Item | Value |
---|---|
geneid | 25936 |
ensemblid | ENSG00000117697.15 |
hgncid | 24548 |
symbol | NSL1 |
name | NSL1 component of MIS12 kinetochore complex |
refseq_nuc | NM_015471.4 |
refseq_prot | NP_056286.3 |
ensembl_nuc | ENST00000366977.8 |
ensembl_prot | ENSP00000355944.3 |
mane_status | MANE Select |
chr | chr1 |
start | 212726153 |
end | 212791777 |
strand | - |
ver | v1.2 |
region | chr1:212726153-212791777 |
region5000 | chr1:212721153-212796777 |
regionname0 | NSL1_chr1_212726153_212791777 |
regionname5000 | NSL1_chr1_212721153_212796777 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 281 | 160 | 33 | 32 | 75 | 6 | 12 | 64 | NSL1_chr1_212721153_212796777 | NSL1 | MAGSP others(276): Show |
chr1 | 212721153 | 212796777 |
a0002 | 0/0 | 281 | 128 | 26 | 17 | 65 | 6 | 14 | 53 | NSL1_chr1_212721153_212796777 | NSL1 | MAGSP others(276): Show |
chr1 | 212721153 | 212796777 |
a0003 | 0/0 | 281 | 73 | 28 | 9 | 28 | 0 | 8 | 22 | NSL1_chr1_212721153_212796777 | NSL1 | MAGFP others(276): Show |
chr1 | 212721153 | 212796777 |
a0004 | 0/0 | 281 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | MAGSP others(276): Show |
chr1 | 212721153 | 212796777 |
a0005 | 0/0 | 281 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | MAGFP others(276): Show |
chr1 | 212721153 | 212796777 |
a0006 | 0/0 | 281 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | MAGSP others(276): Show |
chr1 | 212721153 | 212796777 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 843 | 158 | 33 | 30 | 75 | 6 | 12 | NSL1_chr1_212721153_212796777 | NSL1 | ATGGC others(838): Show |
chr1 | 212721153 | 212796777 | ||
a0001c0005 | 0/0 | 843 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | ATGGC others(838): Show |
chr1 | 212721153 | 212796777 | ||
a0001c0007 | 0/0 | 843 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | ATGGC others(838): Show |
chr1 | 212721153 | 212796777 | ||
a0002c0002 | 0/0 | 843 | 126 | 24 | 17 | 65 | 6 | 14 | NSL1_chr1_212721153_212796777 | NSL1 | ATGGC others(838): Show |
chr1 | 212721153 | 212796777 | ||
a0002c0004 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | ATGGC others(838): Show |
chr1 | 212721153 | 212796777 | ||
a0002c0009 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | ATGGC others(838): Show |
chr1 | 212721153 | 212796777 | ||
a0003c0003 | 0/0 | 843 | 73 | 28 | 9 | 28 | 0 | 8 | NSL1_chr1_212721153_212796777 | NSL1 | ATGGC others(838): Show |
chr1 | 212721153 | 212796777 | ||
a0004c0008 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | ATGGC others(838): Show |
chr1 | 212721153 | 212796777 | ||
a0005c0010 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | ATGGC others(838): Show |
chr1 | 212721153 | 212796777 | ||
a0006c0006 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | ATGGC others(838): Show |
chr1 | 212721153 | 212796777 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 13116 | 37 | 0 | 16 | 20 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0004 | 1/0 | 13115 | 27 | 5 | 2 | 14 | 1 | 4 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0006 | 0/0 | 13117 | 12 | 0 | 1 | 10 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0007 | 0/0 | 13114 | 10 | 9 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0010 | 0/0 | 13115 | 8 | 0 | 3 | 4 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0011 | 0/0 | 13116 | 7 | 0 | 1 | 5 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0016 | 0/0 | 13116 | 4 | 0 | 1 | 0 | 3 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0017 | 0/0 | 13115 | 4 | 4 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0018 | 0/1 | 13117 | 4 | 0 | 1 | 1 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0021 | 0/0 | 13115 | 3 | 3 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0022 | 0/0 | 13116 | 3 | 3 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0023 | 0/0 | 13115 | 3 | 0 | 0 | 3 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0024 | 0/0 | 13116 | 3 | 0 | 0 | 3 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0025 | 0/0 | 13117 | 3 | 0 | 1 | 2 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0036 | 0/0 | 13117 | 2 | 2 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0037 | 0/0 | 13116 | 2 | 0 | 0 | 2 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0071 | 0/0 | 13115 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0072 | 0/0 | 13117 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0073 | 0/0 | 13115 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0074 | 0/0 | 13114 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0075 | 0/0 | 13116 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0076 | 0/0 | 13117 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0077 | 0/0 | 13115 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0078 | 0/0 | 13116 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0079 | 0/0 | 13115 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0080 | 0/0 | 13113 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13108): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0081 | 0/0 | 13114 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0082 | 0/0 | 13114 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0083 | 0/0 | 13117 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0084 | 0/0 | 13113 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13108): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0085 | 0/0 | 13116 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0086 | 0/0 | 13115 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0087 | 0/0 | 13116 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0088 | 0/0 | 13116 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0089 | 0/0 | 13117 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0090 | 0/0 | 13117 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0091 | 0/0 | 13118 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13113): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0092 | 0/0 | 13116 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0096 | 0/0 | 13116 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0097 | 0/0 | 13116 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0119 | 0/0 | 13117 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0001c0001t0120 | 0/0 | 13117 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0001c0005t0007 | 0/0 | 13114 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0001c0007t0070 | 0/0 | 13116 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0002 | 0/0 | 13110 | 28 | 0 | 2 | 22 | 2 | 2 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0005 | 0/0 | 13110 | 15 | 0 | 1 | 14 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0008 | 0/0 | 13111 | 10 | 0 | 1 | 6 | 1 | 2 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13106): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0012 | 0/0 | 13122 | 6 | 1 | 2 | 3 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13117): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0013 | 0/0 | 13111 | 5 | 1 | 3 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13106): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0014 | 0/0 | 13100 | 5 | 5 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13095): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0019 | 0/0 | 13119 | 4 | 0 | 0 | 0 | 0 | 4 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13114): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0026 | 0/0 | 13115 | 3 | 3 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0027 | 0/0 | 13110 | 3 | 0 | 0 | 3 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0035 | 0/0 | 13115 | 2 | 2 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0038 | 0/0 | 13107 | 2 | 2 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13102): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0039 | 0/0 | 13112 | 2 | 1 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13107): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0040 | 0/0 | 13110 | 2 | 0 | 1 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0041 | 0/0 | 13110 | 2 | 0 | 0 | 2 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0042 | 0/0 | 13112 | 2 | 0 | 0 | 2 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13107): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0043 | 0/0 | 13111 | 2 | 0 | 1 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13106): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0044 | 0/0 | 13112 | 2 | 0 | 0 | 1 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13107): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0045 | 0/0 | 13118 | 2 | 0 | 2 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13113): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0046 | 0/0 | 13111 | 2 | 0 | 0 | 2 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13106): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0047 | 0/0 | 13112 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13107): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0065 | 0/0 | 13116 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0066 | 0/0 | 13120 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13115): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0069 | 0/0 | 13119 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13114): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0093 | 0/0 | 13114 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0094 | 0/0 | 13115 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0098 | 0/0 | 13120 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13115): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0099 | 0/0 | 13125 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13120): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0100 | 0/0 | 13111 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13106): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0101 | 0/0 | 13109 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13104): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0102 | 0/0 | 13111 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13106): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0103 | 0/0 | 13111 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13106): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0104 | 0/0 | 13110 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0105 | 0/0 | 13110 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0106 | 0/0 | 13110 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0107 | 0/0 | 13110 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0108 | 0/0 | 13110 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0109 | 0/0 | 13112 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13107): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0110 | 0/0 | 13112 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13107): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0111 | 0/0 | 13113 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13108): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0112 | 0/0 | 13114 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0113 | 0/0 | 13117 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0114 | 0/0 | 13118 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13113): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0115 | 0/0 | 13110 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0116 | 0/0 | 13111 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13106): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0117 | 0/0 | 13109 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13104): Show |
chr1 | 212721153 | 212796777 |
a0002c0002t0118 | 0/0 | 13110 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
a0002c0004t0095 | 0/0 | 13117 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0002c0009t0067 | 0/0 | 13113 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13108): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0003 | 0/0 | 13115 | 27 | 7 | 3 | 13 | 0 | 4 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0009 | 0/0 | 13116 | 7 | 6 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0015 | 0/0 | 13116 | 4 | 0 | 0 | 3 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0020 | 0/0 | 13114 | 3 | 0 | 0 | 3 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0028 | 0/0 | 13117 | 2 | 1 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0029 | 0/0 | 13114 | 2 | 0 | 1 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0030 | 0/0 | 13114 | 2 | 0 | 0 | 2 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0031 | 0/0 | 13116 | 2 | 0 | 1 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0032 | 0/0 | 13114 | 2 | 1 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0033 | 0/0 | 13115 | 2 | 2 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0034 | 0/0 | 13119 | 2 | 0 | 0 | 1 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13114): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0048 | 0/0 | 13116 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0049 | 0/0 | 13115 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0050 | 0/0 | 13114 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0051 | 0/0 | 13115 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0052 | 0/0 | 13116 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0053 | 0/0 | 13116 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0054 | 0/0 | 13116 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0055 | 0/0 | 13112 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13107): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0056 | 0/0 | 13115 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0057 | 0/0 | 13115 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0058 | 0/0 | 13114 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0059 | 0/0 | 13115 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0060 | 0/0 | 13114 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13109): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0061 | 0/0 | 13115 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0062 | 0/0 | 13117 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0063 | 0/0 | 13119 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13114): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0064 | 0/0 | 13117 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13112): Show |
chr1 | 212721153 | 212796777 |
a0003c0003t0068 | 0/0 | 13115 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13110): Show |
chr1 | 212721153 | 212796777 |
a0004c0008t0001 | 0/0 | 13116 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0005c0010t0009 | 0/0 | 13116 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13111): Show |
chr1 | 212721153 | 212796777 |
a0006c0006t0002 | 0/0 | 13110 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | AGTTC others(13105): Show |
chr1 | 212721153 | 212796777 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0007 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0007g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0007g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0010g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0010g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0010g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0010g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0010g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0010g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0011g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0011g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0011g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0011g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0011g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0011g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0016g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0016g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0016g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0016g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0017g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0017g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0017g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0017g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0018g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0018g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0018g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0018g0256 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0021g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0021g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0021g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0022g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0022g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0023g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0023g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0023g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0024g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0024g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0024g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0025g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0025g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0025g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0036g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0036g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0037g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0037g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0071g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0072g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0073g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0074g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0075g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0076g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0077g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0078g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0079g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0080g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0081g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0082g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0083g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0084g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0085g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0086g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0087g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0088g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0089g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0090g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0091g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0092g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0096g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0097g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0119g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0001t0120g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0005t0007g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0001c0007t0070g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0008g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0008g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0008g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0008g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0008g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0008g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0012g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0012g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0012g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0012g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0012g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0012g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0013g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0013g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0013g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0013g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0014g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0014g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0014g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0019g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0019g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0019g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0026g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0026g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0026g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0027g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0027g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0035g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0035g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0038g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0038g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0039g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0039g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0040g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0040g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0041g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0041g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0042g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0042g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0043g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0043g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0044g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0044g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0045g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0045g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0046g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0046g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0047g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0065g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0066g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0069g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0093g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0094g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0098g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0099g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0100g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0101g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0102g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0103g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0104g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0105g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0106g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0107g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0108g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0109g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0110g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0111g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0112g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0113g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0114g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0115g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0116g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0117g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0002t0118g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0004t0095g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0002c0009t0067g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0009g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0009g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0009g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0015g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0015g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0015g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0015g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0020g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0020g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0020g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0028g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0028g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0029g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0029g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0030g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0031g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0032g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0032g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0033g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0033g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0034g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0034g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0048g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0049g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0050g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0051g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0052g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0053g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0054g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0055g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0056g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0057g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0058g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0059g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0060g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0061g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0062g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0063g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0064g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0003c0003t0068g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0004c0008t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0005c0010t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
