Item | Value |
---|---|
geneid | 3938 |
ensemblid | ENSG00000115850.10 |
hgncid | 6530 |
symbol | LCT |
name | lactase |
refseq_nuc | NM_002299.4 |
refseq_prot | NP_002290.2 |
ensembl_nuc | ENST00000264162.7 |
ensembl_prot | ENSP00000264162.2 |
mane_status | MANE Select |
chr | chr2 |
start | 135787850 |
end | 135837184 |
strand | - |
ver | v1.2 |
region | chr2:135787850-135837184 |
region5000 | chr2:135782850-135842184 |
regionname0 | LCT_chr2_135787850_135837184 |
regionname5000 | LCT_chr2_135782850_135842184 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1927 | 127 | 15 | 27 | 66 | 3 | 16 | 48 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0002 | 0/1 | 1927 | 97 | 16 | 19 | 45 | 0 | 16 | 40 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0003 | 0/0 | 1927 | 91 | 15 | 18 | 48 | 3 | 7 | 39 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0004 | 0/0 | 1927 | 16 | 11 | 2 | 3 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0005 | 0/0 | 1927 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0006 | 0/0 | 1927 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0007 | 0/0 | 1927 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0008 | 1/0 | 1927 | 3 | 2 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0009 | 0/0 | 1927 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0010 | 0/0 | 1927 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0011 | 0/0 | 1927 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0012 | 0/0 | 1927 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0013 | 0/0 | 1927 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0014 | 0/0 | 1927 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0015 | 0/0 | 1927 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0016 | 0/0 | 1927 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0017 | 0/0 | 1927 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
a0018 | 0/0 | 1927 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | MELSW others(1922): Show |
chr2 | 135782850 | 135842184 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 5781 | 102 | 13 | 22 | 54 | 3 | 10 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0001c0005 | 0/0 | 5781 | 11 | 2 | 4 | 3 | 0 | 2 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0001c0011 | 0/0 | 5781 | 5 | 0 | 0 | 5 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0001c0019 | 0/0 | 5781 | 3 | 0 | 0 | 0 | 0 | 3 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0001c0038 | 0/0 | 5781 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0001c0039 | 0/0 | 5781 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0001c0042 | 0/0 | 5781 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0001c0044 | 0/0 | 5781 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0001c0045 | 0/0 | 5781 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0001c0047 | 0/0 | 5781 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0002c0002 | 0/0 | 5781 | 72 | 15 | 9 | 38 | 0 | 10 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0002c0008 | 0/1 | 5781 | 7 | 0 | 3 | 1 | 0 | 2 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0002c0009 | 0/0 | 5781 | 7 | 0 | 6 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0002c0015 | 0/0 | 5781 | 4 | 0 | 0 | 2 | 0 | 2 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0002c0023 | 0/0 | 5781 | 2 | 0 | 0 | 2 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0002c0037 | 0/0 | 5781 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0002c0040 | 0/0 | 5781 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0002c0041 | 0/0 | 5781 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0002c0046 | 0/0 | 5781 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0002c0048 | 0/0 | 5781 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0003c0003 | 0/0 | 5781 | 54 | 13 | 13 | 18 | 3 | 7 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0003c0004 | 0/0 | 5781 | 21 | 0 | 2 | 19 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0003c0007 | 0/0 | 5781 | 9 | 2 | 0 | 7 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0003c0013 | 0/0 | 5781 | 4 | 0 | 0 | 4 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0003c0029 | 0/0 | 5781 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0003c0030 | 0/0 | 5781 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0003c0033 | 0/0 | 5781 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0004c0006 | 0/0 | 5781 | 10 | 9 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0004c0014 | 0/0 | 5781 | 4 | 1 | 0 | 3 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0004c0021 | 0/0 | 5781 | 2 | 1 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0005c0012 | 0/0 | 5781 | 4 | 4 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0005c0017 | 0/0 | 5781 | 3 | 3 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0005c0020 | 0/0 | 5781 | 2 | 2 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0005c0026 | 0/0 | 5781 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0006c0010 | 0/0 | 5781 | 5 | 3 | 2 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0007c0016 | 0/0 | 5781 | 4 | 4 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0008c0022 | 1/0 | 5781 | 2 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0008c0035 | 0/0 | 5781 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0009c0018 | 0/0 | 5781 | 3 | 3 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0010c0024 | 0/0 | 5781 | 2 | 2 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0011c0036 | 0/0 | 5781 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0012c0034 | 0/0 | 5781 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0013c0031 | 0/0 | 5781 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0014c0025 | 0/0 | 5781 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0015c0027 | 0/0 | 5781 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0016c0028 | 0/0 | 5781 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0017c0043 | 0/0 | 5781 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 | ||
a0018c0032 | 0/0 | 5781 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | ATGGA others(5776): Show |
chr2 | 135782850 | 135842184 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6273 | 101 | 13 | 22 | 54 | 3 | 9 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0001c0001t0008 | 0/0 | 6273 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0001c0005t0001 | 0/0 | 6273 | 11 | 2 | 4 | 3 | 0 | 2 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0001c0011t0001 | 0/0 | 6273 | 5 | 0 | 0 | 5 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0001c0019t0004 | 0/0 | 6273 | 3 | 0 | 0 | 0 | 0 | 3 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0001c0038t0001 | 0/0 | 6273 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0001c0039t0001 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0001c0042t0001 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0001c0044t0001 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0001c0045t0001 | 0/0 | 6273 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0001c0047t0001 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0002t0001 | 0/0 | 6273 | 52 | 15 | 6 | 24 | 0 | 7 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0002t0002 | 0/0 | 6271 | 6 | 0 | 0 | 6 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0002c0002t0003 | 0/0 | 6273 | 7 | 0 | 0 | 5 | 0 | 2 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0002t0005 | 0/0 | 6273 | 6 | 0 | 3 | 2 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0002t0007 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0008t0001 | 0/1 | 6273 | 7 | 0 | 3 | 1 | 0 | 2 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0009t0001 | 0/0 | 6273 | 7 | 0 | 6 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0015t0001 | 0/0 | 6273 | 4 | 0 | 0 | 2 | 0 | 2 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0023t0001 | 0/0 | 6273 | 2 | 0 | 0 | 2 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0037t0002 | 0/0 | 6271 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0002c0040t0001 | 0/0 | 6273 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0041t0001 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0046t0001 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0002c0048t0001 | 0/0 | 6273 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0003c0003t0001 | 0/0 | 6273 | 6 | 5 | 0 | 0 | 1 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0003c0003t0002 | 0/0 | 6271 | 47 | 8 | 12 | 18 | 2 | 7 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0003c0003t0003 | 0/0 | 6273 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0003c0004t0001 | 0/0 | 6273 | 21 | 0 | 2 | 19 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0003c0007t0001 | 0/0 | 6273 | 9 | 2 | 0 | 7 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0003c0013t0002 | 0/0 | 6271 | 4 | 0 | 0 | 4 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0003c0029t0002 | 0/0 | 6271 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0003c0030t0002 | 0/0 | 6271 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0003c0033t0002 | 0/0 | 6271 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0004c0006t0001 | 0/0 | 6273 | 8 | 7 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0004c0006t0006 | 0/0 | 6273 | 2 | 2 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0004c0014t0001 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0004c0014t0002 | 0/0 | 6271 | 3 | 1 | 0 | 2 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0004c0021t0004 | 0/0 | 6273 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0004c0021t0006 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0005c0012t0001 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0005c0012t0004 | 0/0 | 6273 | 3 | 3 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0005c0017t0001 | 0/0 | 6273 | 3 | 3 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0005c0020t0001 | 0/0 | 6273 | 2 | 2 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0005c0026t0002 | 0/0 | 6271 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0006c0010t0002 | 0/0 | 6271 | 5 | 3 | 2 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0007c0016t0003 | 0/0 | 6273 | 4 | 4 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0008c0022t0003 | 1/0 | 6273 | 2 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0008c0035t0003 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0009c0018t0001 | 0/0 | 6273 | 3 | 3 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0010c0024t0002 | 0/0 | 6271 | 2 | 2 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0011c0036t0002 | 0/0 | 6271 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0012c0034t0002 | 0/0 | 6271 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0013c0031t0002 | 0/0 | 6271 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0014c0025t0004 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0015c0027t0001 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0016c0028t0002 | 0/0 | 6271 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6266): Show |
