Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91694 |
| ensemblid | ENSG00000154359.13 |
| hgncid | 26302 |
| symbol | LONRF1 |
| name | LON peptidase N-terminal domain and ring finger 1 |
| refseq_nuc | NM_152271.5 |
| refseq_prot | NP_689484.3 |
| ensembl_nuc | ENST00000398246.8 |
| ensembl_prot | ENSP00000381298.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 12721906 |
| end | 12755526 |
| strand | - |
| ver | v1.2 |
| region | chr8:12721906-12755526 |
| region5000 | chr8:12716906-12760526 |
| regionname0 | LONRF1_chr8_12721906_12755526 |
| regionname5000 | LONRF1_chr8_12716906_12760526 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 773 | 386 | 92 | 62 | 177 | 12 | 42 | 141 | LONRF1_chr8_12716906_12760526 | LONRF1 | MSSPA others(768): Show |
chr8 | 12716906 | 12760526 |
| a0002 | 0/0 | 773 | 7 | 0 | 0 | 7 | 0 | 0 | 4 | LONRF1_chr8_12716906_12760526 | LONRF1 | MSSPA others(768): Show |
chr8 | 12716906 | 12760526 |
| a0003 | 0/1 | 773 | 7 | 1 | 5 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | MSSPA others(768): Show |
chr8 | 12716906 | 12760526 |
| a0004 | 0/0 | 773 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | MSSPA others(768): Show |
chr8 | 12716906 | 12760526 |
| a0005 | 0/0 | 773 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | MSSPA others(768): Show |
chr8 | 12716906 | 12760526 |
| a0006 | 0/0 | 773 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | MSSPA others(768): Show |
chr8 | 12716906 | 12760526 |
| a0007 | 0/0 | 773 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | MSSPA others(768): Show |
chr8 | 12716906 | 12760526 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2319 | 373 | 89 | 62 | 169 | 12 | 40 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0001c0004 | 0/0 | 2319 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0001c0005 | 0/0 | 2319 | 3 | 0 | 0 | 1 | 0 | 2 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0001c0006 | 0/0 | 2319 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0001c0007 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0001c0008 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0001c0009 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0001c0012 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0002c0002 | 0/0 | 2319 | 7 | 0 | 0 | 7 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0003c0003 | 0/1 | 2319 | 7 | 1 | 5 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0004c0011 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0005c0014 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0006c0010 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 | ||
| a0007c0013 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | ATGTC others(2314): Show |
chr8 | 12716906 | 12760526 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3618 | 302 | 58 | 59 | 141 | 10 | 34 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0002 | 0/0 | 3620 | 6 | 0 | 1 | 0 | 2 | 3 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3615): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0003 | 0/0 | 3618 | 12 | 0 | 0 | 12 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0004 | 0/0 | 3618 | 11 | 11 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0005 | 0/0 | 3617 | 10 | 0 | 1 | 9 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3612): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0006 | 0/0 | 3618 | 8 | 8 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0007 | 0/0 | 3618 | 5 | 5 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0008 | 0/0 | 3618 | 6 | 0 | 1 | 5 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0009 | 1/0 | 3618 | 4 | 3 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0010 | 0/0 | 3618 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0011 | 0/0 | 3618 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0012 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0013 | 0/0 | 3618 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0014 | 0/0 | 3618 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0015 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0016 | 0/0 | 3618 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0001t0017 | 0/0 | 3618 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0004t0001 | 0/0 | 3618 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0005t0001 | 0/0 | 3618 | 3 | 0 | 0 | 1 | 0 | 2 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0006t0001 | 0/0 | 3618 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0007t0006 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0008t0001 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0009t0001 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0001c0012t0001 | 0/0 | 3618 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0002c0002t0001 | 0/0 | 3618 | 7 | 0 | 0 | 7 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0003c0003t0002 | 0/1 | 3620 | 7 | 1 | 5 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3615): Show |
chr8 | 12716906 | 12760526 |
| a0004c0011t0001 | 0/0 | 3618 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0005c0014t0007 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0006c0010t0001 | 0/0 | 3618 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| a0007c0013t0001 | 0/0 | 3618 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | GTCCG others(3613): Show |
chr8 | 12716906 | 12760526 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 29 | 0 | 5 | 15 | 2 | 7 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0002 | 0/0 | 22 | 0 | 4 | 18 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 6 | 3 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0006 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0023 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0047 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0002g0026 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0003g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0004g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0005g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0005g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0006g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0007g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0008g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0009g0029 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0010g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0011g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0012g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0013g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0014g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0015g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0016g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0001t0017g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0004t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0005t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0005t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0006t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0007t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0008t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0009t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0001c0012t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0002c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0003c0003t0002g0013 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0003c0003t0002g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0003c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0003c0003t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0004c0011t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0005c0014t0007g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0006c0010t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| a0007c0013t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | GBR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0240 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01169 | hp2 | a0003 | c0003 | t0002 | g0013 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01243 | hp1 | a0004 | c0011 | t0001 | g0187 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01255 | hp1 | a0003 | c0003 | t0002 | g0013 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01256 | hp1 | a0003 | c0003 | t0002 | g0013 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0013 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | IBS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0239 | EUR | IBS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01928 | hp2 | a0001 | c0001 | t0008 | g0166 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02055 | hp1 | a0005 | c0014 | t0007 | g0262 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0099 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02165 | hp1 | a0001 | c0005 | t0001 | g0260 | EAS | CDX | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02280 | hp2 | a0001 | c0007 | t0006 | g0052 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | PEL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02523 | hp1 | a0006 | c0010 | t0001 | g0057 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0130 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0228 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0223 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02683 | hp1 | a0001 | c0001 | t0011 | g0051 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0046 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02735 | hp1 | a0001 | c0001 | t0016 | g0065 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02809 | hp2 | a0001 | c0008 | t0001 | g0053 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0129 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0081 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0046 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0074 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03490 | hp2 | a0001 | c0001 | t0017 | g0116 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03710 | hp2 | a0001 | c0005 | t0001 | g0261 | SAS | PJL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | STU | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0108 | AFR | YRI | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0172 | AFR | YRI | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18942 | hp2 | a0001 | c0006 | t0001 | g0050 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18944 | hp2 | a0001 | c0001 | t0013 | g0184 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18963 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18971 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18974 | hp1 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18980 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18992 | hp2 | a0007 | c0013 | t0001 | g0258 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19005 | hp2 | a0001 | c0012 | t0001 | g0199 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19007 | hp1 | a0001 | c0001 | t0008 | g0201 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0154 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19062 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19062 | hp2 | a0001 | c0001 | t0008 | g0131 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19078 | hp1 | a0001 | c0001 | t0014 | g0181 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19091 | hp2 | a0001 | c0006 | t0001 | g0050 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0079 | AFR | YRI | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ASW | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0259 | SAS | GIH | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0096 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG02559 | hp2 | a0003 | c0003 | t0002 | g0236 | AFR | ACB | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03471 | hp1 | a0001 | c0009 | t0001 | g0054 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0107 | AFR | USA | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0029 | AFR | USA | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | LWK | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0002 | g0235 | REF | REF | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0009 | g0029 | REF | REF | LONRF1_chr8_12716906_12760526 | LONRF1 | chr8 | 12716906 | 12760526 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:12731782 | A | T | 1 | a0004 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1642T>A | p.Ser548Thr | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/12 | 1748/3618 | 1642/2322 | 548/773 | chr8 | 12731782 | |||
| chr8:12737133 | T | C | 1 | a0006 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1121A>G | p.Glu374Gly | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 5/12 | 1227/3618 | 1121/2322 | 374/773 | chr8 | 12737133 | |||
| chr8:12743211 | T | A | 1 | a0003 | 6 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(3): Show |
missense_variant | MODERATE | c.793A>T | p.Ile265Leu | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/12 | 899/3618 | 793/2322 | 265/773 | chr8 | 12743211 | |||
| chr8:12754931 | G | A | 1 | a0007 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.490C>T | p.Pro164Ser | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/12 | 596/3618 | 490/2322 | 164/773 | chr8 | 12754931 | |||
| chr8:12755093 | C | T | 2 | a0002 a0006 |
8 | HG00621.hp1 HG02027.hp1 HG02027.hp2 others(5): Show |
missense_variant | MODERATE | c.328G>A | p.Val110Ile | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/12 | 434/3618 | 328/2322 | 110/773 | chr8 | 12755093 | |||
| chr8:12755283 | C | A | 1 | a0005 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.138G>T | p.Glu46Asp | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/12 | 244/3618 | 138/2322 | 46/773 | chr8 | 12755283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:12743242 | T | C | 1 | a0001c0012 | 1 | NA19005.hp2 | synonymous_variant | LOW | c.762A>G | p.Ser254Ser | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/12 | 868/3618 | 762/2322 | 254/773 | chr8 | 12743242 | |||
| chr8:12754722 | G | A | 1 | a0001c0004 | 4 | NA18950.hp2 NA18971.hp1 NA18980.hp1 others(1): Show |
synonymous_variant | LOW | c.699C>T | p.Ala233Ala | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/12 | 805/3618 | 699/2322 | 233/773 | chr8 | 12754722 | |||
| chr8:12755004 | G | A | 1 | a0001c0006 | 2 | NA18942.hp2 NA19091.hp2 |
synonymous_variant | LOW | c.417C>T | p.Gly139Gly | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/12 | 523/3618 | 417/2322 | 139/773 | chr8 | 12755004 | |||
| chr8:12755100 | C | T | 1 | a0001c0009 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.321G>A | p.Ala107Ala | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/12 | 427/3618 | 321/2322 | 107/773 | chr8 | 12755100 | |||
