Item | Value |
---|---|
geneid | 164832 |
ensemblid | ENSG00000170500.13 |
hgncid | 24788 |
symbol | LONRF2 |
name | LON peptidase N-terminal domain and ring finger 2 |
refseq_nuc | NM_198461.4 |
refseq_prot | NP_940863.3 |
ensembl_nuc | ENST00000393437.8 |
ensembl_prot | ENSP00000377086.3 |
mane_status | MANE Select |
chr | chr2 |
start | 100271875 |
end | 100322501 |
strand | - |
ver | v1.2 |
region | chr2:100271875-100322501 |
region5000 | chr2:100266875-100327501 |
regionname0 | LONRF2_chr2_100271875_100322501 |
regionname5000 | LONRF2_chr2_100266875_100327501 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 754 | 142 | 10 | 23 | 93 | 5 | 10 | 64 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0002 | 0/0 | 754 | 138 | 67 | 25 | 29 | 3 | 14 | 23 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0003 | 1/0 | 754 | 57 | 9 | 17 | 10 | 4 | 16 | 9 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0004 | 0/0 | 754 | 15 | 0 | 1 | 14 | 0 | 0 | 8 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0005 | 0/0 | 754 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0006 | 0/0 | 754 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0007 | 0/0 | 754 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0008 | 0/0 | 754 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0009 | 0/0 | 754 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0010 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0011 | 0/0 | 754 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0012 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
a0013 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | MSPEP others(749): Show |
chr2 | 100266875 | 100327501 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 2262 | 64 | 0 | 4 | 52 | 2 | 6 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0001c0004 | 0/0 | 2262 | 50 | 0 | 11 | 38 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0001c0006 | 0/1 | 2262 | 18 | 2 | 8 | 1 | 3 | 3 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0001c0008 | 0/0 | 2262 | 8 | 8 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0001c0015 | 0/0 | 2262 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0002c0001 | 0/0 | 2262 | 103 | 58 | 13 | 25 | 1 | 6 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0002c0005 | 0/0 | 2262 | 20 | 0 | 12 | 0 | 2 | 6 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0002c0010 | 0/0 | 2262 | 4 | 0 | 0 | 3 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0002c0012 | 0/0 | 2262 | 3 | 3 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0002c0013 | 0/0 | 2262 | 3 | 3 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0002c0018 | 0/0 | 2262 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0002c0022 | 0/0 | 2262 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0002c0023 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0002c0025 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0003c0003 | 1/0 | 2262 | 57 | 9 | 17 | 10 | 4 | 16 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0004c0007 | 0/0 | 2262 | 10 | 0 | 0 | 10 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0004c0011 | 0/0 | 2262 | 4 | 0 | 1 | 3 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0004c0027 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0005c0009 | 0/0 | 2262 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0006c0014 | 0/0 | 2262 | 3 | 3 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0007c0016 | 0/0 | 2262 | 2 | 1 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0008c0017 | 0/0 | 2262 | 2 | 0 | 0 | 1 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0009c0020 | 0/0 | 2262 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0010c0024 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0011c0019 | 0/0 | 2262 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0012c0021 | 0/0 | 2262 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 | ||
a0013c0026 | 0/0 | 2262 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | ATGAG others(2257): Show |
chr2 | 100266875 | 100327501 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002 | 0/0 | 15046 | 31 | 0 | 0 | 31 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0004 | 0/0 | 15046 | 8 | 0 | 0 | 7 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0013 | 0/0 | 15046 | 6 | 0 | 0 | 6 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0020 | 0/0 | 15046 | 4 | 0 | 1 | 0 | 2 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0025 | 0/0 | 15046 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0026 | 0/0 | 15044 | 3 | 0 | 0 | 1 | 0 | 2 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0027 | 0/0 | 15046 | 3 | 0 | 1 | 0 | 0 | 2 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0116 | 0/0 | 15047 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15042): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0117 | 0/0 | 15046 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0118 | 0/0 | 15046 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0122 | 0/0 | 15046 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0127 | 0/0 | 15046 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0002t0129 | 0/0 | 15046 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0003 | 0/0 | 15044 | 25 | 0 | 0 | 25 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0007 | 0/0 | 15046 | 9 | 0 | 9 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0014 | 0/0 | 15044 | 6 | 0 | 0 | 5 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0038 | 0/0 | 15045 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15040): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0105 | 0/0 | 15046 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0106 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0108 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0109 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0110 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0111 | 0/0 | 15046 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0112 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0001c0004t0113 | 0/0 | 15043 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15038): Show |
chr2 | 100266875 | 100327501 |
a0001c0006t0004 | 0/1 | 15046 | 11 | 0 | 5 | 1 | 2 | 2 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0006t0028 | 0/0 | 15046 | 3 | 1 | 2 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0006t0120 | 0/0 | 15046 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0006t0121 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0006t0123 | 0/0 | 15046 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0006t0130 | 0/0 | 15046 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0008t0039 | 0/0 | 15047 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15042): Show |
chr2 | 100266875 | 100327501 |
a0001c0008t0040 | 0/0 | 15046 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0008t0041 | 0/0 | 15046 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0008t0124 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0008t0125 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0001c0015t0003 | 0/0 | 15044 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0001 | 0/0 | 15044 | 21 | 3 | 1 | 12 | 0 | 5 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0005 | 0/0 | 15044 | 13 | 0 | 9 | 4 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0006 | 0/0 | 15046 | 9 | 9 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0012 | 0/0 | 15050 | 6 | 5 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15045): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0018 | 0/0 | 15052 | 4 | 4 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15047): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0019 | 0/0 | 15046 | 4 | 4 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0022 | 0/0 | 15046 | 3 | 1 | 0 | 2 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0031 | 0/0 | 15045 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15040): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0032 | 0/0 | 15048 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0033 | 0/0 | 15048 | 2 | 1 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0034 | 0/0 | 15048 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0042 | 0/0 | 15048 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0043 | 0/0 | 15048 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0055 | 0/0 | 15049 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15044): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0056 | 0/0 | 15049 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15044): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0057 | 0/0 | 15049 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15044): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0058 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0059 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0060 | 0/0 | 15048 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0062 | 0/0 | 15045 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15040): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0064 | 0/0 | 15044 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0065 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0067 | 0/0 | 15044 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0068 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0071 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0072 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0073 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0074 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0075 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0076 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0077 | 0/0 | 15047 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15042): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0078 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0079 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0080 | 0/0 | 15047 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15042): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0083 | 0/0 | 15048 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0084 | 0/0 | 15048 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0086 | 0/0 | 15048 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0087 | 0/0 | 15048 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0090 | 0/0 | 15048 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0093 | 0/0 | 15050 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15045): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0094 | 0/0 | 15050 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15045): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0095 | 0/0 | 15052 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15047): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0096 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0101 | 0/0 | 15046 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0102 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0001t0103 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0005t0001 | 0/0 | 15044 | 11 | 0 | 8 | 0 | 1 | 2 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0005t0021 | 0/0 | 15046 | 3 | 0 | 2 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0005t0030 | 0/0 | 15044 | 2 | 0 | 1 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0005t0061 | 0/0 | 15044 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0005t0063 | 0/0 | 15044 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0005t0066 | 0/0 | 15044 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0005t0069 | 0/0 | 15044 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0010t0005 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0010t0023 | 0/0 | 15044 | 3 | 0 | 0 | 2 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0002c0012t0035 | 0/0 | 15047 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15042): Show |
chr2 | 100266875 | 100327501 |
a0002c0012t0088 | 0/0 | 15047 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15042): Show |
chr2 | 100266875 | 100327501 |
a0002c0013t0036 | 0/0 | 15046 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0013t0097 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0018t0037 | 0/0 | 15046 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0022t0100 | 0/0 | 15046 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0023t0099 | 0/0 | 15046 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0002c0025t0098 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0008 | 0/0 | 15098 | 6 | 0 | 5 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15093): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0009 | 1/0 | 15096 | 6 | 2 | 2 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15091): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0010 | 0/0 | 15098 | 6 | 0 | 2 | 1 | 0 | 3 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15093): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0011 | 0/0 | 15098 | 6 | 0 | 0 | 6 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15093): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0015 | 0/0 | 15096 | 5 | 0 | 5 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15091): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0016 | 0/0 | 15050 | 5 | 0 | 0 | 0 | 0 | 5 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15045): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0017 | 0/0 | 15050 | 4 | 0 | 0 | 0 | 0 | 4 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15045): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0024 | 0/0 | 15050 | 3 | 3 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15045): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0029 | 0/0 | 15098 | 2 | 0 | 0 | 0 | 1 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15093): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0044 | 0/0 | 15098 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15093): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0045 | 0/0 | 15097 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15092): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0046 | 0/0 | 15096 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15091): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0047 | 0/0 | 15096 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15091): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0048 | 0/0 | 15098 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15093): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0049 | 0/0 | 15096 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15091): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0050 | 0/0 | 15098 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15093): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0051 | 0/0 | 15098 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15093): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0052 | 0/0 | 15098 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15093): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0053 | 0/0 | 15098 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15093): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0054 | 0/0 | 15095 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15090): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0089 | 0/0 | 15050 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15045): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0091 | 0/0 | 15050 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15045): Show |
chr2 | 100266875 | 100327501 |
a0003c0003t0092 | 0/0 | 15050 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15045): Show |
chr2 | 100266875 | 100327501 |
a0004c0007t0002 | 0/0 | 15046 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0004c0007t0004 | 0/0 | 15046 | 6 | 0 | 0 | 6 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0004c0007t0114 | 0/0 | 15049 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15044): Show |
chr2 | 100266875 | 100327501 |
a0004c0007t0119 | 0/0 | 15046 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0004c0007t0128 | 0/0 | 15046 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0004c0011t0004 | 0/0 | 15046 | 4 | 0 | 1 | 3 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0004c0027t0107 | 0/0 | 15045 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15040): Show |
chr2 | 100266875 | 100327501 |
a0005c0009t0003 | 0/0 | 15044 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0006c0014t0001 | 0/0 | 15044 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0006c0014t0070 | 0/0 | 15044 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
a0007c0016t0104 | 0/0 | 15096 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15091): Show |
chr2 | 100266875 | 100327501 |
a0007c0016t0115 | 0/0 | 15050 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15045): Show |
chr2 | 100266875 | 100327501 |
a0008c0017t0081 | 0/0 | 15048 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0008c0017t0082 | 0/0 | 15048 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0009c0020t0126 | 0/0 | 15046 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0010c0024t0006 | 0/0 | 15046 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0011c0019t0004 | 0/0 | 15046 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15041): Show |
chr2 | 100266875 | 100327501 |
a0012c0021t0085 | 0/0 | 15048 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15043): Show |
chr2 | 100266875 | 100327501 |
a0013c0026t0001 | 0/0 | 15044 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | AGTCG others(15039): Show |
chr2 | 100266875 | 100327501 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002g0001 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0004g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0013g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0013g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0013g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0020g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0020g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0020g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0025g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0025g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0025g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0026g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0026g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0027g0020 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0116g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0117g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0118g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0122g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0127g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0002t0129g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0007g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0007g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0007g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0007g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0007g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0014g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0014g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0014g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0038g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0038g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0105g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0106g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0108g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0109g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0110g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0111g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0112g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0004t0113g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0004g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0004g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0028g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0028g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0028g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0120g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0121g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0123g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0006t0130g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0008t0039g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0008t0040g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0008t0041g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0008t0041g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0008t0124g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0008t0125g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0015t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0001c0015t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0005g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0005g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0006g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0012g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0012g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0012g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0018g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0018g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0018g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0019g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0019g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0019g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0019g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0022g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0022g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0022g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0031g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0032g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0032g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0033g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0033g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0034g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0034g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0042g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0043g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0055g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0056g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0057g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0058g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0059g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0060g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0062g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0064g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0065g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0067g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0068g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0071g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0072g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0073g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0074g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0075g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0076g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0077g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0078g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0079g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0080g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0083g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0084g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0086g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0087g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0090g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0093g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0094g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0095g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0096g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0101g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0102g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0001t0103g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0021g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0021g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0030g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0061g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0063g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0066g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0005t0069g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0010t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0010t0023g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0010t0023g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0010t0023g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0012t0035g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0012t0035g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0012t0088g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0013t0036g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0013t0036g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0013t0097g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0018t0037g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0018t0037g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0022t0100g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0023t0099g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0002c0025t0098g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0008g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0008g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0008g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0009g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0009g0030 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0009g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0010g0004 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0010g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0011g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0011g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0015g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0015g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0015g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0016g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0016g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0016g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0016g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0017g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0017g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0017g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0024g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0024g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0024g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0029g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0044g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0045g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0046g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0047g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0048g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0049g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0050g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0051g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0052g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0053g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0054g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0089g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0091g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0003c0003t0092g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0007t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0007t0004g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0007t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0007t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0007t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0007t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0007t0114g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0007t0119g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0007t0128g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0011t0004g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0011t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0004c0027t0107g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0005c0009t0003g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0005c0009t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0006c0014t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0006c0014t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0006c0014t0070g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0007c0016t0104g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0007c0016t0115g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0008c0017t0081g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0008c0017t0082g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0009c0020t0126g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0010c0024t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0011c0019t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0012c0021t0085g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