a0006c0006t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0071 | g0148 | EUR | GBR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0053 | EUR | GBR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00140 | hp1 | a0001 | c0001 | t0016 | g0155 | EUR | GBR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00140 | hp2 | a0002 | c0002 | t0008 | g0042 | EUR | GBR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0089 | EUR | FIN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00323 | hp2 | a0001 | c0001 | t0016 | g0154 | EUR | FIN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | CHS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00423 | hp2 | a0003 | c0003 | t0015 | g0344 | EAS | CHS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | CHS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | CHS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00609 | hp1 | a0004 | c0008 | t0001 | g0280 | EAS | CHS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00609 | hp2 | a0003 | c0003 | t0003 | g0321 | EAS | CHS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00621 | hp1 | a0003 | c0003 | t0015 | g0322 | EAS | CHS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00639 | hp1 | a0003 | c0003 | t0051 | g0291 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00639 | hp2 | a0001 | c0001 | t0007 | g0149 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00733 | hp1 | a0002 | c0002 | t0013 | g0103 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00738 | hp1 | a0002 | c0002 | t0040 | g0054 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00738 | hp2 | a0002 | c0002 | t0012 | g0270 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00741 | hp1 | a0002 | c0002 | t0012 | g0272 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01069 | hp1 | a0002 | c0002 | t0045 | g0173 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01069 | hp2 | a0001 | c0001 | t0025 | g0217 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01071 | hp1 | a0002 | c0002 | t0013 | g0100 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01071 | hp2 | a0002 | c0002 | t0045 | g0174 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01074 | hp2 | a0003 | c0003 | t0003 | g0346 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0085 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01109 | hp1 | a0003 | c0003 | t0028 | g0303 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01109 | hp2 | a0002 | c0002 | t0065 | g0265 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01167 | hp1 | a0003 | c0003 | t0003 | g0334 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01167 | hp2 | a0001 | c0005 | t0007 | g0016 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01168 | hp1 | a0003 | c0003 | t0029 | g0332 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01168 | hp2 | a0002 | c0002 | t0013 | g0098 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01169 | hp1 | a0002 | c0002 | t0108 | g0102 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01169 | hp2 | a0003 | c0003 | t0003 | g0333 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01175 | hp1 | a0001 | c0001 | t0089 | g0208 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01175 | hp2 | a0001 | c0001 | t0011 | g0279 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01192 | hp2 | a0001 | c0001 | t0016 | g0157 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01243 | hp2 | a0003 | c0003 | t0009 | g0003 | AMR | PUR | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01255 | hp1 | a0001 | c0001 | t0092 | g0226 | AMR | CLM | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0125 | AMR | CLM | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01261 | hp2 | a0003 | c0003 | t0031 | g0014 | AMR | CLM | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0253 | AMR | CLM | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01433 | hp2 | a0003 | c0003 | t0032 | g0294 | AMR | CLM | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01496 | hp1 | a0002 | c0002 | t0106 | g0050 | AMR | CLM | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01496 | hp2 | a0001 | c0001 | t0086 | g0204 | AMR | CLM | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01515 | hp1 | a0002 | c0002 | t0105 | g0093 | EUR | IBS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01515 | hp2 | a0002 | c0002 | t0013 | g0101 | EUR | IBS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01516 | hp1 | a0002 | c0002 | t0040 | g0034 | EUR | IBS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01516 | hp2 | a0001 | c0001 | t0018 | g0252 | EUR | IBS | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01884 | hp2 | a0002 | c0002 | t0035 | g0263 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01891 | hp1 | a0002 | c0002 | t0038 | g0104 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01891 | hp2 | a0002 | c0002 | t0026 | g0121 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01952 | hp1 | a0001 | c0001 | t0010 | g0228 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01952 | hp2 | a0002 | c0002 | t0043 | g0023 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01978 | hp2 | a0001 | c0001 | t0010 | g0185 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02004 | hp1 | a0001 | c0001 | t0018 | g0195 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02004 | hp2 | a0001 | c0007 | t0070 | g0221 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02027 | hp1 | a0003 | c0003 | t0015 | g0315 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02027 | hp2 | a0002 | c0002 | t0102 | g0059 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02055 | hp1 | a0001 | c0001 | t0017 | g0160 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02055 | hp2 | a0002 | c0002 | t0111 | g0106 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02056 | hp1 | a0002 | c0002 | t0008 | g0077 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02056 | hp2 | a0002 | c0002 | t0008 | g0081 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02071 | hp1 | a0001 | c0001 | t0078 | g0130 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02071 | hp2 | a0003 | c0003 | t0049 | g0337 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0192 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02074 | hp2 | a0002 | c0002 | t0008 | g0048 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02083 | hp2 | a0002 | c0002 | t0005 | g0065 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02129 | hp1 | a0003 | c0003 | t0003 | g0312 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02132 | hp1 | a0001 | c0001 | t0023 | g0219 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | KHV | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02145 | hp1 | a0001 | c0001 | t0073 | g0268 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02145 | hp2 | a0001 | c0001 | t0074 | g0123 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02148 | hp1 | a0002 | c0002 | t0008 | g0067 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | CDX | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02257 | hp1 | a0003 | c0003 | t0003 | g0287 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02257 | hp2 | a0003 | c0003 | t0061 | g0296 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02258 | hp1 | a0002 | c0002 | t0013 | g0105 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0267 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02273 | hp1 | a0002 | c0002 | t0005 | g0071 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0055 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02300 | hp1 | a0002 | c0002 | t0109 | g0097 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02300 | hp2 | a0001 | c0001 | t0010 | g0227 | AMR | PEL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02451 | hp1 | a0002 | c0002 | t0047 | g0017 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0122 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02572 | hp1 | a0003 | c0003 | t0057 | g0293 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02572 | hp2 | a0002 | c0002 | t0069 | g0177 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02602 | hp1 | a0003 | c0003 | t0003 | g0326 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02602 | hp2 | a0001 | c0001 | t0010 | g0223 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02615 | hp1 | a0001 | c0001 | t0081 | g0171 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02615 | hp2 | a0003 | c0003 | t0009 | g0307 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0161 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02622 | hp2 | a0001 | c0001 | t0021 | g0135 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02630 | hp1 | a0002 | c0002 | t0039 | g0094 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02630 | hp2 | a0003 | c0003 | t0058 | g0284 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02647 | hp1 | a0003 | c0003 | t0003 | g0338 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02647 | hp2 | a0003 | c0003 | t0063 | g0282 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02698 | hp1 | a0003 | c0003 | t0031 | g0014 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02698 | hp2 | a0002 | c0002 | t0039 | g0099 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02738 | hp1 | a0001 | c0001 | t0076 | g0146 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02738 | hp2 | a0002 | c0002 | t0008 | g0021 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02809 | hp1 | a0003 | c0003 | t0009 | g0003 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02809 | hp2 | a0002 | c0002 | t0104 | g0092 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0153 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02886 | hp2 | a0003 | c0003 | t0055 | g0289 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02895 | hp1 | a0002 | c0002 | t0093 | g0118 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02896 | hp2 | a0003 | c0003 | t0032 | g0290 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02897 | hp1 | a0003 | c0003 | t0033 | g0288 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02922 | hp1 | a0002 | c0002 | t0014 | g0004 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02922 | hp2 | a0003 | c0003 | t0050 | g0283 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02965 | hp1 | a0003 | c0003 | t0009 | g0308 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02965 | hp2 | a0001 | c0001 | t0022 | g0008 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02976 | hp1 | a0002 | c0009 | t0067 | g0281 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02976 | hp2 | a0003 | c0003 | t0003 | g0339 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03041 | hp1 | a0002 | c0002 | t0014 | g0090 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03041 | hp2 | a0001 | c0001 | t0022 | g0008 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0266 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03098 | hp2 | a0003 | c0003 | t0053 | g0286 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03130 | hp2 | a0003 | c0003 | t0009 | g0306 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03139 | hp1 | a0003 | c0003 | t0003 | g0013 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03139 | hp2 | a0001 | c0001 | t0083 | g0164 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03195 | hp1 | a0001 | c0001 | t0080 | g0169 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03195 | hp2 | a0002 | c0002 | t0026 | g0119 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03209 | hp1 | a0002 | c0002 | t0094 | g0117 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0142 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03225 | hp1 | a0003 | c0003 | t0068 | g0340 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03225 | hp2 | a0003 | c0003 | t0060 | g0295 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03453 | hp1 | a0001 | c0001 | t0022 | g0145 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03453 | hp2 | a0002 | c0002 | t0014 | g0004 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03486 | hp1 | a0003 | c0003 | t0033 | g0292 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03486 | hp2 | a0001 | c0001 | t0017 | g0141 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03490 | hp1 | a0001 | c0001 | t0006 | g0212 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0138 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03491 | hp1 | a0003 | c0003 | t0003 | g0317 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03491 | hp2 | a0002 | c0002 | t0019 | g0011 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03492 | hp2 | a0002 | c0002 | t0019 | g0011 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0165 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03516 | hp2 | a0002 | c0002 | t0026 | g0120 | AFR | ESN | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03540 | hp1 | a0002 | c0002 | t0114 | g0175 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03540 | hp2 | a0001 | c0001 | t0082 | g0115 | AFR | GWD | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03579 | hp1 | a0003 | c0003 | t0059 | g0285 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0038 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03654 | hp2 | a0003 | c0003 | t0003 | g0318 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03669 | hp1 | a0003 | c0003 | t0003 | g0316 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03669 | hp2 | a0001 | c0001 | t0097 | g0215 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03688 | hp1 | a0002 | c0002 | t0019 | g0276 | SAS | STU | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03688 | hp2 | a0002 | c0002 | t0112 | g0039 | SAS | STU | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0057 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0137 | SAS | PJL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03831 | hp1 | a0002 | c0002 | t0043 | g0052 | SAS | BEB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03831 | hp2 | a0001 | c0001 | t0088 | g0209 | SAS | BEB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03927 | hp1 | a0002 | c0002 | t0008 | g0045 | SAS | BEB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03927 | hp2 | a0002 | c0002 | t0110 | g0096 | SAS | BEB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03942 | hp1 | a0002 | c0002 | t0044 | g0044 | SAS | BEB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03942 | hp2 | a0003 | c0003 | t0034 | g0320 | SAS | BEB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG04115 | hp1 | a0003 | c0003 | t0015 | g0319 | SAS | STU | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG04115 | hp2 | a0001 | c0001 | t0011 | g0116 | SAS | STU | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG04199 | hp1 | a0002 | c0002 | t0019 | g0277 | SAS | STU | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG04199 | hp2 | a0003 | c0003 | t0052 | g0298 | SAS | STU | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG04204 | hp1 | a0001 | c0001 | t0087 | g0180 | SAS | STU | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0159 | SAS | STU | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG04228 | hp1 | a0002 | c0002 | t0100 | g0029 | SAS | STU | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0108 | SAS | STU | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | YRI | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18522 | hp2 | a0003 | c0003 | t0009 | g0304 | AFR | YRI | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | CHB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | CHB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18906 | hp1 | a0002 | c0002 | t0014 | g0091 | AFR | YRI | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18906 | hp2 | a0005 | c0010 | t0009 | g0305 | AFR | YRI | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18939 | hp1 | a0002 | c0002 | t0005 | g0061 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18939 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18941 | hp2 | a0002 | c0002 | t0005 | g0001 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18942 | hp1 | a0001 | c0001 | t0018 | g0201 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18942 | hp2 | a0002 | c0002 | t0027 | g0009 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18943 | hp1 | a0001 | c0001 | t0024 | g0218 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18943 | hp2 | a0003 | c0003 | t0003 | g0297 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18945 | hp1 | a0002 | c0002 | t0005 | g0001 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18947 | hp1 | a0001 | c0001 | t0006 | g0241 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18947 | hp2 | a0002 | c0002 | t0027 | g0178 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18948 | hp1 | a0001 | c0001 | t0006 | g0257 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18948 | hp2 | a0003 | c0003 | t0003 | g0323 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18950 | hp1 | a0001 | c0001 | t0091 | g0234 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18950 | hp2 | a0002 | c0002 | t0046 | g0032 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18951 | hp1 | a0003 | c0003 | t0003 | g0343 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18951 | hp2 | a0001 | c0001 | t0037 | g0251 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18952 | hp2 | a0002 | c0002 | t0098 | g0273 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18953 | hp1 | a0001 | c0001 | t0010 | g0231 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0197 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18954 | hp2 | a0003 | c0003 | t0020 | g0324 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18957 | hp1 | a0002 | c0002 | t0008 | g0082 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18959 | hp1 | a0002 | c0002 | t0101 | g0056 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18959 | hp2 | a0003 | c0003 | t0003 | g0336 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18960 | hp1 | a0002 | c0002 | t0103 | g0041 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18960 | hp2 | a0001 | c0001 | t0023 | g0262 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18961 | hp1 | a0002 | c0002 | t0115 | g0025 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18961 | hp2 | a0001 | c0001 | t0024 | g0184 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18963 | hp2 | a0003 | c0003 | t0020 | g0330 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18964 | hp1 | a0002 | c0002 | t0005 | g0001 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18964 | hp2 | a0001 | c0001 | t0010 | g0245 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18967 | hp1 | a0003 | c0003 | t0003 | g0301 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18968 | hp1 | a0002 | c0002 | t0118 | g0074 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18969 | hp1 | a0002 | c0002 | t0117 | g0069 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18969 | hp2 | a0001 | c0001 | t0023 | g0213 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18970 | hp1 | a0002 | c0002 | t0005 | g0070 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18971 | hp2 | a0003 | c0003 | t0003 | g0325 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18972 | hp1 | a0003 | c0003 | t0034 | g0302 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18973 | hp1 | a0002 | c0002 | t0012 | g0278 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18973 | hp2 | a0003 | c0003 | t0003 | g0314 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0237 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18977 | hp2 | a0003 | c0003 | t0048 | g0313 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18979 | hp1 | a0001 | c0001 | t0025 | g0250 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18979 | hp2 | a0003 | c0003 | t0003 | g0299 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18980 | hp1 | a0002 | c0002 | t0005 | g0001 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18980 | hp2 | a0001 | c0001 | t0006 | g0260 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18982 | hp1 | a0002 | c0002 | t0005 | g0078 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18982 | hp2 | a0003 | c0003 | t0003 | g0311 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18985 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18985 | hp2 | a0001 | c0001 | t0025 | g0243 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18986 | hp2 | a0002 | c0002 | t0116 | g0064 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18989 | hp2 | a0002 | c0002 | t0041 | g0046 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18990 | hp1 | a0002 | c0002 | t0012 | g0275 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18990 | hp2 | a0001 | c0001 | t0011 | g0152 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18992 | hp1 | a0002 | c0002 | t0005 | g0079 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18993 | hp2 | a0002 | c0002 | t0012 | g0274 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18994 | hp1 | a0002 | c0002 | t0027 | g0009 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18998 | hp2 | a0002 | c0002 | t0008 | g0028 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18999 | hp2 | a0001 | c0001 | t0077 | g0128 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19000 | hp1 | a0002 | c0002 | t0099 | g0269 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19000 | hp2 | a0002 | c0002 | t0046 | g0072 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19001 | hp1 | a0003 | c0003 | t0003 | g0335 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19001 | hp2 | a0002 | c0002 | t0005 | g0073 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19002 | hp1 | a0002 | c0002 | t0042 | g0083 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19002 | hp2 | a0001 | c0001 | t0096 | g0131 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19007 | hp1 | a0002 | c0002 | t0042 | g0049 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19007 | hp2 | a0003 | c0003 | t0003 | g0328 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19009 | hp1 | a0003 | c0003 | t0056 | g0329 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19009 | hp2 | a0006 | c0006 | t0002 | g0020 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19011 | hp1 | a0003 | c0003 | t0054 | g0327 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19012 | hp1 | a0001 | c0001 | t0006 | g0261 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19012 | hp2 | a0001 | c0001 | t0011 | g0150 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19030 | hp1 | a0003 | c0003 | t0064 | g0309 | AFR | LWK | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19030 | hp2 | a0002 | c0002 | t0038 | g0095 | AFR | LWK | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19043 | hp1 | a0001 | c0001 | t0036 | g0140 | AFR | LWK | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19043 | hp2 | a0001 | c0001 | t0021 | g0134 | AFR | LWK | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19055 | hp1 | a0001 | c0001 | t0119 | g0259 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19055 | hp2 | a0002 | c0002 | t0008 | g0080 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19056 | hp1 | a0003 | c0003 | t0029 | g0345 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19056 | hp2 | a0001 | c0001 | t0037 | g0246 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19058 | hp1 | a0003 | c0003 | t0062 | g0300 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19062 | hp2 | a0003 | c0003 | t0030 | g0012 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19063 | hp2 | a0002 | c0002 | t0005 | g0033 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19065 | hp1 | a0001 | c0001 | t0010 | g0244 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19068 | hp1 | a0002 | c0002 | t0005 | g0063 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19068 | hp2 | a0001 | c0001 | t0072 | g0258 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19070 | hp1 | a0002 | c0002 | t0107 | g0040 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19070 | hp2 | a0001 | c0001 | t0006 | g0242 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19075 | hp1 | a0001 | c0001 | t0010 | g0188 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19075 | hp2 | a0003 | c0003 | t0020 | g0331 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19078 | hp2 | a0001 | c0001 | t0075 | g0168 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19079 | hp2 | a0001 | c0001 | t0120 | g0193 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19080 | hp2 | a0001 | c0001 | t0011 | g0158 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19081 | hp1 | a0002 | c0002 | t0005 | g0062 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19081 | hp2 | a0001 | c0001 | t0079 | g0230 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19083 | hp1 | a0001 | c0001 | t0024 | g0182 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19084 | hp1 | a0001 | c0001 | t0090 | g0229 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19084 | hp2 | a0001 | c0001 | t0011 | g0124 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19086 | hp2 | a0001 | c0001 | t0085 | g0210 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19088 | hp2 | a0003 | c0003 | t0030 | g0012 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19089 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19090 | hp1 | a0002 | c0002 | t0044 | g0075 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19090 | hp2 | a0001 | c0001 | t0011 | g0151 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19091 | hp2 | a0002 | c0002 | t0005 | g0024 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19240 | hp1 | a0002 | c0002 | t0035 | g0264 | AFR | YRI | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA19240 | hp2 | a0003 | c0003 | t0003 | g0013 | AFR | YRI | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA20129 | hp1 | a0002 | c0002 | t0014 | g0019 | AFR | ASW | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA20129 | hp2 | a0003 | c0003 | t0009 | g0003 | AFR | ASW | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA20805 | hp1 | a0001 | c0001 | t0016 | g0156 | EUR | TSI | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0107 | EUR | TSI | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02109 | hp1 | a0002 | c0004 | t0095 | g0015 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02109 | hp2 | a0003 | c0003 | t0003 | g0342 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02486 | hp1 | a0001 | c0001 | t0084 | g0170 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02486 | hp2 | a0003 | c0003 | t0003 | g0341 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02559 | hp1 | a0003 | c0003 | t0028 | g0310 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG02559 | hp2 | a0001 | c0001 | t0036 | g0139 | AFR | ACB | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03471 | hp1 | a0001 | c0001 | t0017 | g0162 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG03471 | hp2 | a0001 | c0001 | t0021 | g0144 | AFR | MSL | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG06807 | hp1 | a0002 | c0002 | t0113 | g0176 | AFR | USA | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
HG06807 | hp2 | a0002 | c0002 | t0066 | g0018 | AFR | USA | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18955 | hp1 | a0001 | c0001 | t0006 | g0206 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA18955 | hp2 | a0002 | c0002 | t0041 | g0036 | EAS | JPT | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA20300 | hp1 | a0002 | c0002 | t0012 | g0271 | AFR | USA | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
NA20300 | hp2 | a0001 | c0001 | t0017 | g0163 | AFR | USA | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
homoSapiens | chm13v2 | a0001 | c0001 | t0018 | g0256 | REF | REF | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0007 | REF | REF | NSL1_chr1_212721153_212796777 | NSL1 | chr1 | 212721153 | 212796777 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:212738436 | C | T | 1 | a0006 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.818G>A | p.Arg273Gln | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 832/13115 | 818/846 | 273/281 | chr1 | 212738436 | |||
chr1:212738437 | G | A | 1 | a0005 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.817C>T | p.Arg273Trp | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 831/13115 | 817/846 | 273/281 | chr1 | 212738437 | |||
chr1:212738494 | T | C | 4 | a0002 a0003 a0005 others(1): Show |
203 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(200): Show |
missense_variant | MODERATE | c.760A>G | p.Met254Val | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 774/13115 | 760/846 | 254/281 | chr1 | 212738494 | |||
chr1:212791591 | T | C | 1 | a0004 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.173A>G | p.Gln58Arg | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/6 | 187/13115 | 173/846 | 58/281 | chr1 | 212791591 | |||
chr1:212791753 | G | A | 2 | a0003 a0005 |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
missense_variant | MODERATE | c.11C>T | p.Ser4Phe | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/6 | 25/13115 | 11/846 | 4/281 | chr1 | 212791753 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:212738603 | G | A | 1 | a0001c0007 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.651C>T | p.His217His | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 665/13115 | 651/846 | 217/281 | chr1 | 212738603 | |||
chr1:212791551 | G | T | 1 | a0001c0005 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.213C>A | p.Pro71Pro | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/6 | 227/13115 | 213/846 | 71/281 | chr1 | 212791551 | |||
chr1:212791668 | G | T | 1 | a0002c0004 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.96C>A | p.Pro32Pro | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/6 | 110/13115 | 96/846 | 32/281 | chr1 | 212791668 | |||
chr1:212791725 | T | C | 1 | a0002c0009 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.39A>G | p.Pro13Pro | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/6 | 53/13115 | 39/846 | 13/281 | chr1 | 212791725 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:212726172 | G | T | 2 | a0002c0002t0035 a0002c0002t0065 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12236C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 12236 | chr1 | 212726172 | ||||||
chr1:212726181 | A | C | 1 | a0002c0002t0041 | 2 | NA18955.hp2 NA18989.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12227T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 12227 | chr1 | 212726181 | ||||||
chr1:212726189 | A | G | 1 | a0001c0001t0024 | 3 | NA18943.hp1 NA18961.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12219T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 12219 | chr1 | 212726189 | ||||||
chr1:212726425 | C | A | 1 | a0003c0003t0030 | 2 | NA19062.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11983G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11983 | chr1 | 212726425 | ||||||
chr1:212726452 | T | C | 1 | a0001c0001t0021 | 3 | HG02622.hp2 HG03471.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11956A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11956 | chr1 | 212726452 | ||||||
chr1:212726477 | G | A | 1 | a0003c0003t0053 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11931C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11931 | chr1 | 212726477 | ||||||
chr1:212726612 | A | G | 2 | a0002c0002t0109 a0002c0002t0110 |
2 | HG02300.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11796T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11796 | chr1 | 212726612 | ||||||
chr1:212726666 | C | T | 1 | a0001c0001t0086 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11742G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11742 | chr1 | 212726666 | ||||||
chr1:212726712 | C | T | 1 | a0002c0002t0094 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11696G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11696 | chr1 | 212726712 | ||||||
chr1:212726798 | G | A | 2 | a0002c0002t0103 a0002c0002t0107 |
2 | NA18960.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11610C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11610 | chr1 | 212726798 | ||||||
chr1:212726969 | G | C | 79 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(76): Show |
203 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*11439C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11439 | chr1 | 212726969 | ||||||
chr1:212727043 | G | A | 1 | a0003c0003t0054 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11365C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11365 | chr1 | 212727043 | ||||||
chr1:212727068 | C | A | 1 | a0002c0002t0047 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11340G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11340 | chr1 | 212727068 | ||||||
chr1:212727092 | C | CG | 75 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(72): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*11315_*11316insC | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11315 | chr1 | 212727092 | ||||||
chr1:212727121 | G | A | 11 | a0002c0002t0045 a0002c0002t0069 a0002c0002t0113 others(8): Show |
14 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*11287C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11287 | chr1 | 212727121 | ||||||
chr1:212727145 | A | G | 114 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(111): Show |
319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*11263T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 11263 | chr1 | 212727145 | ||||||
chr1:212727715 | A | G | 1 | a0003c0003t0052 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10693T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 10693 | chr1 | 212727715 | ||||||
chr1:212727895 | T | C | 35 | a0002c0002t0035 a0002c0002t0047 a0002c0002t0065 others(32): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*10513A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 10513 | chr1 | 212727895 | ||||||
chr1:212727909 | G | A | 1 | a0002c0002t0066 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10499C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 10499 | chr1 | 212727909 | ||||||
chr1:212727957 | T | C | 1 | a0002c0002t0014 | 5 | HG02922.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*10451A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 10451 | chr1 | 212727957 | ||||||
chr1:212728051 | G | A | 4 | a0003c0003t0009 a0003c0003t0028 a0003c0003t0064 others(1): Show |
11 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*10357C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 10357 | chr1 | 212728051 | ||||||
chr1:212728458 | T | C | 1 | a0003c0003t0031 | 2 | HG01261.hp2 HG02698.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9950A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 9950 | chr1 | 212728458 | ||||||