| chr8:12755157 | G | A | 1 | a0001c0005 | 3 | HG02165.hp1 HG03710.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.264C>T | p.Ala88Ala | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/12 | 370/3618 | 264/2322 | 88/773 | chr8 | 12755157 | |||
| chr8:12755223 | G | T | 1 | a0001c0008 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.198C>A | p.Gly66Gly | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/12 | 304/3618 | 198/2322 | 66/773 | chr8 | 12755223 | |||
| chr8:12755256 | C | T | 1 | a0001c0007 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.165G>A | p.Gly55Gly | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/12 | 271/3618 | 165/2322 | 55/773 | chr8 | 12755256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:12721909 | T | A | 1 | a0001c0001t0008 | 6 | HG01928.hp2 NA18963.hp2 NA18969.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1187A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 1187 | chr8 | 12721909 | ||||||
| chr8:12722013 | T | A | 1 | a0001c0001t0015 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1083A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 1083 | chr8 | 12722013 | ||||||
| chr8:12722133 | A | G | 2 | a0001c0001t0007 a0005c0014t0007 |
6 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*963T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 963 | chr8 | 12722133 | ||||||
| chr8:12722215 | AT | A | 1 | a0001c0001t0005 | 10 | HG02056.hp1 HG02300.hp2 NA18963.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*880delA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 880 | chr8 | 12722215 | ||||||
| chr8:12722387 | A | G | 1 | a0001c0001t0014 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*709T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 709 | chr8 | 12722387 | ||||||
| chr8:12722388 | T | A | 1 | a0001c0001t0016 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*708A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 708 | chr8 | 12722388 | ||||||
| chr8:12722540 | G | A | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
397 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(394): Show |
3_prime_UTR_variant | MODIFIER | c.*556C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 556 | chr8 | 12722540 | ||||||
| chr8:12722563 | A | C | 1 | a0001c0001t0004 | 11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*533T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 533 | chr8 | 12722563 | ||||||
| chr8:12722667 | C | T | 1 | a0001c0001t0013 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*429G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 429 | chr8 | 12722667 | ||||||
| chr8:12722783 | C | G | 1 | a0001c0001t0003 | 12 | HG00558.hp2 NA18941.hp1 NA18979.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*313G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 313 | chr8 | 12722783 | ||||||
| chr8:12722784 | G | GCA | 2 | a0001c0001t0002 a0003c0003t0002 |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*310_*311dupTG | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 311 | chr8 | 12722784 | ||||||
| chr8:12722800 | A | T | 2 | a0001c0001t0006 a0001c0007t0006 |
9 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*296T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 296 | chr8 | 12722800 | ||||||
| chr8:12722801 | C | T | 1 | a0001c0001t0012 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*295G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 295 | chr8 | 12722801 | ||||||
| chr8:12722976 | G | A | 1 | a0001c0001t0010 | 2 | NA18522.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*120C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 120 | chr8 | 12722976 | ||||||
| chr8:12723059 | G | A | 1 | a0001c0001t0017 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*37C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 12/12 | 37 | chr8 | 12723059 | ||||||
| chr8:12755464 | C | G | 1 | a0001c0001t0011 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/12 | 44 | chr8 | 12755464 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:12723276 | T | C | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2164-22A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12723276 | |||||||
| chr8:12723319 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2164-65G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12723319 | |||||||
| chr8:12723440 | T | C | 7 | a0001c0001t0002g0026 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.2164-186A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12723440 | |||||||
| chr8:12723607 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2164-353A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12723607 | |||||||
| chr8:12723661 | G | C | 10 | a0001c0001t0001g0094 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2164-407C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12723661 | |||||||
| chr8:12723673 | C | T | 1 | a0001c0001t0003g0249 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2164-419G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12723673 | |||||||
| chr8:12723926 | T | C | 11 | a0001c0001t0003g0049 a0001c0001t0003g0125 a0001c0001t0003g0241 others(8): Show |
12 | HG00558.hp2 NA18941.hp1 NA18979.hp2 others(9): Show |
intron_variant | MODIFIER | c.2164-672A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12723926 | |||||||
| chr8:12723927 | T | C | 9 | a0001c0001t0001g0066 a0001c0001t0004g0004 a0001c0001t0004g0068 others(6): Show |
13 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2164-673A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12723927 | |||||||
| chr8:12724171 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.2164-917A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12724171 | |||||||
| chr8:12724271 | G | C | 11 | a0001c0001t0003g0049 a0001c0001t0003g0125 a0001c0001t0003g0241 others(8): Show |
12 | HG00558.hp2 NA18941.hp1 NA18979.hp2 others(9): Show |
intron_variant | MODIFIER | c.2164-1017C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12724271 | |||||||
| chr8:12724346 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.2164-1092G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12724346 | |||||||
| chr8:12724355 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.2164-1101T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12724355 | |||||||
| chr8:12724381 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2164-1127A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12724381 | |||||||
| chr8:12724412 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2164-1158G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12724412 | |||||||
| chr8:12724686 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2163+1041A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12724686 | |||||||
| chr8:12724780 | T | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0203 |
2 | HG00738.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.2163+947A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12724780 | |||||||
| chr8:12724822 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2163+905C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12724822 | |||||||
| chr8:12725042 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2163+685C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12725042 | |||||||
| chr8:12725194 | T | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.2163+533A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12725194 | |||||||
| chr8:12725356 | A | G | 20 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0061 others(17): Show |
27 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.2163+371T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12725356 | |||||||
| chr8:12725595 | G | A | 1 | a0001c0001t0015g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2163+132C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12725595 | |||||||
| chr8:12725611 | A | T | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2163+116T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12725611 | |||||||
| chr8:12725628 | A | C | 12 | a0001c0001t0001g0250 a0001c0001t0003g0049 a0001c0001t0003g0125 others(9): Show |
13 | HG00558.hp2 NA18941.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.2163+99T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12725628 | |||||||
| chr8:12725634 | G | C | 1 | a0001c0001t0001g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2163+93C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12725634 | |||||||
| chr8:12725695 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2163+32A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 11/11 | chr8 | 12725695 | |||||||
| chr8:12725976 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2011-97C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12725976 | |||||||
| chr8:12726025 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2011-146G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726025 | |||||||
| chr8:12726035 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.2011-156G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726035 | |||||||
| chr8:12726107 | A | T | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-228T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726107 | |||||||
| chr8:12726119 | A | T | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-240T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726119 | |||||||
| chr8:12726131 | C | A | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-252G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726131 | |||||||
| chr8:12726132 | C | T | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-253G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726132 | |||||||
| chr8:12726133 | C | T | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-254G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726133 | |||||||
| chr8:12726135 | A | G | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-256T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726135 | |||||||
| chr8:12726136 | C | G | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-257G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726136 | |||||||
| chr8:12726138 | A | T | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-259T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726138 | |||||||
| chr8:12726139 | C | T | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-260G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726139 | |||||||
| chr8:12726140 | A | G | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-261T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726140 | |||||||
| chr8:12726143 | C | T | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-264G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726143 | |||||||
| chr8:12726145 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.2011-266A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726145 | |||||||
| chr8:12726146 | C | A | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-267G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726146 | |||||||
| chr8:12726147 | A | T | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-268T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726147 | |||||||
| chr8:12726152 | G | A | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-273C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726152 | |||||||
| chr8:12726156 | G | T | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-277C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726156 | |||||||
| chr8:12726174 | G | T | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2011-295C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726174 | |||||||
| chr8:12726288 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2011-409A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726288 | |||||||
| chr8:12726294 | G | C | 6 | a0001c0001t0002g0026 a0001c0001t0002g0238 a0001c0001t0002g0239 others(3): Show |
11 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.2011-415C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726294 | |||||||
| chr8:12726297 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0015g0074 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2011-418A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726297 | |||||||
| chr8:12726583 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
99 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2011-704A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726583 | |||||||
| chr8:12726651 | C | T | 1 | a0001c0001t0015g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2011-772G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726651 | |||||||
| chr8:12726674 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2011-795A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726674 | |||||||
| chr8:12726736 | A | G | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2011-857T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726736 | |||||||
| chr8:12726745 | T | C | 9 | a0001c0001t0001g0066 a0001c0001t0004g0004 a0001c0001t0004g0068 others(6): Show |
13 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2011-866A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726745 | |||||||
| chr8:12726841 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.2011-962T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726841 | |||||||
| chr8:12726938 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2011-1059T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726938 | |||||||
| chr8:12726950 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2011-1071A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12726950 | |||||||
| chr8:12727119 | C | CT | 78 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
124 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.2011-1241dupA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727119 | |||||||
| chr8:12727119 | C | CTT | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(103): Show |
178 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2011-1242_2011-124 others(6): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727119 | |||||||
| chr8:12727119 | C | CTTT | 7 | a0001c0001t0001g0111 a0001c0001t0001g0123 a0001c0001t0001g0126 others(4): Show |
7 | HG00609.hp2 HG02895.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2011-1243_2011-124 others(7): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727119 | |||||||
| chr8:12727119 | CT | C | 38 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0030 others(35): Show |
