Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 222546 |
| ensemblid | ENSG00000185002.10 |
| hgncid | 21478 |
| symbol | RFX6 |
| name | regulatory factor X6 |
| refseq_nuc | NM_173560.4 |
| refseq_prot | NP_775831.2 |
| ensembl_nuc | ENST00000332958.3 |
| ensembl_prot | ENSP00000332208.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 116877242 |
| end | 116932161 |
| strand | + |
| ver | v1.2 |
| region | chr6:116877242-116932161 |
| region5000 | chr6:116872242-116937161 |
| regionname0 | RFX6_chr6_116877242_116932161 |
| regionname5000 | RFX6_chr6_116872242_116937161 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 928 | 346 | 78 | 53 | 157 | 16 | 40 | 128 | RFX6_chr6_116872242_116937161 | RFX6 | MAKVP others(923): Show |
chr6 | 116872242 | 116937161 |
| a0002 | 0/0 | 928 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | MAKVP others(923): Show |
chr6 | 116872242 | 116937161 |
| a0003 | 0/0 | 928 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | MAKVP others(923): Show |
chr6 | 116872242 | 116937161 |
| a0004 | 0/0 | 928 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | MAKVP others(923): Show |
chr6 | 116872242 | 116937161 |
| a0005 | 0/0 | 928 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | MAKVP others(923): Show |
chr6 | 116872242 | 116937161 |
| a0006 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | MAKVP others(923): Show |
chr6 | 116872242 | 116937161 |
| a0007 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | MAKVP others(923): Show |
chr6 | 116872242 | 116937161 |
| a0008 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | MAKVP others(923): Show |
chr6 | 116872242 | 116937161 |
| a0009 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | MAKVP others(923): Show |
chr6 | 116872242 | 116937161 |
| a0010 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | MAKVP others(923): Show |
chr6 | 116872242 | 116937161 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2784 | 237 | 63 | 43 | 96 | 12 | 21 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0001c0002 | 0/0 | 2784 | 103 | 10 | 10 | 60 | 4 | 19 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0001c0006 | 0/0 | 2784 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0001c0009 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0001c0010 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0001c0012 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0001c0016 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0002c0003 | 0/0 | 2784 | 10 | 9 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0002c0007 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0003c0004 | 0/0 | 2784 | 5 | 4 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0004c0005 | 0/0 | 2784 | 4 | 0 | 4 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0005c0008 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0006c0011 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0007c0015 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0008c0017 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0009c0014 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 | ||
| a0010c0013 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | ATGGC others(2779): Show |
chr6 | 116872242 | 116937161 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3476 | 235 | 62 | 42 | 96 | 12 | 21 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0001c0001t0007 | 0/0 | 3476 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0001c0001t0008 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0001c0002t0002 | 0/0 | 3476 | 100 | 9 | 8 | 60 | 4 | 19 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0001c0002t0003 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0001c0002t0004 | 0/0 | 3476 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0001c0002t0005 | 0/0 | 3476 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0001c0006t0001 | 0/0 | 3476 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0001c0009t0001 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0001c0010t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0001c0012t0002 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0001c0016t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0002c0003t0002 | 0/0 | 3476 | 9 | 8 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0002c0003t0006 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0002c0007t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0003c0004t0002 | 0/0 | 3476 | 5 | 4 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0004c0005t0002 | 0/0 | 3476 | 4 | 0 | 4 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0005c0008t0002 | 0/0 | 3476 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0006c0011t0002 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0007c0015t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0008c0017t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0009c0014t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| a0010c0013t0001 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | GCGGC others(3471): Show |
chr6 | 116872242 | 116937161 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 1 | 3 | 8 | 1 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0003 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0001t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0009 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0002t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0006t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0006t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0009t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0010t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0012t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0001c0016t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0002c0003t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0002c0003t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0002c0003t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0002c0003t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0002c0003t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0002c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0002c0003t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0002c0007t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0003c0004t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0003c0004t0002g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0003c0004t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0004c0005t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0004c0005t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0004c0005t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0005c0008t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0006c0011t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0007c0015t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0008c0017t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0009c0014t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| a0010c0013t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0245 | EUR | GBR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | FIN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0016 | EUR | FIN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00642 | hp1 | a0005 | c0008 | t0002 | g0009 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | CHS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0178 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0048 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG00741 | hp2 | a0002 | c0003 | t0002 | g0075 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01074 | hp1 | a0003 | c0004 | t0002 | g0025 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0050 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0277 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01258 | hp1 | a0004 | c0005 | t0002 | g0054 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0242 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01496 | hp2 | a0001 | c0002 | t0005 | g0048 | AMR | CLM | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0039 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0208 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0276 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG01993 | hp2 | a0004 | c0005 | t0002 | g0021 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0055 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02080 | hp2 | a0006 | c0011 | t0002 | g0212 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02145 | hp2 | a0003 | c0004 | t0002 | g0024 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0183 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02148 | hp2 | a0004 | c0005 | t0002 | g0052 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | CDX | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02273 | hp1 | a0004 | c0005 | t0002 | g0021 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02280 | hp2 | a0003 | c0004 | t0002 | g0049 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0016 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0211 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0090 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0220 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0182 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02615 | hp1 | a0002 | c0007 | t0001 | g0077 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02647 | hp2 | a0001 | c0012 | t0002 | g0184 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0179 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02717 | hp1 | a0002 | c0003 | t0002 | g0011 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02818 | hp1 | a0007 | c0015 | t0001 | g0083 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0089 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02886 | hp2 | a0002 | c0003 | t0002 | g0078 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02895 | hp1 | a0002 | c0003 | t0002 | g0026 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02896 | hp1 | a0002 | c0003 | t0002 | g0073 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02897 | hp1 | a0002 | c0003 | t0002 | g0011 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02897 | hp2 | a0002 | c0003 | t0002 | g0026 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0091 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0068 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0051 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0219 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03098 | hp1 | a0002 | c0003 | t0006 | g0079 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0253 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03139 | hp2 | a0001 | c0010 | t0001 | g0246 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03195 | hp2 | a0002 | c0003 | t0002 | g0074 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0232 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0053 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03486 | hp1 | a0003 | c0004 | t0002 | g0025 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0225 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03540 | hp1 | a0001 | c0006 | t0001 | g0084 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0168 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0181 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0167 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0234 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0235 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0169 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0240 | SAS | BEB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0251 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0177 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0243 | SAS | STU | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18906 | hp1 | a0008 | c0017 | t0001 | g0170 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0172 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18990 | hp2 | a0001 | c0009 | t0001 | g0046 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19030 | hp1 | a0001 | c0006 | t0001 | g0076 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19030 | hp2 | a0009 | c0014 | t0001 | g0116 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19043 | hp2 | a0001 | c0016 | t0001 | g0010 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19059 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA19240 | hp2 | a0003 | c0004 | t0002 | g0024 | AFR | YRI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0061 | AFR | ASW | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | TSI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | TSI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | GIH | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | USA | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | USA | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | USA | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA20300 | hp2 | a0002 | c0003 | t0002 | g0011 | AFR | USA | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| NA21309 | hp2 | a0010 | c0013 | t0001 | g0065 | AFR | LWK | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0265 | REF | REF | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0095 | REF | REF | RFX6_chr6_116872242_116937161 | RFX6 | chr6 | 116872242 | 116937161 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116877325 | C | A | 2 | a0002 a0003 |
16 | HG00741.hp2 HG01074.hp1 HG02145.hp2 others(13): Show |
missense_variant | MODERATE | c.50C>A | p.Ala17Glu | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 1/19 | 84/3476 | 50/2787 | 17/928 | chr6 | 116877325 | |||
| chr6:116877337 | C | A | 1 | a0005 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.62C>A | p.Ser21Tyr | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 1/19 | 96/3476 | 62/2787 | 21/928 | chr6 | 116877337 | |||
| chr6:116918049 | G | A | 1 | a0004 | 4 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(1): Show |
missense_variant | MODERATE | c.985G>A | p.Val329Ile | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/19 | 1019/3476 | 985/2787 | 329/928 | chr6 | 116918049 | |||
| chr6:116920454 | C | T | 1 | a0002 | 11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
missense_variant&splice_region_variant | MODERATE | c.1327C>T | p.His443Tyr | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/19 | 1361/3476 | 1327/2787 | 443/928 | chr6 | 116920454 | |||
| chr6:116925643 | C | A | 1 | a0010 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1869C>A | p.Asp623Glu | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/19 | 1903/3476 | 1869/2787 | 623/928 | chr6 | 116925643 | |||
| chr6:116927317 | C | G | 1 | a0008 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.2176C>G | p.Arg726Gly | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/19 | 2210/3476 | 2176/2787 | 726/928 | chr6 | 116927317 | |||
| chr6:116927402 | C | T | 1 | a0006 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.2261C>T | p.Pro754Leu | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/19 | 2295/3476 | 2261/2787 | 754/928 | chr6 | 116927402 | |||
| chr6:116928759 | G | C | 1 | a0009 | 1 | NA19030.hp2 | missense_variant&splice_region_variant | MODERATE | c.2399G>C | p.Gly800Ala | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/19 | 2433/3476 | 2399/2787 | 800/928 | chr6 | 116928759 | |||
| chr6:116928913 | G | T | 1 | a0007 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.2553G>T | p.Gln851His | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/19 | 2587/3476 | 2553/2787 | 851/928 | chr6 | 116928913 | |||
| chr6:116932161 | A | G | 1 | a0001 | 1 | HG02300.hp1 | splice_region_variant | LOW | c.*655A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | chr6 | 116932161 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116894005 | T | C | 1 | a0001c0009 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.585T>C | p.Ile195Ile | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/19 | 619/3476 | 585/2787 | 195/928 | chr6 | 116894005 | |||
| chr6:116922097 | T | C | 7 | a0001c0002 a0001c0010 a0002c0003 others(4): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
synonymous_variant | LOW | c.1383T>C | p.Thr461Thr | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/19 | 1417/3476 | 1383/2787 | 461/928 | chr6 | 116922097 | |||
| chr6:116923211 | T | C | 8 | a0001c0002 a0001c0010 a0001c0012 others(5): Show |