chr1:212728527 | T | G | 35 | a0002c0002t0035 a0002c0002t0047 a0002c0002t0065 others(32): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*9881A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 9881 | chr1 | 212728527 | ||||||
chr1:212728663 | T | C | 4 | a0002c0002t0045 a0002c0002t0069 a0002c0002t0113 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9745A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 9745 | chr1 | 212728663 | ||||||
chr1:212728846 | T | C | 3 | a0002c0002t0045 a0002c0002t0113 a0002c0002t0114 |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9562A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 9562 | chr1 | 212728846 | ||||||
chr1:212729269 | C | G | 1 | a0001c0001t0037 | 2 | NA18951.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9139G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 9139 | chr1 | 212729269 | ||||||
chr1:212729340 | G | C | 1 | a0001c0001t0087 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9068C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 9068 | chr1 | 212729340 | ||||||
chr1:212729453 | C | T | 1 | a0002c0002t0109 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8955G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8955 | chr1 | 212729453 | ||||||
chr1:212729469 | A | G | 39 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0035 others(36): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*8939T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8939 | chr1 | 212729469 | ||||||
chr1:212729559 | G | A | 30 | a0003c0003t0003 a0003c0003t0009 a0003c0003t0015 others(27): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*8849C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8849 | chr1 | 212729559 | ||||||
chr1:212729709 | C | G | 33 | a0002c0002t0035 a0002c0002t0047 a0002c0002t0065 others(30): Show |
78 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*8699G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8699 | chr1 | 212729709 | ||||||
chr1:212729747 | G | A | 32 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(29): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*8661C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8661 | chr1 | 212729747 | ||||||
chr1:212729945 | A | ATTT | 4 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0098 others(1): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*8460_*8462dupAAA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8462 | chr1 | 212729945 | ||||||
chr1:212729981 | C | T | 2 | a0002c0002t0066 a0002c0002t0106 |
2 | HG01496.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8427G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8427 | chr1 | 212729981 | ||||||
chr1:212730013 | G | A | 1 | a0002c0002t0105 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8395C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8395 | chr1 | 212730013 | ||||||
chr1:212730021 | C | T | 1 | a0002c0002t0040 | 2 | HG00738.hp1 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8387G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8387 | chr1 | 212730021 | ||||||
chr1:212730061 | A | G | 112 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(109): Show |
317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*8347T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8347 | chr1 | 212730061 | ||||||
chr1:212730237 | C | CA | 36 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0011 others(33): Show |
114 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*8170dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8170 | chr1 | 212730237 | ||||||
chr1:212730237 | C | CAA | 24 | a0001c0001t0006 a0001c0001t0022 a0001c0001t0072 others(21): Show |
79 | HG00609.hp2 HG00639.hp1 HG00738.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*8169_*8170dupTT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8170 | chr1 | 212730237 | ||||||
chr1:212730237 | C | CAAA | 18 | a0001c0001t0036 a0001c0001t0083 a0002c0002t0066 others(15): Show |
25 | HG00423.hp2 HG00621.hp1 HG01109.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*8168_*8170dupTTT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8170 | chr1 | 212730237 | ||||||
chr1:212730237 | CA | C | 7 | a0001c0001t0080 a0001c0001t0084 a0002c0002t0101 others(4): Show |
7 | HG01169.hp1 HG02486.hp1 HG03195.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8170delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8170 | chr1 | 212730237 | ||||||
chr1:212730237 | CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0014 | 5 | HG02922.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8159_*8170delTTTT others(8): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8159 | chr1 | 212730237 | ||||||
chr1:212730267 | A | G | 1 | a0001c0001t0083 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8141T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8141 | chr1 | 212730267 | ||||||
chr1:212730273 | G | T | 1 | a0002c0002t0027 | 3 | NA18942.hp2 NA18947.hp2 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8135C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8135 | chr1 | 212730273 | ||||||
chr1:212730314 | G | C | 1 | a0002c0002t0114 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8094C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8094 | chr1 | 212730314 | ||||||
chr1:212730396 | C | T | 1 | a0002c0002t0066 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8012G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 8012 | chr1 | 212730396 | ||||||
chr1:212730721 | T | G | 1 | a0002c0002t0047 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7687A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 7687 | chr1 | 212730721 | ||||||
chr1:212731011 | C | T | 1 | a0002c0002t0116 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7397G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 7397 | chr1 | 212731011 | ||||||
chr1:212731038 | A | T | 1 | a0002c0004t0095 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7370T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 7370 | chr1 | 212731038 | ||||||
chr1:212731059 | T | C | 1 | a0003c0003t0057 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7349A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 7349 | chr1 | 212731059 | ||||||
chr1:212731154 | AATCT | A | 32 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(29): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*7250_*7253delAGAT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 7250 | chr1 | 212731154 | ||||||
chr1:212731186 | G | GA | 23 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0016 others(20): Show |
82 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*7221dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 7221 | chr1 | 212731186 | ||||||
chr1:212731186 | GA | G | 63 | a0001c0001t0074 a0001c0001t0082 a0002c0002t0002 others(60): Show |
174 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*7221delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 7221 | chr1 | 212731186 | ||||||
chr1:212731187 | A | G | 1 | a0002c0002t0115 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7221T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 7221 | chr1 | 212731187 | ||||||
chr1:212731202 | T | C | 4 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0098 others(1): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7206A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 7206 | chr1 | 212731202 | ||||||
chr1:212731219 | G | T | 2 | a0002c0002t0066 a0002c0009t0067 |
2 | HG02976.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7189C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 7189 | chr1 | 212731219 | ||||||
chr1:212731395 | C | T | 2 | a0002c0002t0104 a0002c0002t0105 |
2 | HG01515.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7013G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 7013 | chr1 | 212731395 | ||||||
chr1:212731424 | C | T | 1 | a0002c0009t0067 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6984G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6984 | chr1 | 212731424 | ||||||
chr1:212731647 | C | T | 4 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0098 others(1): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6761G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6761 | chr1 | 212731647 | ||||||
chr1:212731739 | G | A | 1 | a0002c0002t0014 | 5 | HG02922.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6669C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6669 | chr1 | 212731739 | ||||||
chr1:212731776 | G | C | 1 | a0001c0001t0073 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6632C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6632 | chr1 | 212731776 | ||||||
chr1:212732028 | A | AT | 23 | a0001c0001t0018 a0001c0001t0089 a0002c0002t0012 others(20): Show |
64 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*6379dupA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6379 | chr1 | 212732028 | ||||||
chr1:212732028 | A | ATT | 6 | a0002c0002t0035 a0002c0002t0065 a0003c0003t0009 others(3): Show |
14 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6378_*6379dupAA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6379 | chr1 | 212732028 | ||||||
chr1:212732028 | AT | A | 29 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(26): Show |
96 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*6379delA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6379 | chr1 | 212732028 | ||||||
chr1:212732068 | TTTA | T | 32 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(29): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*6337_*6339delTAA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6337 | chr1 | 212732068 | ||||||
chr1:212732107 | C | T | 1 | a0002c0002t0019 | 4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6301G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6301 | chr1 | 212732107 | ||||||
chr1:212732266 | G | A | 4 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0098 others(1): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6142C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6142 | chr1 | 212732266 | ||||||
chr1:212732289 | A | G | 30 | a0003c0003t0003 a0003c0003t0009 a0003c0003t0015 others(27): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*6119T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6119 | chr1 | 212732289 | ||||||
chr1:212732316 | C | CT | 37 | a0001c0001t0085 a0002c0002t0035 a0002c0002t0047 others(34): Show |
82 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*6091dupA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6091 | chr1 | 212732316 | ||||||
chr1:212732316 | C | CTT | 31 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(28): Show |
99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*6090_*6091dupAA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6091 | chr1 | 212732316 | ||||||
chr1:212732316 | C | CTTT | 9 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0045 others(6): Show |
18 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*6089_*6091dupAAA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6091 | chr1 | 212732316 | ||||||
chr1:212732344 | T | C | 113 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(110): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*6064A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6064 | chr1 | 212732344 | ||||||
chr1:212732367 | C | T | 2 | a0001c0001t0080 a0001c0001t0081 |
2 | HG02615.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6041G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6041 | chr1 | 212732367 | ||||||
chr1:212732373 | C | T | 4 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0098 others(1): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6035G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6035 | chr1 | 212732373 | ||||||
chr1:212732374 | G | A | 1 | a0001c0001t0088 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6034C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6034 | chr1 | 212732374 | ||||||
chr1:212732390 | G | A | 4 | a0003c0003t0050 a0003c0003t0058 a0003c0003t0059 others(1): Show |
4 | HG02630.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6018C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 6018 | chr1 | 212732390 | ||||||
chr1:212732438 | G | C | 1 | a0001c0001t0089 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5970C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 5970 | chr1 | 212732438 | ||||||
chr1:212732545 | C | T | 4 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0098 others(1): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5863G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 5863 | chr1 | 212732545 | ||||||
chr1:212732556 | G | A | 102 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(99): Show |
292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*5852C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 5852 | chr1 | 212732556 | ||||||
chr1:212732663 | C | G | 1 | a0003c0003t0050 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5745G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 5745 | chr1 | 212732663 | ||||||
chr1:212732785 | AT | A | 3 | a0002c0002t0045 a0002c0002t0113 a0002c0002t0114 |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5622delA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 5622 | chr1 | 212732785 | ||||||
chr1:212732848 | TTGAC | T | 2 | a0002c0002t0038 a0002c0002t0047 |
3 | HG01891.hp1 HG02451.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5556_*5559delGTCA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 5556 | chr1 | 212732848 | ||||||
chr1:212732871 | T | C | 2 | a0001c0001t0077 a0001c0001t0078 |
2 | HG02071.hp1 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5537A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 5537 | chr1 | 212732871 | ||||||
chr1:212733024 | T | C | 1 | a0002c0002t0066 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5384A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 5384 | chr1 | 212733024 | ||||||
chr1:212733203 | A | C | 4 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0098 others(1): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5205T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 5205 | chr1 | 212733203 | ||||||
chr1:212733252 | C | T | 1 | a0001c0001t0097 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5156G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 5156 | chr1 | 212733252 | ||||||
chr1:212733357 | C | A | 2 | a0003c0003t0060 a0003c0003t0061 |
2 | HG02257.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5051G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 5051 | chr1 | 212733357 | ||||||
chr1:212733430 | TCA | T | 3 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0098 |
11 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4976_*4977delTG | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 4976 | chr1 | 212733430 | ||||||
chr1:212733433 | C | CA | 24 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(21): Show |
86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*4974dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 4974 | chr1 | 212733433 | ||||||
chr1:212733433 | C | CAA | 6 | a0002c0002t0014 a0002c0002t0043 a0002c0002t0044 others(3): Show |
12 | HG01952.hp2 HG02055.hp2 HG02922.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4973_*4974dupTT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 4974 | chr1 | 212733433 | ||||||
chr1:212733433 | CA | C | 39 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(36): Show |
121 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*4974delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 4974 | chr1 | 212733433 | ||||||
chr1:212733433 | CAAAA | C | 30 | a0002c0002t0035 a0002c0002t0065 a0002c0009t0067 others(27): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*4971_*4974delTTTT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 4971 | chr1 | 212733433 | ||||||
chr1:212733819 | C | T | 1 | a0001c0001t0016 | 4 | HG00140.hp1 HG00323.hp2 HG01192.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4589G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 4589 | chr1 | 212733819 | ||||||
chr1:212734114 | G | A | 1 | a0002c0002t0118 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4294C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 4294 | chr1 | 212734114 | ||||||
chr1:212734118 | T | C | 1 | a0003c0003t0064 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4290A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 4290 | chr1 | 212734118 | ||||||
chr1:212734498 | T | C | 1 | a0001c0001t0092 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3910A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 3910 | chr1 | 212734498 | ||||||
chr1:212734524 | T | C | 67 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(64): Show |
180 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*3884A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 3884 | chr1 | 212734524 | ||||||
chr1:212734531 | C | T | 1 | a0003c0003t0049 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3877G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 3877 | chr1 | 212734531 | ||||||
chr1:212734548 | A | G | 1 | a0002c0009t0067 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3860T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 3860 | chr1 | 212734548 | ||||||
chr1:212734621 | A | G | 35 | a0002c0002t0035 a0002c0002t0047 a0002c0002t0065 others(32): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*3787T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 3787 | chr1 | 212734621 | ||||||
chr1:212734692 | A | C | 1 | a0002c0002t0047 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3716T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 3716 | chr1 | 212734692 | ||||||
chr1:212734732 | T | G | 1 | a0002c0009t0067 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3676A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 3676 | chr1 | 212734732 | ||||||
chr1:212734749 | G | C | 1 | a0001c0001t0092 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3659C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 3659 | chr1 | 212734749 | ||||||
chr1:212734835 | A | G | 1 | a0001c0001t0079 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3573T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 3573 | chr1 | 212734835 | ||||||
chr1:212735373 | T | C | 4 | a0002c0002t0045 a0002c0002t0069 a0002c0002t0113 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3035A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 3035 | chr1 | 212735373 | ||||||
chr1:212735491 | C | T | 3 | a0002c0002t0026 a0002c0002t0093 a0002c0002t0094 |
5 | HG01891.hp2 HG02895.hp1 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2917G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 2917 | chr1 | 212735491 | ||||||
chr1:212735580 | T | C | 113 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(110): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*2828A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 2828 | chr1 | 212735580 | ||||||
chr1:212735587 | T | C | 79 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(76): Show |
203 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*2821A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 2821 | chr1 | 212735587 | ||||||
chr1:212735763 | G | A | 1 | a0002c0002t0114 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2645C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 2645 | chr1 | 212735763 | ||||||
chr1:212735892 | G | A | 6 | a0002c0002t0005 a0002c0002t0046 a0002c0002t0115 others(3): Show |
21 | HG02083.hp2 HG02273.hp1 NA18939.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2516C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 2516 | chr1 | 212735892 | ||||||
chr1:212735998 | T | C | 1 | a0001c0001t0096 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2410A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 2410 | chr1 | 212735998 | ||||||
chr1:212736130 | A | T | 39 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0035 others(36): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2278T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 2278 | chr1 | 212736130 | ||||||
chr1:212736315 | G | C | 1 | a0001c0001t0097 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2093C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 2093 | chr1 | 212736315 | ||||||
chr1:212736402 | A | G | 30 | a0003c0003t0003 a0003c0003t0009 a0003c0003t0015 others(27): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2006T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 2006 | chr1 | 212736402 | ||||||
chr1:212736501 | C | T | 1 | a0003c0003t0048 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1907G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 1907 | chr1 | 212736501 | ||||||
chr1:212736707 | C | T | 1 | a0001c0001t0072 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1701G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 1701 | chr1 | 212736707 | ||||||
chr1:212736867 | C | T | 1 | a0001c0001t0071 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1541G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 1541 | chr1 | 212736867 | ||||||
chr1:212737229 | G | T | 1 | a0002c0002t0100 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1179C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 1179 | chr1 | 212737229 | ||||||
chr1:212737235 | C | T | 4 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0098 others(1): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1173G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 1173 | chr1 | 212737235 | ||||||
chr1:212737265 | A | G | 1 | a0001c0007t0070 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1143T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 1143 | chr1 | 212737265 | ||||||
chr1:212737326 | T | A | 1 | a0003c0003t0068 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1082A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 1082 | chr1 | 212737326 | ||||||
chr1:212737578 | C | T | 1 | a0002c0002t0047 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*830G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 830 | chr1 | 212737578 | ||||||
chr1:212737588 | G | A | 75 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0008 others(72): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*820C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 820 | chr1 | 212737588 | ||||||
chr1:212737894 | G | C | 1 | a0001c0001t0119 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*514C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 514 | chr1 | 212737894 | ||||||
chr1:212737977 | A | C | 1 | a0002c0002t0069 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*431T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 431 | chr1 | 212737977 | ||||||
chr1:212738024 | CT | C | 69 | a0001c0001t0010 a0001c0001t0025 a0002c0002t0002 others(66): Show |
180 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*383delA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 383 | chr1 | 212738024 | ||||||
chr1:212738024 | CTT | C | 4 | a0002c0002t0012 a0002c0002t0019 a0002c0002t0098 others(1): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*382_*383delAA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 382 | chr1 | 212738024 | ||||||
chr1:212738033 | T | G | 1 | a0001c0001t0120 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*375A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 375 | chr1 | 212738033 | ||||||
chr1:212738273 | C | T | 35 | a0002c0002t0035 a0002c0002t0047 a0002c0002t0065 others(32): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*135G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 6/6 | 135 | chr1 | 212738273 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:212738755 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.568-69C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 5/5 | chr1 | 212738755 | |||||||
chr1:212738756 | C | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.568-70G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 5/5 | chr1 | 212738756 | |||||||
chr1:212738766 | AT | A | 105 | a0001c0001t0006g0241 a0001c0001t0010g0245 a0002c0002t0012g0270 others(102): Show |
112 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.568-81delA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 5/5 | chr1 | 212738766 | |||||||
chr1:212738766 | ATT | A | 76 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(73): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.568-82_568-81delAA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 5/5 | chr1 | 212738766 | |||||||
chr1:212738905 | G | A | 31 | a0001c0001t0001g0010 a0001c0001t0001g0183 a0001c0001t0001g0191 others(28): Show |
32 | HG00609.hp1 HG00733.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.568-219C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 5/5 | chr1 | 212738905 | |||||||
chr1:212739013 | T | C | 2 | a0001c0001t0007g0006 a0001c0001t0022g0145 |
3 | HG02895.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.568-327A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 5/5 | chr1 | 212739013 | |||||||
chr1:212739089 | T | C | 3 | a0003c0003t0003g0299 a0003c0003t0003g0343 a0003c0003t0020g0324 |
3 | NA18951.hp1 NA18954.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.568-403A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 5/5 | chr1 | 212739089 | |||||||
chr1:212739116 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.567+418T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 5/5 | chr1 | 212739116 | |||||||
chr1:212739190 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.567+344A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 5/5 | chr1 | 212739190 | |||||||
chr1:212739318 | T | C | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.567+216A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 5/5 | chr1 | 212739318 | |||||||
chr1:212739426 | C | T | 1 | a0003c0003t0034g0320 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.567+108G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 5/5 | chr1 | 212739426 | |||||||
chr1:212739726 | C | G | 3 | a0001c0001t0007g0153 a0001c0001t0017g0141 a0001c0005t0007g0016 |
3 | HG01167.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.500-125G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212739726 | |||||||
chr1:212739781 | G | C | 1 | a0001c0001t0084g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.500-180C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212739781 | |||||||
chr1:212739783 | T | C | 27 | a0001c0001t0007g0006 a0001c0001t0007g0122 a0001c0001t0007g0142 others(24): Show |
29 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.500-182A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212739783 | |||||||
chr1:212739812 | A | C | 2 | a0001c0001t0001g0186 a0001c0001t0091g0234 |
2 | NA18950.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.500-211T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212739812 | |||||||
chr1:212739826 | T | C | 54 | a0003c0003t0003g0013 a0003c0003t0003g0297 a0003c0003t0003g0299 others(51): Show |
59 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.500-225A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212739826 | |||||||
chr1:212739856 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-255T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212739856 | |||||||
chr1:212739907 | T | C | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.500-306A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212739907 | |||||||
chr1:212740017 | G | C | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.500-416C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740017 | |||||||
chr1:212740211 | A | G | 1 | a0003c0003t0003g0299 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.500-610T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740211 | |||||||
chr1:212740248 | C | T | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-647G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740248 | |||||||
chr1:212740364 | C | G | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.500-763G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740364 | |||||||
chr1:212740480 | GT | G | 83 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(80): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.500-880delA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740480 | |||||||
chr1:212740490 | T | G | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-889A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740490 | |||||||
chr1:212740491 | G | A | 8 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(5): Show |
8 | HG00738.hp2 HG00741.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.500-890C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740491 | |||||||
chr1:212740558 | C | T | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-957G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740558 | |||||||
chr1:212740678 | T | A | 1 | a0001c0001t0017g0141 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.500-1077A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740678 | |||||||
chr1:212740689 | T | C | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-1088A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740689 | |||||||
chr1:212740693 | A | G | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-1092T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740693 | |||||||
chr1:212740741 | A | G | 3 | a0002c0002t0019g0011 a0002c0002t0019g0276 a0002c0002t0019g0277 |
4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-1140T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740741 | |||||||
chr1:212740782 | A | C | 4 | a0002c0002t0008g0028 a0002c0002t0008g0081 a0002c0002t0008g0082 others(1): Show |
4 | HG02056.hp2 NA18957.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-1181T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740782 | |||||||
chr1:212740810 | T | C | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.500-1209A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740810 | |||||||
chr1:212740832 | T | A | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-1231A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212740832 | |||||||
chr1:212741062 | T | C | 72 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 others(69): Show |
77 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.500-1461A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741062 | |||||||