chr2 | 135782850 | 135842184 |
a0017c0043t0001 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
a0018c0032t0001 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | AACAG others(6268): Show |
chr2 | 135782850 | 135842184 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 13 | 1 | 4 | 5 | 1 | 2 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0002 | 0/0 | 9 | 1 | 1 | 6 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0003 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0005t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0005t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0005t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0005t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0005t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0005t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0005t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0005t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0011t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0011t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0011t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0011t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0011t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0019t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0019t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0019t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0038t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0039t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0042t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0044t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0045t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0001c0047t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0002t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0008t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0008t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0008t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0008t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0008t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0008t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0008t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0009t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0009t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0009t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0009t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0009t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0009t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0009t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0015t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0015t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0015t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0015t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0023t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0023t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0037t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0040t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0041t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0046t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0002c0048t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0003t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0007t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0007t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0007t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0007t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0007t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0013t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0013t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0013t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0013t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0029t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0030t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0003c0033t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0006t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0006t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0006t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0006t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0006t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0006t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0006t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0006t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0014t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0014t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0014t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0014t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0021t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0004c0021t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0005c0012t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0005c0012t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0005c0012t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0005c0012t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0005c0017t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0005c0017t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0005c0017t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0005c0020t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0005c0020t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0005c0026t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0006c0010t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0006c0010t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0006c0010t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0006c0010t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0006c0010t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0007c0016t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0007c0016t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0007c0016t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0007c0016t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0008c0022t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0008c0022t0003g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0008c0035t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0009c0018t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0009c0018t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0009c0018t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0010c0024t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0010c0024t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0011c0036t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0012c0034t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0013c0031t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0014c0025t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0015c0027t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0016c0028t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0017c0043t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
a0018c0032t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | FIN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00280 | hp2 | a0003 | c0003 | t0001 | g0074 | EUR | FIN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00408 | hp1 | a0001 | c0011 | t0001 | g0046 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00408 | hp2 | a0003 | c0004 | t0001 | g0232 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00423 | hp1 | a0003 | c0004 | t0001 | g0205 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00544 | hp2 | a0003 | c0004 | t0001 | g0014 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00558 | hp1 | a0003 | c0004 | t0001 | g0210 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00558 | hp2 | a0001 | c0005 | t0001 | g0034 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00621 | hp1 | a0001 | c0005 | t0001 | g0036 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00639 | hp1 | a0003 | c0003 | t0003 | g0105 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00639 | hp2 | a0001 | c0005 | t0001 | g0039 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00642 | hp2 | a0003 | c0003 | t0002 | g0010 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00733 | hp1 | a0001 | c0045 | t0001 | g0234 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00733 | hp2 | a0003 | c0003 | t0002 | g0085 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00735 | hp1 | a0006 | c0010 | t0002 | g0054 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00735 | hp2 | a0001 | c0005 | t0001 | g0042 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00738 | hp1 | a0003 | c0003 | t0002 | g0011 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00741 | hp1 | a0002 | c0009 | t0001 | g0308 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01069 | hp1 | a0003 | c0003 | t0002 | g0066 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01070 | hp1 | a0002 | c0008 | t0001 | g0133 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01071 | hp2 | a0003 | c0003 | t0002 | g0084 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01099 | hp2 | a0003 | c0003 | t0002 | g0073 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01109 | hp2 | a0002 | c0008 | t0001 | g0165 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01167 | hp1 | a0003 | c0003 | t0002 | g0055 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01175 | hp1 | a0003 | c0003 | t0002 | g0062 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01175 | hp2 | a0004 | c0006 | t0001 | g0225 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01192 | hp1 | a0003 | c0029 | t0002 | g0077 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01192 | hp2 | a0002 | c0008 | t0001 | g0132 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01243 | hp1 | a0001 | c0005 | t0001 | g0035 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01243 | hp2 | a0003 | c0030 | t0002 | g0049 | AMR | PUR | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01255 | hp1 | a0003 | c0033 | t0002 | g0092 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01255 | hp2 | a0003 | c0004 | t0001 | g0206 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01256 | hp1 | a0002 | c0009 | t0001 | g0307 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01257 | hp2 | a0003 | c0003 | t0002 | g0088 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01358 | hp1 | a0002 | c0002 | t0005 | g0109 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01358 | hp2 | a0006 | c0010 | t0002 | g0063 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01433 | hp1 | a0004 | c0021 | t0004 | g0096 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01496 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01515 | hp1 | a0003 | c0003 | t0002 | g0072 | EUR | IBS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01884 | hp2 | a0004 | c0006 | t0001 | g0015 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01928 | hp2 | a0002 | c0009 | t0001 | g0312 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01943 | hp1 | a0002 | c0009 | t0001 | g0309 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01943 | hp2 | a0003 | c0003 | t0002 | g0079 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0160 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01952 | hp2 | a0002 | c0009 | t0001 | g0306 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01975 | hp2 | a0002 | c0009 | t0001 | g0310 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01978 | hp2 | a0001 | c0005 | t0001 | g0043 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01981 | hp2 | a0002 | c0040 | t0001 | g0129 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01993 | hp1 | a0002 | c0002 | t0005 | g0115 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02015 | hp2 | a0004 | c0014 | t0001 | g0083 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02055 | hp1 | a0011 | c0036 | t0002 | g0144 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02055 | hp2 | a0003 | c0003 | t0001 | g0219 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02074 | hp1 | a0003 | c0004 | t0001 | g0212 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02074 | hp2 | a0004 | c0014 | t0002 | g0091 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02080 | hp1 | a0003 | c0003 | t0002 | g0102 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02083 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02129 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02135 | hp2 | a0003 | c0013 | t0002 | g0197 | EAS | KHV | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02145 | hp1 | a0012 | c0034 | t0002 | g0064 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02145 | hp2 | a0001 | c0005 | t0001 | g0037 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02148 | hp1 | a0003 | c0004 | t0001 | g0207 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02165 | hp2 | a0002 | c0002 | t0007 | g0176 | EAS | CDX | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02258 | hp1 | a0007 | c0016 | t0003 | g0316 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02280 | hp1 | a0003 | c0003 | t0001 | g0228 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02293 | hp2 | a0002 | c0002 | t0005 | g0114 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0157 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02615 | hp1 | a0005 | c0020 | t0001 | g0027 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02622 | hp1 | a0001 | c0005 | t0001 | g0041 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0187 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02630 | hp1 | a0010 | c0024 | t0002 | g0304 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02630 | hp2 | a0004 | c0021 | t0006 | g0223 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02647 | hp2 | a0004 | c0006 | t0001 | g0221 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02683 | hp1 | a0003 | c0003 | t0002 | g0076 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02683 | hp2 | a0002 | c0048 | t0001 | g0237 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0122 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02717 | hp1 | a0006 | c0010 | t0002 | g0060 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02717 | hp2 | a0003 | c0003 | t0002 | g0008 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02735 | hp1 | a0013 | c0031 | t0002 | g0068 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02735 | hp2 | a0003 | c0003 | t0002 | g0089 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02818 | hp1 | a0003 | c0007 | t0001 | g0059 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02818 | hp2 | a0014 | c0025 | t0004 | g0024 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02886 | hp1 | a0003 | c0003 | t0002 | g0094 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02895 | hp1 | a0010 | c0024 | t0002 | g0305 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02896 | hp1 | a0005 | c0012 | t0004 | g0025 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02896 | hp2 | a0009 | c0018 | t0001 | g0214 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02897 | hp2 | a0009 | c0018 | t0001 | g0215 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02922 | hp1 | a0009 | c0018 | t0001 | g0216 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02965 | hp1 | a0004 | c0006 | t0006 | g0220 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02965 | hp2 | a0007 | c0016 | t0003 | g0314 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02970 | hp1 | a0005 | c0017 | t0001 | g0020 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0155 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02976 | hp1 | a0005 | c0012 | t0004 | g0023 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0229 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03041 | hp1 | a0003 | c0003 | t0002 | g0058 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03041 | hp2 | a0005 | c0017 | t0001 | g0021 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03098 | hp1 | a0003 | c0007 | t0001 | g0050 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03098 | hp2 | a0003 | c0003 | t0001 | g0218 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03130 | hp2 | a0008 | c0035 | t0003 | g0202 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0145 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03195 | hp1 | a0006 | c0010 | t0002 | g0061 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03209 | hp1 | a0004 | c0006 | t0006 | g0224 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03209 | hp2 | a0005 | c0020 | t0001 | g0029 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0167 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03239 | hp1 | a0001 | c0001 | t0008 | g0260 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03239 | hp2 | a0001 | c0005 | t0001 | g0045 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03453 | hp1 | a0006 | c0010 | t0002 | g0056 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03453 | hp2 | a0004 | c0006 | t0001 | g0222 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03486 | hp2 | a0003 | c0003 | t0002 | g0008 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03490 | hp1 | a0002 | c0008 | t0001 | g0119 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0118 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03491 | hp1 | a0002 | c0015 | t0001 | g0284 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03491 | hp2 | a0001 | c0019 | t0004 | g0033 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03492 | hp1 | a0002 | c0015 | t0001 | g0291 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03492 | hp2 | a0002 | c0008 | t0001 | g0138 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03516 | hp2 | a0007 | c0016 | t0003 | g0313 | AFR | ESN | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03540 | hp1 | a0003 | c0003 | t0001 | g0226 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03579 | hp1 | a0015 | c0027 | t0001 | g0026 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03579 | hp2 | a0003 | c0003 | t0002 | g0052 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03654 | hp1 | a0001 | c0019 | t0004 | g0184 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03654 | hp2 | a0002 | c0002 | t0003 | g0112 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03669 | hp2 | a0001 | c0005 | t0001 | g0048 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0147 | SAS | STU | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0108 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03831 | hp1 | a0003 | c0003 | t0002 | g0070 | SAS | BEB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03831 | hp2 | a0002 | c0009 | t0001 | g0311 | SAS | BEB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03834 | hp1 | a0001 | c0038 | t0001 | g0166 | SAS | BEB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03942 | hp1 | a0003 | c0003 | t0002 | g0090 | SAS | BEB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0142 | SAS | BEB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG04115 | hp1 | a0003 | c0003 | t0002 | g0097 | SAS | STU | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0150 | SAS | STU | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG04184 | hp2 | a0002 | c0002 | t0005 | g0116 | SAS | BEB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG04199 | hp1 | a0003 | c0003 | t0002 | g0065 | SAS | STU | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG04199 | hp2 | a0001 | c0019 | t0004 | g0032 | SAS | STU | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | STU | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG04204 | hp2 | a0003 | c0003 | t0002 | g0078 | SAS | STU | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0163 | SAS | STU | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | STU | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18747 | hp1 | a0001 | c0005 | t0001 | g0040 | EAS | CHB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | CHB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18906 | hp1 | a0004 | c0006 | t0001 | g0016 | AFR | YRI | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18906 | hp2 | a0003 | c0003 | t0002 | g0093 | AFR | YRI | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18941 | hp1 | a0003 | c0007 | t0001 | g0098 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18943 | hp1 | a0003 | c0013 | t0002 | g0195 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18944 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18945 | hp1 | a0003 | c0007 | t0001 | g0099 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18945 | hp2 | a0001 | c0011 | t0001 | g0190 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18950 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18952 | hp2 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18956 | hp1 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18957 | hp1 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18957 | hp2 | a0002 | c0023 | t0001 | g0161 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18963 | hp1 | a0016 | c0028 | t0002 | g0198 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18966 | hp1 | a0003 | c0004 | t0001 | g0203 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18966 | hp2 | a0002 | c0002 | t0003 | g0113 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18968 | hp1 | a0003 | c0004 | t0001 | g0014 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18968 | hp2 | a0003 | c0003 | t0002 | g0069 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18970 | hp1 | a0003 | c0007 | t0001 | g0006 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18970 | hp2 | a0001 | c0011 | t0001 | g0200 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18971 | hp2 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18972 | hp2 | a0002 | c0023 | t0001 | g0174 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18973 | hp1 | a0003 | c0004 | t0001 | g0211 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18973 | hp2 | a0002 | c0008 | t0001 | g0175 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18979 | hp1 | a0003 | c0013 | t0002 | g0194 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18981 | hp1 | a0017 | c0043 | t0001 | g0038 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18981 | hp2 | a0003 | c0004 | t0001 | g0213 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18983 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18986 | hp1 | a0004 | c0014 | t0002 | g0082 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18986 | hp2 | a0001 | c0042 | t0001 | g0047 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18988 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18990 | hp1 | a0002 | c0002 | t0003 | g0110 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18992 | hp1 | a0001 | c0011 | t0001 | g0131 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18992 | hp2 | a0003 | c0007 | t0001 | g0053 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18994 | hp1 | a0003 | c0003 | t0002 | g0086 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18994 | hp2 | a0001 | c0044 | t0001 | g0286 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18998 | hp1 | a0003 | c0003 | t0002 | g0012 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19000 | hp2 | a0003 | c0003 | t0002 | g0095 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19002 | hp1 | a0003 | c0003 | t0002 | g0012 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19002 | hp2 | a0002 | c0002 | t0005 | g0192 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19004 | hp1 | a0003 | c0003 | t0002 | g0011 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19004 | hp2 | a0002 | c0002 | t0003 | g0106 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19007 | hp1 | a0003 | c0003 | t0002 | g0080 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19007 | hp2 | a0002 | c0046 | t0001 | g0303 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19009 | hp2 | a0003 | c0004 | t0001 | g0204 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19010 | hp1 | a0001 | c0011 | t0001 | g0180 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0153 | AFR | LWK | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19030 | hp2 | a0005 | c0012 | t0001 | g0030 | AFR | LWK | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19043 | hp1 | a0007 | c0016 | t0003 | g0315 | AFR | LWK | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19043 | hp2 | a0018 | c0032 | t0001 | g0217 | AFR | LWK | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19054 | hp1 | a0003 | c0004 | t0001 | g0208 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19056 | hp1 | a0003 | c0007 | t0001 | g0006 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19057 | hp2 | a0003 | c0003 | t0002 | g0104 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19058 | hp1 | a0003 | c0004 | t0001 | g0209 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19060 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19062 | hp2 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19064 | hp1 | a0003 | c0007 | t0001 | g0101 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19065 | hp1 | a0003 | c0007 | t0001 | g0006 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19067 | hp1 | a0003 | c0003 | t0002 | g0103 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19070 | hp2 | a0002 | c0015 | t0001 | g0285 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19072 | hp2 | a0003 | c0013 | t0002 | g0196 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19074 | hp1 | a0001 | c0039 | t0001 | g0172 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19074 | hp2 | a0003 | c0003 | t0002 | g0057 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19077 | hp1 | a0002 | c0002 | t0005 | g0189 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19084 | hp1 | a0002 | c0041 | t0001 | g0044 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19084 | hp2 | a0002 | c0015 | t0001 | g0292 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19085 | hp1 | a0003 | c0003 | t0002 | g0067 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19086 | hp1 | a0003 | c0003 | t0002 | g0081 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19087 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19087 | hp2 | a0001 | c0047 | t0001 | g0279 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19240 | hp1 | a0004 | c0006 | t0001 | g0016 | AFR | YRI | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | YRI | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA20129 | hp1 | a0005 | c0026 | t0002 | g0028 | AFR | ASW | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA20129 | hp2 | a0008 | c0022 | t0003 | g0199 | AFR | ASW | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA20805 | hp1 | a0003 | c0003 | t0002 | g0100 | EUR | TSI | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | GIH | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG01123 | hp2 | a0003 | c0003 | t0002 | g0075 | AMR | CLM | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02109 | hp1 | a0004 | c0006 | t0001 | g0227 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02109 | hp2 | a0003 | c0003 | t0002 | g0051 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0164 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02486 | hp2 | a0004 | c0006 | t0001 | g0015 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02559 | hp1 | a0005 | c0017 | t0001 | g0031 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03471 | hp1 | a0005 | c0012 | t0004 | g0022 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18955 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0140 | AFR | USA | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA20300 | hp2 | a0004 | c0014 | t0002 | g0087 | AFR | USA | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA21309 | hp1 | a0002 | c0037 | t0002 | g0123 | AFR | LWK | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
NA21309 | hp2 | a0003 | c0003 | t0002 | g0010 | AFR | LWK | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
homoSapiens | chm13v2 | a0002 | c0008 | t0001 | g0193 | REF | REF | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
homoSapiens | grch38p0 | a0008 | c0022 | t0003 | g0201 | REF | REF | LCT_chr2_135782850_135842184 | LCT | chr2 | 135782850 | 135842184 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135788340 | G | T | 2 | a0009 a0015 |