48 | HG00558.hp2 HG00741.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.2011-1241delA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727119 | |||||||
| chr8:12727119 | CTT | C | 10 | a0001c0001t0001g0028 a0001c0001t0001g0075 a0001c0001t0001g0219 others(7): Show |
16 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.2011-1242_2011-124 others(6): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727119 | |||||||
| chr8:12727121 | T | A | 1 | a0001c0001t0003g0244 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2011-1242A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727121 | |||||||
| chr8:12727122 | T | A | 11 | a0001c0001t0001g0250 a0001c0001t0003g0049 a0001c0001t0003g0125 others(8): Show |
12 | HG00558.hp2 NA18941.hp1 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.2011-1243A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727122 | |||||||
| chr8:12727150 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2011-1271G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727150 | |||||||
| chr8:12727150 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.2011-1271G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727150 | |||||||
| chr8:12727187 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2011-1308G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727187 | |||||||
| chr8:12727192 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2011-1313C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727192 | |||||||
| chr8:12727204 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2011-1325A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727204 | |||||||
| chr8:12727262 | ACG | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
8 | HG02602.hp1 NA18969.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2011-1385_2011-138 others(6): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727262 | |||||||
| chr8:12727269 | T | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
8 | HG02602.hp1 NA18969.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2011-1390A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727269 | |||||||
| chr8:12727272 | A | AGC | 6 | a0001c0001t0001g0022 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
8 | HG02602.hp1 NA18969.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2011-1394_2011-139 others(6): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727272 | |||||||
| chr8:12727419 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2010+1482A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727419 | |||||||
| chr8:12727478 | C | CATT | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
394 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.2010+1422_2010+142 others(7): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727478 | |||||||
| chr8:12727487 | A | T | 12 | a0001c0001t0001g0250 a0001c0001t0003g0049 a0001c0001t0003g0125 others(9): Show |
13 | HG00558.hp2 NA18941.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.2010+1414T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727487 | |||||||
| chr8:12727504 | T | G | 1 | a0001c0001t0001g0133 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2010+1397A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727504 | |||||||
| chr8:12727513 | C | A | 7 | a0001c0001t0002g0026 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.2010+1388G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727513 | |||||||
| chr8:12727525 | G | A | 1 | a0001c0001t0004g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2010+1376C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727525 | |||||||
| chr8:12727600 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2010+1301A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727600 | |||||||
| chr8:12727652 | A | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.2010+1249T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727652 | |||||||
| chr8:12727684 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2010+1217T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727684 | |||||||
| chr8:12727746 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2010+1155T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727746 | |||||||
| chr8:12727826 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2010+1075A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727826 | |||||||
| chr8:12727927 | C | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.2010+974G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727927 | |||||||
| chr8:12727972 | G | A | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2010+929C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727972 | |||||||
| chr8:12727999 | A | C | 1 | a0001c0001t0001g0059 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2010+902T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12727999 | |||||||
| chr8:12728177 | A | T | 1 | a0001c0001t0013g0184 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2010+724T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12728177 | |||||||
| chr8:12728211 | C | T | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2010+690G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12728211 | |||||||
| chr8:12728316 | A | G | 6 | a0001c0001t0001g0091 a0001c0001t0001g0135 a0001c0001t0001g0253 others(3): Show |
6 | HG02258.hp1 HG02615.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010+585T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12728316 | |||||||
| chr8:12728316 | A | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(118): Show |
193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2010+585T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12728316 | |||||||
| chr8:12728436 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2010+465T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12728436 | |||||||
| chr8:12728445 | A | T | 3 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0005c0014t0007g0262 |
3 | HG02055.hp1 HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2010+456T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12728445 | |||||||
| chr8:12728584 | A | G | 37 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0061 others(34): Show |
44 | HG00558.hp2 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.2010+317T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12728584 | |||||||
| chr8:12728752 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(117): Show |
183 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2010+149T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12728752 | |||||||
| chr8:12728755 | A | C | 7 | a0001c0001t0002g0026 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.2010+146T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12728755 | |||||||
| chr8:12728815 | T | G | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2010+86A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 10/11 | chr8 | 12728815 | |||||||
| chr8:12729084 | G | T | 6 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(3): Show |
10 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1848-21C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 9/11 | chr8 | 12729084 | |||||||
| chr8:12729120 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1847+54G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 9/11 | chr8 | 12729120 | |||||||
| chr8:12729450 | A | G | 12 | a0001c0001t0001g0250 a0001c0001t0003g0049 a0001c0001t0003g0125 others(9): Show |
13 | HG00558.hp2 NA18941.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.1689-118T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12729450 | |||||||
| chr8:12729511 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689-179C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12729511 | |||||||
| chr8:12729592 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0149 |
5 | HG02132.hp1 NA18968.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1689-260C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12729592 | |||||||
| chr8:12729803 | G | C | 13 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0045 others(10): Show |
20 | HG00741.hp1 HG02056.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.1689-471C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12729803 | |||||||
| chr8:12729820 | T | C | 7 | a0001c0001t0002g0026 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1689-488A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12729820 | |||||||
| chr8:12729871 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0152 |
2 | NA18982.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1689-539A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12729871 | |||||||
| chr8:12729881 | G | A | 13 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0045 others(10): Show |
20 | HG00741.hp1 HG02056.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.1689-549C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12729881 | |||||||
| chr8:12729986 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1689-654T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12729986 | |||||||
| chr8:12730059 | T | C | 21 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0061 others(18): Show |
28 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1689-727A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730059 | |||||||
| chr8:12730080 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1689-748G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730080 | |||||||
| chr8:12730175 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1689-843G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730175 | |||||||
| chr8:12730203 | A | T | 2 | a0001c0001t0001g0066 a0001c0009t0001g0054 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1689-871T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730203 | |||||||
| chr8:12730353 | T | A | 19 | a0001c0001t0001g0250 a0001c0001t0002g0026 a0001c0001t0002g0237 others(16): Show |
25 | HG00558.hp2 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1689-1021A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730353 | |||||||
| chr8:12730358 | G | A | 1 | a0001c0001t0015g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1689-1026C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730358 | |||||||
| chr8:12730727 | T | C | 1 | a0001c0001t0007g0095 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1688+1009A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730727 | |||||||
| chr8:12730774 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
366 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.1688+962T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730774 | |||||||
| chr8:12730785 | C | T | 1 | a0001c0001t0005g0033 | 2 | NA18963.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1688+951G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730785 | |||||||
| chr8:12730840 | A | C | 1 | a0001c0001t0001g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1688+896T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730840 | |||||||
| chr8:12730847 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1688+889T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730847 | |||||||
| chr8:12730887 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0005g0154 |
2 | NA19004.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1688+849T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730887 | |||||||
| chr8:12730913 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1688+823G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730913 | |||||||
| chr8:12730981 | A | C | 1 | a0001c0001t0004g0213 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1688+755T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12730981 | |||||||
| chr8:12731325 | C | T | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1688+411G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12731325 | |||||||
| chr8:12731379 | C | CCTCA | 12 | a0001c0001t0001g0250 a0001c0001t0003g0049 a0001c0001t0003g0125 others(9): Show |
13 | HG00558.hp2 NA18941.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.1688+353_1688+356d others(6): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12731379 | |||||||
| chr8:12731409 | CAT | C | 12 | a0001c0001t0001g0250 a0001c0001t0003g0049 a0001c0001t0003g0125 others(9): Show |
13 | HG00558.hp2 NA18941.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.1688+325_1688+326d others(4): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12731409 | |||||||
| chr8:12731670 | C | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(117): Show |
195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1688+66G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 8/11 | chr8 | 12731670 | |||||||
| chr8:12731868 | A | G | 2 | a0001c0001t0001g0066 a0001c0009t0001g0054 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1567-11T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12731868 | |||||||
| chr8:12731970 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1567-113A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12731970 | |||||||
| chr8:12732129 | G | T | 6 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(3): Show |
10 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1567-272C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732129 | |||||||
| chr8:12732253 | TTTGCCTT others(1181): Show |
T | 1 | a0001c0001t0004g0070 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1567-1584_1567-397 others(3): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732253 | |||||||
| chr8:12732303 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0161 others(2): Show |
6 | HG00741.hp2 HG02683.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567-446G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732303 | |||||||
| chr8:12732408 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0015g0074 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1567-551G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732408 | |||||||
| chr8:12732469 | T | C | 1 | a0001c0001t0008g0021 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1567-612A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732469 | |||||||
| chr8:12732479 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1567-622G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732479 | |||||||
| chr8:12732497 | A | G | 1 | a0001c0001t0003g0244 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1567-640T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732497 | |||||||
| chr8:12732535 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1567-678G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732535 | |||||||
| chr8:12732582 | C | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02129.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1567-725G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732582 | |||||||