chr1:212741149 | G | C | 4 | a0002c0002t0014g0004 a0002c0002t0014g0019 a0002c0002t0014g0090 others(1): Show |
5 | HG02922.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-1548C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741149 | |||||||
chr1:212741163 | A | G | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-1562T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741163 | |||||||
chr1:212741201 | GTGGTA | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-1605_500-1601d others(7): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741201 | |||||||
chr1:212741410 | A | G | 16 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(13): Show |
17 | HG00738.hp2 HG00741.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.500-1809T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741410 | |||||||
chr1:212741544 | G | A | 1 | a0002c0002t0069g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.500-1943C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741544 | |||||||
chr1:212741603 | A | C | 1 | a0002c0002t0069g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.500-2002T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741603 | |||||||
chr1:212741603 | A | G | 2 | a0002c0002t0005g0024 a0002c0002t0005g0033 |
2 | NA19063.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.500-2002T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741603 | |||||||
chr1:212741727 | T | C | 1 | a0003c0003t0062g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.500-2126A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741727 | |||||||
chr1:212741736 | G | T | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.500-2135C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741736 | |||||||
chr1:212741750 | T | C | 1 | a0002c0002t0098g0273 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.500-2149A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741750 | |||||||
chr1:212741779 | T | C | 1 | a0001c0001t0119g0259 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.500-2178A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741779 | |||||||
chr1:212741999 | C | T | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-2398G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212741999 | |||||||
chr1:212742039 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-2438C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212742039 | |||||||
chr1:212742171 | T | A | 1 | a0001c0001t0004g0132 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.500-2570A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212742171 | |||||||
chr1:212742172 | A | C | 1 | a0001c0001t0004g0132 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.500-2571T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212742172 | |||||||
chr1:212742380 | G | T | 2 | a0003c0003t0020g0330 a0003c0003t0020g0331 |
2 | NA18963.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.500-2779C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212742380 | |||||||
chr1:212742413 | A | C | 1 | a0003c0003t0062g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.500-2812T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212742413 | |||||||
chr1:212742421 | A | C | 1 | a0003c0003t0062g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.500-2820T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212742421 | |||||||
chr1:212742474 | A | C | 1 | a0003c0003t0062g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.500-2873T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212742474 | |||||||
chr1:212743030 | A | T | 1 | a0003c0003t0062g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.500-3429T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743030 | |||||||
chr1:212743031 | T | C | 1 | a0003c0003t0062g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.500-3430A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743031 | |||||||
chr1:212743032 | C | T | 1 | a0002c0004t0095g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.500-3431G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743032 | |||||||
chr1:212743228 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-3627C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743228 | |||||||
chr1:212743337 | G | C | 1 | a0002c0004t0095g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.500-3736C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743337 | |||||||
chr1:212743357 | G | T | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.500-3756C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743357 | |||||||
chr1:212743364 | C | T | 1 | a0002c0002t0112g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.500-3763G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743364 | |||||||
chr1:212743403 | T | A | 1 | a0003c0003t0052g0298 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.500-3802A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743403 | |||||||
chr1:212743406 | G | A | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-3805C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743406 | |||||||
chr1:212743409 | C | T | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-3808G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743409 | |||||||
chr1:212743468 | G | GT | 79 | a0001c0001t0001g0187 a0002c0002t0002g0002 a0002c0002t0002g0022 others(76): Show |
86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.500-3868dupA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743468 | |||||||
chr1:212743468 | G | GTT | 13 | a0002c0002t0005g0070 a0002c0002t0012g0270 a0002c0002t0012g0271 others(10): Show |
14 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(11): Show |
intron_variant | MODIFIER | c.500-3869_500-3868d others(4): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743468 | |||||||
chr1:212743468 | G | T | 1 | a0001c0001t0004g0138 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.500-3867C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743468 | |||||||
chr1:212743532 | T | G | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-3931A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743532 | |||||||
chr1:212743557 | A | C | 1 | a0003c0003t0062g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.500-3956T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743557 | |||||||
chr1:212743749 | C | A | 1 | a0001c0001t0017g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.500-4148G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743749 | |||||||
chr1:212743807 | G | A | 1 | a0003c0003t0050g0283 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.500-4206C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212743807 | |||||||
chr1:212744019 | T | C | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-4418A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744019 | |||||||
chr1:212744111 | C | T | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-4510G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744111 | |||||||
chr1:212744145 | G | A | 1 | a0003c0003t0062g0300 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.500-4544C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744145 | |||||||
chr1:212744164 | T | TGCCTGGC others(12): Show |
1 | a0002c0002t0005g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.500-4582_500-4564d others(21): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744164 | |||||||
chr1:212744271 | C | T | 3 | a0002c0002t0019g0011 a0002c0002t0019g0276 a0002c0002t0019g0277 |
4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-4670G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744271 | |||||||
chr1:212744336 | C | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-4735G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744336 | |||||||
chr1:212744341 | G | A | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.500-4740C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744341 | |||||||
chr1:212744422 | G | A | 1 | a0001c0001t0017g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.500-4821C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744422 | |||||||
chr1:212744426 | C | A | 1 | a0003c0003t0033g0292 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.500-4825G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744426 | |||||||
chr1:212744638 | G | A | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-5037C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744638 | |||||||
chr1:212744961 | C | G | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-5360G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744961 | |||||||
chr1:212744996 | C | T | 72 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 others(69): Show |
77 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.500-5395G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212744996 | |||||||
chr1:212745005 | G | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.500-5404C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745005 | |||||||
chr1:212745023 | C | T | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.500-5422G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745023 | |||||||
chr1:212745068 | C | T | 10 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0225 others(7): Show |
10 | HG00438.hp2 NA18939.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.500-5467G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745068 | |||||||
chr1:212745136 | A | AAAAC | 88 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0183 others(85): Show |
89 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.500-5539_500-5536d others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745136 | |||||||
chr1:212745159 | A | AATATATA others(9): Show |
1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-5559_500-5558i others(18): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745159 | |||||||
chr1:212745160 | C | A | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-5559G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | C | CTA | 32 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0207 others(29): Show |
33 | HG01175.hp1 HG01255.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.500-5561_500-5560d others(4): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | C | CTATA | 10 | a0001c0001t0007g0122 a0001c0001t0007g0149 a0001c0001t0007g0266 others(7): Show |
10 | HG00639.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.500-5563_500-5560d others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | C | CTATATA | 6 | a0001c0001t0004g0137 a0001c0001t0007g0142 a0001c0001t0011g0152 others(3): Show |
6 | HG02486.hp1 HG03209.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.500-5565_500-5560d others(8): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | C | CTATATAT others(3): Show |
1 | a0001c0001t0010g0244 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.500-5569_500-5560d others(12): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | CTA | C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0198 a0001c0001t0001g0202 others(24): Show |
28 | HG00438.hp2 HG00733.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.500-5561_500-5560d others(4): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | CTATA | C | 20 | a0001c0001t0001g0190 a0001c0001t0001g0199 a0001c0001t0001g0200 others(17): Show |
21 | HG00140.hp1 HG01257.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.500-5563_500-5560d others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | CTATATA | C | 10 | a0001c0001t0001g0211 a0001c0001t0004g0113 a0001c0001t0004g0114 others(7): Show |
10 | HG00438.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.500-5565_500-5560d others(8): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | CTATATAT others(3): Show |
C | 2 | a0001c0001t0001g0196 a0001c0001t0004g0138 |
2 | HG03490.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.500-5569_500-5560d others(12): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | CTATATAT others(7): Show |
C | 1 | a0002c0002t0113g0176 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.500-5573_500-5560d others(16): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | CTATATAT others(13): Show |
C | 1 | a0002c0002t0069g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.500-5579_500-5560d others(22): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | CTATATAT others(15): Show |
C | 2 | a0001c0001t0001g0247 a0002c0004t0095g0015 |
2 | HG02109.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.500-5581_500-5560d others(24): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | CTATATAT others(21): Show |
C | 1 | a0001c0001t0004g0127 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.500-5587_500-5560d others(30): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745160 | CTATATAT others(23): Show |
C | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-5589_500-5560d others(32): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745160 | |||||||
chr1:212745165 | T | A | 1 | a0001c0001t0088g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.500-5564A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745165 | |||||||
chr1:212745167 | T | A | 1 | a0001c0001t0088g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.500-5566A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745167 | |||||||
chr1:212745168 | A | C | 1 | a0001c0001t0088g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.500-5567T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745168 | |||||||
chr1:212745175 | TATATATA others(23): Show |
T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-5604_500-5575d others(32): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745175 | |||||||
chr1:212745177 | TATATATA others(21): Show |
T | 57 | a0002c0002t0066g0018 a0003c0003t0003g0013 a0003c0003t0003g0297 others(54): Show |
62 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.500-5604_500-5577d others(30): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745177 | |||||||
chr1:212745179 | TATATATA others(19): Show |
T | 13 | a0003c0003t0003g0287 a0003c0003t0009g0304 a0003c0003t0032g0290 others(10): Show |
13 | HG00639.hp1 HG01433.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.500-5604_500-5579d others(28): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745179 | |||||||
chr1:212745181 | TATATATA others(17): Show |
T | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.500-5604_500-5581d others(26): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745181 | |||||||
chr1:212745185 | TATATATA others(13): Show |
T | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.500-5604_500-5585d others(22): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745185 | |||||||
chr1:212745198 | A | G | 1 | a0001c0001t0022g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.500-5597T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745198 | |||||||
chr1:212745199 | T | C | 1 | a0001c0001t0022g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.500-5598A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745199 | |||||||
chr1:212745358 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-5757T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745358 | |||||||
chr1:212745414 | T | C | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-5813A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745414 | |||||||
chr1:212745463 | CAA | C | 6 | a0002c0002t0002g0022 a0002c0002t0002g0037 a0002c0002t0002g0047 others(3): Show |
6 | NA18955.hp2 NA18966.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-5864_500-5863d others(4): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745463 | |||||||
chr1:212745500 | A | G | 27 | a0001c0001t0007g0006 a0001c0001t0007g0122 a0001c0001t0007g0142 others(24): Show |
29 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.500-5899T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745500 | |||||||
chr1:212745550 | T | C | 1 | a0002c0002t0002g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.500-5949A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745550 | |||||||
chr1:212745582 | C | T | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-5981G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745582 | |||||||
chr1:212745679 | TTGTC | T | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.500-6082_500-6079d others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745679 | |||||||
chr1:212745690 | C | G | 22 | a0001c0001t0004g0005 a0001c0001t0004g0109 a0001c0001t0004g0110 others(19): Show |
23 | HG00438.hp1 HG02071.hp1 HG02132.hp2 others(20): Show |
intron_variant | MODIFIER | c.500-6089G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745690 | |||||||
chr1:212745731 | A | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-6130T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745731 | |||||||
chr1:212745808 | C | CA | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.500-6208dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745808 | |||||||
chr1:212745874 | T | A | 1 | a0002c0002t0069g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.500-6273A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745874 | |||||||
chr1:212745942 | A | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-6341T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745942 | |||||||
chr1:212745943 | A | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-6342T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745943 | |||||||
chr1:212745963 | C | T | 1 | a0002c0002t0040g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.500-6362G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212745963 | |||||||
chr1:212746065 | G | A | 54 | a0003c0003t0003g0013 a0003c0003t0003g0297 a0003c0003t0003g0299 others(51): Show |
59 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.500-6464C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212746065 | |||||||
chr1:212746278 | G | C | 1 | a0001c0001t0083g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.500-6677C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212746278 | |||||||
chr1:212746399 | A | C | 5 | a0002c0002t0012g0274 a0002c0002t0012g0275 a0002c0002t0012g0278 others(2): Show |
5 | NA18952.hp2 NA18973.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-6798T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212746399 | |||||||
chr1:212746455 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-6854A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212746455 | |||||||
chr1:212746474 | T | C | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-6873A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212746474 | |||||||
chr1:212746532 | T | C | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.500-6931A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212746532 | |||||||
chr1:212746801 | T | G | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.500-7200A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212746801 | |||||||
chr1:212746844 | G | A | 12 | a0002c0002t0013g0098 a0002c0002t0013g0100 a0002c0002t0013g0101 others(9): Show |
12 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-7243C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212746844 | |||||||
chr1:212746854 | T | G | 1 | a0001c0001t0087g0180 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.500-7253A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212746854 | |||||||
chr1:212746926 | A | C | 1 | a0002c0002t0098g0273 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.500-7325T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212746926 | |||||||
chr1:212746954 | G | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-7353C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212746954 | |||||||
chr1:212747002 | A | G | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.500-7401T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747002 | |||||||
chr1:212747015 | T | C | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-7414A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747015 | |||||||
chr1:212747128 | C | CA | 104 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0183 others(101): Show |
106 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.500-7528dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747128 | |||||||
chr1:212747128 | C | CAA | 6 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0224 others(3): Show |
6 | HG00597.hp2 HG01192.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-7529_500-7528d others(4): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747128 | |||||||
chr1:212747128 | CA | C | 35 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(32): Show |
39 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.500-7528delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747128 | |||||||
chr1:212747176 | G | C | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.500-7575C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747176 | |||||||
chr1:212747184 | T | C | 12 | a0002c0002t0013g0098 a0002c0002t0013g0100 a0002c0002t0013g0101 others(9): Show |
12 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-7583A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747184 | |||||||
chr1:212747338 | T | C | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.500-7737A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747338 | |||||||
chr1:212747395 | G | A | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.500-7794C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747395 | |||||||
chr1:212747452 | C | A | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-7851G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747452 | |||||||
chr1:212747541 | C | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-7940G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747541 | |||||||
chr1:212747834 | C | T | 6 | a0002c0002t0026g0119 a0002c0002t0026g0120 a0002c0002t0026g0121 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-8233G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747834 | |||||||
chr1:212747908 | G | A | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.500-8307C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212747908 | |||||||
chr1:212748032 | C | T | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-8431G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212748032 | |||||||
chr1:212748033 | T | G | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-8432A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212748033 | |||||||
chr1:212748037 | A | T | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-8436T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212748037 | |||||||
chr1:212748110 | T | G | 2 | a0003c0003t0028g0303 a0003c0003t0028g0310 |
2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.500-8509A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212748110 | |||||||
chr1:212748379 | G | A | 1 | a0001c0001t0004g0138 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.500-8778C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212748379 | |||||||
chr1:212748806 | CA | C | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.500-9206delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212748806 | |||||||
chr1:212748920 | G | A | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-9319C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212748920 | |||||||
chr1:212749003 | T | C | 6 | a0003c0003t0032g0290 a0003c0003t0033g0288 a0003c0003t0055g0289 others(3): Show |
6 | HG02257.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.500-9402A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749003 | |||||||
chr1:212749111 | G | A | 5 | a0002c0002t0026g0119 a0002c0002t0026g0120 a0002c0002t0026g0121 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-9510C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749111 | |||||||
chr1:212749335 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.500-9734A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749335 | |||||||
chr1:212749339 | G | GT | 9 | a0001c0001t0004g0112 a0001c0001t0004g0133 a0001c0001t0011g0116 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.500-9739dupA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749339 | |||||||
chr1:212749339 | G | GTTTTTT | 8 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0274 others(5): Show |
9 | HG00738.hp2 HG03491.hp2 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.500-9744_500-9739d others(8): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749339 | |||||||
chr1:212749339 | GT | G | 157 | a0001c0001t0001g0010 a0001c0001t0001g0183 a0001c0001t0001g0186 others(154): Show |
164 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.500-9739delA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749339 | |||||||
chr1:212749339 | GTT | G | 81 | a0001c0001t0001g0181 a0001c0001t0001g0222 a0001c0001t0001g0239 others(78): Show |
86 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.500-9740_500-9739d others(4): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749339 | |||||||
chr1:212749339 | GTTT | G | 11 | a0001c0001t0007g0142 a0003c0003t0009g0003 a0003c0003t0009g0304 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.500-9741_500-9739d others(5): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749339 | |||||||
chr1:212749348 | T | G | 5 | a0002c0002t0026g0119 a0002c0002t0026g0120 a0002c0002t0026g0121 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-9747A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749348 | |||||||
chr1:212749408 | G | A | 89 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0183 others(86): Show |
90 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.500-9807C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749408 | |||||||
chr1:212749413 | C | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-9812G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749413 | |||||||
chr1:212749420 | G | C | 303 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0183 others(300): Show |
319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.500-9819C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749420 | |||||||
chr1:212749456 | C | CT | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.500-9856dupA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749456 | |||||||
chr1:212749617 | T | A | 2 | a0002c0002t0008g0080 a0002c0002t0042g0049 |
2 | NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.500-10016A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749617 | |||||||
chr1:212749651 | A | G | 3 | a0002c0002t0019g0011 a0002c0002t0019g0276 a0002c0002t0019g0277 |
4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-10050T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749651 | |||||||
chr1:212749758 | C | T | 85 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(82): Show |
91 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.500-10157G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749758 | |||||||
chr1:212749967 | T | C | 2 | a0003c0003t0032g0290 a0003c0003t0033g0288 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.500-10366A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749967 | |||||||
chr1:212749969 | T | TAAG | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-10369_500-1036 others(7): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212749969 | |||||||
chr1:212750102 | C | G | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-10501G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212750102 | |||||||
chr1:212750194 | G | A | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-10593C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212750194 | |||||||
chr1:212750469 | T | C | 1 | a0002c0002t0040g0034 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.500-10868A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212750469 | |||||||
chr1:212750550 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-10949C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212750550 | |||||||
chr1:212750813 | C | T | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.500-11212G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212750813 | |||||||
chr1:212750834 | G | A | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.500-11233C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212750834 | |||||||
chr1:212750898 | G | A | 1 | a0001c0001t0073g0268 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.500-11297C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212750898 | |||||||
chr1:212751065 | T | C | 1 | a0001c0001t0018g0252 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.500-11464A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212751065 | |||||||
chr1:212751088 | A | C | 2 | a0002c0002t0002g0043 a0002c0002t0002g0058 |
2 | NA19065.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.500-11487T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212751088 | |||||||
chr1:212751305 | T | C | 1 | a0002c0004t0095g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.500-11704A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212751305 | |||||||
chr1:212751437 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.500-11836G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212751437 | |||||||
chr1:212751514 | A | C | 1 | a0002c0002t0002g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.500-11913T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212751514 | |||||||
chr1:212751587 | A | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-11986T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212751587 | |||||||
chr1:212751673 | A | G | 190 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(187): Show |
203 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.500-12072T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212751673 | |||||||
chr1:212751708 | AC | A | 4 | a0002c0002t0012g0274 a0002c0002t0012g0275 a0002c0002t0012g0278 others(1): Show |
4 | NA18973.hp1 NA18990.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-12108delG | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212751708 | |||||||
chr1:212751711 | AT | A | 175 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(172): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.500-12111delA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212751711 | |||||||
chr1:212751712 | T | A | 4 | a0002c0002t0012g0274 a0002c0002t0012g0275 a0002c0002t0012g0278 others(1): Show |
