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 5/10 | chr11 | 499782 | |||||||
| chr11:500056 | G | A | 50 | a0001c0001t0001g0023 a0001c0001t0001g0072 a0001c0001t0001g0104 others(47): Show |
97 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.273-57C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500056 | |||||||
| chr11:500060 | GCCAGAGC | G | 2 | a0001c0001t0001g0027 a0001c0001t0009g0140 |
4 | HG02486.hp2 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-68_273-62delGC others(5): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500060 | |||||||
| chr11:500096 | G | A | 7 | a0003c0004t0003g0032 a0003c0004t0003g0033 a0003c0004t0003g0158 others(4): Show |
11 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.273-97C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500096 | |||||||
| chr11:500114 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.273-115G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500114 | |||||||
| chr11:500182 | G | A | 1 | a0001c0002t0002g0126 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.273-183C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500182 | |||||||
| chr11:500182 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.273-183C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500182 | |||||||
| chr11:500225 | T | TC | 8 | a0003c0004t0003g0032 a0003c0004t0003g0033 a0003c0004t0003g0158 others(5): Show |
12 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.273-227dupG | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500225 | |||||||
| chr11:500248 | G | A | 45 | a0001c0002t0001g0075 a0001c0002t0001g0131 a0001c0002t0001g0132 others(42): Show |
84 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.272+236C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500248 | |||||||
| chr11:500278 | C | T | 52 | a0001c0001t0001g0063 a0001c0001t0001g0068 a0001c0001t0001g0080 others(49): Show |
97 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.272+206G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500278 | |||||||
| chr11:500282 | G | A | 11 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(8): Show |
17 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.272+202C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500282 | |||||||
| chr11:500317 | G | A | 2 | a0001c0002t0002g0048 a0001c0002t0002g0049 |
4 | HG02647.hp1 HG03130.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.272+167C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500317 | |||||||
| chr11:500328 | G | A | 2 | a0001c0009t0001g0061 a0001c0009t0001g0097 |
2 | HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.272+156C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500328 | |||||||
| chr11:500362 | T | C | 2 | a0001c0005t0002g0169 a0001c0005t0007g0168 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.272+122A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500362 | |||||||
| chr11:500410 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.272+74G>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500410 | |||||||
| chr11:500411 | G | T | 1 | a0001c0002t0002g0048 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.272+73C>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500411 | |||||||
| chr11:500424 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.272+60C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 4/10 | chr11 | 500424 | |||||||
| chr11:500725 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.102-71C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 500725 | |||||||
| chr11:500774 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0079 |
7 | HG00408.hp1 HG00673.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-120G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 500774 | |||||||
| chr11:500817 | A | T | 2 | a0001c0005t0002g0169 a0001c0005t0007g0168 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.102-163T>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 500817 | |||||||
| chr11:500820 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.102-166T>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 500820 | |||||||
| chr11:500839 | T | C | 1 | a0003c0004t0003g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.102-185A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 500839 | |||||||
| chr11:500845 | G | A | 1 | a0001c0005t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.102-191C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 500845 | |||||||
| chr11:500867 | G | A | 2 | a0003c0004t0003g0031 a0003c0004t0003g0059 |
4 | HG00733.hp1 HG01106.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-213C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 500867 | |||||||
| chr11:500900 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.102-246T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 500900 | |||||||
| chr11:500958 | G | A | 3 | a0001c0002t0002g0058 a0001c0005t0001g0030 a0001c0005t0001g0156 |
5 | HG00597.hp1 HG02622.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-304C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 500958 | |||||||
| chr11:501106 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.102-452T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 501106 | |||||||
| chr11:501152 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.102-498C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 501152 | |||||||
| chr11:501429 | G | A | 11 | a0003c0004t0003g0032 a0003c0004t0003g0033 a0003c0004t0003g0158 others(8): Show |
15 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.101+633C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 501429 | |||||||
| chr11:501468 | G | A | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.101+594C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 501468 | |||||||
| chr11:501647 | T | C | 1 | a0001c0005t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.101+415A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 501647 | |||||||
| chr11:501658 | G | C | 1 | a0001c0001t0004g0069 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.101+404C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 501658 | |||||||
| chr11:501795 | C | G | 1 | a0001c0005t0001g0030 | 3 | HG02622.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.101+267G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 501795 | |||||||
| chr11:501797 | C | T | 1 | a0001c0009t0001g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.101+265G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 501797 | |||||||
| chr11:501841 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0023 others(10): Show |
43 | HG00544.hp2 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.101+221C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 501841 | |||||||