| chr8:12732600 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0127 a0001c0001t0001g0132 others(1): Show |
4 | HG00733.hp1 HG01168.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567-743A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732600 | |||||||
| chr8:12732610 | G | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.1567-753C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732610 | |||||||
| chr8:12732627 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1567-770A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732627 | |||||||
| chr8:12732730 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1567-873C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732730 | |||||||
| chr8:12732828 | G | C | 1 | a0001c0001t0001g0205 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1567-971C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732828 | |||||||
| chr8:12732853 | T | C | 1 | a0001c0001t0001g0028 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1567-996A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732853 | |||||||
| chr8:12732903 | T | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
8 | HG02129.hp1 HG02615.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567-1046A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12732903 | |||||||
| chr8:12733015 | T | C | 4 | a0001c0001t0001g0094 a0001c0001t0007g0095 a0001c0001t0007g0096 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567-1158A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733015 | |||||||
| chr8:12733028 | G | A | 2 | a0001c0001t0004g0004 a0001c0001t0004g0228 |
2 | HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1567-1171C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733028 | |||||||
| chr8:12733060 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(110): Show |
181 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1567-1203C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733060 | |||||||
| chr8:12733099 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1567-1242A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733099 | |||||||
| chr8:12733112 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1567-1255T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733112 | |||||||
| chr8:12733302 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1567-1445A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733302 | |||||||
| chr8:12733305 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1567-1448T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733305 | |||||||
| chr8:12733323 | A | C | 3 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0005c0014t0007g0262 |
3 | HG02055.hp1 HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1567-1466T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733323 | |||||||
| chr8:12733328 | ATG | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.1567-1473_1567-147 others(6): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733328 | |||||||
| chr8:12733483 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1567-1626T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733483 | |||||||
| chr8:12733519 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1567-1662C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733519 | |||||||
| chr8:12733588 | ATATAATA others(4): Show |
A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1566+1687_1566+169 others(15): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733588 | |||||||
| chr8:12733590 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1566+1696T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733590 | |||||||
| chr8:12733601 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1566+1685G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733601 | |||||||
| chr8:12733657 | G | T | 1 | a0001c0001t0001g0072 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1566+1629C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733657 | |||||||
| chr8:12733729 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1566+1557C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733729 | |||||||
| chr8:12733886 | G | A | 3 | a0001c0001t0002g0026 a0001c0001t0002g0238 a0001c0001t0002g0239 |
5 | HG01515.hp2 HG01517.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1566+1400C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733886 | |||||||
| chr8:12733897 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1566+1389C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733897 | |||||||
| chr8:12733922 | G | T | 11 | a0001c0001t0001g0250 a0001c0001t0003g0049 a0001c0001t0003g0125 others(8): Show |
12 | HG00558.hp2 NA18941.hp1 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.1566+1364C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733922 | |||||||
| chr8:12733962 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1566+1324A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12733962 | |||||||
| chr8:12734005 | T | C | 1 | a0001c0001t0003g0251 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1566+1281A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734005 | |||||||
| chr8:12734030 | C | T | 12 | a0001c0001t0001g0250 a0001c0001t0003g0049 a0001c0001t0003g0125 others(9): Show |
13 | HG00558.hp2 NA18941.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.1566+1256G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734030 | |||||||
| chr8:12734078 | A | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1566+1208T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734078 | |||||||
| chr8:12734079 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1566+1207T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734079 | |||||||
| chr8:12734214 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1566+1072G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734214 | |||||||
| chr8:12734262 | A | AT | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1566+1023dupA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734262 | |||||||
| chr8:12734405 | G | T | 1 | a0001c0001t0001g0038 | 2 | HG00639.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1566+881C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734405 | |||||||
| chr8:12734435 | A | G | 2 | a0001c0001t0001g0066 a0001c0009t0001g0054 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1566+851T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734435 | |||||||
| chr8:12734436 | T | A | 2 | a0001c0001t0001g0066 a0001c0009t0001g0054 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1566+850A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734436 | |||||||
| chr8:12734439 | C | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.1566+847G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734439 | |||||||
| chr8:12734508 | G | C | 2 | a0001c0001t0001g0066 a0001c0009t0001g0054 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1566+778C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734508 | |||||||
| chr8:12734559 | T | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0064 others(2): Show |
6 | HG02615.hp1 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1566+727A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734559 | |||||||
| chr8:12734773 | T | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0144 a0001c0001t0001g0153 others(3): Show |
7 | NA18955.hp1 NA18975.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.1566+513A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734773 | |||||||
| chr8:12734780 | T | G | 3 | a0001c0005t0001g0259 a0001c0005t0001g0260 a0001c0005t0001g0261 |
3 | HG02165.hp1 HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1566+506A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734780 | |||||||
| chr8:12734828 | T | C | 1 | a0001c0001t0003g0125 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1566+458A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734828 | |||||||
| chr8:12734855 | T | C | 2 | a0001c0001t0001g0066 a0001c0009t0001g0054 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1566+431A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734855 | |||||||
| chr8:12734999 | T | C | 13 | a0001c0001t0001g0243 a0001c0001t0001g0250 a0001c0001t0003g0049 others(10): Show |
14 | HG00558.hp2 NA18941.hp1 NA18949.hp2 others(11): Show |
intron_variant | MODIFIER | c.1566+287A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12734999 | |||||||
| chr8:12735000 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1566+286A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12735000 | |||||||
| chr8:12735161 | T | A | 1 | a0001c0001t0001g0028 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1566+125A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12735161 | |||||||
| chr8:12735261 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1566+25T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 7/11 | chr8 | 12735261 | |||||||
| chr8:12735447 | C | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1452-47G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12735447 | |||||||
| chr8:12735506 | G | C | 1 | a0001c0001t0001g0028 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1452-106C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12735506 | |||||||
| chr8:12735536 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1452-136T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12735536 | |||||||
| chr8:12735841 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1452-441A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12735841 | |||||||
| chr8:12735860 | T | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
91 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1452-460A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12735860 | |||||||
| chr8:12735920 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(40): Show |
82 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1452-520G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12735920 | |||||||
| chr8:12735971 | T | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0064 others(2): Show |
6 | HG02615.hp1 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1452-571A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12735971 | |||||||
| chr8:12736010 | T | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0064 others(2): Show |
6 | HG02615.hp1 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1452-610A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12736010 | |||||||
| chr8:12736111 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.1451+590A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12736111 | |||||||
| chr8:12736242 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0137 a0001c0001t0001g0139 |
4 | HG00639.hp2 HG01891.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1451+459A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12736242 | |||||||
| chr8:12736288 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1451+413A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12736288 | |||||||
| chr8:12736422 | T | C | 3 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0005c0014t0007g0262 |
3 | HG02055.hp1 HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1451+279A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12736422 | |||||||
| chr8:12736502 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1451+199A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12736502 | |||||||
| chr8:12736506 | T | C | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1451+195A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12736506 | |||||||
| chr8:12736602 | TTG | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0149 |
5 | HG02132.hp1 NA18968.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1451+97_1451+98del others(2): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12736602 | |||||||
| chr8:12736643 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1451+58C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12736643 | |||||||
| chr8:12736652 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1451+49A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 6/11 | chr8 | 12736652 | |||||||
| chr8:12736846 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1355-49C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 5/11 | chr8 | 12736846 | |||||||
| chr8:12737150 | T | C | 1 | a0001c0001t0005g0115 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1114-10A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 4/11 | chr8 | 12737150 | |||||||
| chr8:12737201 | C | A | 2 | a0001c0001t0007g0095 a0001c0001t0007g0096 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1114-61G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 4/11 | chr8 | 12737201 | |||||||
| chr8:12737299 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1114-159C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 4/11 | chr8 | 12737299 | |||||||
| chr8:12737325 | C | T | 1 | a0001c0001t0008g0131 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1114-185G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 4/11 | chr8 | 12737325 | |||||||
| chr8:12737457 | T | C | 1 | a0001c0001t0001g0028 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1114-317A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 4/11 | chr8 | 12737457 | |||||||
| chr8:12737627 | T | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0091 a0001c0001t0015g0074 |
3 | HG02258.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1113+368A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 4/11 | chr8 | 12737627 | |||||||
| chr8:12737656 | T | A | 1 | a0001c0001t0003g0246 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1113+339A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 4/11 | chr8 | 12737656 | |||||||
| chr8:12737665 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1113+330T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 4/11 | chr8 | 12737665 | |||||||
| chr8:12737789 | G | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(52): Show |
104 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1113+206C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 4/11 | chr8 | 12737789 | |||||||
| chr8:12738198 | A | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0157 a0001c0001t0001g0209 |
7 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-54T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738198 | |||||||
| chr8:12738221 | A | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0091 a0001c0001t0015g0074 |
3 | HG02258.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.964-77T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738221 | |||||||