a0013c0026t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0006 | t0004 | g0199 | EUR | GBR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00140 | hp2 | a0003 | c0003 | t0051 | g0106 | EUR | GBR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00280 | hp1 | a0001 | c0002 | t0020 | g0182 | EUR | FIN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00280 | hp2 | a0003 | c0003 | t0008 | g0016 | EUR | FIN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00323 | hp1 | a0003 | c0003 | t0029 | g0028 | EUR | FIN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00323 | hp2 | a0001 | c0006 | t0120 | g0192 | EUR | FIN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00423 | hp1 | a0001 | c0004 | t0014 | g0222 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00423 | hp2 | a0004 | c0007 | t0004 | g0271 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00438 | hp1 | a0001 | c0002 | t0127 | g0219 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00438 | hp2 | a0003 | c0003 | t0047 | g0101 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00544 | hp1 | a0001 | c0004 | t0014 | g0011 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00544 | hp2 | a0004 | c0007 | t0004 | g0043 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00558 | hp1 | a0001 | c0004 | t0003 | g0238 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00597 | hp1 | a0001 | c0002 | t0013 | g0244 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00597 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00609 | hp1 | a0002 | c0001 | t0080 | g0132 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00621 | hp1 | a0001 | c0015 | t0003 | g0193 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00621 | hp2 | a0001 | c0004 | t0014 | g0011 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00639 | hp1 | a0003 | c0003 | t0008 | g0114 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00639 | hp2 | a0001 | c0004 | t0007 | g0234 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00642 | hp1 | a0003 | c0003 | t0015 | g0017 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00642 | hp2 | a0001 | c0006 | t0028 | g0186 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00673 | hp1 | a0001 | c0004 | t0106 | g0231 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00673 | hp2 | a0001 | c0004 | t0108 | g0202 | EAS | CHS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00735 | hp1 | a0002 | c0005 | t0001 | g0175 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00735 | hp2 | a0002 | c0001 | t0005 | g0002 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00738 | hp1 | a0001 | c0006 | t0130 | g0190 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00738 | hp2 | a0002 | c0005 | t0030 | g0035 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00741 | hp1 | a0002 | c0001 | t0005 | g0002 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG00741 | hp2 | a0001 | c0006 | t0004 | g0191 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01069 | hp1 | a0001 | c0006 | t0004 | g0009 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01069 | hp2 | a0003 | c0003 | t0054 | g0100 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01071 | hp1 | a0001 | c0006 | t0004 | g0009 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01071 | hp2 | a0003 | c0003 | t0010 | g0004 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01074 | hp1 | a0001 | c0002 | t0020 | g0037 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01074 | hp2 | a0001 | c0006 | t0028 | g0188 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01081 | hp1 | a0001 | c0006 | t0004 | g0009 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01081 | hp2 | a0002 | c0005 | t0001 | g0018 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01099 | hp1 | a0003 | c0003 | t0049 | g0105 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01099 | hp2 | a0002 | c0005 | t0021 | g0178 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01169 | hp1 | a0001 | c0004 | t0007 | g0005 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01169 | hp2 | a0002 | c0001 | t0057 | g0166 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01175 | hp1 | a0003 | c0003 | t0009 | g0030 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01175 | hp2 | a0002 | c0005 | t0021 | g0034 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01192 | hp1 | a0001 | c0002 | t0027 | g0020 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01192 | hp2 | a0002 | c0005 | t0061 | g0181 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01243 | hp1 | a0002 | c0001 | t0101 | g0052 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01243 | hp2 | a0002 | c0001 | t0005 | g0002 | AMR | PUR | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01255 | hp1 | a0003 | c0003 | t0009 | g0015 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01255 | hp2 | a0002 | c0005 | t0001 | g0018 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01256 | hp1 | a0003 | c0003 | t0008 | g0161 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01256 | hp2 | a0001 | c0006 | t0004 | g0194 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01257 | hp1 | a0001 | c0004 | t0007 | g0005 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01257 | hp2 | a0002 | c0005 | t0001 | g0008 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01258 | hp1 | a0003 | c0003 | t0008 | g0016 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01258 | hp2 | a0002 | c0005 | t0001 | g0008 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01261 | hp1 | a0002 | c0001 | t0012 | g0025 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01261 | hp2 | a0001 | c0002 | t0122 | g0217 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01346 | hp1 | a0003 | c0003 | t0045 | g0110 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01346 | hp2 | a0001 | c0002 | t0116 | g0220 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01358 | hp1 | a0003 | c0003 | t0010 | g0108 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01358 | hp2 | a0009 | c0020 | t0126 | g0263 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01361 | hp1 | a0003 | c0003 | t0008 | g0016 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01361 | hp2 | a0002 | c0001 | t0005 | g0006 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01433 | hp1 | a0007 | c0016 | t0104 | g0214 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01433 | hp2 | a0001 | c0004 | t0007 | g0213 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01516 | hp1 | a0001 | c0006 | t0004 | g0009 | EUR | IBS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01516 | hp2 | a0002 | c0001 | t0033 | g0056 | EUR | IBS | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01884 | hp1 | a0001 | c0008 | t0041 | g0257 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01884 | hp2 | a0002 | c0001 | t0012 | g0033 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01891 | hp1 | a0001 | c0008 | t0125 | g0210 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01891 | hp2 | a0003 | c0003 | t0024 | g0153 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01928 | hp1 | a0001 | c0004 | t0007 | g0215 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01928 | hp2 | a0003 | c0003 | t0015 | g0160 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01934 | hp1 | a0002 | c0005 | t0001 | g0036 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01934 | hp2 | a0003 | c0003 | t0015 | g0017 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01952 | hp1 | a0001 | c0004 | t0111 | g0211 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01952 | hp2 | a0002 | c0005 | t0001 | g0036 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01975 | hp1 | a0002 | c0001 | t0005 | g0002 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01975 | hp2 | a0001 | c0004 | t0007 | g0005 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01981 | hp1 | a0002 | c0001 | t0005 | g0135 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01981 | hp2 | a0003 | c0003 | t0008 | g0049 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01993 | hp1 | a0001 | c0004 | t0007 | g0005 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01993 | hp2 | a0003 | c0003 | t0015 | g0159 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02015 | hp2 | a0002 | c0001 | t0001 | g0137 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02027 | hp2 | a0001 | c0004 | t0109 | g0225 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0140 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02040 | hp2 | a0001 | c0004 | t0110 | g0243 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02055 | hp1 | a0002 | c0001 | t0006 | g0050 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02055 | hp2 | a0002 | c0001 | t0076 | g0078 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02056 | hp2 | a0004 | c0007 | t0004 | g0043 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02074 | hp1 | a0004 | c0007 | t0004 | g0266 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02080 | hp1 | a0002 | c0001 | t0001 | g0124 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02080 | hp2 | a0001 | c0002 | t0025 | g0248 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02083 | hp1 | a0004 | c0007 | t0119 | g0269 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02083 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02129 | hp1 | a0001 | c0004 | t0003 | g0212 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02132 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02132 | hp2 | a0001 | c0004 | t0003 | g0240 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02135 | hp1 | a0001 | c0004 | t0038 | g0224 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02135 | hp2 | a0002 | c0001 | t0072 | g0128 | EAS | KHV | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02148 | hp1 | a0004 | c0011 | t0004 | g0264 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02148 | hp2 | a0001 | c0004 | t0007 | g0205 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02165 | hp1 | a0004 | c0027 | t0107 | g0273 | EAS | CDX | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | CDX | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02257 | hp1 | a0002 | c0001 | t0093 | g0168 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02257 | hp2 | a0001 | c0008 | t0124 | g0249 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02258 | hp1 | a0002 | c0018 | t0037 | g0058 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02258 | hp2 | a0003 | c0003 | t0009 | g0015 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02273 | hp1 | a0001 | c0004 | t0105 | g0209 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02273 | hp2 | a0002 | c0001 | t0005 | g0002 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02280 | hp1 | a0003 | c0003 | t0092 | g0143 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02280 | hp2 | a0002 | c0001 | t0031 | g0026 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02293 | hp1 | a0002 | c0001 | t0005 | g0002 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02293 | hp2 | a0001 | c0004 | t0007 | g0005 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02300 | hp1 | a0002 | c0001 | t0001 | g0131 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02300 | hp2 | a0002 | c0001 | t0005 | g0002 | AMR | PEL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02451 | hp1 | a0010 | c0024 | t0006 | g0066 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02451 | hp2 | a0002 | c0001 | t0094 | g0099 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02572 | hp1 | a0002 | c0001 | t0001 | g0118 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02572 | hp2 | a0002 | c0001 | t0032 | g0061 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02602 | hp1 | a0002 | c0001 | t0001 | g0125 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02602 | hp2 | a0001 | c0006 | t0004 | g0185 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02615 | hp1 | a0002 | c0001 | t0071 | g0095 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02615 | hp2 | a0002 | c0001 | t0006 | g0048 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02622 | hp1 | a0002 | c0012 | t0035 | g0076 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02622 | hp2 | a0002 | c0001 | t0065 | g0139 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02630 | hp1 | a0002 | c0001 | t0022 | g0149 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02630 | hp2 | a0001 | c0006 | t0121 | g0198 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02683 | hp1 | a0002 | c0005 | t0066 | g0179 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02683 | hp2 | a0001 | c0002 | t0020 | g0037 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02698 | hp1 | a0001 | c0002 | t0027 | g0020 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02698 | hp2 | a0003 | c0003 | t0029 | g0028 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02717 | hp1 | a0002 | c0001 | t0064 | g0121 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02717 | hp2 | a0002 | c0001 | t0012 | g0033 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02723 | hp1 | a0002 | c0001 | t0019 | g0069 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02723 | hp2 | a0002 | c0012 | t0035 | g0075 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02735 | hp1 | a0003 | c0003 | t0048 | g0104 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02735 | hp2 | a0002 | c0022 | t0100 | g0148 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02738 | hp1 | a0011 | c0019 | t0004 | g0201 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02738 | hp2 | a0003 | c0003 | t0010 | g0004 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02809 | hp1 | a0002 | c0001 | t0042 | g0074 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02809 | hp2 | a0002 | c0013 | t0036 | g0157 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02886 | hp1 | a0003 | c0003 | t0046 | g0103 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02886 | hp2 | a0002 | c0001 | t0074 | g0129 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02895 | hp1 | a0002 | c0001 | t0087 | g0086 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02895 | hp2 | a0002 | c0001 | t0006 | g0067 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02896 | hp1 | a0002 | c0001 | t0034 | g0165 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02896 | hp2 | a0002 | c0001 | t0019 | g0171 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02897 | hp1 | a0002 | c0001 | t0006 | g0071 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02897 | hp2 | a0002 | c0001 | t0034 | g0164 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02922 | hp1 | a0002 | c0001 | t0006 | g0014 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02922 | hp2 | a0002 | c0001 | t0012 | g0169 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02965 | hp1 | a0006 | c0014 | t0070 | g0155 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02965 | hp2 | a0003 | c0003 | t0091 | g0088 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02970 | hp1 | a0002 | c0001 | t0075 | g0046 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02970 | hp2 | a0002 | c0001 | t0006 | g0070 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02976 | hp1 | a0002 | c0001 | t0090 | g0167 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02976 | hp2 | a0002 | c0001 | t0056 | g0117 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03017 | hp1 | a0003 | c0003 | t0017 | g0150 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03017 | hp2 | a0002 | c0001 | t0001 | g0081 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03041 | hp1 | a0002 | c0001 | t0032 | g0062 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03041 | hp2 | a0002 | c0001 | t0019 | g0072 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03098 | hp1 | a0002 | c0001 | t0006 | g0014 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03098 | hp2 | a0002 | c0001 | t0001 | g0130 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03130 | hp1 | a0001 | c0008 | t0039 | g0039 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03130 | hp2 | a0003 | c0003 | t0024 | g0146 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03139 | hp1 | a0002 | c0012 | t0088 | g0077 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03139 | hp2 | a0002 | c0001 | t0018 | g0047 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03195 | hp1 | a0002 | c0001 | t0084 | g0054 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03195 | hp2 | a0012 | c0021 | t0085 | g0060 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03209 | hp1 | a0003 | c0003 | t0089 | g0094 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03209 | hp2 | a0002 | c0001 | t0086 | g0089 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03225 | hp1 | a0002 | c0001 | t0043 | g0073 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03225 | hp2 | a0002 | c0001 | t0059 | g0173 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03239 | hp1 | a0001 | c0002 | t0027 | g0020 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03239 | hp2 | a0002 | c0001 | t0067 | g0133 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03453 | hp1 | a0002 | c0001 | t0018 | g0087 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03453 | hp2 | a0002 | c0018 | t0037 | g0174 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03486 | hp1 | a0002 | c0001 | t0019 | g0064 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03486 | hp2 | a0002 | c0001 | t0095 | g0051 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03491 | hp1 | a0003 | c0003 | t0016 | g0031 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03491 | hp2 | a0002 | c0001 | t0001 | g0134 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03492 | hp1 | a0003 | c0003 | t0016 | g0031 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03492 | hp2 | a0002 | c0005 | t0030 | g0035 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03516 | hp1 | a0002 | c0001 | t0012 | g0170 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03516 | hp2 | a0002 | c0013 | t0036 | g0158 | AFR | ESN | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03540 | hp1 | a0007 | c0016 | t0115 | g0207 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03540 | hp2 | a0002 | c0001 | t0001 | g0116 | AFR | GWD | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03579 | hp1 | a0002 | c0001 | t0006 | g0063 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03579 | hp2 | a0001 | c0008 | t0041 | g0258 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03654 | hp1 | a0003 | c0003 | t0017 | g0032 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03654 | hp2 | a0002 | c0001 | t0001 | g0098 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03688 | hp1 | a0002 | c0005 | t0001 | g0008 | SAS | STU | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03688 | hp2 | a0003 | c0003 | t0010 | g0004 | SAS | STU | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03704 | hp1 | a0002 | c0001 | t0001 | g0127 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03704 | hp2 | a0003 | c0003 | t0016 | g0154 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03710 | hp1 | a0001 | c0004 | t0014 | g0233 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03710 | hp2 | a0002 | c0005 | t0021 | g0034 | SAS | PJL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03831 | hp1 | a0002 | c0005 | t0001 | g0176 | SAS | BEB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03831 | hp2 | a0003 | c0003 | t0016 | g0147 | SAS | BEB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03834 | hp1 | a0003 | c0003 | t0017 | g0032 | SAS | BEB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03834 | hp2 | a0003 | c0003 | t0044 | g0107 | SAS | BEB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03927 | hp1 | a0003 | c0003 | t0016 | g0152 | SAS | BEB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03927 | hp2 | a0003 | c0003 | t0010 | g0004 | SAS | BEB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG04115 | hp1 | a0001 | c0002 | t0026 | g0042 | SAS | STU | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG04115 | hp2 | a0001 | c0002 | t0004 | g0221 | SAS | STU | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG04184 | hp1 | a0002 | c0010 | t0023 | g0119 | SAS | BEB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG04184 | hp2 | a0008 | c0017 | t0081 | g0044 | SAS | BEB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG04204 | hp1 | a0001 | c0002 | t0026 | g0042 | SAS | STU | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG04204 | hp2 | a0001 | c0006 | t0123 | g0189 | SAS | STU | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG04228 | hp1 | a0001 | c0006 | t0004 | g0197 | SAS | STU | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG04228 | hp2 | a0003 | c0003 | t0017 | g0109 | SAS | STU | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18522 | hp1 | a0002 | c0001 | t0058 | g0172 | AFR | YRI | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18522 | hp2 | a0006 | c0014 | t0001 | g0096 | AFR | YRI | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18612 | hp1 | a0001 | c0002 | t0013 | g0012 | EAS | CHB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18612 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | CHB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0163 | EAS | CHB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18747 | hp2 | a0001 | c0015 | t0003 | g0195 | EAS | CHB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18906 | hp1 | a0006 | c0014 | t0001 | g0097 | AFR | YRI | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18906 | hp2 | a0003 | c0003 | t0024 | g0151 | AFR | YRI | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18939 | hp1 | a0001 | c0002 | t0004 | g0246 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18939 | hp2 | a0002 | c0001 | t0005 | g0006 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18941 | hp1 | a0002 | c0001 | t0078 | g0136 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18941 | hp2 | a0001 | c0002 | t0025 | g0216 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18944 | hp1 | a0002 | c0001 | t0001 | g0162 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18945 | hp1 | a0002 | c0001 | t0005 | g0006 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18945 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18946 | hp1 | a0001 | c0002 | t0004 | g0232 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18946 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18948 | hp1 | a0005 | c0009 | t0003 | g0019 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18948 | hp2 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18951 | hp1 | a0001 | c0002 | t0013 | g0012 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18951 | hp2 | a0003 | c0003 | t0011 | g0007 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18952 | hp1 | a0001 | c0004 | t0003 | g0239 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18953 | hp1 | a0005 | c0009 | t0003 | g0196 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18953 | hp2 | a0004 | c0011 | t0004 | g0023 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18954 | hp1 | a0004 | c0011 | t0004 | g0023 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18954 | hp2 | a0002 | c0001 | t0005 | g0006 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18957 | hp1 | a0002 | c0001 | t0079 | g0091 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18957 | hp2 | a0004 | c0007 | t0114 | g0272 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18959 | hp1 | a0001 | c0004 | t0003 | g0223 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18960 | hp1 | a0003 | c0003 | t0011 | g0007 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18960 | hp2 | a0001 | c0002 | t0025 | g0230 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18961 | hp1 | a0002 | c0010 | t0005 | g0115 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18961 | hp2 | a0005 | c0009 | t0003 | g0019 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18962 | hp1 | a0013 | c0026 | t0001 | g0138 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18964 | hp1 | a0004 | c0007 | t0002 | g0268 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18964 | hp2 | a0001 | c0002 | t0118 | g0254 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18966 | hp1 | a0001 | c0002 | t0117 | g0255 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18966 | hp2 | a0001 | c0004 | t0014 | g0011 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18969 | hp1 | a0001 | c0004 | t0003 | g0206 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18969 | hp2 | a0001 | c0002 | t0013 | g0012 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18973 | hp1 | a0008 | c0017 | t0082 | g0045 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18973 | hp2 | a0001 | c0002 | t0004 | g0251 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18974 | hp1 | a0001 | c0006 | t0004 | g0184 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18974 | hp2 | a0002 | c0001 | t0005 | g0102 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18977 | hp1 | a0002 | c0010 | t0023 | g0120 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18977 | hp2 | a0002 | c0001 | t0022 | g0112 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18978 | hp1 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18979 | hp1 | a0001 | c0004 | t0003 | g0259 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18979 | hp2 | a0002 | c0001 | t0073 | g0111 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18980 | hp1 | a0002 | c0001 | t0062 | g0082 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18980 | hp2 | a0001 | c0004 | t0003 | g0021 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18983 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18985 | hp1 | a0001 | c0004 | t0003 | g0021 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18985 | hp2 | a0001 | c0002 | t0013 | g0245 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18986 | hp2 | a0001 | c0004 | t0112 | g0204 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18991 | hp1 | a0001 | c0004 | t0003 | g0235 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18991 | hp2 | a0002 | c0001 | t0022 | g0144 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18992 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18993 | hp1 | a0001 | c0004 | t0003 | g0247 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18993 | hp2 | a0002 | c0001 | t0068 | g0126 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18994 | hp1 | a0001 | c0004 | t0003 | g0241 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18994 | hp2 | a0002 | c0010 | t0023 | g0090 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18998 | hp1 | a0004 | c0007 | t0004 | g0265 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18998 | hp2 | a0001 | c0004 | t0003 | g0242 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19003 | hp1 | a0001 | c0002 | t0026 | g0218 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19003 | hp2 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19004 | hp2 | a0005 | c0009 | t0003 | g0019 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19005 | hp1 | a0003 | c0003 | t0011 | g0029 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19005 | hp2 | a0001 | c0004 | t0003 | g0228 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19007 | hp1 | a0001 | c0004 | t0003 | g0229 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19009 | hp1 | a0002 | c0001 | t0001 | g0123 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19009 | hp2 | a0003 | c0003 | t0010 | g0004 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19010 | hp2 | a0001 | c0004 | t0038 | g0236 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19030 | hp1 | a0002 | c0001 | t0060 | g0145 | AFR | LWK | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19030 | hp2 | a0002 | c0001 | t0018 | g0024 | AFR | LWK | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19057 | hp1 | a0003 | c0003 | t0011 | g0029 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19060 | hp1 | a0004 | c0007 | t0128 | g0267 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19062 | hp2 | a0003 | c0003 | t0050 | g0093 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19063 | hp1 | a0003 | c0003 | t0011 | g0007 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19063 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19064 | hp1 | a0001 | c0002 | t0013 | g0012 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19065 | hp2 | a0001 | c0004 | t0014 | g0011 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19066 | hp2 | a0001 | c0004 | t0003 | g0227 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19068 | hp1 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19076 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19076 | hp2 | a0001 | c0004 | t0113 | g0226 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19079 | hp1 | a0002 | c0023 | t0099 | g0122 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19079 | hp2 | a0001 | c0004 | t0003 | g0003 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19083 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19083 | hp2 | a0003 | c0003 | t0011 | g0007 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19084 | hp1 | a0002 | c0001 | t0001 | g0141 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19084 | hp2 | a0004 | c0007 | t0004 | g0270 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19085 | hp1 | a0002 | c0001 | t0001 | g0083 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19087 | hp2 | a0001 | c0004 | t0003 | g0021 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19088 | hp1 | a0001 | c0002 | t0129 | g0252 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19088 | hp2 | a0003 | c0003 | t0009 | g0142 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19091 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19091 | hp2 | a0004 | c0011 | t0004 | g0023 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19240 | hp1 | a0002 | c0001 | t0031 | g0026 | AFR | YRI | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA19240 | hp2 | a0001 | c0008 | t0040 | g0038 | AFR | YRI | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA20129 | hp1 | a0001 | c0008 | t0039 | g0039 | AFR | ASW | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA20129 | hp2 | a0002 | c0001 | t0055 | g0059 | AFR | ASW | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA20752 | hp1 | a0003 | c0003 | t0053 | g0113 | EUR | TSI | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA20752 | hp2 | a0002 | c0005 | t0001 | g0008 | EUR | TSI | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA20805 | hp1 | a0001 | c0002 | t0020 | g0183 | EUR | TSI | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA20805 | hp2 | a0002 | c0005 | t0069 | g0180 | EUR | TSI | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA20905 | hp1 | a0003 | c0003 | t0052 | g0092 | SAS | GIH | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA20905 | hp2 | a0002 | c0005 | t0063 | g0177 | SAS | GIH | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01123 | hp1 | a0003 | c0003 | t0015 | g0017 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG01123 | hp2 | a0002 | c0005 | t0001 | g0018 | AMR | CLM | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02109 | hp1 | a0002 | c0025 | t0098 | g0080 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02109 | hp2 | a0001 | c0008 | t0040 | g0038 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02486 | hp1 | a0003 | c0003 | t0009 | g0015 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02486 | hp2 | a0002 | c0001 | t0102 | g0068 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02559 | hp1 | a0002 | c0001 | t0103 | g0065 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG02559 | hp2 | a0002 | c0001 | t0012 | g0025 | AFR | ACB | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03471 | hp1 | a0002 | c0013 | t0097 | g0057 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG03471 | hp2 | a0002 | c0001 | t0006 | g0014 | AFR | MSL | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG06807 | hp1 | a0002 | c0001 | t0096 | g0085 | AFR | USA | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
HG06807 | hp2 | a0002 | c0001 | t0083 | g0053 | AFR | USA | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18955 | hp1 | a0001 | c0004 | t0003 | g0237 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA20300 | hp1 | a0002 | c0001 | t0033 | g0055 | AFR | USA | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA20300 | hp2 | a0002 | c0001 | t0077 | g0079 | AFR | USA | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA21309 | hp1 | a0002 | c0001 | t0018 | g0024 | AFR | LWK | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
NA21309 | hp2 | a0001 | c0006 | t0028 | g0187 | AFR | LWK | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
homoSapiens | chm13v2 | a0001 | c0006 | t0004 | g0200 | REF | REF | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
homoSapiens | grch38p0 | a0003 | c0003 | t0009 | g0030 | REF | REF | LONRF2_chr2_100266875_100327501 | LONRF2 | chr2 | 100266875 | 100327501 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:100287023 | T | C | 1 | a0010 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1961A>G | p.Asp654Gly | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/12 | 2369/15096 | 1961/2265 | 654/754 | chr2 | 100287023 | |||
chr2:100287033 | C | T | 1 | a0006 | 3 | HG02965.hp1 NA18522.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.1951G>A | p.Ala651Thr | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/12 | 2359/15096 | 1951/2265 | 651/754 | chr2 | 100287033 | |||
chr2:100294233 | C | T | 1 | a0009 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1753G>A | p.Ala585Thr | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/12 | 2161/15096 | 1753/2265 | 585/754 | chr2 | 100294233 | |||
chr2:100299310 | A | G | 11 | a0001 a0002 a0004 others(8): Show |
308 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(305): Show |
missense_variant | MODERATE | c.1277T>C | p.Leu426Pro | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 6/12 | 1685/15096 | 1277/2265 | 426/754 | chr2 | 100299310 | |||
chr2:100300766 | A | G | 1 | a0005 | 4 | NA18948.hp1 NA18953.hp1 NA18961.hp2 others(1): Show |
missense_variant | MODERATE | c.943T>C | p.Ser315Pro | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/12 | 1351/15096 | 943/2265 | 315/754 | chr2 | 100300766 | |||
chr2:100309175 | T | G | 1 | a0013 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.730A>C | p.Met244Leu | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/12 | 1138/15096 | 730/2265 | 244/754 | chr2 | 100309175 | |||
chr2:100309195 | C | T | 1 | a0012 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.710G>A | p.Arg237Gln | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/12 | 1118/15096 | 710/2265 | 237/754 | chr2 | 100309195 | |||
chr2:100321601 | G | A | 1 | a0011 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.493C>T | p.Arg165Cys | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/12 | 901/15096 | 493/2265 | 165/754 | chr2 | 100321601 | |||
chr2:100321703 | C | T | 1 | a0008 | 2 | HG04184.hp2 NA18973.hp1 |
missense_variant | MODERATE | c.391G>A | p.Ala131Thr | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/12 | 799/15096 | 391/2265 | 131/754 | chr2 | 100321703 | |||
chr2:100321764 | G | C | 6 | a0001 a0004 a0005 others(3): Show |
164 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(161): Show |
missense_variant | MODERATE | c.330C>G | p.Asp110Glu | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/12 | 738/15096 | 330/2265 | 110/754 | chr2 | 100321764 | |||
chr2:100322019 | C | G | 5 | a0001 a0005 a0007 others(2): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(146): Show |
missense_variant | MODERATE | c.75G>C | p.Gln25His | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/12 | 483/15096 | 75/2265 | 25/754 | chr2 | 100322019 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:100286989 | C | T | 1 | a0002c0025 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1995G>A | p.Ala665Ala | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/12 | 2403/15096 | 1995/2265 | 665/754 | chr2 | 100286989 | |||
chr2:100295518 | C | T | 1 | a0002c0013 | 3 | HG02809.hp2 HG03471.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1512G>A | p.Leu504Leu | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 8/12 | 1920/15096 | 1512/2265 | 504/754 | chr2 | 100295518 | |||
chr2:100299796 | G | A | 2 | a0002c0018 a0002c0025 |
3 | HG02109.hp1 HG02258.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.1188C>T | p.Ser396Ser | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 5/12 | 1596/15096 | 1188/2265 | 396/754 | chr2 | 100299796 | |||
chr2:100299844 | A | G | 25 | a0001c0002 a0001c0004 a0001c0006 others(22): Show |
308 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(305): Show |
synonymous_variant | LOW | c.1140T>C | p.Phe380Phe | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 5/12 | 1548/15096 | 1140/2265 | 380/754 | chr2 | 100299844 | |||
chr2:100299853 | A | G | 6 | a0001c0002 a0001c0006 a0002c0022 others(3): Show |
88 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
synonymous_variant | LOW | c.1131T>C | p.Gly377Gly | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 5/12 | 1539/15096 | 1131/2265 | 377/754 | chr2 | 100299853 | |||
chr2:100300647 | C | T | 9 | a0001c0002 a0001c0004 a0001c0006 others(6): Show |
144 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(141): Show |
synonymous_variant | LOW | c.1062G>A | p.Ser354Ser | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/12 | 1470/15096 | 1062/2265 | 354/754 | chr2 | 100300647 | |||
chr2:100309218 | A | G | 1 | a0002c0012 | 3 | HG02622.hp1 HG02723.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.687T>C | p.Asp229Asp | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/12 | 1095/15096 | 687/2265 | 229/754 | chr2 | 100309218 | |||
chr2:100321743 | G | A | 1 | a0002c0005 | 20 | HG00735.hp1 HG00738.hp2 HG01081.hp2 others(17): Show |
synonymous_variant | LOW | c.351C>T | p.Asn117Asn | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/12 | 759/15096 | 351/2265 | 117/754 | chr2 | 100321743 | |||
chr2:100321779 | G | A | 8 | a0001c0002 a0001c0004 a0001c0008 others(5): Show |
140 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
synonymous_variant | LOW | c.315C>T | p.Ala105Ala | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/12 | 723/15096 | 315/2265 | 105/754 | chr2 | 100321779 | |||
chr2:100321866 | T | C | 12 | a0001c0002 a0001c0004 a0001c0006 others(9): Show |
164 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(161): Show |
synonymous_variant | LOW | c.228A>G | p.Glu76Glu | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/12 | 636/15096 | 228/2265 | 76/754 | chr2 | 100321866 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:100271893 | C | T | 1 | a0002c0012t0088 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12405G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 12405 | chr2 | 100271893 | ||||||
chr2:100271981 | C | T | 1 | a0001c0006t0120 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12317G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 12317 | chr2 | 100271981 | ||||||
chr2:100272035 | T | A | 30 | a0001c0002t0122 a0001c0004t0007 a0001c0004t0105 others(27): Show |
65 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*12263A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 12263 | chr2 | 100272035 | ||||||
chr2:100272235 | T | C | 30 | a0001c0002t0122 a0001c0004t0007 a0001c0004t0105 others(27): Show |
65 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*12063A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 12063 | chr2 | 100272235 | ||||||
chr2:100272335 | T | C | 1 | a0001c0004t0109 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11963A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 11963 | chr2 | 100272335 | ||||||
chr2:100272492 | A | C | 30 | a0001c0002t0122 a0001c0004t0007 a0001c0004t0105 others(27): Show |
65 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*11806T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 11806 | chr2 | 100272492 | ||||||
chr2:100272635 | A | AGT | 94 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(91): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*11661_*11662dupAC | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 11662 | chr2 | 100272635 | ||||||
chr2:100272668 | C | T | 14 | a0001c0002t0122 a0002c0001t0074 a0002c0001t0075 others(11): Show |
32 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*11630G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 11630 | chr2 | 100272668 | ||||||
chr2:100272753 | C | T | 1 | a0002c0005t0069 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11545G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 11545 | chr2 | 100272753 | ||||||
chr2:100272907 | G | A | 1 | a0002c0013t0036 | 2 | HG02809.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11391C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 11391 | chr2 | 100272907 | ||||||
chr2:100272924 | T | C | 30 | a0001c0002t0122 a0001c0004t0007 a0001c0004t0105 others(27): Show |
65 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*11374A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 11374 | chr2 | 100272924 | ||||||
chr2:100273043 | G | A | 2 | a0002c0001t0032 a0012c0021t0085 |
3 | HG02572.hp2 HG03041.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11255C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 11255 | chr2 | 100273043 | ||||||
chr2:100273155 | C | T | 4 | a0002c0001t0055 a0002c0001t0057 a0002c0018t0037 others(1): Show |
5 | HG01169.hp2 HG02109.hp1 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*11143G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 11143 | chr2 | 100273155 | ||||||
chr2:100273173 | C | T | 1 | a0002c0001t0071 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11125G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 11125 | chr2 | 100273173 | ||||||
chr2:100273245 | C | T | 1 | a0002c0025t0098 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11053G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 11053 | chr2 | 100273245 | ||||||
chr2:100273325 | T | A | 1 | a0002c0001t0075 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10973A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 10973 | chr2 | 100273325 | ||||||
chr2:100273479 | T | G | 13 | a0001c0008t0039 a0002c0001t0032 a0002c0001t0033 others(10): Show |
18 | HG01516.hp2 HG02257.hp1 HG02280.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*10819A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 10819 | chr2 | 100273479 | ||||||
chr2:100273572 | T | G | 6 | a0002c0001t0012 a0002c0001t0018 a0002c0001t0042 others(3): Show |
14 | HG01261.hp1 HG01884.hp2 HG02451.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*10726A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 10726 | chr2 | 100273572 | ||||||
chr2:100273850 | G | C | 1 | a0001c0002t0117 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10448C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 10448 | chr2 | 100273850 | ||||||
chr2:100274043 | C | T | 2 | a0002c0001t0031 a0002c0001t0076 |
3 | HG02055.hp2 HG02280.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10255G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 10255 | chr2 | 100274043 | ||||||
chr2:100274340 | C | T | 1 | a0003c0003t0091 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9958G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 9958 | chr2 | 100274340 | ||||||
chr2:100274341 | C | A | 1 | a0003c0003t0091 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9957G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 9957 | chr2 | 100274341 | ||||||
chr2:100274366 | C | T | 1 | a0001c0004t0108 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9932G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 9932 | chr2 | 100274366 | ||||||
chr2:100274843 | C | T | 1 | a0006c0014t0070 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9455G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 9455 | chr2 | 100274843 | ||||||
chr2:100274856 | G | A | 1 | a0001c0004t0105 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9442C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 9442 | chr2 | 100274856 | ||||||
chr2:100274890 | T | C | 1 | a0002c0001t0079 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9408A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 9408 | chr2 | 100274890 | ||||||
chr2:100274941 | C | T | 10 | a0001c0004t0007 a0001c0004t0105 a0002c0001t0042 others(7): Show |
19 | HG00639.hp2 HG00738.hp2 HG01169.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*9357G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 9357 | chr2 | 100274941 | ||||||
chr2:100274949 | C | T | 1 | a0007c0016t0115 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9349G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 9349 | chr2 | 100274949 | ||||||
chr2:100274974 | G | A | 1 | a0003c0003t0011 | 6 | NA18951.hp2 NA18960.hp1 NA19005.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9324C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 9324 | chr2 | 100274974 | ||||||
chr2:100274997 | G | A | 6 | a0001c0008t0041 a0002c0001t0006 a0002c0001t0077 others(3): Show |
15 | HG01884.hp1 HG02055.hp1 HG02451.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*9301C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 9301 | chr2 | 100274997 | ||||||
chr2:100275299 | C | T | 1 | a0004c0007t0119 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8999G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8999 | chr2 | 100275299 | ||||||
chr2:100275341 | G | A | 1 | a0002c0001t0101 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8957C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8957 | chr2 | 100275341 | ||||||
chr2:100275416 | C | T | 1 | a0002c0001t0056 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8882G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8882 | chr2 | 100275416 | ||||||
chr2:100275446 | C | A | 1 | a0002c0001t0087 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8852G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8852 | chr2 | 100275446 | ||||||
chr2:100275511 | G | A | 1 | a0012c0021t0085 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8787C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8787 | chr2 | 100275511 | ||||||
chr2:100275514 | C | T | 118 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(115): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*8784G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8784 | chr2 | 100275514 | ||||||
chr2:100275556 | G | A | 25 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(22): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*8742C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8742 | chr2 | 100275556 | ||||||
chr2:100275826 | T | A | 1 | a0003c0003t0029 | 2 | HG00323.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8472A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8472 | chr2 | 100275826 | ||||||
chr2:100275862 | A | G | 15 | a0001c0002t0026 a0001c0004t0003 a0001c0004t0038 others(12): Show |
58 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*8436T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8436 | chr2 | 100275862 | ||||||
chr2:100275918 | G | A | 1 | a0001c0002t0118 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8380C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8380 | chr2 | 100275918 | ||||||
chr2:100275971 | G | T | 6 | a0002c0001t0006 a0002c0001t0019 a0002c0001t0077 others(3): Show |
17 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*8327C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8327 | chr2 | 100275971 | ||||||
chr2:100275972 | C | T | 1 | a0002c0005t0063 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8326G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8326 | chr2 | 100275972 | ||||||
chr2:100276018 | C | T | 6 | a0001c0004t0007 a0001c0004t0105 a0001c0004t0111 others(3): Show |
14 | HG00639.hp2 HG01169.hp1 HG01257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*8280G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8280 | chr2 | 100276018 | ||||||
chr2:100276054 | C | T | 114 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(111): Show |
308 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*8244G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8244 | chr2 | 100276054 | ||||||
chr2:100276060 | T | C | 6 | a0001c0004t0007 a0001c0004t0105 a0001c0004t0111 others(3): Show |
14 | HG00639.hp2 HG01169.hp1 HG01257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*8238A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 8238 | chr2 | 100276060 | ||||||
chr2:100276412 | G | A | 2 | a0001c0006t0028 a0001c0006t0123 |
4 | HG00642.hp2 HG01074.hp2 HG04204.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7886C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7886 | chr2 | 100276412 | ||||||
chr2:100276651 | C | A | 120 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(117): Show |
322 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*7647G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7647 | chr2 | 100276651 | ||||||
chr2:100276713 | T | C | 6 | a0001c0004t0007 a0001c0004t0105 a0001c0004t0111 others(3): Show |
14 | HG00639.hp2 HG01169.hp1 HG01257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*7585A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7585 | chr2 | 100276713 | ||||||
chr2:100276789 | T | G | 4 | a0002c0001t0012 a0002c0001t0018 a0002c0001t0093 others(1): Show |
12 | HG01261.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7509A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7509 | chr2 | 100276789 | ||||||