4 | NA18973.hp1 NA18990.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-12111A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212751712 | |||||||
chr1:212751755 | C | T | 1 | a0001c0001t0006g0237 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.500-12154G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212751755 | |||||||
chr1:212752019 | T | C | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-12418A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752019 | |||||||
chr1:212752087 | C | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.500-12486G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752087 | |||||||
chr1:212752171 | T | C | 1 | a0003c0003t0050g0283 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.500-12570A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752171 | |||||||
chr1:212752259 | T | G | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-12658A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752259 | |||||||
chr1:212752346 | G | A | 3 | a0002c0002t0005g0070 a0002c0002t0005g0071 a0002c0002t0046g0072 |
3 | HG02273.hp1 NA18970.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.500-12745C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752346 | |||||||
chr1:212752504 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-12903A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752504 | |||||||
chr1:212752515 | C | T | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-12914G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752515 | |||||||
chr1:212752516 | G | A | 1 | a0002c0004t0095g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.500-12915C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752516 | |||||||
chr1:212752562 | TA | T | 179 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(176): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.500-12962delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752562 | |||||||
chr1:212752849 | A | T | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.500-13248T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752849 | |||||||
chr1:212752889 | C | CA | 71 | a0001c0001t0001g0233 a0001c0001t0001g0254 a0001c0001t0004g0132 others(68): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.500-13289dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752889 | |||||||
chr1:212752889 | C | CAA | 15 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 others(12): Show |
17 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.500-13290_500-1328 others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752889 | |||||||
chr1:212752889 | C | CAAAAAAA others(7): Show |
3 | a0002c0002t0019g0011 a0002c0002t0019g0276 a0002c0002t0019g0277 |
4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-13302_500-1328 others(18): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752889 | |||||||
chr1:212752889 | CA | C | 27 | a0002c0002t0013g0098 a0002c0002t0013g0100 a0002c0002t0013g0101 others(24): Show |
28 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.500-13289delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752889 | |||||||
chr1:212752897 | A | G | 18 | a0001c0001t0001g0010 a0001c0001t0001g0191 a0001c0001t0001g0199 others(15): Show |
19 | HG00733.hp2 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.500-13296T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212752897 | |||||||
chr1:212753047 | C | T | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-13446G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753047 | |||||||
chr1:212753064 | C | T | 2 | a0002c0002t0013g0105 a0002c0002t0111g0106 |
2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.500-13463G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753064 | |||||||
chr1:212753084 | G | A | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.500-13483C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753084 | |||||||
chr1:212753148 | T | G | 2 | a0002c0002t0109g0097 a0002c0002t0110g0096 |
2 | HG02300.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.500-13547A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753148 | |||||||
chr1:212753255 | GT | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-13655delA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753255 | |||||||
chr1:212753447 | T | G | 1 | a0001c0001t0001g0249 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.500-13846A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753447 | |||||||
chr1:212753495 | C | T | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-13894G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753495 | |||||||
chr1:212753563 | C | T | 1 | a0003c0003t0003g0326 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.500-13962G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753563 | |||||||
chr1:212753580 | T | A | 1 | a0001c0001t0016g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.500-13979A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753580 | |||||||
chr1:212753596 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-13995T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753596 | |||||||
chr1:212753667 | A | G | 85 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(82): Show |
91 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.500-14066T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753667 | |||||||
chr1:212753697 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-14096A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753697 | |||||||
chr1:212753723 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-14122A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753723 | |||||||
chr1:212753825 | A | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-14224T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753825 | |||||||
chr1:212753829 | T | C | 1 | a0003c0003t0003g0325 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.500-14228A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753829 | |||||||
chr1:212753959 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-14358T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212753959 | |||||||
chr1:212754085 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.500-14484T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754085 | |||||||
chr1:212754156 | C | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-14555G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754156 | |||||||
chr1:212754337 | A | G | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-14736T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754337 | |||||||
chr1:212754460 | C | T | 2 | a0003c0003t0003g0287 a0003c0003t0053g0286 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.500-14859G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754460 | |||||||
chr1:212754500 | G | A | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-14899C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754500 | |||||||
chr1:212754637 | C | T | 3 | a0002c0002t0019g0011 a0002c0002t0019g0276 a0002c0002t0019g0277 |
4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-15036G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754637 | |||||||
chr1:212754769 | C | CA | 7 | a0001c0001t0001g0189 a0001c0001t0001g0233 a0001c0001t0007g0266 others(4): Show |
7 | HG00597.hp2 HG01167.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.500-15169dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754769 | |||||||
chr1:212754769 | C | CAAAAAAA others(1): Show |
11 | a0002c0004t0095g0015 a0003c0003t0003g0287 a0003c0003t0032g0290 others(8): Show |
11 | HG00639.hp1 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.500-15176_500-1516 others(12): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754769 | |||||||
chr1:212754769 | C | CAAAAAAA others(3): Show |
14 | a0002c0002t0002g0053 a0002c0002t0002g0057 a0002c0002t0002g0085 others(11): Show |
14 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.500-15178_500-1516 others(14): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754769 | |||||||
chr1:212754769 | C | CAAAAAAA others(4): Show |
69 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(66): Show |
76 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.500-15179_500-1516 others(15): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754769 | |||||||
chr1:212754769 | C | CAAAAAAA others(5): Show |
57 | a0002c0002t0002g0051 a0002c0002t0002g0076 a0002c0002t0002g0089 others(54): Show |
61 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.500-15180_500-1516 others(16): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754769 | |||||||
chr1:212754769 | C | CAAAAAAA others(6): Show |
18 | a0002c0002t0012g0271 a0002c0002t0012g0272 a0002c0002t0019g0277 others(15): Show |
20 | HG00741.hp1 HG01109.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.500-15181_500-1516 others(17): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754769 | |||||||
chr1:212754769 | C | CAAAAAAA others(7): Show |
5 | a0002c0002t0069g0177 a0003c0003t0009g0306 a0003c0003t0009g0307 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-15182_500-1516 others(18): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754769 | |||||||
chr1:212754769 | C | CAAAAAAA others(8): Show |
5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0066g0018 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-15183_500-1516 others(19): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754769 | |||||||
chr1:212754769 | C | CAAAAAAA others(12): Show |
3 | a0002c0002t0026g0119 a0002c0002t0093g0118 a0002c0002t0094g0117 |
3 | HG02895.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.500-15169_500-1516 others(23): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754769 | |||||||
chr1:212754769 | C | CAAAAAAA others(13): Show |
1 | a0002c0002t0026g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.500-15169_500-1516 others(24): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754769 | |||||||
chr1:212754769 | C | CAAAAAAA others(14): Show |
1 | a0002c0002t0026g0121 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.500-15169_500-1516 others(25): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754769 | |||||||
chr1:212754815 | C | T | 89 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0183 others(86): Show |
90 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.500-15214G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754815 | |||||||
chr1:212754816 | G | A | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.500-15215C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754816 | |||||||
chr1:212754829 | A | G | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.500-15228T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754829 | |||||||
chr1:212754961 | G | A | 1 | a0002c0004t0095g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.500-15360C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212754961 | |||||||
chr1:212755066 | T | TG | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.500-15466dupC | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755066 | |||||||
chr1:212755328 | T | G | 1 | a0003c0003t0015g0344 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.500-15727A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755328 | |||||||
chr1:212755363 | T | C | 1 | a0002c0002t0113g0176 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.500-15762A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755363 | |||||||
chr1:212755498 | A | C | 1 | a0002c0002t0002g0038 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.500-15897T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755498 | |||||||
chr1:212755503 | A | G | 1 | a0001c0001t0004g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.500-15902T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755503 | |||||||
chr1:212755516 | G | A | 1 | a0001c0001t0025g0217 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.500-15915C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755516 | |||||||
chr1:212755574 | G | A | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.500-15973C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755574 | |||||||
chr1:212755592 | ACTAAAAA others(15): Show |
A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-16013_500-1599 others(26): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755592 | |||||||
chr1:212755602 | C | A | 1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.500-16001G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755602 | |||||||
chr1:212755604 | CCT | C | 71 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 others(68): Show |
76 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.500-16005_500-1600 others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755604 | |||||||
chr1:212755690 | T | C | 1 | a0001c0001t0010g0231 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.500-16089A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755690 | |||||||
chr1:212755704 | C | T | 2 | a0001c0001t0004g0114 a0001c0001t0004g0172 |
2 | NA18998.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.500-16103G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755704 | |||||||
chr1:212755719 | A | G | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.500-16118T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755719 | |||||||
chr1:212755764 | T | C | 1 | a0002c0002t0039g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.500-16163A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755764 | |||||||
chr1:212755777 | GTAA | G | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-16179_500-1617 others(7): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755777 | |||||||
chr1:212755864 | A | C | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-16263T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755864 | |||||||
chr1:212755877 | G | A | 1 | a0003c0003t0030g0012 | 2 | NA19062.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.500-16276C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755877 | |||||||
chr1:212755984 | A | C | 1 | a0001c0001t0007g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.500-16383T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755984 | |||||||
chr1:212755991 | T | C | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-16390A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212755991 | |||||||
chr1:212756004 | T | TATATAAG others(30): Show |
1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.500-16440_500-1640 others(41): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756004 | |||||||
chr1:212756085 | A | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-16484T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756085 | |||||||
chr1:212756188 | T | C | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-16587A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756188 | |||||||
chr1:212756255 | A | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-16654T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756255 | |||||||
chr1:212756309 | G | A | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-16708C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756309 | |||||||
chr1:212756358 | G | A | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.500-16757C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756358 | |||||||
chr1:212756410 | G | A | 1 | a0001c0001t0007g0006 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.500-16809C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756410 | |||||||
chr1:212756586 | G | A | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.500-16985C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756586 | |||||||
chr1:212756645 | C | A | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.500-17044G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756645 | |||||||
chr1:212756656 | T | C | 303 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0183 others(300): Show |
319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.500-17055A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756656 | |||||||
chr1:212756799 | G | A | 10 | a0002c0002t0013g0098 a0002c0002t0013g0100 a0002c0002t0013g0101 others(7): Show |
10 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.500-17198C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756799 | |||||||
chr1:212756815 | G | A | 1 | a0003c0003t0003g0317 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.500-17214C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212756815 | |||||||
chr1:212757091 | C | T | 3 | a0002c0002t0002g0066 a0002c0002t0002g0084 a0002c0002t0102g0059 |
3 | HG02027.hp2 HG02135.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.500-17490G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212757091 | |||||||
chr1:212757123 | G | C | 14 | a0001c0001t0007g0122 a0001c0001t0007g0142 a0001c0001t0007g0149 others(11): Show |
14 | HG00639.hp2 HG01167.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.500-17522C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212757123 | |||||||
chr1:212757134 | G | A | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-17533C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212757134 | |||||||
chr1:212757144 | T | C | 3 | a0001c0001t0024g0182 a0001c0001t0024g0184 a0001c0001t0024g0218 |
3 | NA18943.hp1 NA18961.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.500-17543A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212757144 | |||||||
chr1:212757156 | A | G | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.500-17555T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212757156 | |||||||
chr1:212757158 | G | A | 1 | a0003c0003t0003g0325 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.500-17557C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212757158 | |||||||
chr1:212757197 | G | C | 10 | a0001c0001t0004g0005 a0001c0001t0004g0109 a0001c0001t0004g0110 others(7): Show |
11 | HG00438.hp1 NA18953.hp2 NA18966.hp1 others(8): Show |
intron_variant | MODIFIER | c.500-17596C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212757197 | |||||||
chr1:212757329 | A | C | 3 | a0002c0002t0019g0011 a0002c0002t0019g0276 a0002c0002t0019g0277 |
4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-17728T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212757329 | |||||||
chr1:212757575 | G | A | 1 | a0003c0003t0033g0292 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.500-17974C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212757575 | |||||||
chr1:212757666 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-18065A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212757666 | |||||||
chr1:212757873 | T | C | 76 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(73): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.500-18272A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212757873 | |||||||
chr1:212758121 | A | C | 89 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0183 others(86): Show |
90 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.500-18520T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212758121 | |||||||
chr1:212758231 | T | C | 80 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(77): Show |
87 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.500-18630A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212758231 | |||||||
chr1:212758329 | A | G | 1 | a0002c0002t0002g0037 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.500-18728T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212758329 | |||||||
chr1:212758405 | C | G | 1 | a0001c0001t0001g0236 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.500-18804G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212758405 | |||||||
chr1:212758422 | A | G | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-18821T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212758422 | |||||||
chr1:212758528 | A | G | 1 | a0002c0002t0005g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.500-18927T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212758528 | |||||||
chr1:212758718 | C | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-19117G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212758718 | |||||||
chr1:212758794 | T | C | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-19193A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212758794 | |||||||
chr1:212758865 | T | C | 190 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(187): Show |
203 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.500-19264A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212758865 | |||||||
chr1:212758877 | T | C | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.500-19276A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212758877 | |||||||
chr1:212759064 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-19463A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759064 | |||||||
chr1:212759209 | C | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-19608G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759209 | |||||||
chr1:212759417 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-19816C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759417 | |||||||
chr1:212759502 | T | C | 1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.500-19901A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759502 | |||||||
chr1:212759504 | G | T | 1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.500-19903C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759504 | |||||||
chr1:212759506 | C | G | 1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.500-19905G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759506 | |||||||
chr1:212759645 | C | T | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.500-20044G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759645 | |||||||
chr1:212759685 | C | A | 1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.500-20084G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759685 | |||||||
chr1:212759754 | A | G | 1 | a0003c0003t0052g0298 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.500-20153T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759754 | |||||||
chr1:212759787 | G | A | 1 | a0002c0002t0008g0077 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.500-20186C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759787 | |||||||
chr1:212759813 | C | T | 1 | a0001c0001t0120g0193 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.500-20212G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759813 | |||||||
chr1:212759937 | C | T | 15 | a0003c0003t0003g0287 a0003c0003t0032g0290 a0003c0003t0032g0294 others(12): Show |
15 | HG00639.hp1 HG01433.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.500-20336G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212759937 | |||||||
chr1:212760059 | C | G | 1 | a0003c0003t0030g0012 | 2 | NA19062.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.500-20458G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212760059 | |||||||
chr1:212760158 | A | T | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-20557T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212760158 | |||||||
chr1:212760203 | A | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-20602T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212760203 | |||||||
chr1:212760232 | A | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-20631T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212760232 | |||||||
chr1:212760435 | G | A | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.500-20834C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212760435 | |||||||
chr1:212760500 | C | T | 1 | a0001c0001t0006g0241 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.500-20899G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212760500 | |||||||
chr1:212760528 | G | A | 1 | a0002c0002t0002g0022 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.500-20927C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212760528 | |||||||
chr1:212760571 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.500-20970G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212760571 | |||||||
chr1:212760666 | C | T | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.500-21065G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212760666 | |||||||
chr1:212760795 | G | A | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.500-21194C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212760795 | |||||||
chr1:212760857 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-21256A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212760857 | |||||||
chr1:212761030 | C | T | 179 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(176): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.499+21342G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761030 | |||||||
chr1:212761037 | C | A | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499+21335G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761037 | |||||||
chr1:212761080 | T | C | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+21292A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761080 | |||||||
chr1:212761260 | A | C | 1 | a0003c0003t0003g0326 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.499+21112T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761260 | |||||||
chr1:212761397 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+20975T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761397 | |||||||
chr1:212761410 | G | C | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.499+20962C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761410 | |||||||
chr1:212761497 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+20875C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761497 | |||||||
chr1:212761679 | C | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+20693G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761679 | |||||||
chr1:212761748 | AT | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+20623delA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761748 | |||||||
chr1:212761781 | A | G | 1 | a0002c0002t0039g0099 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.499+20591T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761781 | |||||||
chr1:212761876 | C | T | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499+20496G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761876 | |||||||
chr1:212761898 | T | G | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.499+20474A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761898 | |||||||
chr1:212761962 | C | T | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+20410G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761962 | |||||||
chr1:212761971 | T | TA | 10 | a0001c0001t0001g0225 a0001c0001t0004g0112 a0001c0001t0004g0113 others(7): Show |
10 | HG00438.hp1 HG00438.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+20400dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761971 | |||||||
chr1:212761971 | TA | T | 113 | a0001c0001t0001g0199 a0001c0001t0001g0236 a0001c0001t0018g0252 others(110): Show |
121 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.499+20400delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761971 | |||||||
chr1:212761971 | TAA | T | 62 | a0002c0002t0002g0027 a0002c0002t0005g0078 a0002c0002t0039g0099 others(59): Show |
67 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.499+20399_499+2040 others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761971 | |||||||
chr1:212761971 | TAAA | T | 10 | a0003c0003t0003g0317 a0003c0003t0032g0290 a0003c0003t0032g0294 others(7): Show |
10 | HG00639.hp1 HG01433.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.499+20398_499+2040 others(7): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212761971 | |||||||
chr1:212762025 | C | T | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+20347G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762025 | |||||||
chr1:212762026 | G | A | 1 | a0001c0001t0073g0268 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.499+20346C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762026 | |||||||
chr1:212762075 | A | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+20297T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762075 | |||||||
chr1:212762082 | G | A | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+20290C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762082 | |||||||
chr1:212762253 | G | A | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499+20119C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762253 | |||||||
chr1:212762290 | T | C | 4 | a0002c0002t0014g0004 a0002c0002t0014g0019 a0002c0002t0014g0090 others(1): Show |
5 | HG02922.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+20082A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762290 | |||||||
chr1:212762306 | C | CA | 12 | a0001c0001t0001g0181 a0001c0001t0001g0220 a0001c0001t0004g0108 others(9): Show |
12 | HG00609.hp1 HG00741.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+20065dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762306 | |||||||
chr1:212762306 | C | CAA | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0274 others(8): Show |
12 | HG00738.hp2 HG01168.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+20064_499+2006 others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762306 | |||||||
chr1:212762306 | C | CAAA | 55 | a0002c0002t0012g0272 a0002c0002t0035g0263 a0002c0002t0035g0264 others(52): Show |
58 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.499+20063_499+2006 others(7): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762306 | |||||||
chr1:212762306 | C | CAAAA | 16 | a0003c0003t0003g0326 a0003c0003t0009g0003 a0003c0003t0009g0304 others(13): Show |
18 | HG01109.hp1 HG01243.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.499+20062_499+2006 others(8): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762306 | |||||||
chr1:212762306 | CA | C | 94 | a0001c0001t0018g0201 a0002c0002t0002g0002 a0002c0002t0002g0022 others(91): Show |
101 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.499+20065delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762306 | |||||||
chr1:212762306 | CAAAAAAA others(6): Show |
C | 22 | a0001c0001t0004g0005 a0001c0001t0004g0109 a0001c0001t0004g0110 others(19): Show |
23 | HG00438.hp1 HG02071.hp1 HG02132.hp2 others(20): Show |
intron_variant | MODIFIER | c.499+20053_499+2006 others(17): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762306 | |||||||