| chr11:502013 | G | A | 62 | a0001c0001t0001g0006 a0001c0002t0001g0075 a0001c0002t0001g0131 others(59): Show |
118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.101+49C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 3/10 | chr11 | 502013 | |||||||
| chr11:502271 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-87-22G>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 502271 | |||||||
| chr11:502371 | G | A | 14 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(11): Show |
20 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-87-122C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 502371 | |||||||
| chr11:502604 | A | C | 1 | a0001c0012t0001g0077 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-87-355T>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 502604 | |||||||
| chr11:502640 | A | G | 1 | a0006c0010t0006g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-87-391T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 502640 | |||||||
| chr11:502657 | C | T | 1 | a0003c0004t0003g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-87-408G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 502657 | |||||||
| chr11:502704 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-87-455C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 502704 | |||||||
| chr11:502722 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
41 | HG00544.hp2 HG01123.hp1 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.-87-473G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 502722 | |||||||
| chr11:502738 | A | T | 2 | a0001c0001t0001g0027 a0001c0001t0009g0140 |
4 | HG02486.hp2 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-87-489T>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 502738 | |||||||
| chr11:502753 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0100 |
3 | HG02027.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-87-504C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 502753 | |||||||
| chr11:502754 | GC | G | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-87-506delG | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 502754 | |||||||
| chr11:502835 | G | A | 1 | a0001c0005t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-87-586C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 502835 | |||||||
| chr11:503089 | A | G | 3 | a0001c0005t0001g0147 a0001c0005t0002g0169 a0001c0005t0007g0168 |
3 | HG02572.hp1 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-87-840T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 503089 | |||||||
| chr11:503251 | C | T | 1 | a0006c0010t0006g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-87-1002G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 503251 | |||||||
| chr11:503353 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0114 others(1): Show |
6 | HG01884.hp2 HG02630.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-87-1104C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 503353 | |||||||
| chr11:503385 | C | G | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-87-1136G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 503385 | |||||||
| chr11:503467 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-87-1218C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 503467 | |||||||
| chr11:503540 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-88+1284C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 503540 | |||||||
| chr11:503621 | G | A | 1 | a0006c0010t0006g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-88+1203C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 503621 | |||||||
| chr11:503710 | C | T | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-88+1114G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 503710 | |||||||
| chr11:503783 | C | T | 1 | a0001c0005t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-88+1041G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 503783 | |||||||
| chr11:503993 | G | A | 13 | a0001c0001t0001g0130 a0001c0002t0001g0075 a0001c0002t0001g0131 others(10): Show |
32 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.-88+831C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 503993 | |||||||
| chr11:504172 | A | G | 1 | a0006c0010t0006g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-88+652T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504172 | |||||||
| chr11:504239 | T | C | 2 | a0001c0005t0001g0030 a0001c0005t0001g0156 |
4 | HG02622.hp1 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88+585A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504239 | |||||||
| chr11:504333 | A | T | 6 | a0001c0002t0002g0005 a0001c0002t0002g0011 a0001c0002t0002g0073 others(3): Show |
18 | HG01074.hp2 HG02109.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.-88+491T>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504333 | |||||||
| chr11:504384 | C | A | 1 | a0006c0010t0006g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-88+440G>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504384 | |||||||
| chr11:504407 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-88+417C>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504407 | |||||||
| chr11:504411 | C | G | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-88+413G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504411 | |||||||
| chr11:504437 | C | T | 3 | a0001c0002t0002g0118 a0001c0002t0002g0142 a0009c0011t0002g0119 |
3 | NA18967.hp1 NA19072.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-88+387G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504437 | |||||||
| chr11:504507 | C | A | 46 | a0001c0001t0001g0130 a0001c0002t0001g0075 a0001c0002t0001g0131 others(43): Show |
91 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-88+317G>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504507 | |||||||
| chr11:504578 | G | GC | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-88+245dupG | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504578 | |||||||
| chr11:504584 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-88+240C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504584 | |||||||
| chr11:504636 | G | A | 45 | a0001c0001t0001g0130 a0001c0002t0001g0075 a0001c0002t0001g0131 others(42): Show |
89 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.-88+188C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504636 | |||||||
| chr11:504783 | C | G | 1 | a0001c0002t0002g0117 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-88+41G>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504783 | |||||||
| chr11:504794 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-88+30C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 2/10 | chr11 | 504794 | |||||||