chr2:100276820 | T | C | 1 | a0001c0004t0110 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7478A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7478 | chr2 | 100276820 | ||||||
chr2:100276889 | G | A | 1 | a0002c0001t0072 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7409C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7409 | chr2 | 100276889 | ||||||
chr2:100276890 | G | C | 4 | a0002c0001t0012 a0002c0001t0018 a0002c0001t0093 others(1): Show |
12 | HG01261.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7408C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7408 | chr2 | 100276890 | ||||||
chr2:100276937 | C | T | 1 | a0008c0017t0081 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7361G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7361 | chr2 | 100276937 | ||||||
chr2:100276943 | C | T | 1 | a0003c0003t0048 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7355G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7355 | chr2 | 100276943 | ||||||
chr2:100276989 | C | T | 1 | a0002c0001t0101 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7309G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7309 | chr2 | 100276989 | ||||||
chr2:100277018 | C | T | 2 | a0002c0001t0096 a0003c0003t0048 |
2 | HG02735.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7280G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7280 | chr2 | 100277018 | ||||||
chr2:100277106 | C | G | 1 | a0002c0001t0058 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7192G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 7192 | chr2 | 100277106 | ||||||
chr2:100277458 | A | C | 1 | a0002c0001t0068 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6840T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6840 | chr2 | 100277458 | ||||||
chr2:100277550 | G | A | 1 | a0001c0006t0123 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6748C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6748 | chr2 | 100277550 | ||||||
chr2:100277652 | C | G | 91 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(88): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*6646G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6646 | chr2 | 100277652 | ||||||
chr2:100277653 | T | C | 91 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(88): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*6645A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6645 | chr2 | 100277653 | ||||||
chr2:100277678 | T | C | 7 | a0001c0004t0007 a0001c0004t0105 a0001c0004t0111 others(4): Show |
15 | HG00609.hp1 HG00639.hp2 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*6620A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6620 | chr2 | 100277678 | ||||||
chr2:100277705 | C | T | 5 | a0001c0002t0002 a0001c0002t0117 a0001c0002t0118 others(2): Show |
35 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*6593G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6593 | chr2 | 100277705 | ||||||
chr2:100277713 | G | C | 1 | a0002c0001t0043 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6585C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6585 | chr2 | 100277713 | ||||||
chr2:100277925 | C | T | 10 | a0001c0008t0040 a0001c0008t0041 a0001c0008t0124 others(7): Show |
23 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*6373G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6373 | chr2 | 100277925 | ||||||
chr2:100277982 | A | G | 1 | a0001c0002t0027 | 3 | HG01192.hp1 HG02698.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6316T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6316 | chr2 | 100277982 | ||||||
chr2:100277988 | C | T | 1 | a0002c0001t0101 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6310G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6310 | chr2 | 100277988 | ||||||
chr2:100277989 | G | A | 8 | a0002c0001t0032 a0002c0001t0034 a0002c0001t0056 others(5): Show |
10 | HG02280.hp1 HG02572.hp2 HG02895.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6309C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6309 | chr2 | 100277989 | ||||||
chr2:100278029 | C | A | 25 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(22): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*6269G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6269 | chr2 | 100278029 | ||||||
chr2:100278256 | G | C | 1 | a0001c0006t0121 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6042C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 6042 | chr2 | 100278256 | ||||||
chr2:100278300 | G | C | 1 | a0002c0001t0073 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5998C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5998 | chr2 | 100278300 | ||||||
chr2:100278314 | G | A | 1 | a0002c0010t0023 | 3 | HG04184.hp1 NA18977.hp1 NA18994.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5984C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5984 | chr2 | 100278314 | ||||||
chr2:100278340 | C | G | 124 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(121): Show |
326 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*5958G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5958 | chr2 | 100278340 | ||||||
chr2:100278391 | C | T | 3 | a0001c0008t0039 a0002c0012t0035 a0002c0012t0088 |
5 | HG02622.hp1 HG02723.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5907G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5907 | chr2 | 100278391 | ||||||
chr2:100278425 | C | T | 99 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(96): Show |
287 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*5873G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5873 | chr2 | 100278425 | ||||||
chr2:100278443 | G | A | 1 | a0002c0001t0096 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5855C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5855 | chr2 | 100278443 | ||||||
chr2:100278578 | G | C | 4 | a0002c0001t0012 a0002c0001t0018 a0002c0001t0093 others(1): Show |
12 | HG01261.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5720C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5720 | chr2 | 100278578 | ||||||
chr2:100278619 | G | A | 95 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(92): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*5679C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5679 | chr2 | 100278619 | ||||||
chr2:100278679 | C | G | 3 | a0002c0013t0036 a0002c0013t0097 a0002c0025t0098 |
4 | HG02109.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5619G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5619 | chr2 | 100278679 | ||||||
chr2:100278684 | C | T | 1 | a0002c0001t0065 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5614G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5614 | chr2 | 100278684 | ||||||
chr2:100278700 | T | C | 15 | a0001c0002t0020 a0001c0002t0116 a0001c0006t0123 others(12): Show |
20 | HG00280.hp1 HG01074.hp1 HG01346.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*5598A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5598 | chr2 | 100278700 | ||||||
chr2:100278701 | T | C | 1 | a0001c0006t0130 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5597A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5597 | chr2 | 100278701 | ||||||
chr2:100278707 | G | A | 1 | a0001c0004t0112 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5591C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5591 | chr2 | 100278707 | ||||||
chr2:100278809 | C | T | 12 | a0001c0002t0025 a0002c0001t0012 a0002c0001t0032 others(9): Show |
27 | HG01261.hp1 HG01884.hp2 HG02080.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5489G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5489 | chr2 | 100278809 | ||||||
chr2:100278874 | G | A | 3 | a0001c0008t0039 a0002c0012t0035 a0002c0012t0088 |
5 | HG02622.hp1 HG02723.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5424C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5424 | chr2 | 100278874 | ||||||
chr2:100278897 | A | G | 1 | a0003c0003t0046 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5401T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5401 | chr2 | 100278897 | ||||||
chr2:100278949 | A | C | 1 | a0001c0008t0124 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5349T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5349 | chr2 | 100278949 | ||||||
chr2:100279110 | G | T | 1 | a0002c0005t0063 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5188C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5188 | chr2 | 100279110 | ||||||
chr2:100279232 | C | A | 2 | a0008c0017t0081 a0008c0017t0082 |
2 | HG04184.hp2 NA18973.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5066G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5066 | chr2 | 100279232 | ||||||
chr2:100279248 | G | A | 1 | a0002c0001t0062 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5050C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5050 | chr2 | 100279248 | ||||||
chr2:100279260 | G | A | 1 | a0003c0003t0052 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5038C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5038 | chr2 | 100279260 | ||||||
chr2:100279267 | T | A | 11 | a0001c0008t0040 a0001c0008t0041 a0001c0008t0124 others(8): Show |
24 | HG01243.hp1 HG01358.hp2 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5031A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 5031 | chr2 | 100279267 | ||||||
chr2:100279322 | AC | A | 113 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(110): Show |
309 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*4975delG | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4975 | chr2 | 100279322 | ||||||
chr2:100279410 | G | A | 93 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(90): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*4888C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4888 | chr2 | 100279410 | ||||||
chr2:100279589 | C | G | 1 | a0002c0001t0095 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4709G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4709 | chr2 | 100279589 | ||||||
chr2:100279635 | G | A | 1 | a0002c0001t0096 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4663C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4663 | chr2 | 100279635 | ||||||
chr2:100279648 | T | C | 93 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(90): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*4650A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4650 | chr2 | 100279648 | ||||||
chr2:100279650 | C | T | 93 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(90): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*4648G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4648 | chr2 | 100279650 | ||||||
chr2:100279736 | C | T | 1 | a0002c0013t0097 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4562G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4562 | chr2 | 100279736 | ||||||
chr2:100279780 | A | G | 93 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(90): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*4518T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4518 | chr2 | 100279780 | ||||||
chr2:100279849 | G | T | 93 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(90): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*4449C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4449 | chr2 | 100279849 | ||||||
chr2:100279884 | T | C | 1 | a0002c0001t0034 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4414A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4414 | chr2 | 100279884 | ||||||
chr2:100279905 | G | C | 3 | a0002c0001t0012 a0002c0001t0093 a0002c0001t0094 |
8 | HG01261.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4393C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4393 | chr2 | 100279905 | ||||||
chr2:100279914 | G | C | 92 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(89): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*4384C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4384 | chr2 | 100279914 | ||||||
chr2:100279953 | C | T | 92 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(89): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*4345G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4345 | chr2 | 100279953 | ||||||
chr2:100279961 | A | G | 1 | a0002c0005t0061 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4337T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4337 | chr2 | 100279961 | ||||||
chr2:100280050 | G | A | 92 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(89): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*4248C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 4248 | chr2 | 100280050 | ||||||
chr2:100280358 | C | T | 1 | a0003c0003t0044 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3940G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3940 | chr2 | 100280358 | ||||||
chr2:100280501 | C | T | 1 | a0002c0001t0096 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3797G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3797 | chr2 | 100280501 | ||||||
chr2:100280502 | A | G | 122 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(119): Show |
322 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*3796T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3796 | chr2 | 100280502 | ||||||
chr2:100280504 | G | A | 92 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(89): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*3794C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3794 | chr2 | 100280504 | ||||||
chr2:100280546 | C | T | 92 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(89): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*3752G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3752 | chr2 | 100280546 | ||||||
chr2:100280611 | T | TA | 5 | a0002c0001t0018 a0002c0001t0031 a0002c0001t0076 others(2): Show |
9 | HG02055.hp2 HG02280.hp2 HG03139.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3686dupT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3686 | chr2 | 100280611 | ||||||
chr2:100280650 | G | A | 93 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(90): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*3648C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3648 | chr2 | 100280650 | ||||||
chr2:100280692 | A | G | 2 | a0002c0001t0083 a0002c0001t0084 |
2 | HG03195.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3606T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3606 | chr2 | 100280692 | ||||||
chr2:100280738 | G | A | 2 | a0001c0002t0127 a0002c0001t0103 |
2 | HG00438.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3560C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3560 | chr2 | 100280738 | ||||||
chr2:100280752 | G | A | 92 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(89): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*3546C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3546 | chr2 | 100280752 | ||||||
chr2:100280889 | T | A | 92 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(89): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*3409A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3409 | chr2 | 100280889 | ||||||
chr2:100280997 | T | C | 2 | a0002c0001t0018 a0002c0001t0095 |
5 | HG03139.hp2 HG03453.hp1 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3301A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3301 | chr2 | 100280997 | ||||||
chr2:100281089 | G | A | 1 | a0002c0001t0078 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3209C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3209 | chr2 | 100281089 | ||||||
chr2:100281111 | G | A | 92 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(89): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*3187C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3187 | chr2 | 100281111 | ||||||
chr2:100281174 | A | G | 1 | a0001c0004t0106 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3124T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3124 | chr2 | 100281174 | ||||||
chr2:100281212 | T | A | 120 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(117): Show |
320 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*3086A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3086 | chr2 | 100281212 | ||||||
chr2:100281212 | T | G | 1 | a0001c0004t0113 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3086A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3086 | chr2 | 100281212 | ||||||
chr2:100281213 | G | T | 1 | a0001c0004t0113 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3085C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3085 | chr2 | 100281213 | ||||||
chr2:100281214 | T | C | 1 | a0001c0004t0113 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3084A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3084 | chr2 | 100281214 | ||||||
chr2:100281244 | G | A | 1 | a0004c0007t0128 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3054C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3054 | chr2 | 100281244 | ||||||
chr2:100281277 | GTTTT | G | 92 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(89): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*3017_*3020delAAAA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 3017 | chr2 | 100281277 | ||||||
chr2:100281469 | C | T | 2 | a0008c0017t0081 a0008c0017t0082 |
2 | HG04184.hp2 NA18973.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2829G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 2829 | chr2 | 100281469 | ||||||
chr2:100281472 | A | T | 2 | a0002c0001t0080 a0004c0007t0114 |
2 | HG00609.hp1 NA18957.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2826T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 2826 | chr2 | 100281472 | ||||||
chr2:100281619 | T | C | 48 | a0001c0004t0003 a0001c0004t0007 a0001c0004t0014 others(45): Show |
141 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2679A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 2679 | chr2 | 100281619 | ||||||
chr2:100281654 | C | T | 1 | a0003c0003t0089 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2644G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 2644 | chr2 | 100281654 | ||||||
chr2:100281885 | GT | G | 5 | a0001c0004t0113 a0001c0008t0039 a0002c0012t0035 others(2): Show |
7 | HG01069.hp2 HG02622.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2412delA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 2412 | chr2 | 100281885 | ||||||
chr2:100281933 | G | T | 1 | a0001c0004t0105 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2365C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 2365 | chr2 | 100281933 | ||||||
chr2:100282001 | T | C | 1 | a0002c0001t0059 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2297A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 2297 | chr2 | 100282001 | ||||||
chr2:100282172 | G | T | 93 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(90): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*2126C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 2126 | chr2 | 100282172 | ||||||
chr2:100282659 | T | C | 1 | a0001c0002t0129 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1639A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 1639 | chr2 | 100282659 | ||||||
chr2:100282797 | AAAACTAA others(43): Show |
A | 124 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(121): Show |
324 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*1451_*1500delAGTT others(46): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 1451 | chr2 | 100282797 | ||||||
chr2:100282848 | A | G | 124 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(121): Show |
324 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*1450T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 1450 | chr2 | 100282848 | ||||||
chr2:100282849 | C | T | 124 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(121): Show |
324 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*1449G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 1449 | chr2 | 100282849 | ||||||
chr2:100282866 | T | TA | 124 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(121): Show |
324 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*1431dupT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 1431 | chr2 | 100282866 | ||||||
chr2:100283203 | G | A | 92 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(89): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*1095C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 1095 | chr2 | 100283203 | ||||||
chr2:100283214 | T | C | 92 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(89): Show |
270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*1084A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 1084 | chr2 | 100283214 | ||||||
chr2:100283386 | T | G | 1 | a0002c0001t0079 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*912A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 912 | chr2 | 100283386 | ||||||
chr2:100283576 | A | AAT | 102 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(99): Show |
297 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*720_*721dupAT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 721 | chr2 | 100283576 | ||||||
chr2:100283576 | A | AATAT | 4 | a0002c0001t0042 a0002c0001t0043 a0002c0001t0058 others(1): Show |
4 | HG02809.hp1 HG03225.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*718_*721dupATAT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 721 | chr2 | 100283576 | ||||||
chr2:100283803 | G | A | 1 | a0001c0006t0130 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*495C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 495 | chr2 | 100283803 | ||||||
chr2:100283842 | T | C | 106 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(103): Show |
301 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*456A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 456 | chr2 | 100283842 | ||||||
chr2:100283917 | C | T | 48 | a0001c0004t0003 a0001c0004t0007 a0001c0004t0014 others(45): Show |
141 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*381G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 381 | chr2 | 100283917 | ||||||
chr2:100283944 | G | A | 121 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(118): Show |
321 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(318): Show |
3_prime_UTR_variant | MODIFIER | c.*354C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 354 | chr2 | 100283944 | ||||||
chr2:100284114 | C | T | 2 | a0002c0001t0042 a0002c0001t0043 |
2 | HG02809.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*184G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 184 | chr2 | 100284114 | ||||||
chr2:100284229 | C | T | 1 | a0001c0002t0013 | 6 | HG00597.hp1 NA18612.hp1 NA18951.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 12/12 | 69 | chr2 | 100284229 | ||||||
chr2:100322455 | G | C | 48 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(45): Show |
160 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
5_prime_UTR_variant | MODIFIER | c.-362C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/12 | 362 | chr2 | 100322455 | ||||||
chr2:100322490 | T | C | 49 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0013 others(46): Show |
164 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(161): Show |
5_prime_UTR_variant | MODIFIER | c.-397A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/12 | 397 | chr2 | 100322490 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:100284649 | T | G | 4 | a0001c0008t0039g0039 a0002c0012t0035g0075 a0002c0012t0035g0076 others(1): Show |
5 | HG02622.hp1 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2071-157A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100284649 | |||||||
chr2:100284651 | GT | G | 2 | a0001c0008t0040g0038 a0001c0008t0125g0210 |
3 | HG01891.hp1 HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2071-160delA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100284651 | |||||||
chr2:100284669 | C | T | 3 | a0002c0005t0001g0018 a0002c0005t0001g0175 a0002c0005t0061g0181 |
5 | HG00735.hp1 HG01081.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.2071-177G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100284669 | |||||||
chr2:100284723 | C | T | 1 | a0006c0014t0070g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2071-231G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100284723 | |||||||
chr2:100284777 | G | A | 1 | a0001c0006t0121g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2071-285C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100284777 | |||||||
chr2:100284864 | C | T | 2 | a0002c0001t0080g0132 a0004c0007t0114g0272 |
2 | HG00609.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.2071-372G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100284864 | |||||||
chr2:100284898 | A | G | 5 | a0002c0001t0001g0141 a0002c0001t0001g0162 a0002c0001t0001g0163 others(2): Show |
5 | NA18747.hp1 NA18944.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.2071-406T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100284898 | |||||||
chr2:100284977 | G | A | 2 | a0001c0008t0040g0038 a0001c0008t0125g0210 |
3 | HG01891.hp1 HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2071-485C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100284977 | |||||||
chr2:100285095 | C | T | 242 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(239): Show |
321 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.2071-603G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100285095 | |||||||
chr2:100285199 | G | A | 242 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(239): Show |
321 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.2071-707C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100285199 | |||||||
chr2:100285230 | A | C | 2 | a0002c0001t0080g0132 a0004c0007t0114g0272 |
2 | HG00609.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.2071-738T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100285230 | |||||||
chr2:100285402 | G | A | 2 | a0001c0004t0003g0235 a0001c0004t0003g0239 |
2 | NA18952.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.2071-910C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100285402 | |||||||
chr2:100285570 | C | T | 198 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(195): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.2071-1078G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100285570 | |||||||