| chr8:12738227 | T | C | 3 | a0001c0005t0001g0259 a0001c0005t0001g0260 a0001c0005t0001g0261 |
3 | HG02165.hp1 HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.964-83A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738227 | |||||||
| chr8:12738239 | T | G | 1 | a0001c0001t0007g0223 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.964-95A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738239 | |||||||
| chr8:12738314 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.964-170A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738314 | |||||||
| chr8:12738386 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0001g0117 others(1): Show |
6 | HG00423.hp1 HG00673.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-242T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738386 | |||||||
| chr8:12738446 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.964-302T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738446 | |||||||
| chr8:12738479 | G | C | 1 | a0001c0001t0008g0166 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.964-335C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738479 | |||||||
| chr8:12738504 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.964-360C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738504 | |||||||
| chr8:12738751 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.964-607G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738751 | |||||||
| chr8:12738837 | T | C | 1 | a0001c0001t0004g0070 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.964-693A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738837 | |||||||
| chr8:12738847 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0015g0074 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.964-703A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738847 | |||||||
| chr8:12738901 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0015g0074 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.964-757G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12738901 | |||||||
| chr8:12739081 | ATAAAT | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0137 a0001c0001t0001g0139 |
4 | HG00639.hp2 HG01891.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-942_964-938del others(5): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739081 | |||||||
| chr8:12739165 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-1021T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739165 | |||||||
| chr8:12739200 | T | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
9 | HG02129.hp1 HG02615.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.964-1056A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739200 | |||||||
| chr8:12739209 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.964-1065C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739209 | |||||||
| chr8:12739273 | T | C | 2 | a0001c0001t0003g0245 a0001c0001t0003g0247 |
2 | NA18979.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.964-1129A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739273 | |||||||
| chr8:12739274 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.964-1130C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739274 | |||||||
| chr8:12739341 | CA | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.964-1198delT | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739341 | |||||||
| chr8:12739353 | A | C | 1 | a0001c0001t0015g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.964-1209T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739353 | |||||||
| chr8:12739417 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-1273T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739417 | |||||||
| chr8:12739440 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.964-1296T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739440 | |||||||
| chr8:12739535 | C | G | 7 | a0001c0001t0002g0026 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+1339G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739535 | |||||||
| chr8:12739545 | TG | T | 10 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0001g0094 others(7): Show |
11 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.963+1328delC | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739545 | |||||||
| chr8:12739693 | T | C | 1 | a0001c0001t0001g0028 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.963+1181A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739693 | |||||||
| chr8:12739922 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+952G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739922 | |||||||
| chr8:12739939 | G | A | 1 | a0001c0001t0017g0116 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.963+935C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12739939 | |||||||
| chr8:12740134 | G | C | 1 | a0001c0001t0001g0028 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.963+740C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12740134 | |||||||
| chr8:12740243 | A | T | 3 | a0001c0005t0001g0259 a0001c0005t0001g0260 a0001c0005t0001g0261 |
3 | HG02165.hp1 HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.963+631T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12740243 | |||||||
| chr8:12740264 | G | C | 3 | a0001c0005t0001g0259 a0001c0005t0001g0260 a0001c0005t0001g0261 |
3 | HG02165.hp1 HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.963+610C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12740264 | |||||||
| chr8:12740411 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.963+463G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12740411 | |||||||
| chr8:12740453 | G | T | 1 | a0001c0001t0001g0232 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+421C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12740453 | |||||||
| chr8:12740468 | C | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.963+406G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12740468 | |||||||
| chr8:12740623 | A | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.963+251T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12740623 | |||||||
| chr8:12740679 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.963+195A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12740679 | |||||||
| chr8:12740717 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.963+157C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 3/11 | chr8 | 12740717 | |||||||
| chr8:12741099 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.841-103G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741099 | |||||||
| chr8:12741158 | T | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
9 | HG02129.hp1 HG02615.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.841-162A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741158 | |||||||
| chr8:12741246 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.841-250G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741246 | |||||||
| chr8:12741253 | A | G | 13 | a0001c0001t0001g0230 a0001c0001t0001g0243 a0001c0001t0001g0250 others(10): Show |
14 | HG00558.hp2 NA18949.hp2 NA18955.hp2 others(11): Show |
intron_variant | MODIFIER | c.841-257T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741253 | |||||||
| chr8:12741305 | A | T | 3 | a0001c0005t0001g0259 a0001c0005t0001g0260 a0001c0005t0001g0261 |
3 | HG02165.hp1 HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.841-309T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741305 | |||||||
| chr8:12741345 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.841-349T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741345 | |||||||
| chr8:12741442 | T | C | 1 | a0001c0001t0003g0246 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.841-446A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741442 | |||||||
| chr8:12741533 | A | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0032 others(18): Show |
31 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.841-537T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741533 | |||||||
| chr8:12741573 | A | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.841-577T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741573 | |||||||
| chr8:12741603 | T | C | 14 | a0001c0001t0001g0066 a0001c0001t0001g0243 a0001c0001t0001g0250 others(11): Show |
15 | HG00558.hp2 HG02145.hp1 HG03471.hp1 others(12): Show |
intron_variant | MODIFIER | c.841-607A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741603 | |||||||
| chr8:12741762 | A | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.841-766T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741762 | |||||||
| chr8:12741774 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.841-778C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741774 | |||||||
| chr8:12741954 | T | C | 12 | a0001c0001t0001g0243 a0001c0001t0001g0250 a0001c0001t0003g0049 others(9): Show |
13 | HG00558.hp2 NA18949.hp2 NA18979.hp2 others(10): Show |
intron_variant | MODIFIER | c.841-958A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741954 | |||||||
| chr8:12741958 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.841-962A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741958 | |||||||
| chr8:12741960 | T | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
8 | HG02129.hp1 HG02615.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-964A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12741960 | |||||||
| chr8:12742097 | C | T | 1 | a0001c0001t0006g0107 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.840+1067G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742097 | |||||||
| chr8:12742247 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.840+917C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742247 | |||||||
| chr8:12742261 | C | T | 10 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0001g0094 others(7): Show |
11 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.840+903G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742261 | |||||||
| chr8:12742270 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.840+894G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742270 | |||||||
| chr8:12742338 | T | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
9 | HG02129.hp1 HG02615.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.840+826A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742338 | |||||||
| chr8:12742394 | T | C | 1 | a0006c0010t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.840+770A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742394 | |||||||
| chr8:12742541 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG01192.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.840+623G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742541 | |||||||
| chr8:12742565 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.840+599T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742565 | |||||||
| chr8:12742713 | A | T | 1 | a0001c0001t0015g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.840+451T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742713 | |||||||
| chr8:12742746 | A | AT | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.840+417dupA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742746 | |||||||
| chr8:12742812 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.840+352T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742812 | |||||||
| chr8:12742839 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0015g0074 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.840+325G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742839 | |||||||
| chr8:12742969 | G | A | 1 | a0001c0009t0001g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.840+195C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12742969 | |||||||
| chr8:12743087 | T | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0035 others(9): Show |
23 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.840+77A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12743087 | |||||||
| chr8:12743088 | T | G | 1 | a0001c0001t0008g0131 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.840+76A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12743088 | |||||||
| chr8:12743097 | T | A | 6 | a0001c0001t0002g0026 a0001c0001t0002g0238 a0001c0001t0002g0239 others(3): Show |
11 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.840+67A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12743097 | |||||||
| chr8:12743113 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.840+51G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 2/11 | chr8 | 12743113 | |||||||
| chr8:12743391 | T | C | 2 | a0001c0001t0001g0066 a0001c0009t0001g0054 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.722-109A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12743391 | |||||||
| chr8:12743447 | G | C | 10 | a0001c0001t0001g0073 a0001c0001t0001g0091 a0001c0001t0004g0004 others(7): Show |
14 | HG01884.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.722-165C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12743447 | |||||||
| chr8:12743481 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.722-199A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12743481 | |||||||
| chr8:12743525 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.722-243G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12743525 | |||||||
| chr8:12743529 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.722-247T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12743529 | |||||||
| chr8:12743646 | A | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.722-364T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12743646 | |||||||
| chr8:12743716 | T | C | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.722-434A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12743716 | |||||||
| chr8:12743757 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.722-475A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12743757 | |||||||
| chr8:12743805 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.722-523C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12743805 | |||||||
| chr8:12743857 | AT | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.722-576delA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12743857 | |||||||
| chr8:12743899 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.722-617C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12743899 | |||||||
| chr8:12744256 | C | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.722-974G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744256 | |||||||
| chr8:12744400 | G | C | 1 | a0001c0001t0015g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.722-1118C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744400 | |||||||