chr1:212762366 | C | G | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499+20006G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762366 | |||||||
chr1:212762380 | A | G | 6 | a0002c0002t0026g0119 a0002c0002t0026g0120 a0002c0002t0026g0121 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.499+19992T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762380 | |||||||
chr1:212762419 | G | A | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499+19953C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762419 | |||||||
chr1:212762583 | A | C | 1 | a0002c0002t0013g0100 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.499+19789T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762583 | |||||||
chr1:212762708 | G | A | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+19664C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762708 | |||||||
chr1:212762727 | C | A | 5 | a0002c0002t0013g0098 a0002c0002t0013g0100 a0002c0002t0013g0101 others(2): Show |
5 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+19645G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762727 | |||||||
chr1:212762786 | T | A | 1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.499+19586A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762786 | |||||||
chr1:212762849 | T | A | 1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.499+19523A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762849 | |||||||
chr1:212762850 | A | T | 1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.499+19522T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762850 | |||||||
chr1:212762851 | G | A | 1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.499+19521C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762851 | |||||||
chr1:212762889 | G | A | 9 | a0001c0001t0007g0122 a0001c0001t0007g0161 a0001c0001t0007g0165 others(6): Show |
9 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.499+19483C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762889 | |||||||
chr1:212762930 | A | C | 72 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 others(69): Show |
77 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.499+19442T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762930 | |||||||
chr1:212762970 | G | A | 7 | a0001c0001t0001g0200 a0001c0001t0001g0222 a0001c0001t0001g0232 others(4): Show |
7 | HG01081.hp1 HG01255.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.499+19402C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212762970 | |||||||
chr1:212763106 | A | G | 179 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(176): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.499+19266T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763106 | |||||||
chr1:212763137 | C | T | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+19235G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763137 | |||||||
chr1:212763168 | T | C | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+19204A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763168 | |||||||
chr1:212763198 | G | A | 1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.499+19174C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763198 | |||||||
chr1:212763361 | AAAC | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+19008_499+1901 others(7): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763361 | |||||||
chr1:212763369 | A | C | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+19003T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763369 | |||||||
chr1:212763397 | A | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.499+18975T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763397 | |||||||
chr1:212763435 | T | C | 76 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(73): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.499+18937A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763435 | |||||||
chr1:212763581 | G | C | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+18791C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763581 | |||||||
chr1:212763779 | A | T | 1 | a0003c0003t0020g0331 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.499+18593T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763779 | |||||||
chr1:212763823 | C | T | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+18549G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763823 | |||||||
chr1:212763824 | A | C | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+18548T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763824 | |||||||
chr1:212763876 | C | T | 1 | a0002c0002t0014g0090 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.499+18496G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212763876 | |||||||
chr1:212764022 | G | C | 1 | a0001c0001t0004g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.499+18350C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764022 | |||||||
chr1:212764046 | T | C | 1 | a0002c0002t0069g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.499+18326A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764046 | |||||||
chr1:212764074 | A | G | 1 | a0003c0003t0003g0346 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.499+18298T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764074 | |||||||
chr1:212764262 | G | A | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+18110C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764262 | |||||||
chr1:212764339 | C | A | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+18033G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764339 | |||||||
chr1:212764347 | T | C | 12 | a0002c0002t0013g0098 a0002c0002t0013g0100 a0002c0002t0013g0101 others(9): Show |
12 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+18025A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764347 | |||||||
chr1:212764394 | C | T | 1 | a0002c0002t0069g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.499+17978G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764394 | |||||||
chr1:212764538 | C | T | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.499+17834G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764538 | |||||||
chr1:212764679 | C | T | 4 | a0002c0002t0014g0004 a0002c0002t0014g0019 a0002c0002t0014g0090 others(1): Show |
5 | HG02922.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+17693G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764679 | |||||||
chr1:212764783 | T | C | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+17589A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764783 | |||||||
chr1:212764801 | A | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+17571T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764801 | |||||||
chr1:212764843 | C | CA | 15 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0233 others(12): Show |
15 | HG00099.hp1 HG00438.hp2 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.499+17528dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764843 | |||||||
chr1:212764843 | CA | C | 87 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0235 others(84): Show |
92 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.499+17528delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764843 | |||||||
chr1:212764843 | CAA | C | 83 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(80): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.499+17527_499+1752 others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764843 | |||||||
chr1:212764843 | CAAA | C | 7 | a0002c0002t0005g0061 a0002c0002t0005g0063 a0002c0002t0027g0178 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.499+17526_499+1752 others(7): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764843 | |||||||
chr1:212764843 | CAAAAA | C | 6 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(3): Show |
7 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.499+17524_499+1752 others(9): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764843 | |||||||
chr1:212764843 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0190 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.499+17517_499+1752 others(16): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764843 | |||||||
chr1:212764843 | CAAAAAAA others(6): Show |
C | 1 | a0003c0003t0015g0322 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.499+17516_499+1752 others(17): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764843 | |||||||
chr1:212764868 | A | G | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.499+17504T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764868 | |||||||
chr1:212764874 | A | C | 1 | a0002c0002t0005g0078 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.499+17498T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764874 | |||||||
chr1:212764880 | GA | G | 87 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(84): Show |
93 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.499+17491delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212764880 | |||||||
chr1:212765316 | C | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+17056G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765316 | |||||||
chr1:212765318 | T | C | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499+17054A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765318 | |||||||
chr1:212765332 | C | T | 1 | a0003c0003t0048g0313 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.499+17040G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765332 | |||||||
chr1:212765428 | AAC | A | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+16942_499+1694 others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765428 | |||||||
chr1:212765452 | C | T | 1 | a0001c0001t0006g0257 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.499+16920G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765452 | |||||||
chr1:212765479 | A | G | 54 | a0003c0003t0003g0013 a0003c0003t0003g0297 a0003c0003t0003g0299 others(51): Show |
59 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.499+16893T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765479 | |||||||
chr1:212765507 | T | C | 1 | a0003c0003t0003g0346 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.499+16865A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765507 | |||||||
chr1:212765551 | T | G | 3 | a0002c0002t0014g0004 a0002c0002t0014g0019 a0002c0002t0014g0091 |
4 | HG02922.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+16821A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765551 | |||||||
chr1:212765558 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+16814A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765558 | |||||||
chr1:212765563 | A | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.499+16809T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765563 | |||||||
chr1:212765621 | G | A | 1 | a0002c0002t0013g0103 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.499+16751C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765621 | |||||||
chr1:212765671 | A | T | 2 | a0002c0002t0002g0035 a0002c0002t0002g0060 |
2 | NA18952.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.499+16701T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765671 | |||||||
chr1:212765721 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+16651C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765721 | |||||||
chr1:212765728 | C | T | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+16644G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765728 | |||||||
chr1:212765739 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+16633C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765739 | |||||||
chr1:212765760 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+16612C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765760 | |||||||
chr1:212765796 | C | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+16576G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765796 | |||||||
chr1:212765805 | T | TA | 13 | a0001c0001t0001g0198 a0001c0001t0001g0232 a0001c0001t0010g0185 others(10): Show |
13 | HG01255.hp1 HG01255.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.499+16566dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765805 | |||||||
chr1:212765862 | C | T | 1 | a0002c0002t0039g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.499+16510G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765862 | |||||||
chr1:212765918 | C | T | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499+16454G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212765918 | |||||||
chr1:212766029 | C | T | 1 | a0002c0002t0014g0091 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.499+16343G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766029 | |||||||
chr1:212766052 | C | T | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+16320G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766052 | |||||||
chr1:212766115 | G | A | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499+16257C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766115 | |||||||
chr1:212766135 | C | CA | 35 | a0001c0001t0011g0116 a0002c0002t0002g0087 a0002c0002t0008g0028 others(32): Show |
36 | HG00609.hp2 HG00733.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.499+16236dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766135 | |||||||
chr1:212766149 | C | A | 91 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(88): Show |
98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.499+16223G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766149 | |||||||
chr1:212766195 | G | A | 1 | a0002c0002t0014g0019 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.499+16177C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766195 | |||||||
chr1:212766421 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.499+15951A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766421 | |||||||
chr1:212766505 | C | T | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+15867G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766505 | |||||||
chr1:212766506 | A | G | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.499+15866T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766506 | |||||||
chr1:212766518 | G | A | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+15854C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766518 | |||||||
chr1:212766530 | A | G | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+15842T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766530 | |||||||
chr1:212766561 | T | C | 1 | a0001c0001t0007g0149 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.499+15811A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766561 | |||||||
chr1:212766633 | G | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+15739C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766633 | |||||||
chr1:212766645 | T | TA | 10 | a0002c0002t0066g0018 a0003c0003t0009g0003 a0003c0003t0009g0304 others(7): Show |
12 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.499+15726dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766645 | |||||||
chr1:212766645 | TA | T | 6 | a0001c0001t0024g0182 a0001c0001t0037g0246 a0002c0002t0005g0062 others(3): Show |
6 | HG01516.hp1 HG02976.hp1 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.499+15726delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766645 | |||||||
chr1:212766903 | A | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+15469T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766903 | |||||||
chr1:212766939 | G | C | 1 | a0002c0004t0095g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.499+15433C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212766939 | |||||||
chr1:212767038 | C | T | 190 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(187): Show |
203 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.499+15334G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767038 | |||||||
chr1:212767104 | A | G | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+15268T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767104 | |||||||
chr1:212767104 | A | T | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+15268T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767104 | |||||||
chr1:212767168 | T | A | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.499+15204A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767168 | |||||||
chr1:212767194 | C | G | 1 | a0002c0002t0014g0019 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.499+15178G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767194 | |||||||
chr1:212767196 | G | C | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+15176C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767196 | |||||||
chr1:212767208 | T | C | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0240 others(1): Show |
4 | NA18945.hp2 NA18950.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+15164A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767208 | |||||||
chr1:212767220 | C | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+15152G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767220 | |||||||
chr1:212767355 | T | C | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499+15017A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767355 | |||||||
chr1:212767516 | A | T | 6 | a0003c0003t0032g0290 a0003c0003t0033g0288 a0003c0003t0055g0289 others(3): Show |
6 | HG02257.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+14856T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767516 | |||||||
chr1:212767517 | A | C | 6 | a0003c0003t0032g0290 a0003c0003t0033g0288 a0003c0003t0055g0289 others(3): Show |
6 | HG02257.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+14855T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767517 | |||||||
chr1:212767596 | C | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+14776G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767596 | |||||||
chr1:212767638 | A | T | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+14734T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767638 | |||||||
chr1:212767838 | C | A | 1 | a0002c0002t0002g0057 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.499+14534G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212767838 | |||||||
chr1:212768048 | G | A | 1 | a0002c0002t0039g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.499+14324C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768048 | |||||||
chr1:212768050 | C | T | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499+14322G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768050 | |||||||
chr1:212768101 | C | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+14271G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768101 | |||||||
chr1:212768103 | T | C | 3 | a0003c0003t0003g0333 a0003c0003t0003g0334 a0003c0003t0029g0332 |
3 | HG01167.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.499+14269A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768103 | |||||||
chr1:212768236 | C | T | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+14136G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768236 | |||||||
chr1:212768268 | C | T | 1 | a0002c0002t0109g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.499+14104G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768268 | |||||||
chr1:212768307 | G | A | 2 | a0002c0002t0039g0094 a0002c0004t0095g0015 |
2 | HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.499+14065C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768307 | |||||||
chr1:212768319 | C | CA | 75 | a0001c0001t0004g0113 a0001c0001t0007g0153 a0001c0001t0007g0267 others(72): Show |
80 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.499+14052dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768319 | |||||||
chr1:212768319 | C | CAA | 14 | a0002c0002t0047g0017 a0002c0002t0065g0265 a0002c0002t0109g0097 others(11): Show |
14 | HG01109.hp2 HG01433.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.499+14051_499+1405 others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768319 | |||||||
chr1:212768319 | CA | C | 89 | a0001c0001t0001g0010 a0001c0001t0001g0183 a0001c0001t0001g0186 others(86): Show |
91 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.499+14052delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768319 | |||||||
chr1:212768319 | CAA | C | 71 | a0001c0001t0006g0197 a0002c0002t0002g0002 a0002c0002t0002g0026 others(68): Show |
77 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.499+14051_499+1405 others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768319 | |||||||
chr1:212768408 | A | G | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+13964T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768408 | |||||||
chr1:212768461 | A | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+13911T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768461 | |||||||
chr1:212768501 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+13871T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768501 | |||||||
chr1:212768652 | A | G | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499+13720T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768652 | |||||||
chr1:212768678 | G | A | 1 | a0002c0002t0002g0060 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.499+13694C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768678 | |||||||
chr1:212768712 | G | A | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+13660C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768712 | |||||||
chr1:212768791 | G | C | 5 | a0002c0002t0026g0119 a0002c0002t0026g0120 a0002c0002t0026g0121 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+13581C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768791 | |||||||
chr1:212768944 | A | T | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+13428T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768944 | |||||||
chr1:212768958 | C | T | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499+13414G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212768958 | |||||||
chr1:212769046 | A | AAAAC | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.499+13322_499+1332 others(8): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769046 | |||||||
chr1:212769079 | T | TAA | 8 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(5): Show |
8 | HG00738.hp2 HG00741.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+13291_499+1329 others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769079 | |||||||
chr1:212769079 | TA | T | 48 | a0001c0001t0073g0268 a0001c0001t0074g0123 a0002c0002t0005g0061 others(45): Show |
51 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.499+13292delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769079 | |||||||
chr1:212769086 | A | AG | 6 | a0002c0002t0026g0119 a0002c0002t0026g0120 a0002c0002t0026g0121 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.499+13285_499+1328 others(5): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769086 | |||||||
chr1:212769148 | T | G | 1 | a0001c0001t0084g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499+13224A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769148 | |||||||
chr1:212769247 | T | C | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+13125A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769247 | |||||||
chr1:212769253 | T | C | 89 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0183 others(86): Show |
90 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.499+13119A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769253 | |||||||
chr1:212769278 | T | C | 1 | a0001c0001t0037g0251 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.499+13094A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769278 | |||||||
chr1:212769306 | A | G | 1 | a0003c0003t0055g0289 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.499+13066T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769306 | |||||||
chr1:212769626 | A | T | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+12746T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769626 | |||||||
chr1:212769711 | G | A | 1 | a0003c0003t0003g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.499+12661C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769711 | |||||||
chr1:212769792 | G | A | 1 | a0002c0002t0002g0030 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.499+12580C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769792 | |||||||
chr1:212769820 | A | G | 3 | a0002c0002t0019g0011 a0002c0002t0019g0276 a0002c0002t0019g0277 |
4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+12552T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769820 | |||||||
chr1:212769982 | C | A | 38 | a0003c0003t0003g0297 a0003c0003t0003g0299 a0003c0003t0003g0301 others(35): Show |
39 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.499+12390G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212769982 | |||||||
chr1:212770153 | A | G | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499+12219T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770153 | |||||||
chr1:212770239 | A | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.499+12133T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770239 | |||||||
chr1:212770309 | A | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+12063T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770309 | |||||||
chr1:212770340 | CT | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+12031delA | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770340 | |||||||
chr1:212770377 | T | C | 80 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(77): Show |
87 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.499+11995A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770377 | |||||||
chr1:212770454 | C | T | 16 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(13): Show |
17 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.499+11918G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770454 | |||||||
chr1:212770493 | C | A | 10 | a0002c0002t0013g0098 a0002c0002t0013g0100 a0002c0002t0013g0101 others(7): Show |
10 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.499+11879G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770493 | |||||||
chr1:212770501 | C | A | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.499+11871G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770501 | |||||||
chr1:212770529 | A | G | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+11843T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770529 | |||||||
chr1:212770550 | T | C | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.499+11822A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770550 | |||||||
chr1:212770626 | A | G | 1 | a0002c0002t0014g0090 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.499+11746T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770626 | |||||||
chr1:212770715 | T | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+11657A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770715 | |||||||
chr1:212770756 | G | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+11616C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770756 | |||||||
chr1:212770761 | A | G | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+11611T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770761 | |||||||
chr1:212770970 | A | G | 1 | a0001c0001t0007g0006 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.499+11402T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212770970 | |||||||
chr1:212771040 | G | A | 1 | a0003c0003t0003g0318 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.499+11332C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771040 | |||||||
chr1:212771112 | G | A | 76 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(73): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.499+11260C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771112 | |||||||
chr1:212771164 | A | C | 1 | a0003c0003t0003g0321 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.499+11208T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771164 | |||||||
chr1:212771182 | C | T | 5 | a0003c0003t0003g0338 a0003c0003t0003g0339 a0003c0003t0003g0341 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+11190G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771182 | |||||||
chr1:212771212 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+11160T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771212 | |||||||
chr1:212771354 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.499+11018T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771354 | |||||||
chr1:212771535 | C | G | 72 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 others(69): Show |
77 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.499+10837G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771535 | |||||||
chr1:212771587 | TAG | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+10783_499+1078 others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771587 | |||||||
chr1:212771591 | G | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+10781C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771591 | |||||||
chr1:212771611 | C | CA | 24 | a0001c0001t0001g0190 a0001c0001t0001g0194 a0001c0001t0004g0110 others(21): Show |
24 | HG00438.hp1 HG00621.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.499+10760dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771611 | |||||||
chr1:212771611 | C | CAAA | 61 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0027 others(58): Show |
65 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.499+10758_499+1076 others(7): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771611 | |||||||
chr1:212771611 | C | CAAAA | 27 | a0002c0002t0002g0026 a0002c0002t0002g0031 a0002c0002t0002g0066 others(24): Show |
30 | HG00423.hp1 HG02055.hp2 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.499+10757_499+1076 others(8): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771611 | |||||||
chr1:212771624 | A | C | 74 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 others(71): Show |
79 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.499+10748T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771624 | |||||||
chr1:212771683 | A | T | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+10689T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771683 | |||||||