126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
synonymous_variant | LOW | c.1542T>C | p.Asn514Asn | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/19 | 1576/3476 | 1542/2787 | 514/928 | chr6 | 116923211 | |||
| chr6:116925556 | C | T | 7 | a0001c0002 a0001c0012 a0002c0003 others(4): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
synonymous_variant | LOW | c.1782C>T | p.His594His | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/19 | 1816/3476 | 1782/2787 | 594/928 | chr6 | 116925556 | |||
| chr6:116927055 | T | C | 7 | a0001c0002 a0001c0012 a0002c0003 others(4): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
synonymous_variant | LOW | c.1914T>C | p.Gly638Gly | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/19 | 1948/3476 | 1914/2787 | 638/928 | chr6 | 116927055 | |||
| chr6:116927307 | C | T | 1 | a0001c0006 | 2 | HG03540.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.2166C>T | p.Thr722Thr | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/19 | 2200/3476 | 2166/2787 | 722/928 | chr6 | 116927307 | |||
| chr6:116927469 | C | T | 1 | a0001c0016 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.2328C>T | p.Ser776Ser | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/19 | 2362/3476 | 2328/2787 | 776/928 | chr6 | 116927469 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116931509 | C | A | 11 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(8): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*3C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 3 | chr6 | 116931509 | ||||||
| chr6:116931596 | T | G | 10 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(7): Show |
124 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*90T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 90 | chr6 | 116931596 | ||||||
| chr6:116931597 | A | G | 1 | a0002c0003t0006 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 91 | chr6 | 116931597 | ||||||
| chr6:116931964 | C | T | 1 | a0001c0002t0005 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*458C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 458 | chr6 | 116931964 | ||||||
| chr6:116932052 | T | A | 1 | a0002c0003t0006 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 546 | chr6 | 116932052 | ||||||
| chr6:116932067 | C | T | 1 | a0001c0001t0008 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*561C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 561 | chr6 | 116932067 | ||||||
| chr6:116932096 | T | C | 1 | a0001c0001t0007 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 590 | chr6 | 116932096 | ||||||
| chr6:116932128 | G | C | 1 | a0001c0002t0003 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*622G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 19/19 | 622 | chr6 | 116932128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:116877504 | T | G | 1 | a0003c0004t0002g0049 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.223+6T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 1/18 | chr6 | 116877504 | |||||||
| chr6:116877535 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.223+37C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 1/18 | chr6 | 116877535 | |||||||
| chr6:116877734 | A | C | 1 | a0001c0001t0001g0278 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.224-62A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 1/18 | chr6 | 116877734 | |||||||
| chr6:116877991 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.380+39A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116877991 | |||||||
| chr6:116878144 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.380+192G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878144 | |||||||
| chr6:116878228 | C | T | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(36): Show |
57 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.380+276C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878228 | |||||||
| chr6:116878488 | C | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.380+536C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878488 | |||||||
| chr6:116878627 | C | G | 104 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(101): Show |
122 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.380+675C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878627 | |||||||
| chr6:116878660 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.380+708G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878660 | |||||||
| chr6:116878660 | G | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.380+708G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878660 | |||||||
| chr6:116878676 | G | A | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.380+724G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116878676 | |||||||
| chr6:116878828 | TTATTATT others(8): Show |
T | 1 | a0001c0001t0001g0252 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.380+882_380+896del others(15): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 116878828 | ||||||
| chr6:116878870 | G | GT | 182 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.380+924dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 116878870 | ||||||
| chr6:116878900 | CA | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(227): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.380+952delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 116878900 | ||||||
| chr6:116879271 | C | A | 104 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(101): Show |
122 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.381-1273C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116879271 | |||||||
| chr6:116879535 | G | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0057 others(14): Show |
19 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.381-1009G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116879535 | |||||||
| chr6:116879607 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(71): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.381-937C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116879607 | |||||||
| chr6:116879699 | T | G | 2 | a0001c0002t0002g0090 a0001c0002t0002g0091 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.381-845T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116879699 | |||||||
| chr6:116880175 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.381-369A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116880175 | |||||||
| chr6:116880415 | C | T | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.381-129C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116880415 | |||||||
| chr6:116880427 | A | G | 1 | a0001c0002t0002g0251 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.381-117A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 2/18 | chr6 | 116880427 | |||||||
| chr6:116880705 | A | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.504+38A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116880705 | |||||||
| chr6:116880822 | A | C | 17 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0057 others(14): Show |
19 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.504+155A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116880822 | |||||||
| chr6:116881116 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.504+449C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881116 | |||||||
| chr6:116881243 | G | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.504+576G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881243 | |||||||
| chr6:116881297 | C | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG01993.hp1 NA18981.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.504+630C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881297 | |||||||
| chr6:116881312 | C | A | 101 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(98): Show |
119 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.504+645C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881312 | |||||||
| chr6:116881509 | G | A | 2 | a0001c0002t0002g0090 a0001c0002t0002g0091 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.504+842G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881509 | |||||||
| chr6:116881525 | A | G | 1 | a0001c0010t0001g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.505-842A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881525 | |||||||
| chr6:116881534 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0016t0001g0010 |
4 | HG02559.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-833T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881534 | |||||||
| chr6:116881859 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.505-508G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881859 | |||||||
| chr6:116881906 | C | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.505-461C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 3/18 | chr6 | 116881906 | |||||||
| chr6:116882484 | G | T | 1 | a0001c0001t0001g0249 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.566+56G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116882484 | |||||||
| chr6:116882513 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.566+85A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116882513 | |||||||
| chr6:116882569 | G | GA | 43 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0023 others(40): Show |
54 | HG00099.hp1 HG01074.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.566+154dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116882569 | ||||||
| chr6:116882569 | G | GAA | 7 | a0001c0002t0002g0051 a0001c0002t0002g0055 a0001c0006t0001g0076 others(4): Show |
9 | HG00741.hp2 HG02055.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.566+153_566+154dup others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116882569 | ||||||
| chr6:116882569 | GA | G | 104 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(101): Show |
122 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.566+154delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116882569 | ||||||
| chr6:116882648 | C | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0057 others(14): Show |
19 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.566+220C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116882648 | |||||||
| chr6:116882712 | G | A | 1 | a0001c0002t0002g0055 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566+284G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116882712 | |||||||
| chr6:116882972 | TG | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.566+545delG | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116882972 | |||||||
| chr6:116883166 | A | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0080 others(10): Show |
14 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.566+738A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883166 | |||||||
| chr6:116883359 | T | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.566+931T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883359 | |||||||
| chr6:116883402 | C | G | 1 | a0001c0002t0002g0055 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566+974C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883402 | |||||||
| chr6:116883538 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.566+1110T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883538 | |||||||
| chr6:116883548 | T | G | 1 | a0001c0001t0001g0018 | 3 | HG01256.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.566+1120T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883548 | |||||||
| chr6:116883705 | A | C | 2 | a0002c0003t0002g0026 a0002c0003t0006g0079 |
3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.566+1277A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883705 | |||||||
| chr6:116883735 | G | A | 11 | a0002c0003t0002g0011 a0002c0003t0002g0026 a0002c0003t0002g0073 others(8): Show |
16 | HG00741.hp2 HG01074.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.566+1307G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116883735 | |||||||
| chr6:116884122 | G | A | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+1694G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116884122 | |||||||
| chr6:116884230 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.566+1802T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116884230 | |||||||
| chr6:116884974 | T | TA | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0056 others(17): Show |
26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+2551dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116884974 | ||||||
| chr6:116885232 | G | A | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.566+2804G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885232 | |||||||
| chr6:116885240 | G | T | 2 | a0002c0003t0002g0026 a0002c0003t0006g0079 |
3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.566+2812G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885240 | |||||||
| chr6:116885259 | G | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0056 others(17): Show |
26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+2831G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885259 | |||||||
| chr6:116885406 | G | A | 3 | a0001c0002t0002g0168 a0001c0002t0002g0169 a0001c0002t0002g0251 |
3 | HG03654.hp1 HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.566+2978G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885406 | |||||||
| chr6:116885678 | A | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0056 others(17): Show |
26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+3250A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885678 | |||||||
| chr6:116885720 | GT | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0056 others(17): Show |
26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+3301delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116885720 | ||||||
| chr6:116885883 | C | A | 1 | a0001c0001t0001g0256 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.566+3455C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116885883 | |||||||
| chr6:116886158 | G | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0056 others(17): Show |
26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+3730G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886158 | |||||||
| chr6:116886374 | G | A | 14 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(11): Show |
15 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.566+3946G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886374 | |||||||
| chr6:116886482 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.566+4054T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886482 | |||||||
| chr6:116886514 | A | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0032 others(4): Show |
16 | HG00621.hp2 HG02083.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.566+4086A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886514 | |||||||
| chr6:116886519 | A | G | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.566+4091A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886519 | |||||||
| chr6:116886669 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566+4241C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886669 | |||||||
| chr6:116886762 | A | C | 1 | a0001c0002t0002g0055 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566+4334A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886762 | |||||||
| chr6:116886771 | C | CA | 8 | a0001c0001t0001g0171 a0001c0002t0002g0051 a0001c0002t0002g0053 others(5): Show |
9 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.566+4352dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116886771 | ||||||
| chr6:116886934 | G | T | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.566+4506G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886934 | |||||||
| chr6:116886993 | G | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0056 others(17): Show |
26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.566+4565G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886993 | |||||||
| chr6:116886995 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.566+4567G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116886995 | |||||||
| chr6:116887168 | A | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.566+4740A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887168 | |||||||
| chr6:116887191 | T | G | 1 | a0001c0001t0001g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.566+4763T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887191 | |||||||