| chr8:12744431 | C | T | 4 | a0001c0001t0001g0106 a0001c0001t0005g0017 a0001c0001t0005g0098 others(1): Show |
6 | HG02056.hp1 NA18989.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.722-1149G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744431 | |||||||
| chr8:12744462 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.722-1180A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744462 | |||||||
| chr8:12744546 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.722-1264A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744546 | |||||||
| chr8:12744568 | A | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(65): Show |
95 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.722-1286T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744568 | |||||||
| chr8:12744672 | G | C | 16 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(13): Show |
21 | HG01884.hp2 HG02129.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.722-1390C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744672 | |||||||
| chr8:12744722 | T | G | 10 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
11 | HG02129.hp1 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.722-1440A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744722 | |||||||
| chr8:12744741 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.722-1459T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744741 | |||||||
| chr8:12744796 | G | C | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.722-1514C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744796 | |||||||
| chr8:12744808 | C | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
8 | HG02129.hp1 HG02615.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.722-1526G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744808 | |||||||
| chr8:12744862 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.722-1580T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744862 | |||||||
| chr8:12744876 | A | AT | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.722-1595dupA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744876 | |||||||
| chr8:12744876 | A | T | 8 | a0001c0001t0001g0145 a0001c0001t0001g0158 a0001c0001t0002g0026 others(5): Show |
13 | HG00423.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.722-1594T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744876 | |||||||
| chr8:12744921 | C | CT | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.722-1640dupA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12744921 | |||||||
| chr8:12745016 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.722-1734C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745016 | |||||||
| chr8:12745032 | G | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.722-1750C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745032 | |||||||
| chr8:12745083 | C | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02486.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.722-1801G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745083 | |||||||
| chr8:12745091 | AG | A | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.722-1810delC | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745091 | |||||||
| chr8:12745093 | C | T | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.722-1811G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745093 | |||||||
| chr8:12745135 | C | T | 12 | a0001c0001t0001g0243 a0001c0001t0001g0250 a0001c0001t0003g0049 others(9): Show |
13 | HG00558.hp2 NA18949.hp2 NA18979.hp2 others(10): Show |
intron_variant | MODIFIER | c.722-1853G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745135 | |||||||
| chr8:12745140 | T | A | 1 | a0001c0001t0001g0200 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.722-1858A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745140 | |||||||
| chr8:12745319 | T | C | 9 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
10 | HG02129.hp1 HG02145.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.722-2037A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745319 | |||||||
| chr8:12745321 | GA | G | 17 | a0001c0001t0001g0064 a0001c0001t0001g0243 a0001c0001t0001g0250 others(14): Show |
22 | HG00558.hp2 HG01884.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.722-2040delT | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745321 | |||||||
| chr8:12745321 | GAA | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(3): Show |
7 | HG02129.hp1 HG02615.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.722-2041_722-2040d others(4): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745321 | |||||||
| chr8:12745321 | GAAAA | G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0040 others(18): Show |
27 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.722-2043_722-2040d others(6): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745321 | |||||||
| chr8:12745321 | GAAAAA | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.722-2044_722-2040d others(7): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745321 | |||||||
| chr8:12745321 | GAAAAAA | G | 38 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0032 others(35): Show |
49 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.722-2045_722-2040d others(8): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745321 | |||||||
| chr8:12745327 | A | G | 1 | a0001c0001t0006g0103 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.722-2045T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745327 | |||||||
| chr8:12745390 | A | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02129.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.722-2108T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745390 | |||||||
| chr8:12745391 | G | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
6 | NA18941.hp1 NA18944.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.722-2109C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745391 | |||||||
| chr8:12745391 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.722-2109C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745391 | |||||||
| chr8:12745405 | C | CACTT | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.722-2124_722-2123i others(6): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745405 | |||||||
| chr8:12745426 | C | T | 1 | a0001c0001t0006g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.722-2144G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745426 | |||||||
| chr8:12745460 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.722-2178T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745460 | |||||||
| chr8:12745548 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0230 |
2 | HG02132.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.722-2266T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745548 | |||||||
| chr8:12745550 | A | C | 1 | a0001c0001t0001g0212 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.722-2268T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745550 | |||||||
| chr8:12745567 | T | C | 6 | a0001c0001t0002g0026 a0001c0001t0002g0238 a0001c0001t0002g0239 others(3): Show |
11 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.722-2285A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745567 | |||||||
| chr8:12745599 | C | A | 13 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0032 others(10): Show |
20 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.722-2317G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745599 | |||||||
| chr8:12745680 | C | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.722-2398G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745680 | |||||||
| chr8:12745696 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.722-2414A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745696 | |||||||
| chr8:12745734 | A | G | 1 | a0001c0001t0001g0012 | 4 | HG00741.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-2452T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745734 | |||||||
| chr8:12745846 | A | G | 1 | a0001c0001t0001g0042 | 2 | NA18952.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.722-2564T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745846 | |||||||
| chr8:12745963 | T | C | 6 | a0001c0001t0002g0026 a0001c0001t0002g0238 a0001c0001t0002g0239 others(3): Show |
11 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.722-2681A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12745963 | |||||||
| chr8:12746008 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.722-2726A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746008 | |||||||
| chr8:12746036 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0220 |
5 | HG00741.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.722-2754A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746036 | |||||||
| chr8:12746068 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.722-2786G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746068 | |||||||
| chr8:12746102 | A | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.722-2820T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746102 | |||||||
| chr8:12746209 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.722-2927T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746209 | |||||||
| chr8:12746449 | G | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.722-3167C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746449 | |||||||
| chr8:12746542 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.722-3260A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746542 | |||||||
| chr8:12746555 | C | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0032 others(15): Show |
27 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.722-3273G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746555 | |||||||
| chr8:12746713 | TG | T | 6 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(3): Show |
10 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.722-3432delC | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746713 | |||||||
| chr8:12746730 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.722-3448T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746730 | |||||||
| chr8:12746774 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.722-3492T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746774 | |||||||
| chr8:12746783 | T | C | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG01255.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.722-3501A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746783 | |||||||
| chr8:12746852 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.722-3570C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746852 | |||||||
| chr8:12746900 | C | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.722-3618G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746900 | |||||||
| chr8:12746919 | C | A | 1 | a0001c0001t0001g0041 | 2 | HG02129.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.722-3637G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746919 | |||||||
| chr8:12746929 | T | C | 7 | a0001c0001t0002g0026 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.722-3647A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746929 | |||||||
| chr8:12746983 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.722-3701T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12746983 | |||||||
| chr8:12747038 | T | G | 12 | a0001c0001t0001g0243 a0001c0001t0001g0250 a0001c0001t0003g0049 others(9): Show |
13 | HG00558.hp2 NA18949.hp2 NA18979.hp2 others(10): Show |
intron_variant | MODIFIER | c.722-3756A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747038 | |||||||
| chr8:12747066 | T | C | 1 | a0002c0002t0001g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.722-3784A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747066 | |||||||
| chr8:12747085 | A | G | 6 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(3): Show |
10 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.722-3803T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747085 | |||||||
| chr8:12747182 | G | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.722-3900C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747182 | |||||||
| chr8:12747237 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.722-3955C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747237 | |||||||
| chr8:12747295 | TTCTA | T | 12 | a0001c0001t0001g0243 a0001c0001t0001g0250 a0001c0001t0003g0049 others(9): Show |
13 | HG00558.hp2 NA18949.hp2 NA18979.hp2 others(10): Show |
intron_variant | MODIFIER | c.722-4017_722-4014d others(6): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747295 | |||||||
| chr8:12747322 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.722-4040A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747322 | |||||||
| chr8:12747538 | A | C | 1 | a0001c0001t0005g0099 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.722-4256T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747538 | |||||||
| chr8:12747618 | TA | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
101 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.722-4337delT | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747618 | |||||||
| chr8:12747666 | T | C | 1 | a0001c0001t0001g0012 | 4 | HG00741.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.722-4384A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747666 | |||||||
| chr8:12747688 | C | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
9 | HG02129.hp1 HG02615.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.722-4406G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747688 | |||||||
| chr8:12747707 | CAG | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
9 | HG02129.hp1 HG02615.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.722-4427_722-4426d others(4): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747707 | |||||||
| chr8:12747715 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.722-4433C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747715 | |||||||
| chr8:12747752 | CTCTCT | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.722-4475_722-4471d others(7): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747752 | |||||||
| chr8:12747754 | C | G | 6 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(3): Show |
10 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.722-4472G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747754 | |||||||
| chr8:12747756 | CT | C | 62 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0028 others(59): Show |