chr2:100285689 | C | T | 2 | a0005c0009t0003g0019 a0005c0009t0003g0196 |
4 | NA18948.hp1 NA18953.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.2071-1197G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100285689 | |||||||
chr2:100285704 | G | A | 198 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(195): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.2070+1210C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100285704 | |||||||
chr2:100285731 | C | T | 3 | a0001c0004t0014g0011 a0001c0004t0014g0233 a0001c0004t0110g0243 |
6 | HG00544.hp1 HG00621.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.2070+1183G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100285731 | |||||||
chr2:100285762 | C | T | 15 | a0001c0008t0039g0039 a0002c0001t0032g0061 a0002c0001t0032g0062 others(12): Show |
16 | HG01516.hp2 HG02572.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.2070+1152G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100285762 | |||||||
chr2:100285956 | T | C | 1 | a0002c0001t0012g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2070+958A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100285956 | |||||||
chr2:100286546 | C | G | 198 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(195): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.2070+368G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100286546 | |||||||
chr2:100286601 | C | A | 2 | a0002c0001t0080g0132 a0004c0007t0114g0272 |
2 | HG00609.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.2070+313G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100286601 | |||||||
chr2:100286826 | T | C | 2 | a0008c0017t0081g0044 a0008c0017t0082g0045 |
2 | HG04184.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2070+88A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100286826 | |||||||
chr2:100286885 | G | T | 1 | a0004c0011t0004g0023 | 3 | NA18953.hp2 NA18954.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2070+29C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100286885 | |||||||
chr2:100286895 | G | T | 19 | a0001c0008t0039g0039 a0002c0001t0032g0061 a0002c0001t0032g0062 others(16): Show |
20 | HG00609.hp1 HG01516.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.2070+19C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 11/11 | chr2 | 100286895 | |||||||
chr2:100287158 | G | T | 1 | a0002c0001t0096g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1921-95C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100287158 | |||||||
chr2:100287288 | A | T | 3 | a0002c0018t0037g0058 a0002c0018t0037g0174 a0002c0025t0098g0080 |
3 | HG02109.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1921-225T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100287288 | |||||||
chr2:100287347 | C | T | 1 | a0002c0001t0001g0083 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1921-284G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100287347 | |||||||
chr2:100287349 | T | C | 1 | a0001c0004t0003g0241 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1921-286A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100287349 | |||||||
chr2:100287465 | T | C | 1 | a0002c0001t0042g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1921-402A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100287465 | |||||||
chr2:100287466 | T | C | 1 | a0002c0001t0042g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1921-403A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100287466 | |||||||
chr2:100287467 | T | C | 1 | a0002c0001t0042g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1921-404A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100287467 | |||||||
chr2:100287468 | T | A | 1 | a0002c0001t0042g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1921-405A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100287468 | |||||||
chr2:100287580 | T | C | 1 | a0002c0001t0095g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1921-517A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100287580 | |||||||
chr2:100287592 | C | T | 1 | a0008c0017t0081g0044 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1921-529G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100287592 | |||||||
chr2:100287971 | T | C | 1 | a0002c0012t0035g0076 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1921-908A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100287971 | |||||||
chr2:100288055 | T | A | 1 | a0002c0010t0023g0120 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1921-992A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288055 | |||||||
chr2:100288095 | C | T | 1 | a0003c0003t0047g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1921-1032G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288095 | |||||||
chr2:100288180 | T | C | 3 | a0002c0001t0055g0059 a0002c0001t0056g0117 a0002c0001t0057g0166 |
3 | HG01169.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1921-1117A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288180 | |||||||
chr2:100288186 | T | C | 1 | a0002c0001t0096g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1921-1123A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288186 | |||||||
chr2:100288340 | C | T | 1 | a0002c0001t0096g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1921-1277G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288340 | |||||||
chr2:100288379 | G | T | 1 | a0002c0010t0023g0120 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1921-1316C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288379 | |||||||
chr2:100288400 | A | T | 1 | a0002c0001t0075g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1921-1337T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288400 | |||||||
chr2:100288446 | C | T | 1 | a0002c0001t0043g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1921-1383G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288446 | |||||||
chr2:100288639 | A | C | 221 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(218): Show |
299 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.1921-1576T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288639 | |||||||
chr2:100288639 | A | T | 2 | a0002c0001t0001g0123 a0013c0026t0001g0138 |
2 | NA18962.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1921-1576T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288639 | |||||||
chr2:100288733 | G | A | 1 | a0004c0007t0119g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1920+1525C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288733 | |||||||
chr2:100288812 | C | A | 198 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(195): Show |
271 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.1920+1446G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100288812 | |||||||
chr2:100289051 | G | A | 107 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(104): Show |
143 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1920+1207C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289051 | |||||||
chr2:100289153 | A | C | 9 | a0002c0001t0032g0061 a0002c0001t0032g0062 a0002c0001t0034g0164 others(6): Show |
9 | HG02572.hp2 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1920+1105T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289153 | |||||||
chr2:100289173 | C | T | 3 | a0003c0003t0024g0146 a0003c0003t0024g0151 a0003c0003t0024g0153 |
3 | HG01891.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1920+1085G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289173 | |||||||
chr2:100289175 | CCAT | C | 93 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(90): Show |
130 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1920+1080_1920+108 others(7): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289175 | |||||||
chr2:100289239 | G | T | 4 | a0002c0001t0005g0002 a0002c0001t0005g0006 a0002c0001t0005g0135 others(1): Show |
13 | HG00735.hp2 HG00741.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1920+1019C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289239 | |||||||
chr2:100289352 | A | G | 1 | a0009c0020t0126g0263 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1920+906T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289352 | |||||||
chr2:100289366 | A | G | 200 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(197): Show |
273 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.1920+892T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289366 | |||||||
chr2:100289414 | A | G | 1 | a0002c0001t0093g0168 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1920+844T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289414 | |||||||
chr2:100289430 | CT | C | 127 | a0001c0002t0002g0041 a0001c0002t0013g0245 a0001c0004t0003g0003 others(124): Show |
167 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(164): Show |
intron_variant | MODIFIER | c.1920+827delA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289430 | |||||||
chr2:100289430 | CTT | C | 103 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(100): Show |
142 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1920+826_1920+827d others(4): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289430 | |||||||
chr2:100289475 | G | A | 3 | a0002c0001t0055g0059 a0002c0001t0056g0117 a0002c0001t0057g0166 |
3 | HG01169.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1920+783C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289475 | |||||||
chr2:100289599 | T | C | 118 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(115): Show |
160 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1920+659A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289599 | |||||||
chr2:100289602 | A | AT | 93 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(90): Show |
130 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1920+655dupA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289602 | |||||||
chr2:100289620 | T | C | 1 | a0002c0001t0101g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1920+638A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289620 | |||||||
chr2:100289622 | G | C | 118 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(115): Show |
160 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1920+636C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289622 | |||||||
chr2:100289638 | G | A | 5 | a0002c0001t0096g0085 a0002c0013t0097g0057 a0002c0018t0037g0058 others(2): Show |
5 | HG02109.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1920+620C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289638 | |||||||
chr2:100289690 | C | T | 4 | a0001c0008t0039g0039 a0002c0012t0035g0075 a0002c0012t0035g0076 others(1): Show |
5 | HG02622.hp1 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1920+568G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289690 | |||||||
chr2:100289754 | G | C | 3 | a0002c0018t0037g0058 a0002c0018t0037g0174 a0002c0025t0098g0080 |
3 | HG02109.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1920+504C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289754 | |||||||
chr2:100289813 | T | C | 6 | a0001c0008t0039g0039 a0002c0001t0033g0055 a0002c0001t0033g0056 others(3): Show |
7 | HG01516.hp2 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1920+445A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289813 | |||||||
chr2:100289860 | C | T | 1 | a0001c0004t0007g0205 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1920+398G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289860 | |||||||
chr2:100289861 | A | G | 233 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(230): Show |
312 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(309): Show |
intron_variant | MODIFIER | c.1920+397T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289861 | |||||||
chr2:100289869 | T | C | 233 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(230): Show |
312 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(309): Show |
intron_variant | MODIFIER | c.1920+389A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289869 | |||||||
chr2:100289965 | T | C | 3 | a0002c0001t0055g0059 a0002c0001t0056g0117 a0002c0001t0057g0166 |
3 | HG01169.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1920+293A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289965 | |||||||
chr2:100289999 | C | T | 2 | a0001c0004t0003g0235 a0001c0004t0003g0239 |
2 | NA18952.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1920+259G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100289999 | |||||||
chr2:100290021 | C | A | 16 | a0001c0008t0041g0257 a0001c0008t0041g0258 a0002c0001t0006g0014 others(13): Show |
18 | HG01884.hp1 HG02055.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1920+237G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100290021 | |||||||
chr2:100290108 | A | AAAAT | 79 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(76): Show |
115 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1920+146_1920+149d others(6): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100290108 | |||||||
chr2:100290116 | C | T | 156 | a0001c0002t0122g0217 a0001c0004t0003g0003 a0001c0004t0003g0021 others(153): Show |
199 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.1920+142G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100290116 | |||||||
chr2:100290120 | T | C | 4 | a0001c0002t0122g0217 a0001c0006t0004g0194 a0001c0006t0004g0199 others(1): Show |
4 | HG00140.hp1 HG01256.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1920+138A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100290120 | |||||||
chr2:100290122 | G | A | 4 | a0001c0002t0122g0217 a0001c0006t0004g0194 a0001c0006t0004g0199 others(1): Show |
4 | HG00140.hp1 HG01256.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1920+136C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100290122 | |||||||
chr2:100290126 | A | G | 4 | a0001c0002t0122g0217 a0001c0006t0004g0194 a0001c0006t0004g0199 others(1): Show |
4 | HG00140.hp1 HG01256.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1920+132T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100290126 | |||||||
chr2:100290134 | AC | A | 4 | a0001c0002t0122g0217 a0001c0006t0004g0194 a0001c0006t0004g0199 others(1): Show |
4 | HG00140.hp1 HG01256.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1920+123delG | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100290134 | |||||||
chr2:100290136 | T | A | 4 | a0001c0002t0122g0217 a0001c0006t0004g0194 a0001c0006t0004g0199 others(1): Show |
4 | HG00140.hp1 HG01256.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1920+122A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 10/11 | chr2 | 100290136 | |||||||
chr2:100290666 | G | A | 130 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(127): Show |
171 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.1758-246C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100290666 | |||||||
chr2:100290675 | G | A | 133 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(130): Show |
174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1758-255C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100290675 | |||||||
chr2:100290736 | T | G | 2 | a0008c0017t0081g0044 a0008c0017t0082g0045 |
2 | HG04184.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1758-316A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100290736 | |||||||
chr2:100290783 | G | A | 1 | a0002c0010t0023g0120 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1758-363C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100290783 | |||||||
chr2:100290841 | A | G | 1 | a0002c0001t0096g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1758-421T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100290841 | |||||||
chr2:100290889 | A | G | 233 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(230): Show |
312 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(309): Show |
intron_variant | MODIFIER | c.1758-469T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100290889 | |||||||
chr2:100290892 | C | T | 1 | a0002c0001t0001g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1758-472G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100290892 | |||||||
chr2:100290913 | T | C | 2 | a0002c0001t0006g0067 a0002c0001t0006g0071 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1758-493A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100290913 | |||||||
chr2:100291000 | T | C | 133 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(130): Show |
174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1758-580A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291000 | |||||||
chr2:100291136 | A | G | 245 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(242): Show |
324 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.1758-716T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291136 | |||||||
chr2:100291177 | A | AT | 180 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(177): Show |
253 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.1758-758dupA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291177 | |||||||
chr2:100291187 | T | A | 1 | a0002c0001t0006g0070 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1758-767A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291187 | |||||||
chr2:100291256 | G | A | 7 | a0003c0003t0016g0031 a0003c0003t0016g0147 a0003c0003t0016g0152 others(4): Show |
9 | HG03017.hp1 HG03491.hp1 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.1758-836C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291256 | |||||||
chr2:100291262 | T | G | 3 | a0001c0002t0020g0037 a0001c0002t0020g0182 a0001c0002t0020g0183 |
4 | HG00280.hp1 HG01074.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1758-842A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291262 | |||||||
chr2:100291337 | G | C | 4 | a0002c0001t0001g0141 a0002c0001t0001g0162 a0002c0001t0005g0102 others(1): Show |
4 | NA18944.hp1 NA18974.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1758-917C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291337 | |||||||
chr2:100291437 | C | T | 133 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(130): Show |
174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1758-1017G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291437 | |||||||
chr2:100291458 | A | G | 3 | a0002c0018t0037g0058 a0002c0018t0037g0174 a0002c0025t0098g0080 |
3 | HG02109.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1758-1038T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291458 | |||||||
chr2:100291499 | G | A | 1 | a0001c0004t0003g0212 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1758-1079C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291499 | |||||||
chr2:100291854 | C | T | 2 | a0001c0008t0040g0038 a0001c0008t0125g0210 |
3 | HG01891.hp1 HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1758-1434G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291854 | |||||||
chr2:100291885 | G | A | 2 | a0002c0001t0086g0089 a0002c0001t0087g0086 |
2 | HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1758-1465C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291885 | |||||||
chr2:100291914 | C | T | 1 | a0002c0001t0075g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1758-1494G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291914 | |||||||
chr2:100291935 | C | T | 14 | a0003c0003t0016g0031 a0003c0003t0016g0147 a0003c0003t0016g0152 others(11): Show |
16 | HG01891.hp2 HG02280.hp1 HG02965.hp2 others(13): Show |
intron_variant | MODIFIER | c.1758-1515G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291935 | |||||||
chr2:100291955 | C | T | 7 | a0001c0004t0007g0005 a0001c0004t0007g0205 a0001c0004t0007g0213 others(4): Show |
11 | HG00639.hp2 HG01169.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1758-1535G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100291955 | |||||||
chr2:100292046 | G | A | 268 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(265): Show |
360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.1758-1626C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100292046 | |||||||
chr2:100292137 | A | G | 4 | a0001c0008t0039g0039 a0002c0012t0035g0075 a0002c0012t0035g0076 others(1): Show |
5 | HG02622.hp1 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1758-1717T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100292137 | |||||||
chr2:100292148 | T | A | 1 | a0002c0001t0057g0166 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1758-1728A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100292148 | |||||||
chr2:100292172 | A | C | 67 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(64): Show |
101 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1758-1752T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100292172 | |||||||
chr2:100292262 | C | T | 12 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0063 others(9): Show |
14 | HG02451.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1758-1842G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100292262 | |||||||
chr2:100292288 | G | A | 1 | a0001c0002t0002g0022 | 3 | HG00558.hp2 NA18986.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1758-1868C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100292288 | |||||||
chr2:100292534 | C | T | 133 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(130): Show |
174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1757+1695G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100292534 | |||||||
chr2:100292578 | T | C | 1 | a0001c0004t0003g0227 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1757+1651A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100292578 | |||||||
chr2:100292751 | T | C | 1 | a0002c0005t0021g0178 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1757+1478A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100292751 | |||||||
chr2:100292962 | G | A | 2 | a0008c0017t0081g0044 a0008c0017t0082g0045 |
2 | HG04184.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1757+1267C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100292962 | |||||||
chr2:100293060 | G | A | 10 | a0002c0001t0080g0132 a0004c0007t0002g0268 a0004c0007t0004g0043 others(7): Show |
11 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.1757+1169C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100293060 | |||||||
chr2:100293115 | T | C | 1 | a0001c0002t0004g0221 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1757+1114A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100293115 | |||||||
chr2:100293247 | T | A | 133 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(130): Show |
174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1757+982A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100293247 | |||||||
chr2:100293579 | A | G | 2 | a0002c0001t0034g0164 a0002c0001t0034g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1757+650T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100293579 | |||||||
chr2:100293607 | T | G | 3 | a0003c0003t0009g0142 a0003c0003t0011g0007 a0003c0003t0011g0029 |
7 | NA18951.hp2 NA18960.hp1 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1757+622A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100293607 | |||||||
chr2:100293724 | C | T | 1 | a0002c0001t0006g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1757+505G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100293724 | |||||||
chr2:100293780 | A | G | 2 | a0005c0009t0003g0019 a0005c0009t0003g0196 |
4 | NA18948.hp1 NA18953.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.1757+449T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100293780 | |||||||
chr2:100294015 | T | G | 2 | a0002c0001t0033g0055 a0002c0001t0033g0056 |
2 | HG01516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1757+214A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100294015 | |||||||
chr2:100294116 | C | T | 133 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(130): Show |
174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1757+113G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100294116 | |||||||
chr2:100294213 | T | C | 4 | a0001c0008t0039g0039 a0002c0012t0035g0075 a0002c0012t0035g0076 others(1): Show |
5 | HG02622.hp1 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1757+16A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 9/11 | chr2 | 100294213 | |||||||
chr2:100294477 | C | T | 2 | a0002c0001t0033g0055 a0002c0001t0033g0056 |
2 | HG01516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1599-90G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 8/11 | chr2 | 100294477 | |||||||
chr2:100294552 | A | T | 14 | a0003c0003t0016g0031 a0003c0003t0016g0147 a0003c0003t0016g0152 others(11): Show |
16 | HG01891.hp2 HG02280.hp1 HG02965.hp2 others(13): Show |
intron_variant | MODIFIER | c.1599-165T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 8/11 | chr2 | 100294552 | |||||||
chr2:100294664 | A | G | 1 | a0001c0002t0020g0182 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1599-277T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 8/11 | chr2 | 100294664 | |||||||
chr2:100294805 | C | T | 4 | a0001c0002t0002g0040 a0001c0002t0002g0250 a0001c0002t0002g0253 others(1): Show |
5 | NA18959.hp2 NA18978.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.1599-418G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 8/11 | chr2 | 100294805 | |||||||
chr2:100294806 | G | A | 1 | a0001c0002t0013g0245 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1599-419C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 8/11 | chr2 | 100294806 | |||||||
chr2:100295034 | G | C | 1 | a0002c0001t0032g0062 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1598+398C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 8/11 | chr2 | 100295034 | |||||||
chr2:100295120 | G | T | 79 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(76): Show |
115 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1598+312C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 8/11 | chr2 | 100295120 | |||||||
chr2:100295273 | G | T | 133 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(130): Show |
174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1598+159C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 8/11 | chr2 | 100295273 | |||||||
chr2:100295421 | T | G | 1 | a0002c0001t0001g0162 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1598+11A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 8/11 | chr2 | 100295421 | |||||||