| chr6:116887295 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | NA18949.hp2 NA18991.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.566+4867T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887295 | |||||||
| chr6:116887346 | G | T | 101 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(98): Show |
119 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.566+4918G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887346 | |||||||
| chr6:116887360 | C | T | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+4932C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887360 | |||||||
| chr6:116887558 | T | C | 1 | a0001c0002t0002g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.566+5130T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887558 | |||||||
| chr6:116887763 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(253): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.566+5335C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887763 | |||||||
| chr6:116887820 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.566+5392C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116887820 | |||||||
| chr6:116888082 | A | C | 1 | a0001c0002t0002g0245 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.566+5654A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888082 | |||||||
| chr6:116888327 | T | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.567-5660T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888327 | |||||||
| chr6:116888346 | A | G | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-5641A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888346 | |||||||
| chr6:116888547 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.567-5440G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888547 | |||||||
| chr6:116888697 | A | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0056 others(17): Show |
26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.567-5290A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888697 | |||||||
| chr6:116888889 | T | C | 101 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(98): Show |
119 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.567-5098T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888889 | |||||||
| chr6:116888959 | G | T | 12 | a0001c0002t0002g0068 a0002c0003t0002g0011 a0002c0003t0002g0026 others(9): Show |
17 | HG00741.hp2 HG01074.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.567-5028G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116888959 | |||||||
| chr6:116889006 | G | A | 12 | a0001c0002t0002g0068 a0002c0003t0002g0011 a0002c0003t0002g0026 others(9): Show |
17 | HG00741.hp2 HG01074.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.567-4981G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889006 | |||||||
| chr6:116889092 | A | G | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-4895A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889092 | |||||||
| chr6:116889187 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.567-4800A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889187 | |||||||
| chr6:116889238 | T | C | 26 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(23): Show |
32 | HG00741.hp2 HG01074.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.567-4749T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889238 | |||||||
| chr6:116889300 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.567-4687T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889300 | |||||||
| chr6:116889336 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0107 a0001c0001t0001g0108 others(7): Show |
12 | HG01496.hp1 HG02132.hp2 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.567-4651G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889336 | |||||||
| chr6:116889343 | T | G | 1 | a0001c0002t0002g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.567-4644T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889343 | |||||||
| chr6:116889354 | G | C | 26 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(23): Show |
32 | HG00741.hp2 HG01074.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.567-4633G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889354 | |||||||
| chr6:116889374 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.567-4613T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889374 | |||||||
| chr6:116889443 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(70): Show |
109 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.567-4544A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889443 | |||||||
| chr6:116889573 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.567-4414T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889573 | |||||||
| chr6:116889676 | T | C | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-4311T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889676 | |||||||
| chr6:116889729 | C | A | 1 | a0001c0001t0007g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.567-4258C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889729 | |||||||
| chr6:116889936 | G | A | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.567-4051G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889936 | |||||||
| chr6:116889945 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.567-4042C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116889945 | |||||||
| chr6:116890043 | A | AAG | 230 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(227): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.567-3943_567-3942d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr6 | 116890043 | ||||||
| chr6:116890399 | G | T | 1 | a0001c0002t0002g0244 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.567-3588G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890399 | |||||||
| chr6:116890547 | C | T | 1 | a0001c0002t0002g0243 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.567-3440C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890547 | |||||||
| chr6:116890553 | C | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02300.hp2 NA18966.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.567-3434C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890553 | |||||||
| chr6:116890646 | T | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.567-3341T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890646 | |||||||
| chr6:116890653 | C | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.567-3334C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890653 | |||||||
| chr6:116890896 | G | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0056 others(17): Show |
26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.567-3091G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890896 | |||||||
| chr6:116890990 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.567-2997T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116890990 | |||||||
| chr6:116891017 | T | C | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.567-2970T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891017 | |||||||
| chr6:116891037 | T | A | 11 | a0001c0002t0002g0048 a0001c0002t0002g0176 a0001c0002t0002g0177 others(8): Show |
11 | HG00735.hp1 HG00741.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.567-2950T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891037 | |||||||
| chr6:116891095 | T | C | 101 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(98): Show |
119 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.567-2892T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891095 | |||||||
| chr6:116891321 | T | A | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG02258.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.567-2666T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891321 | |||||||
| chr6:116891371 | A | T | 26 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(23): Show |
32 | HG00741.hp2 HG01074.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.567-2616A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891371 | |||||||
| chr6:116891452 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.567-2535T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891452 | |||||||
| chr6:116891458 | A | G | 1 | a0001c0002t0002g0242 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.567-2529A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891458 | |||||||
| chr6:116891526 | A | G | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.567-2461A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891526 | |||||||
| chr6:116891756 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.567-2231A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891756 | |||||||
| chr6:116891819 | T | C | 1 | a0001c0001t0001g0043 | 2 | NA18983.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.567-2168T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116891819 | |||||||
| chr6:116892068 | T | C | 1 | a0001c0002t0002g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.567-1919T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892068 | |||||||
| chr6:116892145 | T | C | 2 | a0002c0003t0002g0026 a0002c0003t0006g0079 |
3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.567-1842T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892145 | |||||||
| chr6:116892290 | G | C | 2 | a0001c0001t0001g0115 a0009c0014t0001g0116 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.567-1697G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892290 | |||||||
| chr6:116892308 | T | C | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.567-1679T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892308 | |||||||
| chr6:116892434 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0257 a0001c0001t0001g0274 |
5 | HG01891.hp1 HG02486.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.567-1553A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892434 | |||||||
| chr6:116892447 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(201): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.567-1540A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892447 | |||||||
| chr6:116892451 | T | C | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.567-1536T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892451 | |||||||
| chr6:116892563 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.567-1424G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892563 | |||||||
| chr6:116892746 | G | A | 1 | a0001c0002t0002g0022 | 2 | NA18957.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.567-1241G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892746 | |||||||
| chr6:116892832 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(213): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.567-1155C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116892832 | |||||||
| chr6:116893016 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.567-971T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893016 | |||||||
| chr6:116893054 | G | A | 1 | a0001c0002t0002g0183 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.567-933G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893054 | |||||||
| chr6:116893085 | A | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.567-902A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893085 | |||||||
| chr6:116893510 | T | G | 1 | a0001c0001t0001g0258 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.567-477T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893510 | |||||||
| chr6:116893512 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.567-475G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893512 | |||||||
| chr6:116893534 | G | T | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.567-453G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893534 | |||||||
| chr6:116893543 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.567-444T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893543 | |||||||
| chr6:116893559 | A | T | 3 | a0002c0003t0002g0026 a0002c0003t0002g0078 a0002c0003t0006g0079 |
4 | HG02886.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-428A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893559 | |||||||
| chr6:116893703 | A | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.567-284A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893703 | |||||||
| chr6:116893741 | G | A | 1 | a0001c0012t0002g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.567-246G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893741 | |||||||
| chr6:116893776 | A | C | 3 | a0001c0001t0001g0258 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | NA18993.hp2 NA18994.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.567-211A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893776 | |||||||
| chr6:116893951 | T | C | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.567-36T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 4/18 | chr6 | 116893951 | |||||||
| chr6:116894120 | T | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.644+56T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894120 | |||||||
| chr6:116894137 | G | A | 16 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0057 others(13): Show |
18 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.644+73G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894137 | |||||||
| chr6:116894217 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(77): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.644+153T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894217 | |||||||
| chr6:116894257 | T | A | 1 | a0001c0002t0002g0126 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.644+193T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894257 | |||||||
| chr6:116894464 | T | G | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.644+400T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894464 | |||||||
| chr6:116894496 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.644+432T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894496 | |||||||
| chr6:116894508 | A | G | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.644+444A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894508 | |||||||
| chr6:116894647 | A | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(11): Show |
15 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.645-533A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894647 | |||||||
| chr6:116894657 | T | TGA | 113 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0038 others(110): Show |
134 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.645-522_645-521dup others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 116894657 | ||||||
| chr6:116894658 | G | GAA | 10 | a0001c0001t0001g0036 a0001c0002t0002g0015 a0001c0002t0002g0185 others(7): Show |
13 | HG02074.hp1 HG02129.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-521_645-520ins others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 116894658 | ||||||
| chr6:116894718 | T | A | 1 | a0001c0001t0001g0019 | 3 | NA18942.hp2 NA18977.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.645-462T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894718 | |||||||
| chr6:116894754 | C | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(11): Show |
15 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.645-426C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894754 | |||||||
| chr6:116894962 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.645-218G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 5/18 | chr6 | 116894962 | |||||||
| chr6:116895238 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG01071.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.672+31C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116895238 | |||||||
| chr6:116895503 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.672+296C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116895503 | |||||||
| chr6:116895645 | T | TAC | 26 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0058 others(23): Show |
29 | HG01081.hp2 HG01109.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.672+469_672+470dup others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | ||||||
| chr6:116895645 | T | TACAC | 74 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(71): Show |
87 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.672+467_672+470dup others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | ||||||