4 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.5768C>A | p.Pro1923Gln | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 17/17 | 5783/6273 | 5768/5784 | 1923/1927 | chr2 | 135788340 | |||
chr2:135798089 | T | C | 6 | a0001 a0004 a0005 others(3): Show |
156 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(153): Show |
missense_variant | MODERATE | c.4916A>G | p.Asn1639Ser | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/17 | 4931/6273 | 4916/5784 | 1639/1927 | chr2 | 135798089 | |||
chr2:135800696 | C | T | 3 | a0006 a0011 a0012 |
7 | HG00735.hp1 HG01358.hp2 HG02055.hp1 others(4): Show |
missense_variant | MODERATE | c.4777G>A | p.Val1593Met | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/17 | 4792/6273 | 4777/5784 | 1593/1927 | chr2 | 135800696 | |||
chr2:135808505 | G | A | 1 | a0017 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.3842C>T | p.Pro1281Leu | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/17 | 3857/6273 | 3842/5784 | 1281/1927 | chr2 | 135808505 | |||
chr2:135809006 | T | C | 1 | a0013 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.3341A>G | p.Gln1114Arg | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/17 | 3356/6273 | 3341/5784 | 1114/1927 | chr2 | 135809006 | |||
chr2:135809633 | T | C | 3 | a0009 a0015 a0018 |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
missense_variant | MODERATE | c.2714A>G | p.Asp905Gly | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/17 | 2729/6273 | 2714/5784 | 905/1927 | chr2 | 135809633 | |||
chr2:135809636 | C | T | 1 | a0016 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.2711G>A | p.Arg904Gln | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/17 | 2726/6273 | 2711/5784 | 904/1927 | chr2 | 135809636 | |||
chr2:135817354 | A | C | 1 | a0016 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.1694T>G | p.Val565Gly | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/17 | 1709/6273 | 1694/5784 | 565/1927 | chr2 | 135817354 | |||
chr2:135817730 | C | T | 1 | a0007 | 4 | HG02258.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
missense_variant | MODERATE | c.1318G>A | p.Val440Ile | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/17 | 1333/6273 | 1318/5784 | 440/1927 | chr2 | 135817730 | |||
chr2:135817964 | T | C | 17 | a0001 a0002 a0003 others(14): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
missense_variant | MODERATE | c.1084A>G | p.Ile362Val | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/17 | 1099/6273 | 1084/5784 | 362/1927 | chr2 | 135817964 | |||
chr2:135817966 | C | T | 1 | a0014 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1082G>A | p.Arg361Lys | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/17 | 1097/6273 | 1082/5784 | 361/1927 | chr2 | 135817966 | |||
chr2:135823969 | T | C | 1 | a0012 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.839A>G | p.Asn280Ser | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/17 | 854/6273 | 839/5784 | 280/1927 | chr2 | 135823969 | |||
chr2:135833176 | C | T | 13 | a0003 a0004 a0005 others(10): Show |
137 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(134): Show |
missense_variant | MODERATE | c.655G>A | p.Val219Ile | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/17 | 670/6273 | 655/5784 | 219/1927 | chr2 | 135833176 | |||
chr2:135836601 | G | A | 1 | a0010 | 2 | HG02630.hp1 HG02895.hp1 |
missense_variant | MODERATE | c.569C>T | p.Ser190Leu | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/17 | 584/6273 | 569/5784 | 190/1927 | chr2 | 135836601 | |||
chr2:135836716 | C | T | 3 | a0005 a0014 a0015 |
12 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(9): Show |
missense_variant | MODERATE | c.454G>A | p.Ala152Thr | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/17 | 469/6273 | 454/5784 | 152/1927 | chr2 | 135836716 | |||
chr2:135836869 | T | C | 1 | a0007 | 4 | HG02258.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
missense_variant | MODERATE | c.301A>G | p.Ser101Gly | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/17 | 316/6273 | 301/5784 | 101/1927 | chr2 | 135836869 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135788540 | A | G | 19 | a0001c0001 a0001c0005 a0001c0011 others(16): Show |
161 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(158): Show |
synonymous_variant | LOW | c.5568T>C | p.Ala1856Ala | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 17/17 | 5583/6273 | 5568/5784 | 1856/1927 | chr2 | 135788540 | |||
chr2:135789629 | G | A | 1 | a0003c0029 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.5505C>T | p.Val1835Val | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/17 | 5520/6273 | 5505/5784 | 1835/1927 | chr2 | 135789629 | |||
chr2:135800712 | G | A | 1 | a0002c0040 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.4761C>T | p.Arg1587Arg | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/17 | 4776/6273 | 4761/5784 | 1587/1927 | chr2 | 135800712 | |||
chr2:135803987 | G | A | 23 | a0001c0001 a0001c0011 a0001c0019 others(20): Show |
250 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(247): Show |
synonymous_variant | LOW | c.4606C>T | p.Leu1536Leu | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/17 | 4621/6273 | 4606/5784 | 1536/1927 | chr2 | 135803987 | |||
chr2:135804017 | G | A | 1 | a0003c0030 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.4576C>T | p.Leu1526Leu | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/17 | 4591/6273 | 4576/5784 | 1526/1927 | chr2 | 135804017 | |||
chr2:135804884 | A | G | 1 | a0001c0045 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.4347T>C | p.Phe1449Phe | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 10/17 | 4362/6273 | 4347/5784 | 1449/1927 | chr2 | 135804884 | |||
chr2:135804902 | G | A | 8 | a0001c0038 a0001c0039 a0002c0002 others(5): Show |
98 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(95): Show |
synonymous_variant | LOW | c.4329C>T | p.Gly1443Gly | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 10/17 | 4344/6273 | 4329/5784 | 1443/1927 | chr2 | 135804902 | |||
chr2:135805046 | C | T | 1 | a0001c0044 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.4185G>A | p.Ala1395Ala | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 10/17 | 4200/6273 | 4185/5784 | 1395/1927 | chr2 | 135805046 | |||
chr2:135808750 | C | T | 1 | a0008c0035 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.3597G>A | p.Ala1199Ala | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/17 | 3612/6273 | 3597/5784 | 1199/1927 | chr2 | 135808750 | |||
chr2:135808864 | G | A | 1 | a0001c0047 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.3483C>T | p.Asn1161Asn | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/17 | 3498/6273 | 3483/5784 | 1161/1927 | chr2 | 135808864 | |||
chr2:135809341 | C | T | 1 | a0005c0017 | 3 | HG02559.hp1 HG02970.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.3006G>A | p.Arg1002Arg | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/17 | 3021/6273 | 3006/5784 | 1002/1927 | chr2 | 135809341 | |||
chr2:135809584 | C | T | 3 | a0001c0019 a0003c0013 a0016c0028 |
8 | HG02135.hp2 HG03491.hp2 HG03654.hp1 others(5): Show |
synonymous_variant | LOW | c.2763G>A | p.Ala921Ala | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/17 | 2778/6273 | 2763/5784 | 921/1927 | chr2 | 135809584 | |||
chr2:135809641 | C | T | 1 | a0005c0020 | 2 | HG02615.hp1 HG03209.hp2 |
synonymous_variant | LOW | c.2706G>A | p.Thr902Thr | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/17 | 2721/6273 | 2706/5784 | 902/1927 | chr2 | 135809641 | |||
chr2:135809890 | G | A | 1 | a0003c0033 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.2457C>T | p.His819His | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/17 | 2472/6273 | 2457/5784 | 819/1927 | chr2 | 135809890 | |||
chr2:135817398 | G | C | 5 | a0001c0005 a0001c0042 a0002c0041 others(2): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
synonymous_variant | LOW | c.1650C>G | p.Gly550Gly | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/17 | 1665/6273 | 1650/5784 | 550/1927 | chr2 | 135817398 | |||
chr2:135817629 | G | T | 8 | a0001c0001 a0001c0011 a0001c0044 others(5): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
synonymous_variant | LOW | c.1419C>A | p.Gly473Gly | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/17 | 1434/6273 | 1419/5784 | 473/1927 | chr2 | 135817629 | |||
chr2:135829668 | G | C | 5 | a0001c0005 a0001c0042 a0002c0041 others(2): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
synonymous_variant | LOW | c.729C>G | p.Val243Val | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/17 | 744/6273 | 729/5784 | 243/1927 | chr2 | 135829668 | |||
chr2:135836588 | G | A | 7 | a0001c0001 a0001c0044 a0001c0045 others(4): Show |
111 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(108): Show |
synonymous_variant | LOW | c.582C>T | p.Thr194Thr | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/17 | 597/6273 | 582/5784 | 194/1927 | chr2 | 135836588 | |||
chr2:135836852 | G | A | 1 | a0002c0009 | 7 | HG00741.hp1 HG01256.hp1 HG01928.hp2 others(4): Show |
synonymous_variant | LOW | c.318C>T | p.Asp106Asp | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/17 | 333/6273 | 318/5784 | 106/1927 | chr2 | 135836852 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135787878 | AAC | A | 15 | a0002c0002t0002 a0002c0037t0002 a0003c0003t0002 others(12): Show |
76 | HG00642.hp2 HG00673.hp1 HG00733.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*444_*445delGT | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 17/17 | 444 | chr2 | 135787878 | ||||||
chr2:135787893 | G | A | 1 | a0002c0002t0007 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*431C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 17/17 | 431 | chr2 | 135787893 | ||||||
chr2:135787895 | T | G | 4 | a0001c0019t0004 a0004c0021t0004 a0005c0012t0004 others(1): Show |