chr2:100295674 | G | A | 1 | a0002c0001t0033g0056 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1477-121C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100295674 | |||||||
chr2:100295690 | C | T | 7 | a0002c0001t0001g0123 a0002c0001t0001g0124 a0002c0001t0001g0156 others(4): Show |
7 | HG02080.hp1 HG04184.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477-137G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100295690 | |||||||
chr2:100295716 | G | A | 4 | a0002c0001t0096g0085 a0002c0018t0037g0058 a0002c0018t0037g0174 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477-163C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100295716 | |||||||
chr2:100295757 | A | G | 45 | a0001c0004t0014g0011 a0001c0004t0014g0222 a0001c0004t0014g0233 others(42): Show |
57 | HG00423.hp1 HG00544.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1477-204T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100295757 | |||||||
chr2:100295825 | G | C | 3 | a0002c0001t0055g0059 a0002c0001t0056g0117 a0002c0001t0057g0166 |
3 | HG01169.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1477-272C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100295825 | |||||||
chr2:100295840 | A | G | 1 | a0001c0002t0122g0217 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1477-287T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100295840 | |||||||
chr2:100295932 | T | C | 133 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(130): Show |
174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1477-379A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100295932 | |||||||
chr2:100296001 | A | G | 231 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(228): Show |
308 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.1477-448T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296001 | |||||||
chr2:100296003 | G | GT | 4 | a0001c0002t0002g0013 a0001c0002t0002g0022 a0001c0002t0002g0208 others(1): Show |
9 | HG00558.hp2 HG02015.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.1477-451dupA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296003 | |||||||
chr2:100296206 | G | A | 1 | a0001c0008t0041g0257 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1477-653C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296206 | |||||||
chr2:100296232 | G | A | 1 | a0001c0002t0004g0246 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1477-679C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296232 | |||||||
chr2:100296280 | A | T | 18 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(15): Show |
37 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.1477-727T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296280 | |||||||
chr2:100296524 | C | T | 11 | a0002c0001t0012g0025 a0002c0001t0012g0033 a0002c0001t0012g0169 others(8): Show |
14 | HG01261.hp1 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1477-971G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296524 | |||||||
chr2:100296553 | G | T | 1 | a0003c0003t0017g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1477-1000C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296553 | |||||||
chr2:100296567 | G | A | 5 | a0002c0001t0001g0137 a0002c0001t0005g0002 a0002c0001t0005g0006 others(2): Show |
14 | HG00735.hp2 HG00741.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1477-1014C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296567 | |||||||
chr2:100296589 | G | A | 1 | a0002c0001t0005g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1477-1036C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296589 | |||||||
chr2:100296641 | C | T | 1 | a0003c0003t0016g0031 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1477-1088G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296641 | |||||||
chr2:100296797 | A | C | 5 | a0002c0001t0001g0137 a0002c0001t0005g0002 a0002c0001t0005g0006 others(2): Show |
14 | HG00735.hp2 HG00741.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1477-1244T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296797 | |||||||
chr2:100296800 | A | G | 3 | a0001c0002t0020g0037 a0001c0002t0020g0182 a0001c0002t0020g0183 |
4 | HG00280.hp1 HG01074.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477-1247T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296800 | |||||||
chr2:100296899 | T | C | 245 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(242): Show |
324 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.1477-1346A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100296899 | |||||||
chr2:100297096 | T | C | 10 | a0002c0001t0080g0132 a0004c0007t0002g0268 a0004c0007t0004g0043 others(7): Show |
11 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.1477-1543A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297096 | |||||||
chr2:100297128 | CT | C | 135 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(132): Show |
176 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.1477-1576delA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297128 | |||||||
chr2:100297168 | G | A | 2 | a0002c0001t0033g0055 a0002c0001t0033g0056 |
2 | HG01516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1477-1615C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297168 | |||||||
chr2:100297180 | G | C | 133 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(130): Show |
174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1477-1627C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297180 | |||||||
chr2:100297273 | T | C | 244 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(241): Show |
323 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1476+1563A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297273 | |||||||
chr2:100297278 | G | A | 135 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(132): Show |
176 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.1476+1558C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297278 | |||||||
chr2:100297300 | GTTTTTGT others(7): Show |
G | 1 | a0011c0019t0004g0201 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1476+1522_1476+153 others(18): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297300 | |||||||
chr2:100297308 | AT | A | 243 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(240): Show |
322 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.1476+1527delA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297308 | |||||||
chr2:100297337 | C | T | 2 | a0008c0017t0081g0044 a0008c0017t0082g0045 |
2 | HG04184.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1476+1499G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297337 | |||||||
chr2:100297339 | G | T | 1 | a0003c0003t0024g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1476+1497C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297339 | |||||||
chr2:100297366 | C | T | 133 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(130): Show |
174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1476+1470G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297366 | |||||||
chr2:100297368 | C | A | 245 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(242): Show |
324 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.1476+1468G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297368 | |||||||
chr2:100297384 | G | A | 1 | a0002c0001t0001g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1476+1452C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297384 | |||||||
chr2:100297435 | C | A | 9 | a0002c0001t0032g0061 a0002c0001t0032g0062 a0002c0001t0034g0164 others(6): Show |
9 | HG02572.hp2 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1476+1401G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297435 | |||||||
chr2:100297436 | C | A | 1 | a0003c0003t0008g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1476+1400G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297436 | |||||||
chr2:100297458 | C | T | 1 | a0001c0008t0041g0258 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1476+1378G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297458 | |||||||
chr2:100297608 | A | C | 7 | a0001c0004t0007g0005 a0001c0004t0007g0205 a0001c0004t0007g0213 others(4): Show |
11 | HG00639.hp2 HG01169.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1476+1228T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297608 | |||||||
chr2:100297629 | G | A | 4 | a0002c0001t0096g0085 a0002c0018t0037g0058 a0002c0018t0037g0174 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476+1207C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297629 | |||||||
chr2:100297687 | A | G | 135 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(132): Show |
176 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.1476+1149T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297687 | |||||||
chr2:100297738 | A | G | 133 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(130): Show |
174 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1476+1098T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297738 | |||||||
chr2:100297740 | C | T | 2 | a0002c0001t0033g0055 a0002c0001t0033g0056 |
2 | HG01516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1476+1096G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297740 | |||||||
chr2:100297741 | G | A | 1 | a0003c0003t0045g0110 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1476+1095C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297741 | |||||||
chr2:100297755 | T | C | 2 | a0002c0001t0086g0089 a0002c0001t0087g0086 |
2 | HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1476+1081A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297755 | |||||||
chr2:100297987 | GA | G | 136 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(133): Show |
177 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.1476+848delT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100297987 | |||||||
chr2:100298129 | G | A | 2 | a0002c0001t0033g0055 a0002c0001t0033g0056 |
2 | HG01516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1476+707C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100298129 | |||||||
chr2:100298331 | G | A | 1 | a0003c0003t0015g0160 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1476+505C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100298331 | |||||||
chr2:100298337 | A | G | 10 | a0002c0001t0080g0132 a0004c0007t0002g0268 a0004c0007t0004g0043 others(7): Show |
11 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.1476+499T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100298337 | |||||||
chr2:100298464 | T | C | 2 | a0002c0001t0042g0074 a0002c0001t0043g0073 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1476+372A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100298464 | |||||||
chr2:100298542 | A | G | 44 | a0001c0004t0014g0011 a0001c0004t0014g0222 a0001c0004t0014g0233 others(41): Show |
56 | HG00423.hp1 HG00544.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1476+294T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 7/11 | chr2 | 100298542 | |||||||
chr2:100299010 | C | T | 1 | a0002c0001t0083g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1362-60G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 6/11 | chr2 | 100299010 | |||||||
chr2:100299075 | A | G | 1 | a0001c0004t0003g0240 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1362-125T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 6/11 | chr2 | 100299075 | |||||||
chr2:100299138 | G | A | 13 | a0002c0001t0032g0061 a0002c0001t0032g0062 a0002c0001t0034g0164 others(10): Show |
13 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1361+88C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 6/11 | chr2 | 100299138 | |||||||
chr2:100299167 | T | C | 218 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(215): Show |
295 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.1361+59A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 6/11 | chr2 | 100299167 | |||||||
chr2:100299376 | C | T | 13 | a0002c0001t0032g0061 a0002c0001t0032g0062 a0002c0001t0034g0164 others(10): Show |
13 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1268-57G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 5/11 | chr2 | 100299376 | |||||||
chr2:100299453 | G | C | 4 | a0002c0001t0096g0085 a0002c0018t0037g0058 a0002c0018t0037g0174 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1268-134C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 5/11 | chr2 | 100299453 | |||||||
chr2:100299581 | C | T | 13 | a0002c0001t0032g0061 a0002c0001t0032g0062 a0002c0001t0034g0164 others(10): Show |
13 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1267+136G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 5/11 | chr2 | 100299581 | |||||||
chr2:100299589 | T | C | 231 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(228): Show |
308 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.1267+128A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 5/11 | chr2 | 100299589 | |||||||
chr2:100299983 | T | A | 4 | a0002c0001t0001g0118 a0002c0001t0001g0130 a0002c0001t0001g0131 others(1): Show |
4 | HG02300.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-65A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100299983 | |||||||
chr2:100300008 | T | TG | 103 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(100): Show |
139 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.1066-91dupC | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300008 | |||||||
chr2:100300011 | A | G | 1 | a0004c0027t0107g0273 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1066-93T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300011 | |||||||
chr2:100300019 | A | AG | 40 | a0001c0002t0002g0253 a0002c0001t0012g0025 a0002c0001t0012g0033 others(37): Show |
44 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1066-102dupC | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300019 | |||||||
chr2:100300019 | A | AGG | 63 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(60): Show |
97 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1066-103_1066-102d others(4): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300019 | |||||||
chr2:100300019 | A | AGGG | 17 | a0001c0006t0004g0191 a0001c0008t0040g0038 a0001c0008t0041g0257 others(14): Show |
20 | HG00741.hp2 HG01358.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1066-104_1066-102d others(5): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300019 | |||||||
chr2:100300019 | A | G | 103 | a0001c0004t0003g0003 a0001c0004t0003g0021 a0001c0004t0003g0206 others(100): Show |
139 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.1066-101T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300019 | |||||||
chr2:100300126 | G | T | 2 | a0002c0001t0042g0074 a0002c0001t0043g0073 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1066-208C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300126 | |||||||
chr2:100300153 | ATCTG | A | 226 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(223): Show |
301 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.1066-239_1066-236d others(6): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300153 | |||||||
chr2:100300165 | G | A | 1 | a0002c0001t0067g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1066-247C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300165 | |||||||
chr2:100300176 | T | C | 1 | a0002c0001t0067g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1066-258A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300176 | |||||||
chr2:100300252 | A | AT | 207 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(204): Show |
282 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.1066-335dupA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300252 | |||||||
chr2:100300262 | A | T | 215 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(212): Show |
290 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.1066-344T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300262 | |||||||
chr2:100300298 | C | T | 11 | a0002c0001t0005g0002 a0002c0001t0005g0135 a0002c0001t0032g0061 others(8): Show |
17 | HG00735.hp2 HG00741.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1065+346G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300298 | |||||||
chr2:100300305 | G | C | 1 | a0012c0021t0085g0060 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1065+339C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300305 | |||||||
chr2:100300592 | C | A | 14 | a0002c0001t0022g0149 a0003c0003t0016g0031 a0003c0003t0016g0147 others(11): Show |
16 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1065+52G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300592 | |||||||
chr2:100300637 | G | A | 3 | a0002c0013t0097g0057 a0002c0018t0037g0058 a0002c0025t0098g0080 |
3 | HG02109.hp1 HG02258.hp1 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.1065+7C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 4/11 | chr2 | 100300637 | |||||||
chr2:100300815 | T | A | 9 | a0002c0001t0032g0061 a0002c0001t0032g0062 a0002c0001t0033g0055 others(6): Show |
9 | HG01516.hp2 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.922-28A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100300815 | |||||||
chr2:100300958 | C | A | 1 | a0007c0016t0115g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.922-171G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100300958 | |||||||
chr2:100301042 | A | G | 14 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(11): Show |
16 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.922-255T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301042 | |||||||
chr2:100301112 | G | T | 9 | a0002c0001t0032g0061 a0002c0001t0032g0062 a0002c0001t0033g0055 others(6): Show |
9 | HG01516.hp2 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.922-325C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301112 | |||||||
chr2:100301274 | T | C | 2 | a0002c0001t0034g0164 a0002c0001t0034g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.922-487A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301274 | |||||||
chr2:100301277 | C | A | 139 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(136): Show |
193 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.922-490G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301277 | |||||||
chr2:100301284 | G | T | 1 | a0001c0002t0013g0245 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.922-497C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301284 | |||||||
chr2:100301480 | T | C | 29 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(26): Show |
33 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.922-693A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301480 | |||||||
chr2:100301498 | C | A | 1 | a0001c0004t0003g0228 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.922-711G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301498 | |||||||
chr2:100301499 | T | C | 168 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(165): Show |
226 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.922-712A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301499 | |||||||
chr2:100301630 | G | A | 1 | a0001c0004t0007g0215 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.922-843C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301630 | |||||||
chr2:100301692 | C | T | 1 | a0002c0001t0101g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.922-905G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301692 | |||||||
chr2:100301718 | G | A | 1 | a0001c0004t0106g0231 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.922-931C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301718 | |||||||
chr2:100301758 | A | C | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.922-971T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301758 | |||||||
chr2:100301901 | G | A | 139 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(136): Show |
193 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.921+1020C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301901 | |||||||
chr2:100301916 | T | C | 20 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(17): Show |
23 | HG01261.hp1 HG01516.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.921+1005A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301916 | |||||||
chr2:100301982 | G | A | 1 | a0002c0001t0001g0137 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.921+939C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100301982 | |||||||
chr2:100302162 | A | G | 29 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(26): Show |
33 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.921+759T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100302162 | |||||||
chr2:100302550 | C | G | 168 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(165): Show |
226 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.921+371G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100302550 | |||||||
chr2:100302619 | T | C | 6 | a0002c0001t0001g0141 a0002c0001t0001g0162 a0002c0001t0001g0163 others(3): Show |
6 | NA18747.hp1 NA18944.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.921+302A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100302619 | |||||||
chr2:100302644 | A | G | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.921+277T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100302644 | |||||||
chr2:100302790 | G | A | 2 | a0008c0017t0081g0044 a0008c0017t0082g0045 |
2 | HG04184.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.921+131C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 3/11 | chr2 | 100302790 | |||||||
chr2:100303146 | T | A | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-103A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100303146 | |||||||
chr2:100303273 | G | A | 139 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(136): Show |
193 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.799-230C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100303273 | |||||||
chr2:100303372 | C | A | 1 | a0001c0004t0003g0229 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.799-329G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100303372 | |||||||
chr2:100303426 | A | C | 139 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(136): Show |
193 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.799-383T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100303426 | |||||||
chr2:100303629 | T | C | 3 | a0002c0005t0030g0035 a0002c0005t0066g0179 a0002c0005t0069g0180 |
4 | HG00738.hp2 HG02683.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-586A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100303629 | |||||||
chr2:100303757 | T | C | 9 | a0002c0001t0032g0061 a0002c0001t0032g0062 a0002c0001t0033g0055 others(6): Show |
9 | HG01516.hp2 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-714A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100303757 | |||||||
chr2:100303989 | T | C | 182 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(179): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.799-946A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100303989 | |||||||
chr2:100304098 | A | C | 12 | a0002c0001t0012g0033 a0002c0001t0012g0169 a0002c0001t0018g0047 others(9): Show |
13 | HG01169.hp2 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.799-1055T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304098 | |||||||
chr2:100304153 | C | CT | 168 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(165): Show |
226 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.799-1111dupA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304153 | |||||||
chr2:100304171 | G | A | 6 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(3): Show |
9 | HG01261.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.799-1128C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304171 | |||||||
chr2:100304205 | C | T | 182 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(179): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.799-1162G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304205 | |||||||
chr2:100304243 | C | T | 139 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(136): Show |
193 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.799-1200G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304243 | |||||||
chr2:100304312 | C | CTAATTTT others(1): Show |
181 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(178): Show |
240 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.799-1277_799-1270d others(10): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304312 | |||||||
chr2:100304328 | C | T | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1285G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304328 | |||||||
chr2:100304350 | C | A | 17 | a0002c0001t0012g0170 a0002c0001t0022g0149 a0002c0001t0086g0089 others(14): Show |
19 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.799-1307G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304350 | |||||||
chr2:100304505 | A | C | 1 | a0004c0007t0004g0271 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.799-1462T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304505 | |||||||
chr2:100304623 | C | T | 2 | a0002c0001t0034g0164 a0002c0001t0034g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.799-1580G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304623 | |||||||
chr2:100304625 | G | GTT | 6 | a0002c0001t0006g0070 a0002c0013t0097g0057 a0002c0018t0037g0058 others(3): Show |
6 | HG02109.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-1584_799-1583d others(4): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304625 | |||||||
chr2:100304625 | G | GTTGT | 8 | a0001c0002t0004g0232 a0001c0002t0013g0012 a0001c0002t0013g0244 others(5): Show |
11 | HG00597.hp1 HG02080.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.799-1583_799-1582i others(6): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304625 | |||||||
chr2:100304625 | G | GTTT | 25 | a0001c0008t0039g0039 a0001c0008t0040g0038 a0001c0008t0041g0257 others(22): Show |
29 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.799-1585_799-1583d others(5): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304625 | |||||||
chr2:100304625 | G | GTTTT | 94 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(91): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.799-1586_799-1583d others(6): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304625 | |||||||
chr2:100304625 | G | GTTTTT | 23 | a0001c0004t0003g0235 a0001c0004t0014g0233 a0001c0006t0028g0186 others(20): Show |