| chr6:116895645 | T | TACACAC | 16 | a0001c0001t0001g0107 a0001c0001t0001g0171 a0001c0001t0001g0175 others(13): Show |
21 | HG00673.hp1 HG00673.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+465_672+470dup others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | ||||||
| chr6:116895645 | T | TACACACA others(1): Show |
4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0002t0002g0193 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+463_672+470dup others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | ||||||
| chr6:116895645 | T | TACACACA others(3): Show |
1 | a0001c0002t0002g0244 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.672+461_672+470dup others(10): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | ||||||
| chr6:116895645 | TAC | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0081 a0001c0001t0001g0082 others(18): Show |
28 | HG00099.hp2 HG00642.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.672+469_672+470del others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | ||||||
| chr6:116895645 | TACAC | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0069 others(5): Show |
9 | HG02559.hp2 HG02886.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.672+467_672+470del others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116895645 | ||||||
| chr6:116895741 | A | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0056 others(17): Show |
26 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.672+534A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116895741 | |||||||
| chr6:116896219 | C | T | 145 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0023 others(142): Show |
173 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.672+1012C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896219 | |||||||
| chr6:116896411 | A | G | 2 | a0001c0001t0001g0031 a0001c0002t0002g0126 |
3 | HG02155.hp1 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.672+1204A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896411 | |||||||
| chr6:116896582 | G | A | 1 | a0001c0002t0002g0202 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.672+1375G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896582 | |||||||
| chr6:116896597 | CA | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.672+1392delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116896597 | ||||||
| chr6:116896602 | A | T | 1 | a0001c0012t0002g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.672+1395A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896602 | |||||||
| chr6:116896627 | G | C | 1 | a0001c0006t0001g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.672+1420G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896627 | |||||||
| chr6:116896707 | CA | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(221): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.672+1512delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116896707 | ||||||
| chr6:116896707 | CAA | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.672+1511_672+1512d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116896707 | ||||||
| chr6:116896787 | C | T | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.672+1580C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896787 | |||||||
| chr6:116896974 | G | C | 1 | a0001c0001t0001g0161 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.672+1767G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116896974 | |||||||
| chr6:116897163 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | NA18972.hp2 NA19078.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.672+1956G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897163 | |||||||
| chr6:116897192 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(77): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.672+1985G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897192 | |||||||
| chr6:116897278 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.672+2071A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897278 | |||||||
| chr6:116897316 | C | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(77): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.672+2109C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897316 | |||||||
| chr6:116897383 | C | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+2176C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897383 | |||||||
| chr6:116897405 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672+2198C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897405 | |||||||
| chr6:116897449 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672+2242G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897449 | |||||||
| chr6:116897459 | T | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(11): Show |
15 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.672+2252T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897459 | |||||||
| chr6:116897479 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.672+2272T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897479 | |||||||
| chr6:116897530 | T | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.672+2323T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897530 | |||||||
| chr6:116897545 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.672+2338G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897545 | |||||||
| chr6:116897638 | C | T | 1 | a0001c0001t0007g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.672+2431C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897638 | |||||||
| chr6:116897695 | C | A | 1 | a0001c0001t0001g0261 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.672+2488C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897695 | |||||||
| chr6:116897730 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.672+2523C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897730 | |||||||
| chr6:116897836 | T | A | 1 | a0001c0002t0002g0204 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.672+2629T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897836 | |||||||
| chr6:116897927 | T | C | 1 | a0001c0001t0007g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.672+2720T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116897927 | |||||||
| chr6:116898022 | A | T | 1 | a0001c0002t0002g0251 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.672+2815A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898022 | |||||||
| chr6:116898253 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.672+3046T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898253 | |||||||
| chr6:116898361 | A | C | 145 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0023 others(142): Show |
173 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.672+3154A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898361 | |||||||
| chr6:116898693 | A | G | 1 | a0001c0001t0001g0047 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.672+3486A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898693 | |||||||
| chr6:116898731 | A | G | 1 | a0003c0004t0002g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.672+3524A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898731 | |||||||
| chr6:116898892 | C | A | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.672+3685C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898892 | |||||||
| chr6:116898908 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.672+3701T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116898908 | |||||||
| chr6:116899090 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.672+3883T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899090 | |||||||
| chr6:116899136 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.672+3929G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899136 | |||||||
| chr6:116899248 | T | C | 1 | a0001c0001t0008g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.672+4041T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899248 | |||||||
| chr6:116899484 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.672+4277A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899484 | |||||||
| chr6:116899494 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.672+4287T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899494 | |||||||
| chr6:116899506 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.672+4299G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899506 | |||||||
| chr6:116899751 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.672+4544T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116899751 | |||||||
| chr6:116900023 | C | T | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.672+4816C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900023 | |||||||
| chr6:116900079 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.672+4872A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900079 | |||||||
| chr6:116900166 | T | G | 1 | a0001c0002t0002g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.672+4959T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900166 | |||||||
| chr6:116900287 | G | T | 8 | a0002c0003t0002g0011 a0002c0003t0002g0026 a0002c0003t0002g0073 others(5): Show |
11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.672+5080G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900287 | |||||||
| chr6:116900340 | C | T | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.672+5133C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900340 | |||||||
| chr6:116900341 | G | A | 8 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0119 others(5): Show |
8 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.672+5134G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900341 | |||||||
| chr6:116900379 | C | T | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.672+5172C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900379 | |||||||
| chr6:116900429 | G | A | 22 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(19): Show |
26 | HG00741.hp2 HG01884.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.672+5222G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900429 | |||||||
| chr6:116900551 | G | A | 3 | a0001c0002t0002g0205 a0001c0002t0002g0206 a0001c0002t0002g0207 |
3 | NA19003.hp1 NA19005.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.672+5344G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900551 | |||||||
| chr6:116900603 | A | T | 2 | a0001c0001t0001g0115 a0009c0014t0001g0116 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.672+5396A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900603 | |||||||
| chr6:116900604 | T | A | 1 | a0001c0001t0001g0257 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.672+5397T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900604 | |||||||
| chr6:116900904 | C | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.672+5697C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900904 | |||||||
| chr6:116900998 | CTG | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0085 a0001c0006t0001g0076 others(1): Show |
4 | HG02717.hp2 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+5793_672+5794d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116900998 | ||||||
| chr6:116900999 | T | G | 123 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0036 others(120): Show |
147 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.672+5792T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116900999 | |||||||
| chr6:116901066 | T | C | 145 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0023 others(142): Show |
173 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.672+5859T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901066 | |||||||
| chr6:116901115 | C | A | 1 | a0001c0001t0001g0058 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.672+5908C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901115 | |||||||
| chr6:116901364 | A | ATTTAGT | 225 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.672+6158_672+6159i others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116901364 | ||||||
| chr6:116901510 | A | G | 5 | a0001c0001t0001g0114 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | HG02451.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.672+6303A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901510 | |||||||
| chr6:116901532 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.672+6325T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901532 | |||||||
| chr6:116901690 | A | G | 1 | a0001c0002t0002g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.672+6483A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901690 | |||||||
| chr6:116901710 | T | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.672+6503T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901710 | |||||||
| chr6:116901715 | C | T | 1 | a0001c0002t0002g0277 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.672+6508C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901715 | |||||||
| chr6:116901818 | AT | A | 123 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0036 others(120): Show |
147 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.672+6614delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116901818 | ||||||
| chr6:116901828 | T | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0002t0002g0061 |
3 | HG02965.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672+6621T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901828 | |||||||
| chr6:116901994 | A | G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0002t0002g0061 |
3 | HG02965.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672+6787A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116901994 | |||||||
| chr6:116902153 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.672+6946A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902153 | |||||||
| chr6:116902160 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.672+6953G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902160 | |||||||
| chr6:116902577 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.672+7370C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902577 | |||||||
| chr6:116902631 | G | A | 1 | a0001c0001t0007g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.672+7424G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902631 | |||||||
| chr6:116902659 | A | T | 1 | a0001c0002t0002g0234 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.672+7452A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902659 | |||||||
| chr6:116902806 | T | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0107 a0001c0001t0001g0108 others(7): Show |
12 | HG01496.hp1 HG02132.hp2 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.672+7599T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902806 | |||||||
| chr6:116902986 | A | G | 5 | a0001c0002t0002g0055 a0001c0002t0002g0068 a0003c0004t0002g0024 others(2): Show |
7 | HG01074.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.672+7779A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116902986 | |||||||
| chr6:116903014 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.672+7807A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903014 | |||||||
| chr6:116903049 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0233 |
3 | HG00738.hp2 HG01261.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.672+7842C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903049 | |||||||
| chr6:116903085 | C | T | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.673-7850C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903085 | |||||||
| chr6:116903140 | A | G | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.673-7795A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903140 | |||||||
| chr6:116903221 | G | C | 8 | a0002c0003t0002g0011 a0002c0003t0002g0026 a0002c0003t0002g0073 others(5): Show |
11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-7714G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903221 | |||||||
| chr6:116903286 | T | G | 1 | a0001c0002t0002g0186 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.673-7649T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903286 | |||||||
| chr6:116903414 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.673-7521T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903414 | |||||||