chr1:212771697 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+10675A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771697 | |||||||
chr1:212771766 | TA | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+10605delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771766 | |||||||
chr1:212771959 | T | C | 6 | a0002c0002t0002g0002 a0002c0002t0002g0026 a0002c0002t0002g0076 others(3): Show |
8 | HG00423.hp1 HG02056.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+10413A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212771959 | |||||||
chr1:212772097 | C | T | 1 | a0001c0001t0006g0197 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.499+10275G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772097 | |||||||
chr1:212772116 | T | C | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.499+10256A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772116 | |||||||
chr1:212772161 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+10211T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772161 | |||||||
chr1:212772278 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+10094A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772278 | |||||||
chr1:212772406 | C | A | 1 | a0002c0002t0069g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.499+9966G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772406 | |||||||
chr1:212772463 | C | T | 76 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(73): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.499+9909G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772463 | |||||||
chr1:212772502 | A | AAAAT | 5 | a0001c0001t0007g0161 a0001c0001t0007g0165 a0001c0001t0017g0162 others(2): Show |
5 | HG02622.hp1 HG03139.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+9866_499+9869d others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772502 | |||||||
chr1:212772502 | AAAAT | A | 3 | a0002c0002t0039g0094 a0003c0003t0058g0284 a0003c0003t0063g0282 |
3 | HG02630.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.499+9866_499+9869d others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772502 | |||||||
chr1:212772526 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.499+9846T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772526 | |||||||
chr1:212772625 | T | C | 179 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(176): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.499+9747A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772625 | |||||||
chr1:212772676 | C | CA | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+9695dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772676 | |||||||
chr1:212772688 | A | G | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.499+9684T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772688 | |||||||
chr1:212772777 | A | G | 179 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(176): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.499+9595T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772777 | |||||||
chr1:212772874 | C | G | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+9498G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212772874 | |||||||
chr1:212773007 | A | G | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499+9365T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773007 | |||||||
chr1:212773009 | T | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+9363A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773009 | |||||||
chr1:212773134 | G | T | 1 | a0001c0001t0087g0180 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.499+9238C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773134 | |||||||
chr1:212773162 | A | G | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+9210T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773162 | |||||||
chr1:212773192 | T | A | 3 | a0001c0001t0010g0188 a0001c0001t0010g0244 a0001c0001t0010g0245 |
3 | NA18964.hp2 NA19065.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.499+9180A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773192 | |||||||
chr1:212773252 | T | G | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+9120A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773252 | |||||||
chr1:212773302 | C | G | 3 | a0002c0002t0019g0011 a0002c0002t0019g0276 a0002c0002t0019g0277 |
4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+9070G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773302 | |||||||
chr1:212773306 | T | C | 2 | a0003c0003t0058g0284 a0003c0003t0063g0282 |
2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.499+9066A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773306 | |||||||
chr1:212773310 | C | T | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.499+9062G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773310 | |||||||
chr1:212773340 | G | GA | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+9031dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773340 | |||||||
chr1:212773409 | T | G | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+8963A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773409 | |||||||
chr1:212773423 | A | G | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.499+8949T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773423 | |||||||
chr1:212773554 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+8818C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773554 | |||||||
chr1:212773577 | T | C | 73 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(70): Show |
78 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.499+8795A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773577 | |||||||
chr1:212773602 | T | C | 1 | a0003c0003t0049g0337 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.499+8770A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773602 | |||||||
chr1:212773634 | C | CA | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0247 others(6): Show |
9 | HG00597.hp2 NA18951.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.499+8737dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773634 | |||||||
chr1:212773643 | A | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+8729T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773643 | |||||||
chr1:212773731 | C | T | 4 | a0002c0002t0014g0004 a0002c0002t0014g0019 a0002c0002t0014g0090 others(1): Show |
5 | HG02922.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+8641G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773731 | |||||||
chr1:212773732 | A | G | 190 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(187): Show |
203 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.499+8640T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773732 | |||||||
chr1:212773772 | G | A | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+8600C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773772 | |||||||
chr1:212773844 | T | C | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499+8528A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212773844 | |||||||
chr1:212774049 | G | A | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+8323C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774049 | |||||||
chr1:212774057 | C | T | 1 | a0001c0001t0087g0180 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.499+8315G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774057 | |||||||
chr1:212774097 | G | C | 1 | a0001c0001t0004g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.499+8275C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774097 | |||||||
chr1:212774100 | G | A | 1 | a0001c0001t0004g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.499+8272C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774100 | |||||||
chr1:212774178 | G | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+8194C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774178 | |||||||
chr1:212774209 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+8163T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774209 | |||||||
chr1:212774341 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+8031T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774341 | |||||||
chr1:212774447 | A | C | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+7925T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774447 | |||||||
chr1:212774547 | A | AAAG | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+7822_499+7824d others(5): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774547 | |||||||
chr1:212774564 | G | A | 1 | a0001c0001t0018g0252 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.499+7808C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774564 | |||||||
chr1:212774639 | C | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+7733G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774639 | |||||||
chr1:212774722 | T | C | 6 | a0003c0003t0003g0287 a0003c0003t0050g0283 a0003c0003t0053g0286 others(3): Show |
6 | HG02257.hp1 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+7650A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774722 | |||||||
chr1:212774785 | C | T | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499+7587G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774785 | |||||||
chr1:212774983 | TA | T | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+7388delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212774983 | |||||||
chr1:212775186 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.499+7186T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775186 | |||||||
chr1:212775192 | G | C | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+7180C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775192 | |||||||
chr1:212775473 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+6899A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775473 | |||||||
chr1:212775611 | AC | A | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.499+6760delG | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775611 | |||||||
chr1:212775637 | G | T | 1 | a0001c0001t0018g0195 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.499+6735C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775637 | |||||||
chr1:212775717 | A | C | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.499+6655T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775717 | |||||||
chr1:212775764 | A | T | 1 | a0003c0003t0063g0282 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.499+6608T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775764 | |||||||
chr1:212775793 | T | A | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+6579A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775793 | |||||||
chr1:212775797 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+6575A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775797 | |||||||
chr1:212775816 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+6556T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775816 | |||||||
chr1:212775824 | GTGGTTTT others(4): Show |
G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+6537_499+6547d others(13): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775824 | |||||||
chr1:212775827 | G | T | 162 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(159): Show |
174 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.499+6545C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775827 | |||||||
chr1:212775828 | T | G | 4 | a0001c0001t0007g0149 a0001c0001t0007g0153 a0001c0001t0017g0141 others(1): Show |
4 | HG00639.hp2 HG01167.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+6544A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775828 | |||||||
chr1:212775850 | C | T | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+6522G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775850 | |||||||
chr1:212775893 | T | C | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+6479A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775893 | |||||||
chr1:212775942 | C | T | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+6430G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775942 | |||||||
chr1:212775949 | T | A | 1 | a0002c0002t0113g0176 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.499+6423A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212775949 | |||||||
chr1:212776017 | C | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+6355G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776017 | |||||||
chr1:212776107 | G | A | 1 | a0003c0003t0003g0343 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.499+6265C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776107 | |||||||
chr1:212776114 | C | T | 6 | a0003c0003t0003g0287 a0003c0003t0050g0283 a0003c0003t0053g0286 others(3): Show |
6 | HG02257.hp1 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+6258G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776114 | |||||||
chr1:212776228 | T | C | 2 | a0002c0002t0038g0095 a0002c0002t0038g0104 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.499+6144A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776228 | |||||||
chr1:212776250 | C | A | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499+6122G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776250 | |||||||
chr1:212776295 | G | A | 2 | a0002c0002t0013g0105 a0002c0002t0111g0106 |
2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.499+6077C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776295 | |||||||
chr1:212776351 | G | C | 2 | a0002c0002t0013g0105 a0002c0002t0111g0106 |
2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.499+6021C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776351 | |||||||
chr1:212776370 | A | T | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.499+6002T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776370 | |||||||
chr1:212776534 | G | T | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+5838C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776534 | |||||||
chr1:212776627 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.499+5745G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776627 | |||||||
chr1:212776632 | C | G | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+5740G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776632 | |||||||
chr1:212776700 | C | T | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+5672G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776700 | |||||||
chr1:212776703 | TAAAAC | T | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+5664_499+5668d others(7): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776703 | |||||||
chr1:212776718 | CAA | C | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+5652_499+5653d others(4): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776718 | |||||||
chr1:212776720 | AAAC | A | 12 | a0001c0001t0001g0236 a0001c0001t0004g0107 a0001c0001t0004g0108 others(9): Show |
12 | HG00099.hp1 HG01175.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+5649_499+5651d others(5): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776720 | |||||||
chr1:212776737 | AC | A | 14 | a0003c0003t0032g0290 a0003c0003t0032g0294 a0003c0003t0033g0288 others(11): Show |
14 | HG00639.hp1 HG01433.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.499+5634delG | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776737 | |||||||
chr1:212776738 | C | A | 5 | a0001c0001t0016g0154 a0001c0001t0016g0155 a0001c0001t0016g0156 others(2): Show |
5 | HG00140.hp1 HG00323.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+5634G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776738 | |||||||
chr1:212776738 | CAAA | C | 5 | a0002c0002t0026g0119 a0002c0002t0026g0120 a0002c0002t0026g0121 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+5631_499+5633d others(5): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776738 | |||||||
chr1:212776741 | A | C | 1 | a0002c0004t0095g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.499+5631T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776741 | |||||||
chr1:212776746 | A | C | 1 | a0003c0003t0009g0304 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.499+5626T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776746 | |||||||
chr1:212776757 | C | G | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.499+5615G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776757 | |||||||
chr1:212776767 | T | G | 76 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(73): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.499+5605A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776767 | |||||||
chr1:212776821 | C | A | 1 | a0003c0003t0003g0013 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.499+5551G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776821 | |||||||
chr1:212776962 | A | T | 4 | a0002c0002t0014g0004 a0002c0002t0014g0019 a0002c0002t0014g0090 others(1): Show |
5 | HG02922.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+5410T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212776962 | |||||||
chr1:212777068 | A | C | 19 | a0001c0001t0007g0122 a0001c0001t0007g0266 a0001c0001t0007g0267 others(16): Show |
21 | HG00738.hp2 HG00741.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.499+5304T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777068 | |||||||
chr1:212777068 | A | T | 1 | a0002c0002t0069g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.499+5304T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777068 | |||||||
chr1:212777095 | C | A | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+5277G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777095 | |||||||
chr1:212777191 | T | C | 1 | a0003c0003t0015g0315 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.499+5181A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777191 | |||||||
chr1:212777219 | A | T | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.499+5153T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777219 | |||||||
chr1:212777308 | T | C | 1 | a0003c0003t0058g0284 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.499+5064A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777308 | |||||||
chr1:212777317 | C | T | 1 | a0002c0002t0005g0078 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.499+5055G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777317 | |||||||
chr1:212777371 | C | CA | 10 | a0001c0001t0007g0122 a0001c0001t0007g0161 a0001c0001t0007g0165 others(7): Show |
10 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.499+5000dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777371 | |||||||
chr1:212777550 | T | C | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.499+4822A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777550 | |||||||
chr1:212777590 | C | T | 1 | a0001c0001t0075g0168 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.499+4782G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777590 | |||||||
chr1:212777699 | G | A | 3 | a0002c0002t0008g0028 a0002c0002t0008g0082 a0002c0002t0042g0083 |
3 | NA18957.hp1 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.499+4673C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777699 | |||||||
chr1:212777735 | C | G | 2 | a0003c0003t0015g0319 a0003c0003t0034g0320 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.499+4637G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777735 | |||||||
chr1:212777736 | T | G | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.499+4636A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777736 | |||||||
chr1:212777737 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.499+4635T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777737 | |||||||
chr1:212777827 | T | C | 1 | a0001c0001t0004g0166 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.499+4545A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777827 | |||||||
chr1:212777883 | G | A | 1 | a0001c0001t0004g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.499+4489C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777883 | |||||||
chr1:212777910 | T | C | 1 | a0001c0001t0006g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.499+4462A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777910 | |||||||
chr1:212777912 | T | A | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+4460A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777912 | |||||||
chr1:212777963 | G | A | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+4409C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777963 | |||||||
chr1:212777990 | A | C | 1 | a0002c0002t0046g0032 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.499+4382T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212777990 | |||||||
chr1:212778022 | A | G | 15 | a0003c0003t0003g0287 a0003c0003t0032g0290 a0003c0003t0032g0294 others(12): Show |
15 | HG00639.hp1 HG01433.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.499+4350T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778022 | |||||||
chr1:212778090 | TG | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+4281delC | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778090 | |||||||
chr1:212778110 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+4262C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778110 | |||||||
chr1:212778149 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+4223A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778149 | |||||||
chr1:212778166 | TACTC | T | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+4202_499+4205d others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778166 | |||||||
chr1:212778174 | C | T | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+4198G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778174 | |||||||
chr1:212778326 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.499+4046A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778326 | |||||||
chr1:212778393 | C | T | 2 | a0002c0002t0109g0097 a0002c0002t0110g0096 |
2 | HG02300.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.499+3979G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778393 | |||||||
chr1:212778394 | GCTCTCTC | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+3971_499+3977d others(9): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778394 | |||||||
chr1:212778429 | C | T | 4 | a0003c0003t0003g0316 a0003c0003t0003g0317 a0003c0003t0003g0318 others(1): Show |
4 | HG03491.hp1 HG03654.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+3943G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778429 | |||||||
chr1:212778469 | C | T | 8 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(5): Show |
8 | HG00738.hp2 HG00741.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+3903G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778469 | |||||||
chr1:212778547 | C | T | 1 | a0001c0001t0120g0193 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.499+3825G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778547 | |||||||
chr1:212778551 | G | A | 1 | a0003c0003t0059g0285 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.499+3821C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778551 | |||||||
chr1:212778661 | G | A | 1 | a0002c0004t0095g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.499+3711C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778661 | |||||||
chr1:212778681 | G | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+3691C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778681 | |||||||
chr1:212778719 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+3653C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778719 | |||||||
chr1:212778758 | C | A | 1 | a0003c0003t0003g0336 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.499+3614G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778758 | |||||||
chr1:212778824 | G | A | 1 | a0002c0002t0002g0027 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.499+3548C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778824 | |||||||
chr1:212778891 | G | A | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.499+3481C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778891 | |||||||
chr1:212778891 | G | C | 1 | a0002c0002t0005g0079 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.499+3481C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778891 | |||||||
chr1:212778918 | G | A | 1 | a0001c0001t0004g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.499+3454C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778918 | |||||||
chr1:212778967 | C | T | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499+3405G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212778967 | |||||||
chr1:212779005 | C | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+3367G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779005 | |||||||
chr1:212779054 | A | AC | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+3317dupG | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779054 | |||||||
chr1:212779091 | G | A | 1 | a0003c0003t0048g0313 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.499+3281C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779091 | |||||||
chr1:212779131 | G | A | 1 | a0001c0001t0006g0179 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.499+3241C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779131 | |||||||
chr1:212779217 | G | C | 1 | a0003c0003t0003g0338 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.499+3155C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779217 | |||||||
chr1:212779238 | T | G | 3 | a0002c0002t0019g0011 a0002c0002t0019g0276 a0002c0002t0019g0277 |
4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+3134A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779238 | |||||||
chr1:212779241 | G | C | 1 | a0001c0001t0004g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.499+3131C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779241 | |||||||
chr1:212779242 | G | C | 5 | a0002c0002t0012g0274 a0002c0002t0012g0275 a0002c0002t0012g0278 others(2): Show |
5 | NA18952.hp2 NA18973.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+3130C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779242 | |||||||
chr1:212779270 | G | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+3102C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779270 | |||||||
chr1:212779304 | A | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.499+3068T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779304 | |||||||
chr1:212779304 | AGCCAGCC others(492): Show |
A | 4 | a0001c0001t0006g0257 a0001c0001t0006g0260 a0001c0001t0072g0258 others(1): Show |
4 | NA18948.hp1 NA18980.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+2569_499+3067d others(2): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779304 | |||||||
chr1:212779321 | G | A | 2 | a0003c0003t0003g0312 a0003c0003t0048g0313 |
2 | HG02129.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.499+3051C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779321 | |||||||
chr1:212779322 | G | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+3050C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779322 | |||||||
chr1:212779337 | G | A | 1 | a0002c0002t0008g0080 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.499+3035C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779337 | |||||||
chr1:212779348 | C | G | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+3024G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779348 | |||||||
chr1:212779348 | C | T | 1 | a0003c0003t0003g0297 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.499+3024G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779348 | |||||||
chr1:212779360 | C | T | 9 | a0003c0003t0032g0290 a0003c0003t0032g0294 a0003c0003t0033g0288 others(6): Show |
9 | HG00639.hp1 HG01433.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.499+3012G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779360 | |||||||
chr1:212779366 | A | G | 1 | a0001c0001t0007g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.499+3006T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779366 | |||||||
chr1:212779378 | G | T | 1 | a0001c0001t0006g0192 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.499+2994C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779378 | |||||||
chr1:212779419 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.499+2953C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779419 | |||||||
chr1:212779478 | A | C | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+2894T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779478 | |||||||
chr1:212779508 | G | T | 1 | a0002c0002t0094g0117 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.499+2864C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779508 | |||||||
chr1:212779513 | GGTCAGCC others(42): Show |
G | 7 | a0002c0002t0026g0119 a0002c0002t0026g0120 a0002c0002t0026g0121 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.499+2810_499+2858d others(51): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779513 | |||||||
chr1:212779537 | GCCCCGTC others(42): Show |
G | 3 | a0001c0001t0022g0008 a0001c0001t0036g0139 a0001c0001t0036g0140 |
3 | HG02559.hp2 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.499+2786_499+2834d others(51): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779537 | |||||||
chr1:212779546 | G | C | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.499+2826C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779546 | |||||||
chr1:212779562 | T | G | 289 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0183 others(286): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.499+2810A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779562 | |||||||
chr1:212779591 | G | A | 1 | a0003c0003t0049g0337 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.499+2781C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779591 | |||||||
chr1:212779608 | G | T | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+2764C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779608 | |||||||
chr1:212779622 | C | T | 1 | a0003c0003t0055g0289 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.499+2750G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779622 | |||||||
chr1:212779643 | T | C | 103 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(100): Show |
110 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.499+2729A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779643 | |||||||