26 | HG00642.hp2 HG00738.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.799-1587_799-1583d others(7): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304625 | |||||||
chr2:100304625 | G | GTTTTTTT | 6 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(3): Show |
7 | HG00544.hp2 HG02056.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-1589_799-1583d others(9): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304625 | |||||||
chr2:100304625 | G | T | 2 | a0002c0001t0034g0164 a0002c0001t0034g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.799-1582C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304625 | |||||||
chr2:100304663 | G | A | 168 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(165): Show |
226 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.799-1620C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304663 | |||||||
chr2:100304669 | G | A | 3 | a0002c0005t0001g0018 a0002c0005t0001g0175 a0002c0005t0061g0181 |
5 | HG00735.hp1 HG01081.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-1626C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304669 | |||||||
chr2:100304674 | C | A | 168 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(165): Show |
226 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.799-1631G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304674 | |||||||
chr2:100304755 | C | G | 3 | a0002c0012t0035g0075 a0002c0012t0035g0076 a0002c0012t0088g0077 |
3 | HG02622.hp1 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.799-1712G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304755 | |||||||
chr2:100304790 | A | AT | 9 | a0002c0001t0001g0141 a0002c0001t0022g0144 a0002c0001t0034g0165 others(6): Show |
9 | HG01169.hp2 HG02896.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-1748dupA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304790 | |||||||
chr2:100304790 | A | ATT | 27 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(24): Show |
31 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.799-1749_799-1748d others(4): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304790 | |||||||
chr2:100304790 | A | ATTT | 26 | a0001c0002t0004g0232 a0001c0002t0020g0183 a0001c0002t0118g0254 others(23): Show |
28 | HG00558.hp1 HG00673.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.799-1750_799-1748d others(5): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304790 | |||||||
chr2:100304790 | A | ATTTT | 95 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(92): Show |
143 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.799-1751_799-1748d others(6): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304790 | |||||||
chr2:100304790 | A | ATTTTT | 15 | a0001c0002t0002g0250 a0001c0002t0025g0216 a0001c0004t0003g0212 others(12): Show |
19 | HG01169.hp1 HG01257.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.799-1752_799-1748d others(7): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304790 | |||||||
chr2:100304844 | G | C | 1 | a0002c0001t0005g0102 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-1801C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304844 | |||||||
chr2:100304845 | C | G | 1 | a0002c0001t0005g0102 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.799-1802G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304845 | |||||||
chr2:100304862 | A | T | 2 | a0008c0017t0081g0044 a0008c0017t0082g0045 |
2 | HG04184.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.799-1819T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100304862 | |||||||
chr2:100305108 | G | A | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2065C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305108 | |||||||
chr2:100305130 | C | T | 2 | a0003c0003t0008g0114 a0003c0003t0053g0113 |
2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.799-2087G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305130 | |||||||
chr2:100305219 | C | A | 1 | a0006c0014t0070g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.799-2176G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305219 | |||||||
chr2:100305314 | T | A | 139 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(136): Show |
193 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.799-2271A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305314 | |||||||
chr2:100305355 | G | C | 1 | a0002c0001t0077g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.799-2312C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305355 | |||||||
chr2:100305357 | C | T | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2314G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305357 | |||||||
chr2:100305431 | A | AAAT | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2391_799-2389d others(5): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305431 | |||||||
chr2:100305653 | A | G | 3 | a0002c0005t0001g0008 a0002c0005t0001g0036 a0002c0005t0001g0176 |
7 | HG01257.hp2 HG01258.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-2610T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305653 | |||||||
chr2:100305710 | C | G | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2667G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305710 | |||||||
chr2:100305819 | A | G | 1 | a0002c0001t0001g0084 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.799-2776T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305819 | |||||||
chr2:100305851 | T | C | 122 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(119): Show |
174 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.799-2808A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305851 | |||||||
chr2:100305896 | T | C | 1 | a0003c0003t0092g0143 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.799-2853A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305896 | |||||||
chr2:100305919 | C | T | 29 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(26): Show |
33 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.799-2876G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305919 | |||||||
chr2:100305928 | G | A | 122 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(119): Show |
174 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.799-2885C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100305928 | |||||||
chr2:100306012 | C | T | 11 | a0002c0001t0001g0118 a0002c0001t0012g0033 a0002c0001t0012g0169 others(8): Show |
12 | HG01884.hp2 HG02257.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.799-2969G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306012 | |||||||
chr2:100306051 | G | T | 1 | a0002c0001t0001g0098 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.799-3008C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306051 | |||||||
chr2:100306074 | T | G | 17 | a0002c0001t0012g0170 a0002c0001t0022g0149 a0002c0001t0086g0089 others(14): Show |
19 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.799-3031A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306074 | |||||||
chr2:100306076 | G | T | 60 | a0001c0002t0117g0255 a0001c0006t0028g0186 a0001c0006t0028g0187 others(57): Show |
70 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.798+3031C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306076 | |||||||
chr2:100306078 | G | T | 3 | a0002c0005t0001g0018 a0002c0005t0001g0175 a0002c0005t0061g0181 |
5 | HG00735.hp1 HG01081.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+3029C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306078 | |||||||
chr2:100306086 | G | A | 2 | a0006c0014t0001g0097 a0006c0014t0070g0155 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.798+3021C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306086 | |||||||
chr2:100306132 | T | G | 122 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(119): Show |
174 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.798+2975A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306132 | |||||||
chr2:100306196 | G | A | 11 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(8): Show |
14 | HG01261.hp1 HG02055.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.798+2911C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306196 | |||||||
chr2:100306207 | C | T | 29 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(26): Show |
33 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.798+2900G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306207 | |||||||
chr2:100306368 | C | T | 122 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(119): Show |
174 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.798+2739G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306368 | |||||||
chr2:100306492 | T | G | 17 | a0002c0001t0012g0170 a0002c0001t0022g0149 a0002c0001t0086g0089 others(14): Show |
19 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.798+2615A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306492 | |||||||
chr2:100306575 | T | C | 1 | a0003c0003t0024g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.798+2532A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306575 | |||||||
chr2:100306600 | G | T | 3 | a0002c0001t0018g0047 a0002c0001t0018g0087 a0002c0001t0095g0051 |
3 | HG03139.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.798+2507C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306600 | |||||||
chr2:100306653 | G | A | 29 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(26): Show |
33 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.798+2454C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306653 | |||||||
chr2:100306862 | C | T | 29 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(26): Show |
33 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.798+2245G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306862 | |||||||
chr2:100306894 | CT | C | 145 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(142): Show |
201 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.798+2212delA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306894 | |||||||
chr2:100306894 | CTT | C | 6 | a0001c0004t0003g0239 a0002c0001t0033g0055 a0002c0001t0033g0056 others(3): Show |
6 | HG01516.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.798+2211_798+2212d others(4): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306894 | |||||||
chr2:100306895 | T | C | 17 | a0002c0001t0012g0170 a0002c0001t0022g0149 a0002c0001t0086g0089 others(14): Show |
19 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.798+2212A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306895 | |||||||
chr2:100306908 | T | G | 1 | a0002c0001t0001g0083 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.798+2199A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306908 | |||||||
chr2:100306925 | CT | C | 181 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(178): Show |
240 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.798+2181delA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306925 | |||||||
chr2:100306942 | G | A | 3 | a0003c0003t0008g0049 a0003c0003t0008g0114 a0003c0003t0053g0113 |
3 | HG00639.hp1 HG01981.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.798+2165C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306942 | |||||||
chr2:100306994 | C | T | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.798+2113G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100306994 | |||||||
chr2:100307013 | C | T | 6 | a0001c0004t0003g0021 a0001c0004t0003g0235 a0001c0004t0003g0237 others(3): Show |
8 | HG00558.hp1 NA18952.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.798+2094G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307013 | |||||||
chr2:100307021 | C | T | 29 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(26): Show |
33 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.798+2086G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307021 | |||||||
chr2:100307065 | C | T | 1 | a0001c0002t0013g0244 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.798+2042G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307065 | |||||||
chr2:100307092 | T | G | 2 | a0008c0017t0081g0044 a0008c0017t0082g0045 |
2 | HG04184.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.798+2015A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307092 | |||||||
chr2:100307179 | G | C | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.798+1928C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307179 | |||||||
chr2:100307252 | A | G | 1 | a0002c0001t0101g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.798+1855T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307252 | |||||||
chr2:100307290 | C | T | 1 | a0003c0003t0047g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.798+1817G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307290 | |||||||
chr2:100307524 | T | C | 6 | a0001c0004t0003g0021 a0001c0004t0003g0235 a0001c0004t0003g0237 others(3): Show |
8 | HG00558.hp1 NA18952.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.798+1583A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307524 | |||||||
chr2:100307567 | G | A | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.798+1540C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307567 | |||||||
chr2:100307603 | C | A | 122 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(119): Show |
174 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.798+1504G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307603 | |||||||
chr2:100307667 | T | C | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.798+1440A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307667 | |||||||
chr2:100307813 | A | AT | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.798+1293dupA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307813 | |||||||
chr2:100307859 | T | G | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.798+1248A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307859 | |||||||
chr2:100307942 | C | CT | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.798+1164dupA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100307942 | |||||||
chr2:100308097 | T | C | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.798+1010A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308097 | |||||||
chr2:100308135 | T | C | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.798+972A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308135 | |||||||
chr2:100308136 | G | A | 1 | a0001c0004t0003g0240 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.798+971C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308136 | |||||||
chr2:100308193 | C | A | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.798+914G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308193 | |||||||
chr2:100308228 | GGT | G | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.798+877_798+878del others(2): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308228 | |||||||
chr2:100308299 | A | G | 122 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(119): Show |
174 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.798+808T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308299 | |||||||
chr2:100308360 | G | A | 3 | a0001c0006t0004g0194 a0001c0006t0004g0199 a0011c0019t0004g0201 |
3 | HG00140.hp1 HG01256.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.798+747C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308360 | |||||||
chr2:100308475 | G | A | 1 | a0002c0001t0001g0081 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.798+632C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308475 | |||||||
chr2:100308502 | C | T | 17 | a0002c0001t0012g0170 a0002c0001t0022g0149 a0002c0001t0086g0089 others(14): Show |
19 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.798+605G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308502 | |||||||
chr2:100308598 | C | T | 9 | a0002c0001t0032g0061 a0002c0001t0032g0062 a0002c0001t0033g0055 others(6): Show |
9 | HG01516.hp2 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+509G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308598 | |||||||
chr2:100308644 | A | T | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.798+463T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308644 | |||||||
chr2:100308706 | G | A | 29 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(26): Show |
33 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.798+401C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308706 | |||||||
chr2:100308841 | AT | A | 94 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(91): Show |
142 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.798+265delA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308841 | |||||||
chr2:100308878 | A | G | 122 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(119): Show |
174 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.798+229T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308878 | |||||||
chr2:100308937 | T | C | 122 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(119): Show |
174 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.798+170A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308937 | |||||||
chr2:100308977 | G | A | 122 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(119): Show |
174 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.798+130C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 2/11 | chr2 | 100308977 | |||||||
chr2:100309341 | A | G | 150 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(147): Show |
206 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.680-116T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100309341 | |||||||
chr2:100309409 | A | G | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.680-184T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100309409 | |||||||
chr2:100309472 | C | A | 121 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(118): Show |
173 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.680-247G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100309472 | |||||||
chr2:100309670 | A | AT | 10 | a0002c0001t0012g0033 a0002c0001t0012g0169 a0002c0001t0018g0047 others(7): Show |
11 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.680-446dupA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100309670 | |||||||
chr2:100309807 | G | A | 2 | a0002c0001t0055g0059 a0002c0001t0057g0166 |
2 | HG01169.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.680-582C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100309807 | |||||||
chr2:100309865 | G | T | 2 | a0008c0017t0081g0044 a0008c0017t0082g0045 |
2 | HG04184.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.680-640C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100309865 | |||||||
chr2:100310032 | C | T | 29 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(26): Show |
33 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.680-807G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100310032 | |||||||
chr2:100310161 | C | CT | 150 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(147): Show |
206 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.680-937_680-936ins others(1): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100310161 | |||||||
chr2:100310590 | CATATGTG others(4): Show |
C | 2 | a0002c0001t0055g0059 a0002c0001t0057g0166 |
2 | HG01169.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.680-1376_680-1366d others(13): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100310590 | |||||||
chr2:100310669 | T | G | 150 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(147): Show |
206 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.680-1444A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100310669 | |||||||
chr2:100310798 | C | T | 43 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(40): Show |
49 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.680-1573G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100310798 | |||||||
chr2:100310855 | G | A | 43 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(40): Show |
49 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.680-1630C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100310855 | |||||||
chr2:100310913 | T | C | 107 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(104): Show |
157 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.680-1688A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100310913 | |||||||
chr2:100311035 | T | C | 12 | a0002c0001t0012g0033 a0002c0001t0012g0169 a0002c0001t0018g0047 others(9): Show |
13 | HG01169.hp2 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.680-1810A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311035 | |||||||
chr2:100311157 | C | T | 2 | a0008c0017t0081g0044 a0008c0017t0082g0045 |
2 | HG04184.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.680-1932G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311157 | |||||||
chr2:100311260 | C | A | 34 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(31): Show |
39 | HG01261.hp1 HG01516.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.680-2035G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311260 | |||||||
chr2:100311323 | C | T | 2 | a0001c0006t0004g0185 a0001c0006t0004g0197 |
2 | HG02602.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.680-2098G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311323 | |||||||
chr2:100311357 | G | GA | 118 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(115): Show |
169 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.680-2133dupT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311357 | |||||||
chr2:100311367 | T | A | 42 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(39): Show |
48 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(45): Show |
intron_variant | MODIFIER | c.680-2142A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311367 | |||||||
chr2:100311371 | G | T | 43 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(40): Show |
49 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.680-2146C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311371 | |||||||
chr2:100311373 | A | G | 43 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(40): Show |
49 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.680-2148T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311373 | |||||||
chr2:100311411 | C | T | 1 | a0003c0003t0091g0088 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.680-2186G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311411 | |||||||
chr2:100311440 | G | A | 2 | a0002c0001t0055g0059 a0002c0001t0057g0166 |
2 | HG01169.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.680-2215C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311440 | |||||||
chr2:100311446 | G | A | 3 | a0002c0012t0035g0075 a0002c0012t0035g0076 a0002c0012t0088g0077 |
3 | HG02622.hp1 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.680-2221C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311446 | |||||||
chr2:100311448 | A | C | 107 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(104): Show |
157 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.680-2223T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311448 | |||||||
chr2:100311586 | A | C | 1 | a0001c0004t0105g0209 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.680-2361T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311586 | |||||||
chr2:100311588 | G | A | 1 | a0002c0013t0036g0158 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.680-2363C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311588 | |||||||
chr2:100311624 | T | C | 43 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(40): Show |
49 | HG00423.hp2 HG00544.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.680-2399A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311624 | |||||||
chr2:100311645 | A | G | 1 | a0003c0003t0054g0100 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.680-2420T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311645 | |||||||
chr2:100311753 | A | G | 1 | a0003c0003t0092g0143 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.680-2528T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311753 | |||||||
chr2:100311875 | T | C | 107 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(104): Show |
157 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.680-2650A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311875 | |||||||
chr2:100311931 | A | G | 107 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(104): Show |
157 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.680-2706T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100311931 | |||||||
chr2:100312115 | G | A | 9 | a0002c0001t0012g0025 a0002c0001t0018g0024 a0002c0001t0031g0026 others(6): Show |
12 | HG01261.hp1 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.680-2890C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100312115 | |||||||
chr2:100312187 | T | C | 1 | a0007c0016t0115g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.680-2962A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100312187 | |||||||
chr2:100312204 | T | C | 1 | a0002c0001t0006g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.680-2979A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100312204 | |||||||
chr2:100312610 | C | G | 182 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(179): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.680-3385G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100312610 | |||||||
chr2:100312661 | G | T | 3 | a0003c0003t0016g0031 a0003c0003t0016g0147 a0003c0003t0016g0154 |
4 | HG03491.hp1 HG03492.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-3436C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100312661 | |||||||
chr2:100312919 | T | C | 1 | a0013c0026t0001g0138 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.680-3694A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100312919 | |||||||
chr2:100313064 | A | T | 231 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(228): Show |
308 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.680-3839T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313064 | |||||||
chr2:100313269 | C | T | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.680-4044G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313269 | |||||||