| chr6:116903478 | A | T | 103 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0042 others(100): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.673-7457A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903478 | |||||||
| chr6:116903564 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(86): Show |
130 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.673-7371C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903564 | |||||||
| chr6:116903598 | T | C | 1 | a0001c0002t0002g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.673-7337T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903598 | |||||||
| chr6:116903657 | ATATTGTT | A | 6 | a0001c0002t0002g0016 a0001c0002t0002g0208 a0001c0002t0002g0235 others(3): Show |
7 | HG00140.hp1 HG00323.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.673-7273_673-7267d others(9): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116903657 | ||||||
| chr6:116903699 | G | C | 2 | a0001c0001t0001g0031 a0001c0002t0002g0126 |
3 | HG02155.hp1 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.673-7236G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903699 | |||||||
| chr6:116903749 | G | C | 1 | a0001c0002t0002g0177 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.673-7186G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903749 | |||||||
| chr6:116903831 | C | T | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-7104C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116903831 | |||||||
| chr6:116904180 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.673-6755G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904180 | |||||||
| chr6:116904188 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.673-6747T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904188 | |||||||
| chr6:116904236 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.673-6699A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904236 | |||||||
| chr6:116904249 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.673-6686C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904249 | |||||||
| chr6:116904382 | C | A | 1 | a0001c0001t0001g0019 | 3 | NA18942.hp2 NA18977.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.673-6553C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904382 | |||||||
| chr6:116904404 | A | G | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-6531A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904404 | |||||||
| chr6:116904450 | A | C | 1 | a0002c0007t0001g0077 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.673-6485A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904450 | |||||||
| chr6:116904505 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(203): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.673-6430A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904505 | |||||||
| chr6:116904947 | C | T | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-5988C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116904947 | |||||||
| chr6:116905082 | T | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(86): Show |
130 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.673-5853T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905082 | |||||||
| chr6:116905300 | T | A | 1 | a0001c0001t0001g0209 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.673-5635T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905300 | |||||||
| chr6:116905333 | T | C | 1 | a0001c0002t0002g0187 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.673-5602T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905333 | |||||||
| chr6:116905434 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.673-5501T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905434 | |||||||
| chr6:116905437 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.673-5498A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905437 | |||||||
| chr6:116905556 | C | CT | 6 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0001c0006t0001g0076 others(3): Show |
7 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-5364dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116905556 | ||||||
| chr6:116905556 | CT | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0114 a0001c0001t0001g0165 others(2): Show |
7 | HG01256.hp1 HG01433.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-5364delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116905556 | ||||||
| chr6:116905604 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.673-5331G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905604 | |||||||
| chr6:116905646 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.673-5289G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905646 | |||||||
| chr6:116905699 | G | A | 5 | a0001c0002t0002g0055 a0001c0002t0002g0068 a0003c0004t0002g0024 others(2): Show |
7 | HG01074.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-5236G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905699 | |||||||
| chr6:116905784 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.673-5151T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905784 | |||||||
| chr6:116905792 | C | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.673-5143C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905792 | |||||||
| chr6:116905911 | A | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(204): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.673-5024A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116905911 | |||||||
| chr6:116905952 | C | CTA | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(203): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.673-4982_673-4981i others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116905952 | ||||||
| chr6:116906121 | T | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(59): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.673-4814T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906121 | |||||||
| chr6:116906135 | C | T | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-4800C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906135 | |||||||
| chr6:116906187 | G | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0057 others(12): Show |
17 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.673-4748G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906187 | |||||||
| chr6:116906291 | A | C | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.673-4644A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906291 | |||||||
| chr6:116906511 | TA | T | 8 | a0002c0003t0002g0011 a0002c0003t0002g0026 a0002c0003t0002g0073 others(5): Show |
11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-4423delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906511 | |||||||
| chr6:116906610 | T | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0057 a0001c0001t0001g0066 others(1): Show |
5 | HG00099.hp1 HG01358.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.673-4325T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906610 | |||||||
| chr6:116906691 | G | T | 2 | a0002c0003t0002g0026 a0002c0003t0006g0079 |
3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.673-4244G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906691 | |||||||
| chr6:116906743 | T | TTG | 21 | a0001c0001t0001g0029 a0001c0001t0001g0203 a0001c0002t0002g0015 others(18): Show |
28 | HG00741.hp2 HG01258.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.673-4170_673-4169d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116906743 | ||||||
| chr6:116906743 | TTG | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.673-4170_673-4169d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116906743 | ||||||
| chr6:116906858 | T | TTTG | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-4076_673-4075i others(5): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116906858 | ||||||
| chr6:116906860 | G | GT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0110 others(25): Show |
34 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.673-4062dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116906860 | ||||||
| chr6:116906860 | G | T | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-4075G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116906860 | |||||||
| chr6:116906860 | GT | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(70): Show |
110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.673-4062delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116906860 | ||||||
| chr6:116907080 | G | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0254 a0001c0001t0001g0255 |
7 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-3855G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907080 | |||||||
| chr6:116907127 | A | AT | 125 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0038 others(122): Show |
147 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.673-3801dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116907127 | ||||||
| chr6:116907178 | T | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(77): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.673-3757T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907178 | |||||||
| chr6:116907339 | T | A | 8 | a0002c0003t0002g0011 a0002c0003t0002g0026 a0002c0003t0002g0073 others(5): Show |
11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-3596T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907339 | |||||||
| chr6:116907384 | C | T | 1 | a0001c0002t0002g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.673-3551C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907384 | |||||||
| chr6:116907422 | G | C | 15 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0057 others(12): Show |
17 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.673-3513G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907422 | |||||||
| chr6:116907488 | G | T | 1 | a0001c0002t0002g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.673-3447G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907488 | |||||||
| chr6:116907489 | C | A | 8 | a0002c0003t0002g0011 a0002c0003t0002g0026 a0002c0003t0002g0073 others(5): Show |
11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-3446C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907489 | |||||||
| chr6:116907519 | C | T | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.673-3416C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907519 | |||||||
| chr6:116907644 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.673-3291C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907644 | |||||||
| chr6:116907753 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.673-3182A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907753 | |||||||
| chr6:116907776 | T | C | 8 | a0002c0003t0002g0011 a0002c0003t0002g0026 a0002c0003t0002g0073 others(5): Show |
11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-3159T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907776 | |||||||
| chr6:116907869 | AATTTT | A | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-3065_673-3061d others(7): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116907869 | |||||||
| chr6:116908028 | C | T | 2 | a0001c0002t0002g0180 a0001c0002t0002g0181 |
2 | HG02083.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.673-2907C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908028 | |||||||
| chr6:116908092 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(73): Show |
113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.673-2843G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908092 | |||||||
| chr6:116908126 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(74): Show |
114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.673-2809T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908126 | |||||||
| chr6:116908430 | G | C | 125 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0038 others(122): Show |
147 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.673-2505G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908430 | |||||||
| chr6:116908490 | C | A | 1 | a0001c0001t0001g0007 | 4 | NA18945.hp1 NA18975.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-2445C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908490 | |||||||
| chr6:116908580 | A | C | 1 | a0001c0002t0002g0041 | 2 | NA18975.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.673-2355A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908580 | |||||||
| chr6:116908643 | G | A | 130 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0038 others(127): Show |
153 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.673-2292G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908643 | |||||||
| chr6:116908669 | T | TAC | 11 | a0001c0001t0001g0085 a0001c0002t0002g0048 a0001c0002t0002g0166 others(8): Show |
11 | HG00735.hp1 HG00741.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.673-2248_673-2247d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908669 | ||||||
| chr6:116908669 | T | TACAC | 7 | a0001c0001t0001g0038 a0001c0001t0001g0082 a0001c0001t0001g0086 others(4): Show |
8 | HG01884.hp2 HG02148.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.673-2250_673-2247d others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908669 | ||||||
| chr6:116908669 | T | TACACAC | 3 | a0001c0001t0001g0081 a0001c0001t0001g0203 a0001c0002t0002g0202 |
3 | HG02809.hp1 HG03195.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.673-2252_673-2247d others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908669 | ||||||
| chr6:116908669 | TAC | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0057 a0001c0001t0001g0058 others(12): Show |
17 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.673-2248_673-2247d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908669 | ||||||
| chr6:116908669 | TACACACA others(15): Show |
T | 4 | a0002c0003t0002g0011 a0002c0003t0002g0073 a0002c0003t0002g0074 others(1): Show |
6 | HG00741.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-2246_673-2225d others(24): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908669 | ||||||
| chr6:116908673 | CACACACA others(9): Show |
C | 1 | a0001c0001t0001g0210 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.673-2246_673-2231d others(18): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908673 | ||||||
| chr6:116908677 | CACACACA others(5): Show |
C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0002t0002g0051 others(5): Show |
10 | HG01993.hp2 HG02148.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.673-2246_673-2235d others(14): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908677 | ||||||
| chr6:116908679 | CACACACA others(3): Show |
C | 2 | a0001c0001t0001g0071 a0001c0002t0002g0182 |
2 | HG02559.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.673-2246_673-2237d others(12): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908679 | ||||||
| chr6:116908681 | CACACACA others(1): Show |
C | 6 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0248 others(3): Show |
6 | HG01258.hp1 HG01516.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-2246_673-2239d others(10): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908681 | ||||||
| chr6:116908683 | CACACAG | C | 18 | a0001c0001t0001g0042 a0001c0001t0001g0216 a0001c0001t0001g0218 others(15): Show |
19 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.673-2246_673-2241d others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908683 | ||||||
| chr6:116908685 | CACAG | C | 39 | a0001c0001t0001g0036 a0001c0001t0001g0171 a0001c0001t0001g0175 others(36): Show |
48 | HG00558.hp1 HG00609.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.673-2246_673-2243d others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908685 | ||||||
| chr6:116908687 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.673-2248C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908687 | |||||||
| chr6:116908687 | CAG | C | 19 | a0001c0001t0001g0072 a0001c0001t0001g0201 a0001c0001t0001g0226 others(16): Show |
19 | HG00140.hp1 HG00323.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.673-2246_673-2245d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908687 | ||||||
| chr6:116908689 | G | C | 40 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0001t0001g0081 others(37): Show |
45 | HG00673.hp2 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.673-2246G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908689 | |||||||
| chr6:116908689 | G | GAC | 15 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0031 others(12): Show |