78 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.722-4475delA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747756 | |||||||
| chr8:12747758 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.722-4476A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747758 | |||||||
| chr8:12747762 | T | C | 1 | a0001c0001t0012g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.722-4480A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747762 | |||||||
| chr8:12747764 | T | C | 1 | a0001c0001t0005g0099 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.722-4482A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747764 | |||||||
| chr8:12747765 | T | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.722-4483A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747765 | |||||||
| chr8:12747766 | T | C | 1 | a0001c0001t0006g0129 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.722-4484A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747766 | |||||||
| chr8:12747781 | C | G | 1 | a0001c0001t0005g0098 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.722-4499G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747781 | |||||||
| chr8:12747799 | A | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
9 | HG02129.hp1 HG02615.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.722-4517T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747799 | |||||||
| chr8:12747863 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.722-4581A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747863 | |||||||
| chr8:12747874 | C | G | 6 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(3): Show |
10 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.722-4592G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747874 | |||||||
| chr8:12747878 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.722-4596A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747878 | |||||||
| chr8:12747955 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.722-4673A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12747955 | |||||||
| chr8:12748139 | T | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
11 | HG02129.hp1 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.722-4857A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748139 | |||||||
| chr8:12748150 | T | C | 1 | a0001c0001t0015g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.722-4868A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748150 | |||||||
| chr8:12748172 | T | C | 7 | a0001c0001t0002g0026 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.722-4890A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748172 | |||||||
| chr8:12748209 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.722-4927A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748209 | |||||||
| chr8:12748225 | T | C | 1 | a0001c0001t0003g0249 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.722-4943A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748225 | |||||||
| chr8:12748265 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.722-4983G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748265 | |||||||
| chr8:12748305 | A | G | 6 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(3): Show |
10 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.722-5023T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748305 | |||||||
| chr8:12748326 | G | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.722-5044C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748326 | |||||||
| chr8:12748398 | TG | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(118): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.722-5117delC | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748398 | |||||||
| chr8:12748571 | C | T | 3 | a0001c0005t0001g0259 a0001c0005t0001g0260 a0001c0005t0001g0261 |
3 | HG02165.hp1 HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.722-5289G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748571 | |||||||
| chr8:12748795 | A | G | 2 | a0001c0001t0001g0076 a0001c0008t0001g0053 |
2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.722-5513T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748795 | |||||||
| chr8:12748797 | C | G | 2 | a0001c0001t0003g0241 a0001c0001t0003g0242 |
2 | NA19067.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.722-5515G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748797 | |||||||
| chr8:12748807 | A | AT | 34 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(31): Show |
41 | HG00558.hp2 HG01167.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.722-5526dupA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748807 | |||||||
| chr8:12748807 | A | ATT | 6 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(3): Show |
10 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.722-5527_722-5526d others(4): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748807 | |||||||
| chr8:12748807 | A | ATTT | 90 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
146 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.722-5528_722-5526d others(5): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748807 | |||||||
| chr8:12748807 | A | ATTTT | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.722-5529_722-5526d others(6): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748807 | |||||||
| chr8:12748807 | A | ATTTTT | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0175 others(2): Show |
6 | HG02080.hp1 NA18963.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.722-5530_722-5526d others(7): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748807 | |||||||
| chr8:12748807 | A | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0075 |
2 | HG03579.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.722-5525T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748807 | |||||||
| chr8:12748820 | G | T | 1 | a0001c0001t0001g0016 | 3 | HG01074.hp2 HG01192.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.722-5538C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748820 | |||||||
| chr8:12748830 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.722-5548G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748830 | |||||||
| chr8:12748909 | A | T | 3 | a0001c0005t0001g0259 a0001c0005t0001g0260 a0001c0005t0001g0261 |
3 | HG02165.hp1 HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.722-5627T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748909 | |||||||
| chr8:12748922 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.722-5640T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12748922 | |||||||
| chr8:12749088 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.721+5612C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749088 | |||||||
| chr8:12749142 | T | A | 1 | a0001c0001t0001g0089 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.721+5558A>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749142 | |||||||
| chr8:12749182 | T | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.721+5518A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749182 | |||||||
| chr8:12749251 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.721+5449A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749251 | |||||||
| chr8:12749269 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.721+5431A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749269 | |||||||
| chr8:12749336 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.721+5364T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749336 | |||||||
| chr8:12749386 | G | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0178 a0001c0001t0001g0179 others(1): Show |
6 | HG02602.hp1 NA18969.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.721+5314C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749386 | |||||||
| chr8:12749410 | T | C | 1 | a0001c0005t0001g0260 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.721+5290A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749410 | |||||||
| chr8:12749532 | A | G | 12 | a0001c0001t0001g0243 a0001c0001t0001g0250 a0001c0001t0003g0049 others(9): Show |
13 | HG00558.hp2 NA18949.hp2 NA18979.hp2 others(10): Show |
intron_variant | MODIFIER | c.721+5168T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749532 | |||||||
| chr8:12749611 | T | C | 1 | a0001c0001t0015g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.721+5089A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749611 | |||||||
| chr8:12749677 | C | G | 7 | a0001c0001t0002g0026 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.721+5023G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749677 | |||||||
| chr8:12749723 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0139 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.721+4977A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749723 | |||||||
| chr8:12749725 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.721+4975C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749725 | |||||||
| chr8:12749739 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.721+4961G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749739 | |||||||
| chr8:12749800 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.721+4900G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749800 | |||||||
| chr8:12749955 | A | T | 2 | a0001c0001t0001g0093 a0001c0006t0001g0050 |
3 | NA18942.hp2 NA18962.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.721+4745T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12749955 | |||||||
| chr8:12750017 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0167 |
3 | HG02886.hp1 HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.721+4683C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750017 | |||||||
| chr8:12750108 | A | C | 24 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0032 others(21): Show |
34 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.721+4592T>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750108 | |||||||
| chr8:12750120 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
395 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.721+4580G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750120 | |||||||
| chr8:12750211 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.721+4489C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750211 | |||||||
| chr8:12750289 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721+4411T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750289 | |||||||
| chr8:12750354 | T | G | 1 | a0001c0001t0008g0166 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.721+4346A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750354 | |||||||
| chr8:12750404 | C | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.721+4296G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750404 | |||||||
| chr8:12750460 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.721+4240A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750460 | |||||||
| chr8:12750477 | G | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0221 a0001c0009t0001g0054 |
3 | HG02145.hp1 HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.721+4223C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750477 | |||||||
| chr8:12750484 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0226 a0001c0009t0001g0054 |
3 | HG02145.hp1 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.721+4216T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750484 | |||||||
| chr8:12750549 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.721+4151G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750549 | |||||||
| chr8:12750611 | T | C | 1 | a0001c0001t0006g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.721+4089A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750611 | |||||||
| chr8:12750764 | C | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
9 | HG02129.hp1 HG02615.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.721+3936G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750764 | |||||||
| chr8:12750793 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.721+3907C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750793 | |||||||
| chr8:12750972 | C | G | 1 | a0001c0001t0015g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.721+3728G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12750972 | |||||||
| chr8:12751043 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.721+3657T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751043 | |||||||
| chr8:12751054 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.721+3646C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751054 | |||||||
| chr8:12751068 | G | A | 7 | a0001c0001t0002g0026 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.721+3632C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751068 | |||||||
| chr8:12751089 | C | A | 2 | a0001c0001t0001g0222 a0001c0001t0007g0223 |
2 | HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.721+3611G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751089 | |||||||
| chr8:12751128 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
8 | HG00408.hp1 NA18961.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.721+3572C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751128 | |||||||
| chr8:12751134 | T | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
9 | HG02129.hp1 HG02615.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.721+3566A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751134 | |||||||
| chr8:12751219 | T | C | 1 | a0001c0001t0008g0131 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.721+3481A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751219 | |||||||
| chr8:12751222 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.721+3478C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751222 | |||||||
| chr8:12751294 | A | ATGGTTTT others(8): Show |
2 | a0001c0001t0007g0095 a0001c0001t0007g0096 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.721+3405_721+3406i others(17): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751294 | |||||||
| chr8:12751294 | A | ATGTTTTT others(8): Show |
1 | a0001c0001t0001g0114 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.721+3405_721+3406i others(17): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751294 | |||||||
| chr8:12751294 | A | ATGTTTTT others(8): Show |
48 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(45): Show |
95 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.721+3405_721+3406i others(17): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751294 | |||||||
| chr8:12751294 | A | ATGTTTTT others(8): Show |