chr1:212779658 | G | A | 4 | a0002c0002t0008g0028 a0002c0002t0008g0081 a0002c0002t0008g0082 others(1): Show |
4 | HG02056.hp2 NA18957.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+2714C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779658 | |||||||
chr1:212779662 | C | T | 5 | a0002c0002t0026g0119 a0002c0002t0026g0120 a0002c0002t0026g0121 others(2): Show |
5 | HG01891.hp2 HG02895.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+2710G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779662 | |||||||
chr1:212779667 | T | C | 182 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(179): Show |
195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.499+2705A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779667 | |||||||
chr1:212779672 | G | A | 1 | a0002c0004t0095g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.499+2700C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779672 | |||||||
chr1:212779700 | T | TGCCCGGC others(189): Show |
7 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+2671_499+2672i others(198): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779700 | |||||||
chr1:212779700 | T | TGCCCGGC others(238): Show |
4 | a0002c0002t0012g0274 a0002c0002t0012g0275 a0002c0002t0012g0278 others(1): Show |
4 | NA18973.hp1 NA18990.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+2671_499+2672i others(247): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779700 | |||||||
chr1:212779705 | GGCCAGCC others(42): Show |
G | 80 | a0002c0002t0013g0098 a0002c0002t0013g0100 a0002c0002t0013g0101 others(77): Show |
85 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.499+2618_499+2666d others(51): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779705 | |||||||
chr1:212779707 | C | T | 80 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(77): Show |
87 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.499+2665G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779707 | |||||||
chr1:212779712 | C | T | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+2660G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779712 | |||||||
chr1:212779718 | A | G | 100 | a0001c0001t0006g0237 a0002c0002t0002g0002 a0002c0002t0002g0022 others(97): Show |
108 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.499+2654T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779718 | |||||||
chr1:212779718 | ATCCGGGA others(42): Show |
A | 1 | a0001c0001t0025g0217 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.499+2605_499+2653d others(51): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779718 | |||||||
chr1:212779754 | A | G | 91 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(88): Show |
99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.499+2618T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779754 | |||||||
chr1:212779754 | AGCCAGCC others(42): Show |
A | 4 | a0001c0001t0004g0159 a0001c0001t0080g0169 a0001c0001t0081g0171 others(1): Show |
4 | HG02486.hp1 HG02615.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+2569_499+2617d others(51): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779754 | |||||||
chr1:212779756 | C | T | 13 | a0002c0002t0013g0098 a0002c0002t0013g0100 a0002c0002t0013g0101 others(10): Show |
13 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.499+2616G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779756 | |||||||
chr1:212779766 | C | T | 1 | a0001c0001t0006g0179 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.499+2606G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779766 | |||||||
chr1:212779771 | G | A | 2 | a0001c0001t0075g0168 a0002c0002t0039g0094 |
2 | HG02630.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.499+2601C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779771 | |||||||
chr1:212779803 | G | A | 67 | a0003c0003t0003g0013 a0003c0003t0003g0297 a0003c0003t0003g0299 others(64): Show |
72 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.499+2569C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779803 | |||||||
chr1:212779803 | G | GACCAGCC others(218): Show |
2 | a0003c0003t0003g0287 a0003c0003t0053g0286 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.499+2568_499+2569i others(227): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779803 | |||||||
chr1:212779804 | GCCAGCCG others(42): Show |
G | 1 | a0001c0001t0001g0191 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.499+2519_499+2567d others(51): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779804 | |||||||
chr1:212779820 | G | A | 9 | a0003c0003t0009g0003 a0003c0003t0009g0304 a0003c0003t0009g0306 others(6): Show |
11 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.499+2552C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779820 | |||||||
chr1:212779847 | C | A | 3 | a0001c0001t0024g0182 a0001c0001t0024g0184 a0001c0001t0024g0218 |
3 | NA18943.hp1 NA18961.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.499+2525G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779847 | |||||||
chr1:212779847 | C | T | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+2525G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779847 | |||||||
chr1:212779852 | G | A | 1 | a0002c0002t0039g0099 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.499+2520C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779852 | |||||||
chr1:212779853 | A | G | 2 | a0001c0001t0001g0233 a0001c0001t0088g0209 |
2 | HG03831.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.499+2519T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779853 | |||||||
chr1:212779869 | G | A | 12 | a0002c0002t0013g0098 a0002c0002t0013g0100 a0002c0002t0013g0101 others(9): Show |
12 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+2503C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779869 | |||||||
chr1:212779903 | A | C | 179 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(176): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.499+2469T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779903 | |||||||
chr1:212779918 | G | A | 3 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 |
3 | HG02451.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+2454C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779918 | |||||||
chr1:212779949 | C | T | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+2423G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779949 | |||||||
chr1:212779986 | A | AC | 36 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0186 others(33): Show |
36 | HG00597.hp2 HG00741.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.499+2385dupG | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212779986 | |||||||
chr1:212780004 | A | G | 3 | a0003c0003t0003g0311 a0003c0003t0003g0312 a0003c0003t0048g0313 |
3 | HG02129.hp1 NA18977.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.499+2368T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780004 | |||||||
chr1:212780039 | A | G | 1 | a0002c0002t0002g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.499+2333T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780039 | |||||||
chr1:212780105 | G | A | 1 | a0003c0003t0059g0285 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.499+2267C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780105 | |||||||
chr1:212780132 | G | A | 1 | a0001c0005t0007g0016 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.499+2240C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780132 | |||||||
chr1:212780203 | C | T | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+2169G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780203 | |||||||
chr1:212780265 | T | C | 1 | a0002c0002t0039g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.499+2107A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780265 | |||||||
chr1:212780310 | C | T | 1 | a0002c0002t0002g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.499+2062G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780310 | |||||||
chr1:212780368 | G | A | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+2004C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780368 | |||||||
chr1:212780500 | T | TA | 58 | a0001c0001t0006g0261 a0003c0003t0003g0013 a0003c0003t0003g0287 others(55): Show |
61 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.499+1871dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780500 | |||||||
chr1:212780516 | G | A | 9 | a0003c0003t0009g0003 a0003c0003t0009g0304 a0003c0003t0009g0306 others(6): Show |
11 | HG01109.hp1 HG01243.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.499+1856C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780516 | |||||||
chr1:212780517 | G | A | 1 | a0003c0003t0034g0302 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.499+1855C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780517 | |||||||
chr1:212780517 | GA | G | 83 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(80): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.499+1854delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780517 | |||||||
chr1:212780518 | A | G | 11 | a0002c0002t0002g0085 a0002c0002t0066g0018 a0003c0003t0009g0003 others(8): Show |
13 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.499+1854T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780518 | |||||||
chr1:212780525 | A | T | 1 | a0002c0002t0002g0022 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.499+1847T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780525 | |||||||
chr1:212780592 | A | G | 12 | a0002c0002t0013g0098 a0002c0002t0013g0100 a0002c0002t0013g0101 others(9): Show |
12 | HG00733.hp1 HG01071.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+1780T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780592 | |||||||
chr1:212780885 | T | C | 2 | a0003c0003t0060g0295 a0003c0003t0061g0296 |
2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.499+1487A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780885 | |||||||
chr1:212780889 | C | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+1483G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780889 | |||||||
chr1:212780928 | C | T | 3 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 |
3 | HG01109.hp2 HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.499+1444G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212780928 | |||||||
chr1:212781087 | A | G | 6 | a0001c0001t0004g0005 a0001c0001t0004g0109 a0001c0001t0004g0110 others(3): Show |
7 | HG00438.hp1 NA18966.hp1 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.499+1285T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212781087 | |||||||
chr1:212781172 | T | G | 3 | a0002c0002t0019g0011 a0002c0002t0019g0276 a0002c0002t0019g0277 |
4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+1200A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212781172 | |||||||
chr1:212781342 | T | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.499+1030A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212781342 | |||||||
chr1:212781489 | A | G | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.499+883T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212781489 | |||||||
chr1:212781538 | T | TA | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.499+833_499+834ins others(1): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212781538 | |||||||
chr1:212781538 | T | TC | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+833dupG | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212781538 | |||||||
chr1:212781703 | T | C | 1 | a0001c0001t0073g0268 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.499+669A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212781703 | |||||||
chr1:212781861 | T | C | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+511A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212781861 | |||||||
chr1:212781889 | A | C | 104 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(101): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.499+483T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212781889 | |||||||
chr1:212782112 | G | A | 80 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(77): Show |
87 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.499+260C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 4/5 | chr1 | 212782112 | |||||||
chr1:212782568 | G | A | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-142C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212782568 | |||||||
chr1:212782577 | A | G | 72 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 others(69): Show |
77 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.445-151T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212782577 | |||||||
chr1:212782627 | C | T | 1 | a0003c0003t0063g0282 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.445-201G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212782627 | |||||||
chr1:212782630 | G | A | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.445-204C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212782630 | |||||||
chr1:212782788 | G | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-362C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212782788 | |||||||
chr1:212783027 | C | T | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.445-601G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212783027 | |||||||
chr1:212783070 | G | A | 72 | a0002c0002t0047g0017 a0002c0002t0066g0018 a0002c0009t0067g0281 others(69): Show |
77 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.445-644C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212783070 | |||||||
chr1:212783147 | C | CGCAGG | 4 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0113g0176 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-726_445-722dup others(5): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212783147 | |||||||
chr1:212783190 | G | T | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-764C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212783190 | |||||||
chr1:212783261 | C | A | 5 | a0003c0003t0003g0338 a0003c0003t0003g0339 a0003c0003t0003g0341 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-835G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212783261 | |||||||
chr1:212783808 | C | T | 2 | a0002c0002t0027g0009 a0002c0002t0027g0178 |
3 | NA18942.hp2 NA18947.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.444+555G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212783808 | |||||||
chr1:212783831 | G | A | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.444+532C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212783831 | |||||||
chr1:212783856 | T | C | 72 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 others(69): Show |
77 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.444+507A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212783856 | |||||||
chr1:212783907 | A | T | 1 | a0001c0001t0004g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.444+456T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212783907 | |||||||
chr1:212783995 | CA | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.444+367delT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212783995 | |||||||
chr1:212784012 | A | G | 72 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0065g0265 others(69): Show |
77 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.444+351T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212784012 | |||||||
chr1:212784095 | T | C | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.444+268A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212784095 | |||||||
chr1:212784291 | G | A | 3 | a0002c0002t0002g0086 a0002c0002t0002g0087 a0002c0002t0002g0088 |
3 | NA18999.hp1 NA19078.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.444+72C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 3/5 | chr1 | 212784291 | |||||||
chr1:212784518 | T | C | 1 | a0003c0003t0003g0013 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.314-25A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212784518 | |||||||
chr1:212784571 | A | G | 1 | a0002c0002t0066g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.314-78T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212784571 | |||||||
chr1:212784683 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.314-190T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212784683 | |||||||
chr1:212784798 | T | A | 1 | a0002c0002t0002g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.314-305A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212784798 | |||||||
chr1:212784829 | T | C | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.314-336A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212784829 | |||||||
chr1:212784869 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.314-376T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212784869 | |||||||
chr1:212784950 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.314-457T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212784950 | |||||||
chr1:212785061 | T | C | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.314-568A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212785061 | |||||||
chr1:212785207 | A | G | 1 | a0001c0001t0004g0107 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.314-714T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212785207 | |||||||
chr1:212785493 | C | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.314-1000G>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212785493 | |||||||
chr1:212785627 | G | A | 1 | a0003c0003t0003g0343 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.314-1134C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212785627 | |||||||
chr1:212785639 | G | T | 1 | a0002c0004t0095g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.314-1146C>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212785639 | |||||||
chr1:212786017 | C | T | 1 | a0002c0002t0008g0021 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.314-1524G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786017 | |||||||
chr1:212786112 | C | T | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.313+1447G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786112 | |||||||
chr1:212786120 | CTAGA | C | 76 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(73): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.313+1435_313+1438d others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786120 | |||||||
chr1:212786129 | T | G | 1 | a0002c0002t0039g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.313+1430A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786129 | |||||||
chr1:212786133 | T | G | 81 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.313+1426A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786133 | |||||||
chr1:212786143 | G | C | 4 | a0002c0002t0104g0092 a0002c0002t0105g0093 a0003c0003t0003g0287 others(1): Show |
4 | HG01515.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+1416C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786143 | |||||||
chr1:212786416 | T | TA | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+1142dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786416 | |||||||
chr1:212786432 | A | C | 1 | a0006c0006t0002g0020 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.313+1127T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786432 | |||||||
chr1:212786577 | G | A | 1 | a0003c0003t0015g0344 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.313+982C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786577 | |||||||
chr1:212786744 | G | A | 3 | a0001c0001t0080g0169 a0001c0001t0081g0171 a0001c0001t0084g0170 |
3 | HG02486.hp1 HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.313+815C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786744 | |||||||
chr1:212786795 | A | G | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.313+764T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786795 | |||||||
chr1:212786801 | G | A | 8 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(5): Show |
8 | HG00738.hp2 HG00741.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.313+758C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786801 | |||||||
chr1:212786869 | T | A | 1 | a0003c0003t0031g0014 | 2 | HG01261.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.313+690A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212786869 | |||||||
chr1:212787007 | T | C | 1 | a0002c0002t0039g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.313+552A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212787007 | |||||||
chr1:212787023 | G | A | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+536C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212787023 | |||||||
chr1:212787029 | GC | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+529delG | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212787029 | |||||||
chr1:212787160 | C | CA | 64 | a0001c0001t0004g0172 a0002c0002t0035g0263 a0002c0002t0035g0264 others(61): Show |
69 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.313+398dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212787160 | |||||||
chr1:212787226 | G | A | 1 | a0002c0009t0067g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.313+333C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212787226 | |||||||
chr1:212787524 | C | T | 85 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0183 others(82): Show |
86 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.313+35G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 2/5 | chr1 | 212787524 | |||||||
chr1:212787738 | T | TAAAG | 86 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(83): Show |
92 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.235-102_235-101ins others(4): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212787738 | |||||||
chr1:212787801 | T | C | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.235-164A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212787801 | |||||||
chr1:212787991 | T | A | 1 | a0002c0004t0095g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.235-354A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212787991 | |||||||
chr1:212788078 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-441T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212788078 | |||||||
chr1:212788084 | C | T | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.235-447G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212788084 | |||||||
chr1:212788107 | G | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-470C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212788107 | |||||||
chr1:212788111 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-474A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212788111 | |||||||
chr1:212788339 | G | A | 184 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(181): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.235-702C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212788339 | |||||||
chr1:212788368 | G | A | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.235-731C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212788368 | |||||||
chr1:212788543 | C | T | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.235-906G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212788543 | |||||||
chr1:212788704 | T | C | 54 | a0003c0003t0003g0013 a0003c0003t0003g0297 a0003c0003t0003g0299 others(51): Show |
59 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.235-1067A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212788704 | |||||||
chr1:212788735 | T | C | 1 | a0003c0003t0015g0344 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.235-1098A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212788735 | |||||||
chr1:212788748 | C | T | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.235-1111G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212788748 | |||||||
chr1:212788865 | A | G | 81 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.235-1228T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212788865 | |||||||
chr1:212789201 | TTTTG | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-1568_235-1565d others(6): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212789201 | |||||||
chr1:212789464 | A | G | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-1827T>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212789464 | |||||||
chr1:212789479 | TG | T | 75 | a0002c0002t0035g0263 a0002c0002t0035g0264 a0002c0002t0047g0017 others(72): Show |
80 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.235-1843delC | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212789479 | |||||||
chr1:212789612 | T | C | 1 | a0003c0003t0029g0345 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.234+1918A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212789612 | |||||||
chr1:212789657 | C | T | 93 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(90): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.234+1873G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212789657 | |||||||
chr1:212789737 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.234+1793A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212789737 | |||||||
chr1:212789918 | T | A | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.234+1612A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212789918 | |||||||
chr1:212790172 | G | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.234+1358C>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790172 | |||||||
chr1:212790307 | G | A | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.234+1223C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790307 | |||||||
chr1:212790341 | T | C | 2 | a0002c0002t0027g0009 a0002c0002t0027g0178 |
3 | NA18942.hp2 NA18947.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.234+1189A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790341 | |||||||
chr1:212790498 | C | G | 179 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(176): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.234+1032G>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790498 | |||||||
chr1:212790553 | T | TA | 3 | a0002c0002t0019g0011 a0002c0002t0019g0276 a0002c0002t0019g0277 |
4 | HG03491.hp2 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+976_234+977ins others(1): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790553 | |||||||
chr1:212790553 | T | TG | 8 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(5): Show |
8 | HG00738.hp2 HG00741.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.234+976_234+977ins others(1): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790553 | |||||||
chr1:212790614 | T | G | 1 | a0001c0001t0023g0262 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.234+916A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790614 | |||||||
chr1:212790639 | T | C | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.234+891A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790639 | |||||||
chr1:212790661 | G | A | 5 | a0002c0002t0045g0173 a0002c0002t0045g0174 a0002c0002t0069g0177 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+869C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790661 | |||||||
chr1:212790734 | A | C | 1 | a0002c0002t0047g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.234+796T>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790734 | |||||||
chr1:212790799 | T | C | 2 | a0002c0002t0027g0009 a0002c0002t0027g0178 |
3 | NA18942.hp2 NA18947.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.234+731A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790799 | |||||||
chr1:212790876 | T | C | 85 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0183 others(82): Show |
86 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.234+654A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790876 | |||||||
chr1:212790896 | C | T | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.234+634G>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790896 | |||||||
chr1:212790912 | G | A | 1 | a0002c0002t0012g0278 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.234+618C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790912 | |||||||
chr1:212790930 | A | AAT | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.234+599_234+600ins others(2): Show |
NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790930 | |||||||
chr1:212790930 | A | T | 70 | a0002c0002t0014g0019 a0003c0003t0003g0013 a0003c0003t0003g0287 others(67): Show |
75 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.234+600T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790930 | |||||||
chr1:212790931 | A | T | 2 | a0002c0002t0047g0017 a0002c0009t0067g0281 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.234+599T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790931 | |||||||
chr1:212790935 | T | A | 7 | a0001c0001t0007g0266 a0001c0001t0007g0267 a0001c0001t0073g0268 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+595A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790935 | |||||||
chr1:212790940 | T | A | 2 | a0002c0002t0047g0017 a0002c0002t0066g0018 |
2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.234+590A>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790940 | |||||||
chr1:212790941 | A | T | 2 | a0002c0002t0047g0017 a0002c0002t0066g0018 |
2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.234+589T>A | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212790941 | |||||||
chr1:212791083 | T | G | 1 | a0003c0003t0003g0346 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.234+447A>C | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212791083 | |||||||
chr1:212791085 | T | C | 69 | a0003c0003t0003g0013 a0003c0003t0003g0287 a0003c0003t0003g0297 others(66): Show |
74 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.234+445A>G | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212791085 | |||||||
chr1:212791116 | G | GA | 11 | a0002c0002t0012g0270 a0002c0002t0012g0271 a0002c0002t0012g0272 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.234+413dupT | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212791116 | |||||||
chr1:212791520 | G | A | 1 | a0001c0001t0011g0279 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.234+10C>T | NSL1 | ENSG00000117697.15 | transcript | ENST00000366977.8 | protein_coding | 1/5 | chr1 | 212791520 |