22 | HG00733.hp1 HG01074.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.673-2220_673-2219d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908689 | ||||||
| chr6:116908689 | GACAC | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(44): Show |
72 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.673-2222_673-2219d others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908689 | ||||||
| chr6:116908689 | GACACAC | G | 26 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
38 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.673-2224_673-2219d others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116908689 | ||||||
| chr6:116908691 | C | G | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.673-2244C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908691 | |||||||
| chr6:116908695 | C | G | 1 | a0001c0001t0001g0271 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.673-2240C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908695 | |||||||
| chr6:116908699 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.673-2236C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908699 | |||||||
| chr6:116908719 | G | A | 1 | a0001c0002t0002g0214 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.673-2216G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908719 | |||||||
| chr6:116908793 | T | C | 4 | a0002c0003t0002g0011 a0002c0003t0002g0073 a0002c0003t0002g0074 others(1): Show |
6 | HG00741.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-2142T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908793 | |||||||
| chr6:116908795 | A | G | 130 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0038 others(127): Show |
153 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.673-2140A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908795 | |||||||
| chr6:116908797 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.673-2138A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908797 | |||||||
| chr6:116908902 | C | T | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.673-2033C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908902 | |||||||
| chr6:116908935 | T | A | 1 | a0001c0001t0001g0209 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.673-2000T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116908935 | |||||||
| chr6:116909176 | G | C | 125 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0038 others(122): Show |
147 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.673-1759G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116909176 | |||||||
| chr6:116909197 | T | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.673-1738T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116909197 | |||||||
| chr6:116909558 | T | A | 125 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0038 others(122): Show |
147 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.673-1377T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116909558 | |||||||
| chr6:116909630 | TA | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(73): Show |
113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.673-1299delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909630 | ||||||
| chr6:116909735 | C | CT | 71 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0028 others(68): Show |
91 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.673-1171dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | ||||||
| chr6:116909735 | C | CTT | 10 | a0001c0001t0001g0230 a0001c0002t0002g0172 a0001c0002t0002g0189 others(7): Show |
10 | HG00609.hp2 HG02129.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.673-1172_673-1171d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | ||||||
| chr6:116909735 | C | CTTTTTTT others(3): Show |
4 | a0002c0003t0002g0011 a0002c0003t0002g0026 a0002c0003t0002g0073 others(1): Show |
7 | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.673-1180_673-1171d others(12): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | ||||||
| chr6:116909735 | C | CTTTTTTT others(4): Show |
1 | a0002c0003t0002g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.673-1181_673-1171d others(13): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | ||||||
| chr6:116909735 | C | CTTTTTTT others(5): Show |
1 | a0002c0003t0006g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.673-1182_673-1171d others(14): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | ||||||
| chr6:116909735 | CT | C | 50 | a0001c0001t0001g0032 a0001c0001t0001g0042 a0001c0001t0001g0046 others(47): Show |
56 | HG00323.hp1 HG00639.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.673-1171delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | ||||||
| chr6:116909735 | CTT | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0081 others(10): Show |
14 | HG00733.hp2 HG01884.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.673-1172_673-1171d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | ||||||
| chr6:116909735 | CTTT | C | 6 | a0001c0001t0001g0072 a0001c0001t0001g0085 a0001c0001t0001g0088 others(3): Show |
6 | HG02717.hp2 HG02818.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-1173_673-1171d others(5): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | ||||||
| chr6:116909735 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0097 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.673-1180_673-1171d others(12): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | ||||||
| chr6:116909735 | CTTTTTTT others(7): Show |
C | 1 | a0001c0010t0001g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.673-1184_673-1171d others(16): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr6 | 116909735 | ||||||
| chr6:116909770 | G | A | 3 | a0001c0001t0001g0109 a0002c0003t0002g0026 a0002c0003t0006g0079 |
4 | HG02132.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-1165G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116909770 | |||||||
| chr6:116910018 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.673-917A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910018 | |||||||
| chr6:116910453 | A | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.673-482A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910453 | |||||||
| chr6:116910461 | T | G | 1 | a0001c0001t0001g0036 | 2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.673-474T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910461 | |||||||
| chr6:116910513 | C | T | 5 | a0001c0002t0002g0055 a0001c0002t0002g0068 a0003c0004t0002g0024 others(2): Show |
7 | HG01074.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-422C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910513 | |||||||
| chr6:116910514 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.673-421G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910514 | |||||||
| chr6:116910706 | T | C | 1 | a0001c0002t0002g0169 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.673-229T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910706 | |||||||
| chr6:116910932 | T | C | 2 | a0002c0003t0002g0026 a0002c0003t0006g0079 |
3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.673-3T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 6/18 | chr6 | 116910932 | |||||||
| chr6:116911103 | G | T | 1 | a0001c0002t0002g0055 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.780+61G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116911103 | |||||||
| chr6:116911519 | C | T | 8 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0111 others(5): Show |
8 | HG03688.hp1 HG04184.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+477C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116911519 | |||||||
| chr6:116911671 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.780+629G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116911671 | |||||||
| chr6:116911691 | G | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(20): Show |
32 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.780+649G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116911691 | |||||||
| chr6:116912031 | C | T | 1 | a0001c0002t0002g0244 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.780+989C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912031 | |||||||
| chr6:116912045 | C | A | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.780+1003C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912045 | |||||||
| chr6:116912262 | C | T | 2 | a0001c0001t0001g0171 a0008c0017t0001g0170 |
2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.780+1220C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912262 | |||||||
| chr6:116912309 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02074.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.780+1267G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912309 | |||||||
| chr6:116912336 | C | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(203): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.780+1294C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912336 | |||||||
| chr6:116912343 | G | GA | 16 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(13): Show |
17 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.780+1311dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 116912343 | ||||||
| chr6:116912481 | C | T | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+1439C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912481 | |||||||
| chr6:116912510 | T | C | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.780+1468T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912510 | |||||||
| chr6:116912722 | C | A | 1 | a0001c0001t0001g0047 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.780+1680C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116912722 | |||||||
| chr6:116912847 | G | GGT | 125 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0038 others(122): Show |
147 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.780+1806_780+1807d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 116912847 | ||||||
| chr6:116913207 | GC | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.780+2167delC | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 116913207 | ||||||
| chr6:116913250 | C | T | 2 | a0001c0002t0002g0211 a0001c0002t0002g0232 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.780+2208C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913250 | |||||||
| chr6:116913354 | G | A | 130 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0038 others(127): Show |
153 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.780+2312G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913354 | |||||||
| chr6:116913383 | G | A | 4 | a0002c0003t0002g0011 a0002c0003t0002g0073 a0002c0003t0002g0074 others(1): Show |
6 | HG00741.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+2341G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913383 | |||||||
| chr6:116913463 | C | G | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.780+2421C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913463 | |||||||
| chr6:116913489 | G | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(3): Show |
6 | HG02258.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+2447G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913489 | |||||||
| chr6:116913548 | T | A | 3 | a0001c0002t0002g0040 a0001c0002t0002g0199 a0001c0002t0002g0229 |
4 | NA18956.hp2 NA18957.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-2460T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913548 | |||||||
| chr6:116913548 | T | C | 102 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0038 others(99): Show |
120 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.781-2460T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913548 | |||||||
| chr6:116913557 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.781-2451T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913557 | |||||||
| chr6:116913620 | G | A | 1 | a0001c0002t0002g0126 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.781-2388G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913620 | |||||||
| chr6:116913680 | A | C | 5 | a0001c0002t0002g0055 a0001c0002t0002g0068 a0003c0004t0002g0024 others(2): Show |
7 | HG01074.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-2328A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913680 | |||||||
| chr6:116913799 | G | T | 2 | a0001c0002t0002g0180 a0001c0002t0002g0181 |
2 | HG02083.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.781-2209G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913799 | |||||||
| chr6:116913870 | G | T | 1 | a0001c0002t0002g0193 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.781-2138G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116913870 | |||||||
| chr6:116914094 | T | C | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.781-1914T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914094 | |||||||
| chr6:116914115 | C | G | 1 | a0001c0002t0002g0126 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.781-1893C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914115 | |||||||
| chr6:116914133 | C | A | 5 | a0001c0002t0002g0055 a0001c0002t0002g0068 a0003c0004t0002g0024 others(2): Show |
7 | HG01074.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-1875C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914133 | |||||||
| chr6:116914493 | G | C | 132 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0036 others(129): Show |
156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.781-1515G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914493 | |||||||
| chr6:116914595 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.781-1413T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914595 | |||||||
| chr6:116914684 | C | A | 1 | a0001c0002t0002g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.781-1324C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914684 | |||||||
| chr6:116914757 | C | A | 2 | a0001c0002t0002g0217 a0006c0011t0002g0212 |
2 | HG02080.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.781-1251C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914757 | |||||||
| chr6:116914933 | T | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0002t0002g0061 |
3 | HG02965.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.781-1075T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116914933 | |||||||
| chr6:116915214 | A | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0056 others(16): Show |
25 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.781-794A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915214 | |||||||
| chr6:116915384 | T | G | 4 | a0002c0003t0002g0011 a0002c0003t0002g0073 a0002c0003t0002g0074 others(1): Show |
6 | HG00741.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-624T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915384 | |||||||
| chr6:116915412 | A | T | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.781-596A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915412 | |||||||
| chr6:116915482 | G | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.781-526G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915482 | |||||||
| chr6:116915523 | T | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-485T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915523 | |||||||
| chr6:116915545 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.781-463A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915545 | |||||||
| chr6:116915659 | T | G | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-349T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915659 | |||||||
| chr6:116915690 | T | A | 132 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0036 others(129): Show |
156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.781-318T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915690 | |||||||
| chr6:116915760 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.781-248G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915760 | |||||||
| chr6:116915769 | T | C | 2 | a0002c0003t0002g0026 a0002c0003t0006g0079 |
3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.781-239T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 7/18 | chr6 | 116915769 | |||||||
| chr6:116916361 | G | A | 132 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0036 others(129): Show |
156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.972+47G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916361 | |||||||