chr2:100313270 | G | A | 2 | a0002c0001t0034g0164 a0002c0001t0034g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.680-4045C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313270 | |||||||
chr2:100313316 | G | A | 1 | a0004c0007t0004g0271 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.680-4091C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313316 | |||||||
chr2:100313398 | G | A | 1 | a0001c0015t0003g0195 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.680-4173C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313398 | |||||||
chr2:100313437 | G | A | 2 | a0002c0001t0034g0164 a0002c0001t0034g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.680-4212C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313437 | |||||||
chr2:100313450 | G | A | 2 | a0008c0017t0081g0044 a0008c0017t0082g0045 |
2 | HG04184.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.680-4225C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313450 | |||||||
chr2:100313486 | C | A | 3 | a0001c0004t0003g0206 a0001c0004t0003g0241 a0001c0004t0003g0242 |
3 | NA18969.hp1 NA18994.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.680-4261G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313486 | |||||||
chr2:100313592 | C | T | 2 | a0002c0001t0056g0117 a0002c0001t0064g0121 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.680-4367G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313592 | |||||||
chr2:100313654 | A | G | 3 | a0006c0014t0001g0096 a0006c0014t0001g0097 a0006c0014t0070g0155 |
3 | HG02965.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.680-4429T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313654 | |||||||
chr2:100313659 | T | C | 1 | a0002c0001t0001g0116 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.680-4434A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313659 | |||||||
chr2:100313672 | G | A | 196 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(193): Show |
268 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.680-4447C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100313672 | |||||||
chr2:100314040 | G | A | 36 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(33): Show |
41 | HG01243.hp1 HG01261.hp1 HG01516.hp2 others(38): Show |
intron_variant | MODIFIER | c.680-4815C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100314040 | |||||||
chr2:100314200 | T | C | 152 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(149): Show |
210 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.680-4975A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100314200 | |||||||
chr2:100314412 | C | T | 1 | a0002c0001t0071g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.680-5187G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100314412 | |||||||
chr2:100314488 | T | C | 1 | a0001c0004t0110g0243 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.680-5263A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100314488 | |||||||
chr2:100314499 | T | C | 3 | a0002c0001t0042g0074 a0002c0001t0043g0073 a0002c0001t0065g0139 |
3 | HG02622.hp2 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-5274A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100314499 | |||||||
chr2:100314647 | T | C | 1 | a0009c0020t0126g0263 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.680-5422A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100314647 | |||||||
chr2:100314788 | CA | C | 4 | a0002c0001t0033g0055 a0002c0001t0033g0056 a0002c0001t0083g0053 others(1): Show |
4 | HG01516.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-5564delT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100314788 | |||||||
chr2:100314860 | A | G | 1 | a0003c0003t0089g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.680-5635T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100314860 | |||||||
chr2:100315057 | T | C | 3 | a0001c0002t0013g0012 a0001c0002t0013g0244 a0001c0002t0013g0245 |
6 | HG00597.hp1 NA18612.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.680-5832A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100315057 | |||||||
chr2:100315119 | C | T | 1 | a0003c0003t0050g0093 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.680-5894G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100315119 | |||||||
chr2:100315276 | G | C | 152 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(149): Show |
210 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.680-6051C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100315276 | |||||||
chr2:100315298 | CT | C | 49 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(46): Show |
57 | HG00423.hp2 HG00544.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.680-6074delA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100315298 | |||||||
chr2:100315468 | T | C | 49 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(46): Show |
57 | HG00423.hp2 HG00544.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.679+5947A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100315468 | |||||||
chr2:100315603 | TGA | T | 103 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(100): Show |
153 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.679+5810_679+5811d others(4): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100315603 | |||||||
chr2:100315610 | T | C | 1 | a0002c0001t0096g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.679+5805A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100315610 | |||||||
chr2:100315660 | T | C | 2 | a0001c0002t0002g0256 a0001c0002t0117g0255 |
2 | NA18966.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.679+5755A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100315660 | |||||||
chr2:100315790 | C | T | 1 | a0003c0003t0052g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.679+5625G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100315790 | |||||||
chr2:100315835 | T | C | 103 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(100): Show |
153 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.679+5580A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100315835 | |||||||
chr2:100316026 | T | C | 152 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(149): Show |
210 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.679+5389A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316026 | |||||||
chr2:100316042 | C | T | 1 | a0002c0001t0079g0091 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.679+5373G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316042 | |||||||
chr2:100316043 | G | A | 1 | a0002c0001t0001g0140 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.679+5372C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316043 | |||||||
chr2:100316074 | A | T | 1 | a0003c0003t0024g0146 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.679+5341T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316074 | |||||||
chr2:100316103 | G | A | 1 | a0005c0009t0003g0196 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.679+5312C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316103 | |||||||
chr2:100316120 | G | C | 152 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(149): Show |
210 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.679+5295C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316120 | |||||||
chr2:100316126 | T | C | 1 | a0002c0018t0037g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.679+5289A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316126 | |||||||
chr2:100316180 | G | T | 1 | a0002c0010t0023g0090 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.679+5235C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316180 | |||||||
chr2:100316263 | G | A | 2 | a0002c0001t0034g0164 a0002c0001t0034g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.679+5152C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316263 | |||||||
chr2:100316273 | C | T | 12 | a0002c0001t0012g0033 a0002c0001t0012g0169 a0002c0001t0012g0170 others(9): Show |
13 | HG01169.hp2 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.679+5142G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316273 | |||||||
chr2:100316318 | C | CA | 7 | a0002c0001t0012g0025 a0002c0001t0031g0026 a0002c0001t0076g0078 others(4): Show |
9 | HG01261.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.679+5096dupT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316318 | |||||||
chr2:100316318 | C | CAA | 30 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(27): Show |
33 | HG01516.hp2 HG02055.hp1 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.679+5095_679+5096d others(4): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316318 | |||||||
chr2:100316318 | CA | C | 101 | a0002c0001t0001g0027 a0002c0001t0001g0081 a0002c0001t0001g0083 others(98): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.679+5096delT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316318 | |||||||
chr2:100316318 | CAA | C | 7 | a0002c0001t0018g0087 a0002c0001t0057g0166 a0002c0001t0086g0089 others(4): Show |
7 | HG01169.hp2 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.679+5095_679+5096d others(4): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316318 | |||||||
chr2:100316335 | A | AAG | 100 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(97): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.679+5079_679+5080i others(4): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316335 | |||||||
chr2:100316335 | A | G | 1 | a0002c0001t0075g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.679+5080T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316335 | |||||||
chr2:100316337 | AAG | A | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
12 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.679+5076_679+5077d others(4): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316337 | |||||||
chr2:100316349 | T | TTTCTAAT others(21): Show |
30 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(27): Show |
33 | HG01243.hp1 HG01516.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.679+5038_679+5065d others(30): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316349 | |||||||
chr2:100316368 | A | ATTCTAAT others(21): Show |
8 | a0002c0001t0012g0025 a0002c0001t0031g0026 a0002c0001t0076g0078 others(5): Show |
10 | HG01261.hp1 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.679+5046_679+5047i others(30): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316368 | |||||||
chr2:100316612 | A | G | 1 | a0002c0001t0087g0086 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.679+4803T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316612 | |||||||
chr2:100316620 | G | A | 7 | a0002c0001t0012g0025 a0002c0001t0031g0026 a0002c0001t0076g0078 others(4): Show |
9 | HG01261.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.679+4795C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316620 | |||||||
chr2:100316623 | A | G | 152 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(149): Show |
210 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.679+4792T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316623 | |||||||
chr2:100316631 | CG | C | 11 | a0002c0001t0022g0149 a0002c0022t0100g0148 a0003c0003t0016g0031 others(8): Show |
13 | HG01891.hp2 HG02630.hp1 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.679+4783delC | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316631 | |||||||
chr2:100316632 | G | A | 11 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(8): Show |
14 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.679+4783C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316632 | |||||||
chr2:100316641 | A | G | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.679+4774T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316641 | |||||||
chr2:100316893 | C | T | 1 | a0002c0001t0001g0084 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.679+4522G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316893 | |||||||
chr2:100316994 | A | G | 1 | a0004c0007t0004g0265 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.679+4421T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100316994 | |||||||
chr2:100317171 | A | C | 1 | a0003c0003t0008g0161 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.679+4244T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317171 | |||||||
chr2:100317241 | C | A | 48 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(45): Show |
56 | HG00423.hp2 HG00544.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.679+4174G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317241 | |||||||
chr2:100317243 | T | C | 1 | a0006c0014t0070g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.679+4172A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317243 | |||||||
chr2:100317296 | T | A | 30 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(27): Show |
33 | HG01243.hp1 HG01516.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.679+4119A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317296 | |||||||
chr2:100317305 | C | T | 9 | a0002c0001t0012g0033 a0002c0001t0012g0169 a0002c0001t0012g0170 others(6): Show |
10 | HG01169.hp2 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.679+4110G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317305 | |||||||
chr2:100317347 | T | C | 1 | a0002c0001t0001g0156 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.679+4068A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317347 | |||||||
chr2:100317430 | C | A | 1 | a0001c0008t0040g0038 | 2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.679+3985G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317430 | |||||||
chr2:100317576 | C | T | 114 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(111): Show |
167 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.679+3839G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317576 | |||||||
chr2:100317605 | C | T | 1 | a0007c0016t0115g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.679+3810G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317605 | |||||||
chr2:100317737 | GT | G | 30 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(27): Show |
33 | HG01243.hp1 HG01516.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.679+3677delA | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317737 | |||||||
chr2:100317803 | T | G | 11 | a0002c0001t0012g0033 a0002c0001t0012g0169 a0002c0001t0012g0170 others(8): Show |
12 | HG01169.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.679+3612A>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317803 | |||||||
chr2:100317961 | C | T | 30 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(27): Show |
33 | HG01243.hp1 HG01516.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.679+3454G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100317961 | |||||||
chr2:100318026 | C | A | 2 | a0001c0008t0039g0039 a0001c0008t0124g0249 |
3 | HG02257.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.679+3389G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318026 | |||||||
chr2:100318073 | C | A | 18 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(15): Show |
37 | HG00558.hp2 HG00609.hp2 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.679+3342G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318073 | |||||||
chr2:100318080 | C | T | 1 | a0002c0001t0001g0163 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.679+3335G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318080 | |||||||
chr2:100318114 | T | A | 2 | a0002c0001t0034g0164 a0002c0001t0034g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.679+3301A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318114 | |||||||
chr2:100318168 | T | C | 3 | a0002c0001t0031g0026 a0002c0001t0076g0078 a0002c0001t0077g0079 |
4 | HG02055.hp2 HG02280.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+3247A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318168 | |||||||
chr2:100318274 | G | C | 2 | a0002c0025t0098g0080 a0007c0016t0115g0207 |
2 | HG02109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.679+3141C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318274 | |||||||
chr2:100318344 | A | G | 3 | a0002c0012t0035g0075 a0002c0012t0035g0076 a0002c0012t0088g0077 |
3 | HG02622.hp1 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.679+3071T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318344 | |||||||
chr2:100318445 | C | T | 14 | a0002c0001t0001g0027 a0002c0001t0001g0083 a0002c0001t0012g0033 others(11): Show |
16 | HG01169.hp2 HG01884.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.679+2970G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318445 | |||||||
chr2:100318657 | C | G | 1 | a0002c0001t0018g0047 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.679+2758G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318657 | |||||||
chr2:100318667 | C | A | 114 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(111): Show |
167 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.679+2748G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318667 | |||||||
chr2:100318673 | C | T | 1 | a0002c0025t0098g0080 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.679+2742G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318673 | |||||||
chr2:100318674 | A | G | 114 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(111): Show |
167 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.679+2741T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318674 | |||||||
chr2:100318686 | C | T | 3 | a0002c0001t0006g0050 a0004c0011t0004g0023 a0004c0011t0004g0264 |
5 | HG02055.hp1 HG02148.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.679+2729G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318686 | |||||||
chr2:100318738 | C | T | 1 | a0001c0008t0041g0257 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.679+2677G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318738 | |||||||
chr2:100318786 | C | A | 2 | a0002c0001t0034g0164 a0002c0001t0034g0165 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.679+2629G>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318786 | |||||||
chr2:100318818 | C | T | 3 | a0001c0002t0002g0208 a0002c0001t0057g0166 a0002c0001t0090g0167 |
3 | HG01169.hp2 HG02129.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.679+2597G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318818 | |||||||
chr2:100318831 | C | CA | 10 | a0002c0001t0012g0033 a0002c0001t0012g0169 a0002c0001t0012g0170 others(7): Show |
11 | HG01256.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.679+2583dupT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318831 | |||||||
chr2:100318831 | C | CAAA | 11 | a0002c0025t0098g0080 a0004c0007t0002g0268 a0004c0007t0004g0043 others(8): Show |
14 | HG00544.hp2 HG02056.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.679+2581_679+2583d others(5): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318831 | |||||||
chr2:100318831 | C | CAAAA | 101 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(98): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.679+2580_679+2583d others(6): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318831 | |||||||
chr2:100318858 | A | G | 151 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(148): Show |
209 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.679+2557T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318858 | |||||||
chr2:100318867 | T | C | 162 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(159): Show |
221 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.679+2548A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318867 | |||||||
chr2:100318883 | G | C | 7 | a0002c0001t0012g0025 a0002c0001t0031g0026 a0002c0001t0076g0078 others(4): Show |
9 | HG01261.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.679+2532C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318883 | |||||||
chr2:100318902 | C | T | 1 | a0001c0004t0112g0204 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.679+2513G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318902 | |||||||
chr2:100318907 | G | A | 2 | a0002c0001t0057g0166 a0002c0001t0090g0167 |
2 | HG01169.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.679+2508C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100318907 | |||||||
chr2:100319078 | C | T | 1 | a0002c0001t0001g0081 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.679+2337G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319078 | |||||||
chr2:100319120 | T | A | 1 | a0003c0003t0008g0161 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.679+2295A>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319120 | |||||||
chr2:100319120 | T | TA | 48 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(45): Show |
54 | HG01243.hp1 HG01261.hp1 HG01516.hp2 others(51): Show |
intron_variant | MODIFIER | c.679+2294dupT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319120 | |||||||
chr2:100319120 | T | TAA | 103 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(100): Show |
156 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.679+2293_679+2294d others(4): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319120 | |||||||
chr2:100319120 | T | TAAA | 10 | a0001c0002t0002g0260 a0001c0002t0002g0261 a0001c0002t0002g0262 others(7): Show |
10 | HG01884.hp1 HG02148.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.679+2292_679+2294d others(5): Show |
LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319120 | |||||||
chr2:100319331 | C | T | 9 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.679+2084G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319331 | |||||||
chr2:100319355 | G | A | 112 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(109): Show |
165 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.679+2060C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319355 | |||||||
chr2:100319428 | G | A | 1 | a0002c0001t0075g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.679+1987C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319428 | |||||||
chr2:100319662 | A | G | 37 | a0002c0001t0006g0014 a0002c0001t0006g0048 a0002c0001t0006g0050 others(34): Show |
42 | HG01243.hp1 HG01261.hp1 HG01516.hp2 others(39): Show |
intron_variant | MODIFIER | c.679+1753T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319662 | |||||||
chr2:100319700 | G | A | 1 | a0009c0020t0126g0263 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.679+1715C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319700 | |||||||
chr2:100319706 | T | C | 1 | a0002c0001t0001g0162 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.679+1709A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319706 | |||||||
chr2:100319713 | T | C | 1 | a0002c0001t0001g0163 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.679+1702A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319713 | |||||||
chr2:100319814 | A | C | 111 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(108): Show |
164 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.679+1601T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319814 | |||||||
chr2:100319857 | A | G | 1 | a0002c0001t0018g0047 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.679+1558T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319857 | |||||||
chr2:100319907 | T | C | 1 | a0001c0006t0004g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.679+1508A>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100319907 | |||||||
chr2:100320088 | T | TA | 3 | a0002c0001t0019g0171 a0002c0001t0058g0172 a0002c0001t0059g0173 |
3 | HG02896.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.679+1326dupT | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100320088 | |||||||
chr2:100320140 | A | C | 1 | a0003c0003t0008g0049 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.679+1275T>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100320140 | |||||||
chr2:100320175 | C | T | 111 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(108): Show |
164 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.679+1240G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100320175 | |||||||
chr2:100320229 | G | A | 1 | a0002c0018t0037g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.679+1186C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100320229 | |||||||
chr2:100320254 | A | G | 1 | a0002c0001t0006g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.679+1161T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100320254 | |||||||
chr2:100320346 | A | G | 1 | a0001c0002t0002g0203 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.679+1069T>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100320346 | |||||||
chr2:100320551 | G | T | 1 | a0001c0004t0108g0202 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.679+864C>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100320551 | |||||||
chr2:100320849 | A | T | 1 | a0002c0001t0018g0047 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.679+566T>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100320849 | |||||||
chr2:100320945 | G | A | 12 | a0002c0001t0012g0033 a0002c0001t0012g0169 a0002c0001t0012g0170 others(9): Show |
13 | HG01169.hp2 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.679+470C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100320945 | |||||||
chr2:100321188 | C | T | 1 | a0002c0001t0075g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.679+227G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100321188 | |||||||
chr2:100321195 | C | T | 12 | a0004c0007t0002g0268 a0004c0007t0004g0043 a0004c0007t0004g0265 others(9): Show |
15 | HG00423.hp2 HG00544.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.679+220G>A | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100321195 | |||||||
chr2:100321245 | G | A | 111 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0022 others(108): Show |
164 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.679+170C>T | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100321245 | |||||||
chr2:100321331 | C | G | 2 | a0004c0011t0004g0023 a0004c0011t0004g0264 |
4 | HG02148.hp1 NA18953.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+84G>C | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100321331 | |||||||
chr2:100321369 | G | C | 8 | a0002c0001t0012g0033 a0002c0001t0012g0169 a0002c0001t0012g0170 others(5): Show |
9 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.679+46C>G | LONRF2 | ENSG00000170500.13 | transcript | ENST00000393437.8 | protein_coding | 1/11 | chr2 | 100321369 |