1 | a0001c0001t0001g0100 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.721+3405_721+3406i others(17): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751294 | |||||||
| chr8:12751294 | A | ATGTTTTT others(7): Show |
2 | a0001c0001t0005g0033 a0001c0001t0005g0097 |
3 | NA18963.hp1 NA18974.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.721+3392_721+3405d others(16): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751294 | |||||||
| chr8:12751294 | A | ATGTTTTT others(8): Show |
30 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0034 others(27): Show |
38 | HG00597.hp1 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.721+3391_721+3405d others(17): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751294 | |||||||
| chr8:12751296 | G | GGTTTTTT others(9): Show |
1 | a0005c0014t0007g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.721+3403_721+3404i others(18): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751296 | G | GGTTTTTT others(9): Show |
1 | a0001c0001t0001g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.721+3403_721+3404i others(18): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751296 | G | GT | 13 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0028 others(10): Show |
18 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.721+3403dupA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751296 | G | GTT | 15 | a0001c0001t0001g0215 a0001c0001t0001g0218 a0001c0001t0001g0219 others(12): Show |
20 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.721+3402_721+3403d others(4): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751296 | G | GTTT | 14 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0061 others(11): Show |
15 | HG01081.hp2 HG01109.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.721+3401_721+3403d others(5): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751296 | G | GTTTTTTT others(9): Show |
14 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(11): Show |
18 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.721+3403_721+3404i others(18): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751296 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0001g0090 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.721+3403_721+3404i others(19): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751296 | G | GTTTTTTT others(13): Show |
1 | a0001c0001t0001g0072 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.721+3403_721+3404i others(22): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751296 | G | GTTTTTTT others(9): Show |
12 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0037 others(9): Show |
15 | HG01884.hp1 HG01891.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.721+3403_721+3404i others(18): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751296 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0005g0099 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.721+3403_721+3404i others(19): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751296 | G | GTTTTTTT others(8): Show |
1 | a0001c0001t0001g0118 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.721+3389_721+3403d others(17): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751296 | GTTTT | G | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.721+3400_721+3403d others(6): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751296 | |||||||
| chr8:12751297 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.721+3403A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751297 | |||||||
| chr8:12751297 | T | TTTTTTTT others(7): Show |
3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0209 |
3 | HG00639.hp1 HG02922.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.721+3402_721+3403i others(16): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751297 | |||||||
| chr8:12751297 | T | TTTTTTTT others(7): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.721+3402_721+3403i others(16): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751297 | |||||||
| chr8:12751300 | T | TTTTTTTG others(8): Show |
1 | a0001c0001t0001g0210 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.721+3399_721+3400i others(17): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751300 | |||||||
| chr8:12751301 | T | TTTTTTGT others(10): Show |
2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.721+3398_721+3399i others(19): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751301 | |||||||
| chr8:12751302 | T | TTTTTGTT others(9): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0138 a0001c0001t0001g0139 |
4 | HG00639.hp2 HG01891.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.721+3397_721+3398i others(18): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751302 | |||||||
| chr8:12751302 | T | TTTTTTTT others(8): Show |
1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.721+3397_721+3398i others(17): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751302 | |||||||
| chr8:12751304 | T | TTTGTTTG | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0020 others(52): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.721+3395_721+3396i others(9): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751304 | |||||||
| chr8:12751308 | T | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0175 |
3 | NA18978.hp2 NA19063.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.721+3392A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751308 | |||||||
| chr8:12751368 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.721+3332C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751368 | |||||||
| chr8:12751371 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.721+3329C>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751371 | |||||||
| chr8:12751400 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.721+3300C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751400 | |||||||
| chr8:12751455 | C | CA | 7 | a0001c0001t0004g0004 a0001c0001t0004g0068 a0001c0001t0004g0069 others(4): Show |
11 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.721+3244dupT | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751455 | |||||||
| chr8:12751460 | C | A | 1 | a0001c0005t0001g0261 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.721+3240G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751460 | |||||||
| chr8:12751481 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.721+3219G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751481 | |||||||
| chr8:12751524 | C | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0230 |
3 | HG02132.hp2 HG02148.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.721+3176G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751524 | |||||||
| chr8:12751540 | T | G | 1 | a0001c0001t0016g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.721+3160A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751540 | |||||||
| chr8:12751573 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.721+3127C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751573 | |||||||
| chr8:12751608 | C | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.721+3092G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751608 | |||||||
| chr8:12751679 | C | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
99 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.721+3021G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751679 | |||||||
| chr8:12751688 | C | CTT | 10 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0061 others(7): Show |
12 | HG01081.hp2 HG01109.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.721+3010_721+3011d others(4): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751688 | |||||||
| chr8:12751688 | CT | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
8 | HG01167.hp1 HG01517.hp2 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.721+3011delA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751688 | |||||||
| chr8:12751754 | G | C | 22 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0045 others(19): Show |
31 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.721+2946C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751754 | |||||||
| chr8:12751825 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.721+2875C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12751825 | |||||||
| chr8:12752082 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.721+2618A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12752082 | |||||||
| chr8:12752120 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.721+2580G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12752120 | |||||||
| chr8:12752335 | T | C | 1 | a0001c0001t0015g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.721+2365A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12752335 | |||||||
| chr8:12752445 | G | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(46): Show |
91 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.721+2255C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12752445 | |||||||
| chr8:12752571 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0015g0074 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.721+2129A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12752571 | |||||||
| chr8:12752691 | T | C | 1 | a0007c0013t0001g0258 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.721+2009A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12752691 | |||||||
| chr8:12752832 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.721+1868T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12752832 | |||||||
| chr8:12752957 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.721+1743G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12752957 | |||||||
| chr8:12752973 | G | A | 23 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0045 others(20): Show |
32 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.721+1727C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12752973 | |||||||
| chr8:12753061 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
13 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.721+1639G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12753061 | |||||||
| chr8:12753092 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.721+1608T>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12753092 | |||||||
| chr8:12753121 | T | C | 12 | a0001c0001t0001g0243 a0001c0001t0001g0250 a0001c0001t0003g0049 others(9): Show |
13 | HG00558.hp2 NA18949.hp2 NA18979.hp2 others(10): Show |
intron_variant | MODIFIER | c.721+1579A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12753121 | |||||||
| chr8:12753267 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.721+1433A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12753267 | |||||||
| chr8:12753303 | C | T | 12 | a0001c0001t0001g0243 a0001c0001t0001g0250 a0001c0001t0003g0049 others(9): Show |
13 | HG00558.hp2 NA18949.hp2 NA18979.hp2 others(10): Show |
intron_variant | MODIFIER | c.721+1397G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12753303 | |||||||
| chr8:12753681 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.721+1019A>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12753681 | |||||||
| chr8:12753794 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.721+906C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12753794 | |||||||
| chr8:12753828 | C | CT | 7 | a0001c0001t0002g0026 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.721+871dupA | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12753828 | |||||||
| chr8:12753888 | A | T | 3 | a0001c0005t0001g0259 a0001c0005t0001g0260 a0001c0005t0001g0261 |
3 | HG02165.hp1 HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.721+812T>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12753888 | |||||||
| chr8:12753902 | CTCA | C | 7 | a0001c0001t0002g0026 a0001c0001t0002g0237 a0001c0001t0002g0238 others(4): Show |
12 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.721+795_721+797del others(3): Show |
LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12753902 | |||||||
| chr8:12753966 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0225 |
4 | HG03490.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.721+734C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12753966 | |||||||
| chr8:12754081 | G | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0233 a0001c0001t0001g0234 |
5 | HG00642.hp1 HG00738.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.721+619C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754081 | |||||||
| chr8:12754094 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.721+606C>G | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754094 | |||||||
| chr8:12754221 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.721+479C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754221 | |||||||
| chr8:12754252 | T | G | 1 | a0001c0001t0004g0228 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.721+448A>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754252 | |||||||
| chr8:12754277 | T | TC | 4 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
4 | HG03831.hp1 NA18955.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.721+422dupG | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754277 | |||||||
| chr8:12754324 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG01255.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.721+376C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754324 | |||||||
| chr8:12754378 | G | A | 19 | a0001c0001t0001g0243 a0001c0001t0001g0250 a0001c0001t0002g0026 others(16): Show |
25 | HG00558.hp2 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.721+322C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754378 | |||||||
| chr8:12754606 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.721+94C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754606 | |||||||
| chr8:12754667 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.721+33G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754667 | |||||||
| chr8:12754669 | G | A | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
4 | HG02615.hp2 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.721+31C>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754669 | |||||||
| chr8:12754681 | C | G | 1 | a0001c0007t0006g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.721+19G>C | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754681 | |||||||
| chr8:12754687 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.721+13G>T | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754687 | |||||||
| chr8:12754691 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.721+9G>A | LONRF1 | ENSG00000154359.13 | transcript | ENST00000398246.8 | protein_coding | 1/11 | chr8 | 12754691 |