8 | HG01433.hp1 HG02818.hp2 HG02896.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*429A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 17/17 | 429 | chr2 | 135787895 | ||||||
chr2:135787999 | C | G | 1 | a0002c0002t0005 | 6 | HG01358.hp1 HG01993.hp1 HG02293.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*325G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 17/17 | 325 | chr2 | 135787999 | ||||||
chr2:135788169 | G | C | 1 | a0001c0001t0008 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*155C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 17/17 | 155 | chr2 | 135788169 | ||||||
chr2:135788197 | A | G | 2 | a0004c0006t0006 a0004c0021t0006 |
3 | HG02630.hp2 HG02965.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*127T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 17/17 | 127 | chr2 | 135788197 | ||||||
chr2:135788274 | C | G | 39 | a0001c0001t0001 a0001c0001t0008 a0001c0005t0001 others(36): Show |
274 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*50G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 17/17 | 50 | chr2 | 135788274 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135788561 | C | T | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5564-17G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/16 | chr2 | 135788561 | |||||||
chr2:135788568 | G | A | 7 | a0006c0010t0002g0054 a0006c0010t0002g0056 a0006c0010t0002g0060 others(4): Show |
7 | HG00735.hp1 HG01358.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.5564-24C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/16 | chr2 | 135788568 | |||||||
chr2:135788581 | C | T | 11 | a0002c0002t0001g0148 a0002c0002t0001g0167 a0002c0002t0001g0178 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.5564-37G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/16 | chr2 | 135788581 | |||||||
chr2:135788642 | G | A | 7 | a0002c0009t0001g0306 a0002c0009t0001g0307 a0002c0009t0001g0308 others(4): Show |
7 | HG00741.hp1 HG01256.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.5564-98C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/16 | chr2 | 135788642 | |||||||
chr2:135788779 | T | C | 1 | a0002c0002t0001g0120 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5564-235A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/16 | chr2 | 135788779 | |||||||
chr2:135789065 | C | T | 84 | a0001c0039t0001g0172 a0001c0042t0001g0047 a0002c0002t0001g0117 others(81): Show |
86 | HG00280.hp2 HG00741.hp1 HG01256.hp1 others(83): Show |
intron_variant | MODIFIER | c.5563+506G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/16 | chr2 | 135789065 | |||||||
chr2:135789163 | G | C | 17 | a0002c0048t0001g0237 a0003c0004t0001g0004 a0003c0004t0001g0013 others(14): Show |
23 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.5563+408C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/16 | chr2 | 135789163 | |||||||
chr2:135789206 | C | T | 17 | a0002c0048t0001g0237 a0003c0004t0001g0004 a0003c0004t0001g0013 others(14): Show |
23 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.5563+365G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/16 | chr2 | 135789206 | |||||||
chr2:135789340 | T | C | 6 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0240 others(3): Show |
6 | HG02895.hp2 HG02897.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.5563+231A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/16 | chr2 | 135789340 | |||||||
chr2:135789357 | C | T | 69 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0136 others(66): Show |
76 | HG00642.hp2 HG00673.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.5563+214G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/16 | chr2 | 135789357 | |||||||
chr2:135789497 | A | G | 64 | a0001c0039t0001g0172 a0001c0042t0001g0047 a0002c0002t0001g0117 others(61): Show |
67 | HG00741.hp1 HG01256.hp1 HG01261.hp1 others(64): Show |
intron_variant | MODIFIER | c.5563+74T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 16/16 | chr2 | 135789497 | |||||||
chr2:135789912 | G | A | 1 | a0002c0037t0002g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5336-114C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 15/16 | chr2 | 135789912 | |||||||
chr2:135789913 | G | A | 11 | a0002c0002t0001g0148 a0002c0002t0001g0167 a0002c0002t0001g0178 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.5336-115C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 15/16 | chr2 | 135789913 | |||||||
chr2:135790388 | G | A | 1 | a0001c0005t0001g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5335+270C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 15/16 | chr2 | 135790388 | |||||||
chr2:135790449 | C | A | 1 | a0015c0027t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5335+209G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 15/16 | chr2 | 135790449 | |||||||
chr2:135790527 | C | A | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5335+131G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 15/16 | chr2 | 135790527 | |||||||
chr2:135790546 | G | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
351 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.5335+112C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 15/16 | chr2 | 135790546 | |||||||
chr2:135790579 | C | T | 2 | a0005c0020t0001g0027 a0005c0020t0001g0029 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5335+79G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 15/16 | chr2 | 135790579 | |||||||
chr2:135790599 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
351 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.5335+59T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 15/16 | chr2 | 135790599 | |||||||
chr2:135790609 | G | C | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5335+49C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 15/16 | chr2 | 135790609 | |||||||
chr2:135790622 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
351 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.5335+36C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 15/16 | chr2 | 135790622 | |||||||
chr2:135790636 | G | T | 11 | a0002c0002t0001g0148 a0002c0002t0001g0167 a0002c0002t0001g0178 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.5335+22C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 15/16 | chr2 | 135790636 | |||||||
chr2:135791128 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.5112-247G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135791128 | |||||||
chr2:135791134 | A | G | 1 | a0003c0007t0001g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5112-253T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135791134 | |||||||
chr2:135791147 | G | A | 3 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 |
3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.5112-266C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135791147 | |||||||
chr2:135791241 | C | T | 3 | a0001c0005t0001g0036 a0002c0041t0001g0044 a0003c0003t0003g0105 |
3 | HG00621.hp1 HG00639.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.5112-360G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135791241 | |||||||
chr2:135791381 | T | C | 4 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5112-500A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135791381 | |||||||
chr2:135791543 | A | G | 1 | a0005c0012t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5112-662T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135791543 | |||||||
chr2:135791561 | GA | G | 72 | a0001c0039t0001g0172 a0001c0042t0001g0047 a0002c0002t0001g0117 others(69): Show |
74 | HG00741.hp1 HG01256.hp1 HG01261.hp1 others(71): Show |
intron_variant | MODIFIER | c.5112-681delT | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135791561 | |||||||
chr2:135792039 | C | T | 1 | a0005c0017t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5112-1158G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135792039 | |||||||
chr2:135792238 | T | C | 1 | a0003c0003t0002g0072 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.5112-1357A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135792238 | |||||||
chr2:135792247 | C | G | 1 | a0005c0012t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5112-1366G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135792247 | |||||||
chr2:135792254 | G | C | 5 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 others(2): Show |
5 | HG01433.hp1 HG02818.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.5112-1373C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135792254 | |||||||
chr2:135792418 | G | A | 1 | a0002c0002t0001g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.5112-1537C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135792418 | |||||||
chr2:135792539 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
123 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.5112-1658G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135792539 | |||||||
chr2:135792767 | A | G | 1 | a0002c0037t0002g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5111+1874T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135792767 | |||||||
chr2:135792928 | G | A | 2 | a0005c0020t0001g0027 a0005c0020t0001g0029 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5111+1713C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135792928 | |||||||
chr2:135792935 | G | A | 2 | a0003c0004t0001g0206 a0003c0004t0001g0207 |
2 | HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.5111+1706C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135792935 | |||||||
chr2:135793107 | A | G | 2 | a0005c0020t0001g0027 a0005c0020t0001g0029 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5111+1534T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793107 | |||||||
chr2:135793113 | G | A | 1 | a0005c0012t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5111+1528C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793113 | |||||||