| chr6:116916403 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.972+89A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916403 | |||||||
| chr6:116916421 | T | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.972+107T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916421 | |||||||
| chr6:116916524 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.972+210A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916524 | |||||||
| chr6:116916564 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0002t0002g0061 |
3 | HG02965.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.972+250C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916564 | |||||||
| chr6:116916663 | T | C | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.972+349T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916663 | |||||||
| chr6:116916735 | C | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.972+421C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916735 | |||||||
| chr6:116916770 | A | T | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.972+456A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916770 | |||||||
| chr6:116916791 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.972+477G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116916791 | |||||||
| chr6:116917158 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.972+844A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917158 | |||||||
| chr6:116917317 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(206): Show |
270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.973-720G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917317 | |||||||
| chr6:116917338 | G | GT | 18 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0082 others(15): Show |
22 | HG00323.hp1 HG00741.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.973-684dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116917338 | ||||||
| chr6:116917338 | G | GTT | 7 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG02717.hp2 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.973-685_973-684dup others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116917338 | ||||||
| chr6:116917338 | GT | G | 118 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0031 others(115): Show |
142 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.973-684delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116917338 | ||||||
| chr6:116917343 | T | TTG | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.973-693_973-692ins others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116917343 | ||||||
| chr6:116917371 | G | A | 8 | a0002c0003t0002g0011 a0002c0003t0002g0026 a0002c0003t0002g0073 others(5): Show |
11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.973-666G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917371 | |||||||
| chr6:116917505 | A | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.973-532A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917505 | |||||||
| chr6:116917763 | T | G | 1 | a0001c0001t0001g0047 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.973-274T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917763 | |||||||
| chr6:116917861 | ACACT | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0057 a0001c0001t0001g0066 others(1): Show |
5 | HG00099.hp1 HG01358.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.973-172_973-169del others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116917861 | ||||||
| chr6:116917923 | A | C | 6 | a0001c0001t0001g0042 a0001c0001t0001g0216 a0001c0001t0001g0218 others(3): Show |
7 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.973-114A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917923 | |||||||
| chr6:116917978 | T | C | 132 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0036 others(129): Show |
156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.973-59T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | chr6 | 116917978 | |||||||
| chr6:116918001 | T | TAAAG | 8 | a0002c0003t0002g0011 a0002c0003t0002g0026 a0002c0003t0002g0073 others(5): Show |
11 | HG00741.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.973-34_973-31dupAA others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 116918001 | ||||||
| chr6:116918177 | C | A | 1 | a0001c0012t0002g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1022+91C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918177 | |||||||
| chr6:116918301 | C | T | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1022+215C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918301 | |||||||
| chr6:116918336 | T | C | 132 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0036 others(129): Show |
156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.1022+250T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918336 | |||||||
| chr6:116918518 | A | T | 1 | a0001c0001t0001g0151 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1022+432A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918518 | |||||||
| chr6:116918558 | CA | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0057 others(31): Show |
38 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1022+484delA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 116918558 | ||||||
| chr6:116918588 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1022+502C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918588 | |||||||
| chr6:116918600 | G | GA | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(80): Show |
121 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1022+524dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 116918600 | ||||||
| chr6:116918600 | G | GAA | 104 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0042 others(101): Show |
125 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.1022+523_1022+524d others(4): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 116918600 | ||||||
| chr6:116918646 | T | C | 2 | a0001c0002t0002g0168 a0001c0002t0002g0169 |
2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1023-491T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116918646 | |||||||
| chr6:116919103 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1023-34C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 10/18 | chr6 | 116919103 | |||||||
| chr6:116919322 | A | T | 1 | a0001c0002t0002g0126 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1182+26A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919322 | |||||||
| chr6:116919427 | C | T | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182+131C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919427 | |||||||
| chr6:116919430 | G | A | 132 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0036 others(129): Show |
156 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.1182+134G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919430 | |||||||
| chr6:116919494 | G | C | 1 | a0001c0002t0002g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1182+198G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919494 | |||||||
| chr6:116919562 | TAAG | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(74): Show |
114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1182+270_1182+272d others(5): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 116919562 | ||||||
| chr6:116919737 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1182+441A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919737 | |||||||
| chr6:116919817 | T | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(206): Show |
270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1183-493T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919817 | |||||||
| chr6:116919856 | A | G | 3 | a0001c0001t0001g0085 a0001c0006t0001g0076 a0001c0006t0001g0084 |
3 | HG02717.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1183-454A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919856 | |||||||
| chr6:116919879 | G | C | 1 | a0001c0001t0001g0060 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1183-431G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116919879 | |||||||
| chr6:116920041 | T | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1183-269T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116920041 | |||||||
| chr6:116920114 | A | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0275 |
2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1183-196A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 11/18 | chr6 | 116920114 | |||||||
| chr6:116920510 | C | T | 2 | a0001c0001t0001g0115 a0009c0014t0001g0116 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1327+56C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116920510 | |||||||
| chr6:116920584 | C | CCTGA | 19 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(16): Show |
21 | HG01258.hp1 HG01884.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.1327+131_1327+132i others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 116920584 | ||||||
| chr6:116920587 | A | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0072 others(16): Show |
21 | HG01258.hp1 HG01884.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.1327+133A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116920587 | |||||||
| chr6:116920609 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1327+155C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116920609 | |||||||
| chr6:116920772 | T | C | 5 | a0001c0002t0002g0196 a0001c0002t0002g0236 a0001c0002t0002g0237 others(2): Show |
5 | HG00673.hp1 NA19000.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1327+318T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116920772 | |||||||
| chr6:116920858 | T | C | 116 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0038 others(113): Show |
136 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.1327+404T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116920858 | |||||||
| chr6:116921093 | T | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1327+639T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921093 | |||||||
| chr6:116921138 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0201 a0001c0001t0001g0254 others(27): Show |
38 | HG00673.hp2 HG01243.hp2 HG02080.hp2 others(35): Show |
intron_variant | MODIFIER | c.1327+684A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921138 | |||||||
| chr6:116921301 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1328-741C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921301 | |||||||
| chr6:116921389 | A | G | 1 | a0006c0011t0002g0212 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1328-653A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921389 | |||||||
| chr6:116921501 | A | G | 1 | a0001c0002t0003g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1328-541A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921501 | |||||||
| chr6:116921523 | T | C | 1 | a0004c0005t0002g0052 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1328-519T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921523 | |||||||
| chr6:116921550 | A | G | 1 | a0001c0002t0002g0055 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1328-492A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921550 | |||||||
| chr6:116921591 | G | A | 2 | a0001c0002t0002g0205 a0001c0002t0002g0207 |
2 | NA19003.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1328-451G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921591 | |||||||
| chr6:116921619 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0224 |
2 | HG00639.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1328-423G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921619 | |||||||
| chr6:116921655 | AT | A | 120 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0035 others(117): Show |
147 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(144): Show |
intron_variant | MODIFIER | c.1328-372delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 116921655 | ||||||
| chr6:116921693 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1328-349C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921693 | |||||||
| chr6:116921694 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1328-348G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921694 | |||||||
| chr6:116921857 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1328-185G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921857 | |||||||
| chr6:116921911 | A | T | 1 | a0001c0012t0002g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1328-131A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116921911 | |||||||
| chr6:116922018 | C | CTT | 6 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0001c0002t0003g0089 others(3): Show |
7 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1328-11_1328-10dup others(2): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 116922018 | ||||||
| chr6:116922032 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG01106.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1328-10T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 12/18 | chr6 | 116922032 | |||||||
| chr6:116922236 | AG | A | 16 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0057 others(13): Show |
17 | HG00099.hp1 HG01109.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1437+89delG | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 116922236 | ||||||
| chr6:116922288 | G | A | 4 | a0002c0003t0002g0011 a0002c0003t0002g0073 a0002c0003t0002g0075 others(1): Show |
7 | HG00741.hp2 HG02145.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1437+137G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116922288 | |||||||
| chr6:116922554 | G | C | 2 | a0002c0003t0002g0026 a0002c0003t0006g0079 |
3 | HG02895.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1437+403G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116922554 | |||||||
| chr6:116922788 | T | C | 1 | a0001c0002t0002g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1438-319T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116922788 | |||||||
| chr6:116922798 | A | G | 1 | a0001c0001t0001g0013 | 3 | NA18947.hp2 NA18952.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1438-309A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116922798 | |||||||
| chr6:116922944 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1438-163G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116922944 | |||||||
| chr6:116923047 | G | A | 1 | a0001c0002t0002g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1438-60G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 13/18 | chr6 | 116923047 | |||||||
| chr6:116923319 | C | A | 1 | a0001c0012t0002g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1555+95C>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923319 | |||||||
| chr6:116923391 | C | T | 1 | a0001c0006t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1555+167C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923391 | |||||||
| chr6:116923425 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1555+201T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923425 | |||||||
| chr6:116923475 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1555+251C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923475 | |||||||
| chr6:116923513 | T | C | 104 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(101): Show |
126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1555+289T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923513 | |||||||
| chr6:116923693 | A | G | 104 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(101): Show |
126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1555+469A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923693 | |||||||
| chr6:116923734 | G | C | 104 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(101): Show |
126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1555+510G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923734 | |||||||
| chr6:116923838 | T | C | 104 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(101): Show |
126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1555+614T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116923838 | |||||||
| chr6:116924064 | A | G | 8 | a0001c0001t0001g0042 a0001c0001t0001g0216 a0001c0001t0001g0218 others(5): Show |
9 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1556-605A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116924064 | |||||||