| chr11:505006 | G | C | 46 | a0001c0001t0001g0130 a0001c0002t0001g0075 a0001c0002t0001g0131 others(43): Show |
91 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-260-10C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505006 | |||||||
| chr11:505025 | T | A | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-260-29A>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505025 | |||||||
| chr11:505113 | T | C | 42 | a0001c0001t0001g0130 a0001c0002t0001g0075 a0001c0002t0001g0131 others(39): Show |
79 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-260-117A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505113 | |||||||
| chr11:505131 | C | A | 4 | a0003c0004t0003g0033 a0003c0004t0003g0165 a0003c0004t0003g0166 others(1): Show |
6 | HG00099.hp2 HG01175.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-135G>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505131 | |||||||
| chr11:505337 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0103 |
2 | HG00735.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-260-341C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505337 | |||||||
| chr11:505583 | A | G | 1 | a0006c0010t0006g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-260-587T>C | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505583 | |||||||
| chr11:505619 | T | C | 2 | a0004c0006t0002g0050 a0004c0006t0002g0133 |
3 | HG01167.hp2 HG01169.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-260-623A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505619 | |||||||
| chr11:505780 | T | C | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-260-784A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505780 | |||||||
| chr11:505808 | G | A | 2 | a0003c0004t0003g0031 a0003c0004t0003g0059 |
4 | HG00733.hp1 HG01106.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-812C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505808 | |||||||
| chr11:505851 | G | GCAC | 107 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0023 others(104): Show |
210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.-260-856_-260-855i others(5): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505851 | |||||||
| chr11:505874 | C | CT | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0062 others(19): Show |
30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.-260-879dupA | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505874 | |||||||
| chr11:505874 | CT | C | 28 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0027 others(25): Show |
52 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.-260-879delA | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505874 | |||||||
| chr11:505874 | CTT | C | 19 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0005t0001g0029 others(16): Show |
27 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.-260-880_-260-879d others(4): Show |
RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505874 | |||||||
| chr11:505911 | G | C | 1 | a0001c0002t0002g0151 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-260-915C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505911 | |||||||
| chr11:505975 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-260-979C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 505975 | |||||||
| chr11:506184 | C | T | 4 | a0001c0002t0002g0019 a0001c0002t0002g0035 a0001c0002t0002g0058 others(1): Show |
7 | HG00597.hp1 NA18939.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.-261+929G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506184 | |||||||
| chr11:506191 | T | C | 3 | a0001c0005t0002g0169 a0001c0005t0007g0168 a0006c0010t0006g0170 |
3 | HG01109.hp1 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-261+922A>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506191 | |||||||
| chr11:506229 | C | T | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-261+884G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506229 | |||||||
| chr11:506268 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-261+845C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506268 | |||||||
| chr11:506279 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-261+834C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506279 | |||||||
| chr11:506295 | G | A | 2 | a0001c0005t0001g0030 a0001c0005t0001g0156 |
4 | HG02622.hp1 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+818C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506295 | |||||||
| chr11:506442 | G | T | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-261+671C>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506442 | |||||||
| chr11:506596 | C | T | 13 | a0003c0004t0003g0031 a0003c0004t0003g0032 a0003c0004t0003g0033 others(10): Show |
19 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-261+517G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506596 | |||||||
| chr11:506747 | C | T | 2 | a0003c0004t0003g0031 a0003c0004t0003g0059 |
4 | HG00733.hp1 HG01106.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+366G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506747 | |||||||
| chr11:506780 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0157 |
3 | HG02630.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-261+333C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506780 | |||||||
| chr11:506826 | G | C | 15 | a0001c0005t0002g0169 a0001c0005t0007g0168 a0003c0004t0003g0031 others(12): Show |
21 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-261+287C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506826 | |||||||
| chr11:506859 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-261+254C>G | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506859 | |||||||
| chr11:506880 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-261+233C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506880 | |||||||
| chr11:506969 | C | T | 1 | a0001c0002t0002g0058 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-261+144G>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506969 | |||||||
| chr11:506990 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-261+123C>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 506990 | |||||||
| chr11:507020 | C | A | 1 | a0001c0005t0001g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-261+93G>T | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 507020 | |||||||
| chr11:507064 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0057 |
3 | HG00597.hp2 HG02135.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-261+49C>A | RNH1 | ENSG00000023191.17 | transcript | ENST00000354420.7 | protein_coding | 1/10 | chr11 | 507064 |