chr2:135793172 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5111+1469G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793172 | |||||||
chr2:135793174 | G | A | 1 | a0003c0007t0001g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5111+1467C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793174 | |||||||
chr2:135793236 | G | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
351 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.5111+1405C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793236 | |||||||
chr2:135793297 | CT | C | 8 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 others(5): Show |
8 | HG01433.hp1 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.5111+1343delA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793297 | |||||||
chr2:135793300 | T | C | 8 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 others(5): Show |
8 | HG01433.hp1 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.5111+1341A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793300 | |||||||
chr2:135793545 | G | C | 2 | a0005c0020t0001g0027 a0005c0020t0001g0029 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5111+1096C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793545 | |||||||
chr2:135793643 | A | G | 4 | a0005c0012t0004g0022 a0005c0012t0004g0023 a0005c0012t0004g0025 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5111+998T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793643 | |||||||
chr2:135793737 | T | G | 1 | a0005c0012t0004g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5111+904A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793737 | |||||||
chr2:135793967 | A | T | 70 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0136 others(67): Show |
77 | HG00280.hp2 HG00642.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.5111+674T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793967 | |||||||
chr2:135793971 | CA | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
224 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.5111+669delT | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135793971 | |||||||
chr2:135794008 | T | C | 1 | a0001c0011t0001g0131 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5111+633A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135794008 | |||||||
chr2:135794012 | C | T | 1 | a0003c0003t0002g0075 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.5111+629G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135794012 | |||||||
chr2:135794063 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.5111+578G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135794063 | |||||||
chr2:135794124 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
125 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.5111+517G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135794124 | |||||||
chr2:135794150 | T | A | 1 | a0002c0002t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.5111+491A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135794150 | |||||||
chr2:135794150 | T | TAAAATA | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
350 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(347): Show |
intron_variant | MODIFIER | c.5111+485_5111+490d others(8): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135794150 | |||||||
chr2:135794428 | T | C | 2 | a0005c0020t0001g0027 a0005c0020t0001g0029 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5111+213A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135794428 | |||||||
chr2:135794618 | G | A | 70 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0136 others(67): Show |
77 | HG00280.hp2 HG00642.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.5111+23C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 14/16 | chr2 | 135794618 | |||||||
chr2:135794801 | A | G | 34 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0136 others(31): Show |
39 | HG00673.hp1 HG00738.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.4977-26T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135794801 | |||||||
chr2:135794841 | T | C | 1 | a0003c0003t0002g0090 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4977-66A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135794841 | |||||||
chr2:135794894 | G | A | 1 | a0002c0002t0001g0145 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4977-119C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135794894 | |||||||
chr2:135794947 | G | A | 71 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0136 others(68): Show |
78 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.4977-172C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135794947 | |||||||
chr2:135794956 | A | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
273 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.4977-181T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135794956 | |||||||
chr2:135794974 | G | C | 1 | a0003c0003t0002g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4977-199C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135794974 | |||||||
chr2:135794981 | T | G | 1 | a0014c0025t0004g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4977-206A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135794981 | |||||||
chr2:135795006 | C | G | 1 | a0001c0001t0001g0243 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4977-231G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795006 | |||||||
chr2:135795033 | A | ACG | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
326 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.4977-260_4977-259d others(4): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795033 | |||||||
chr2:135795045 | G | GCA | 10 | a0002c0002t0003g0106 a0002c0002t0003g0107 a0002c0002t0003g0110 others(7): Show |
10 | HG02258.hp1 HG02965.hp2 HG03516.hp2 others(7): Show |
intron_variant | MODIFIER | c.4977-272_4977-271d others(4): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795045 | |||||||
chr2:135795045 | G | GCGCA | 19 | a0001c0001t0001g0245 a0001c0001t0001g0257 a0001c0001t0001g0262 others(16): Show |
19 | HG00735.hp1 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.4977-271_4977-270i others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795045 | |||||||
chr2:135795047 | A | G | 3 | a0003c0003t0002g0075 a0003c0003t0003g0105 a0005c0026t0002g0028 |
3 | HG00639.hp1 HG01123.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4977-272T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795047 | |||||||
chr2:135795059 | A | T | 72 | a0001c0001t0001g0259 a0001c0039t0001g0172 a0001c0042t0001g0047 others(69): Show |
74 | HG00741.hp1 HG01256.hp1 HG01261.hp1 others(71): Show |
intron_variant | MODIFIER | c.4977-284T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795059 | |||||||
chr2:135795133 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4977-358T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795133 | |||||||
chr2:135795213 | AT | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
351 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(348): Show |
intron_variant | MODIFIER | c.4977-439delA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795213 | |||||||
chr2:135795452 | G | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
273 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.4977-677C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795452 | |||||||
chr2:135795535 | G | A | 3 | a0002c0002t0001g0117 a0002c0002t0001g0126 a0002c0002t0001g0152 |
3 | HG01261.hp1 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4977-760C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795535 | |||||||
chr2:135795604 | C | CTAA | 27 | a0002c0037t0002g0123 a0003c0003t0001g0074 a0003c0003t0002g0008 others(24): Show |
29 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.4977-832_4977-830d others(5): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795604 | |||||||
chr2:135795604 | C | CTAATAA | 31 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0136 others(28): Show |
34 | HG00673.hp1 HG00738.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.4977-835_4977-830d others(8): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795604 | |||||||
chr2:135795604 | C | CTAATAAT others(2): Show |
8 | a0003c0003t0002g0005 a0003c0003t0002g0057 a0003c0003t0002g0066 others(5): Show |
10 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.4977-838_4977-830d others(11): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795604 | |||||||
chr2:135795604 | C | CTAATAAT others(2): Show |
24 | a0002c0002t0001g0118 a0002c0002t0001g0124 a0002c0002t0001g0127 others(21): Show |
24 | HG00741.hp1 HG01256.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.4977-830_4977-829i others(11): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795604 | |||||||
chr2:135795604 | C | CTAATAAT others(5): Show |
26 | a0001c0039t0001g0172 a0001c0042t0001g0047 a0002c0002t0001g0121 others(23): Show |
28 | HG01952.hp1 HG01978.hp1 HG01981.hp2 others(25): Show |
intron_variant | MODIFIER | c.4977-830_4977-829i others(14): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795604 | |||||||
chr2:135795604 | C | CTAATAAT others(8): Show |
14 | a0002c0002t0001g0139 a0002c0002t0001g0140 a0002c0002t0001g0141 others(11): Show |
14 | HG01993.hp1 HG02280.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.4977-830_4977-829i others(17): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795604 | |||||||
chr2:135795604 | C | CTAATAAT others(11): Show |
5 | a0002c0002t0001g0117 a0002c0002t0001g0157 a0002c0002t0001g0186 others(2): Show |
5 | HG01261.hp1 HG01346.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.4977-830_4977-829i others(20): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795604 | |||||||