| chr6:116924226 | T | C | 104 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(101): Show |
126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1556-443T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116924226 | |||||||
| chr6:116924354 | C | T | 1 | a0001c0002t0002g0022 | 2 | NA18957.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1556-315C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 14/18 | chr6 | 116924354 | |||||||
| chr6:116924850 | A | G | 4 | a0001c0001t0001g0175 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+59A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | chr6 | 116924850 | |||||||
| chr6:116924895 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA18949.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1678+104T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | chr6 | 116924895 | |||||||
| chr6:116925035 | T | C | 1 | a0001c0002t0002g0188 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1678+244T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | chr6 | 116925035 | |||||||
| chr6:116925145 | A | C | 1 | a0001c0002t0002g0225 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1679-308A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | chr6 | 116925145 | |||||||
| chr6:116925266 | A | C | 104 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(101): Show |
126 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1679-187A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | chr6 | 116925266 | |||||||
| chr6:116925413 | G | GA | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(77): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1679-34dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr6 | 116925413 | ||||||
| chr6:116925897 | ATTAG | A | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1885+242_1885+245d others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 116925897 | ||||||
| chr6:116925936 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0254 |
6 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1885+277A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116925936 | |||||||
| chr6:116926034 | G | C | 1 | a0001c0002t0002g0055 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1885+375G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926034 | |||||||
| chr6:116926095 | G | T | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1885+436G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926095 | |||||||
| chr6:116926132 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1885+473C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926132 | |||||||
| chr6:116926251 | A | G | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1885+592A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926251 | |||||||
| chr6:116926388 | T | A | 1 | a0009c0014t0001g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1886-639T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926388 | |||||||
| chr6:116926529 | A | G | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1886-498A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926529 | |||||||
| chr6:116926552 | C | T | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1886-475C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926552 | |||||||
| chr6:116926743 | C | T | 1 | a0002c0003t0006g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1886-284C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926743 | |||||||
| chr6:116926744 | A | C | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1886-283A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 16/18 | chr6 | 116926744 | |||||||
| chr6:116927547 | T | C | 1 | a0001c0002t0002g0251 | 1 | HG04199.hp2 | splice_region_variant&intron_variant | LOW | c.2398+8T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927547 | |||||||
| chr6:116927556 | G | T | 1 | a0008c0017t0001g0170 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2398+17G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927556 | |||||||
| chr6:116927583 | A | G | 10 | a0001c0001t0001g0072 a0001c0001t0001g0118 a0001c0001t0001g0127 others(7): Show |
13 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2398+44A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927583 | |||||||
| chr6:116927743 | C | CT | 4 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0155 others(1): Show |
8 | HG00621.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2398+223dupT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | ||||||
| chr6:116927743 | C | CTTTT | 78 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(75): Show |
96 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.2398+220_2398+223d others(6): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | ||||||
| chr6:116927743 | C | CTTTTT | 13 | a0001c0002t0002g0061 a0001c0002t0002g0149 a0001c0002t0002g0166 others(10): Show |
13 | HG01516.hp2 HG02056.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.2398+219_2398+223d others(7): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | ||||||
| chr6:116927743 | C | CTTTTTTT others(2): Show |
3 | a0002c0003t0002g0011 a0002c0003t0002g0078 a0003c0004t0002g0024 |
6 | HG02145.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2398+215_2398+223d others(11): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | ||||||
| chr6:116927743 | C | CTTTTTTT others(3): Show |
2 | a0001c0002t0002g0055 a0002c0003t0002g0075 |
2 | HG00741.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2398+214_2398+223d others(12): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | ||||||
| chr6:116927743 | C | CTTTTTTT others(6): Show |
3 | a0001c0002t0002g0051 a0004c0005t0002g0021 a0004c0005t0002g0052 |
4 | HG01993.hp2 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.2398+211_2398+223d others(15): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | ||||||
| chr6:116927743 | C | CTTTTTTT others(7): Show |
2 | a0001c0002t0002g0053 a0004c0005t0002g0054 |
2 | HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2398+210_2398+223d others(16): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | ||||||
| chr6:116927743 | CT | C | 8 | a0001c0001t0001g0072 a0001c0001t0001g0105 a0001c0001t0001g0111 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2398+223delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116927743 | ||||||
| chr6:116927769 | A | G | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2398+230A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927769 | |||||||
| chr6:116927796 | G | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(77): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2398+257G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927796 | |||||||
| chr6:116927810 | C | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0032 others(4): Show |
16 | HG00621.hp2 HG02083.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.2398+271C>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116927810 | |||||||
| chr6:116928038 | A | C | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2398+499A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928038 | |||||||
| chr6:116928045 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2398+506C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928045 | |||||||
| chr6:116928080 | T | TA | 212 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(209): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.2398+555dupA | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 116928080 | ||||||
| chr6:116928161 | A | G | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.2399-598A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928161 | |||||||
| chr6:116928221 | A | C | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2399-538A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928221 | |||||||
| chr6:116928260 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2399-499G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928260 | |||||||
| chr6:116928395 | C | T | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2399-364C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928395 | |||||||
| chr6:116928411 | C | T | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2399-348C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928411 | |||||||
| chr6:116928462 | T | C | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2399-297T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928462 | |||||||
| chr6:116928522 | A | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2399-237A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928522 | |||||||
| chr6:116928684 | A | G | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2399-75A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 17/18 | chr6 | 116928684 | |||||||
| chr6:116929010 | G | C | 1 | a0009c0014t0001g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2611+39G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929010 | |||||||
| chr6:116929017 | A | C | 1 | a0002c0003t0006g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2611+46A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929017 | |||||||
| chr6:116929019 | C | T | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2611+48C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929019 | |||||||
| chr6:116929031 | A | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0062 a0001c0001t0001g0064 |
3 | HG02257.hp2 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2611+60A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929031 | |||||||
| chr6:116929139 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0216 a0001c0001t0001g0218 others(5): Show |
9 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2611+168G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929139 | |||||||
| chr6:116929223 | G | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0216 a0001c0001t0001g0218 others(3): Show |
7 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2611+252G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929223 | |||||||
| chr6:116929224 | G | A | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2611+253G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929224 | |||||||
| chr6:116929296 | A | G | 5 | a0001c0002t0002g0051 a0001c0002t0002g0053 a0004c0005t0002g0021 others(2): Show |
6 | HG01258.hp1 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.2611+325A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929296 | |||||||
| chr6:116929352 | G | C | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2611+381G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929352 | |||||||
| chr6:116929407 | A | T | 2 | a0001c0002t0002g0221 a0001c0002t0002g0244 |
2 | NA18951.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2611+436A>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929407 | |||||||
| chr6:116929414 | A | AC | 3 | a0001c0001t0001g0063 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG01106.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2611+444dupC | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr6 | 116929414 | ||||||
| chr6:116929544 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0171 |
3 | HG02572.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2611+573G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929544 | |||||||
| chr6:116929956 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2611+985A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929956 | |||||||
| chr6:116929996 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0171 |
3 | HG02572.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2611+1025T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116929996 | |||||||
| chr6:116930027 | G | T | 1 | a0001c0002t0002g0220 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2611+1056G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930027 | |||||||
| chr6:116930088 | C | T | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2611+1117C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930088 | |||||||
| chr6:116930113 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0216 a0001c0001t0001g0218 others(5): Show |
9 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2611+1142G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930113 | |||||||
| chr6:116930113 | G | T | 1 | a0008c0017t0001g0170 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2611+1142G>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930113 | |||||||
| chr6:116930138 | A | C | 1 | a0002c0003t0006g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2611+1167A>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930138 | |||||||
| chr6:116930280 | TAGAC | T | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-1047_2612-104 others(8): Show |
RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr6 | 116930280 | ||||||
| chr6:116930332 | A | G | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(99): Show |
124 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.2612-999A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930332 | |||||||
| chr6:116930363 | AT | A | 91 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(88): Show |
109 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.2612-964delT | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr6 | 116930363 | ||||||
| chr6:116930500 | C | T | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-831C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930500 | |||||||
| chr6:116930554 | A | G | 1 | a0002c0003t0006g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2612-777A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930554 | |||||||
| chr6:116930565 | G | A | 2 | a0001c0002t0002g0221 a0001c0002t0002g0244 |
2 | NA18951.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2612-766G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930565 | |||||||
| chr6:116930707 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0133 a0001c0001t0001g0138 others(5): Show |
11 | NA18962.hp1 NA18972.hp2 NA18981.hp2 others(8): Show |
intron_variant | MODIFIER | c.2612-624C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930707 | |||||||
| chr6:116930724 | A | G | 102 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(99): Show |
124 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.2612-607A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930724 | |||||||
| chr6:116930725 | T | G | 1 | a0002c0003t0006g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2612-606T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930725 | |||||||
| chr6:116930792 | G | C | 2 | a0001c0002t0002g0222 a0001c0002t0002g0223 |
2 | NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2612-539G>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930792 | |||||||
| chr6:116930826 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2612-505C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930826 | |||||||
| chr6:116930928 | T | C | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-403T>C | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930928 | |||||||
| chr6:116930973 | G | A | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-358G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116930973 | |||||||
| chr6:116931034 | C | T | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-297C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931034 | |||||||
| chr6:116931035 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2612-296C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931035 | |||||||
| chr6:116931084 | C | T | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-247C>T | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931084 | |||||||
| chr6:116931085 | G | A | 1 | a0008c0017t0001g0170 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2612-246G>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931085 | |||||||
| chr6:116931178 | A | G | 103 | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0015 others(100): Show |
125 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.2612-153A>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931178 | |||||||
| chr6:116931224 | T | A | 1 | a0001c0001t0007g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2612-107T>A | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931224 | |||||||
| chr6:116931235 | T | G | 1 | a0002c0003t0006g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2612-96T>G | RFX6 | ENSG00000185002.10 | transcript | ENST00000332958.3 | protein_coding | 18/18 | chr6 | 116931235 |