chr2:135795604 | C | CTAATAAT others(14): Show |
1 | a0002c0002t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4977-830_4977-829i others(23): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795604 | |||||||
chr2:135795609 | A | AATT | 26 | a0001c0001t0001g0246 a0001c0011t0001g0200 a0002c0002t0003g0106 others(23): Show |
32 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.4977-835_4977-834i others(5): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795609 | |||||||
chr2:135795612 | A | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
164 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.4977-837T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795612 | |||||||
chr2:135795615 | A | T | 2 | a0001c0001t0001g0246 a0001c0011t0001g0200 |
2 | HG00423.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.4977-840T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795615 | |||||||
chr2:135795618 | A | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
126 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.4977-843T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795618 | |||||||
chr2:135795753 | T | A | 22 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.4977-978A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795753 | |||||||
chr2:135795795 | C | T | 2 | a0002c0002t0001g0122 a0003c0030t0002g0049 |
2 | HG01243.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.4977-1020G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795795 | |||||||
chr2:135795868 | C | T | 83 | a0001c0039t0001g0172 a0001c0042t0001g0047 a0002c0002t0001g0117 others(80): Show |
85 | HG00741.hp1 HG01256.hp1 HG01261.hp1 others(82): Show |
intron_variant | MODIFIER | c.4977-1093G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795868 | |||||||
chr2:135795959 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
184 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.4977-1184G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135795959 | |||||||
chr2:135796069 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
123 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.4977-1294C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796069 | |||||||
chr2:135796098 | G | A | 4 | a0007c0016t0003g0313 a0007c0016t0003g0314 a0007c0016t0003g0315 others(1): Show |
4 | HG02258.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.4977-1323C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796098 | |||||||
chr2:135796171 | G | A | 4 | a0007c0016t0003g0313 a0007c0016t0003g0314 a0007c0016t0003g0315 others(1): Show |
4 | HG02258.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.4977-1396C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796171 | |||||||
chr2:135796209 | G | A | 1 | a0002c0002t0001g0150 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4977-1434C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796209 | |||||||
chr2:135796355 | C | T | 83 | a0001c0039t0001g0172 a0001c0042t0001g0047 a0002c0002t0001g0117 others(80): Show |
85 | HG00741.hp1 HG01256.hp1 HG01261.hp1 others(82): Show |
intron_variant | MODIFIER | c.4977-1580G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796355 | |||||||
chr2:135796471 | C | T | 4 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.4976+1558G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796471 | |||||||
chr2:135796550 | T | C | 1 | a0002c0002t0001g0120 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4976+1479A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796550 | |||||||
chr2:135796627 | C | G | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4976+1402G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796627 | |||||||
chr2:135796737 | G | A | 1 | a0002c0048t0001g0237 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4976+1292C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796737 | |||||||
chr2:135796907 | T | C | 4 | a0003c0003t0002g0066 a0003c0003t0002g0072 a0003c0003t0002g0073 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.4976+1122A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796907 | |||||||
chr2:135796929 | G | A | 20 | a0002c0002t0001g0118 a0002c0002t0001g0120 a0002c0002t0001g0124 others(17): Show |
20 | HG00741.hp1 HG01256.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.4976+1100C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796929 | |||||||
chr2:135796941 | A | AT | 46 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0240 others(43): Show |
46 | HG01123.hp1 HG01433.hp1 HG01978.hp1 others(43): Show |
intron_variant | MODIFIER | c.4976+1087dupA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796941 | |||||||
chr2:135796941 | A | ATT | 21 | a0001c0001t0001g0257 a0001c0001t0001g0263 a0001c0001t0001g0298 others(18): Show |
27 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.4976+1086_4976+108 others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796941 | |||||||
chr2:135796941 | AT | A | 58 | a0001c0001t0001g0296 a0001c0011t0001g0180 a0002c0002t0002g0134 others(55): Show |
64 | HG00639.hp1 HG00642.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.4976+1087delA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796941 | |||||||
chr2:135796941 | ATT | A | 9 | a0002c0002t0002g0136 a0002c0037t0002g0123 a0003c0003t0001g0074 others(6): Show |
9 | HG00280.hp2 HG00735.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.4976+1086_4976+108 others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796941 | |||||||
chr2:135796987 | G | A | 4 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 others(1): Show |
4 | HG01433.hp1 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.4976+1042C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135796987 | |||||||
chr2:135797227 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
270 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(267): Show |
intron_variant | MODIFIER | c.4976+802A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797227 | |||||||
chr2:135797230 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
126 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.4976+799C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797230 | |||||||
chr2:135797320 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
272 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.4976+709C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797320 | |||||||
chr2:135797423 | C | G | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4976+606G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797423 | |||||||
chr2:135797451 | G | A | 3 | a0005c0020t0001g0027 a0005c0020t0001g0029 a0005c0026t0002g0028 |
3 | HG02615.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4976+578C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797451 | |||||||
chr2:135797484 | A | G | 4 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.4976+545T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797484 | |||||||
chr2:135797658 | A | C | 16 | a0002c0048t0001g0237 a0003c0004t0001g0004 a0003c0004t0001g0013 others(13): Show |
22 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.4976+371T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797658 | |||||||
chr2:135797861 | C | A | 1 | a0008c0022t0003g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4976+168G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797861 | |||||||
chr2:135797914 | T | C | 132 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(129): Show |
136 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.4976+115A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797914 | |||||||
chr2:135797955 | T | G | 65 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0136 others(62): Show |
71 | HG00280.hp2 HG00642.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.4976+74A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797955 | |||||||
chr2:135797973 | A | T | 2 | a0003c0003t0002g0010 a0003c0003t0002g0100 |
3 | HG00642.hp2 NA20805.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.4976+56T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797973 | |||||||
chr2:135797988 | C | T | 1 | a0002c0037t0002g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4976+41G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 13/16 | chr2 | 135797988 | |||||||
chr2:135798387 | G | A | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.4867-249C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135798387 | |||||||
chr2:135798457 | C | T | 3 | a0002c0002t0001g0121 a0002c0002t0001g0143 a0002c0002t0001g0169 |
3 | NA18963.hp2 NA19058.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.4867-319G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135798457 | |||||||
chr2:135798497 | C | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(293): Show |
346 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(343): Show |
intron_variant | MODIFIER | c.4867-359G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135798497 | |||||||
chr2:135798612 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
289 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(286): Show |
intron_variant | MODIFIER | c.4867-474A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135798612 | |||||||
chr2:135798910 | G | A | 63 | a0003c0003t0002g0005 a0003c0003t0002g0008 a0003c0003t0002g0009 others(60): Show |
70 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.4867-772C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135798910 | |||||||
chr2:135799235 | C | T | 100 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 others(97): Show |
102 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(99): Show |
intron_variant | MODIFIER | c.4867-1097G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135799235 | |||||||
chr2:135799239 | G | A | 1 | a0003c0003t0002g0067 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4867-1101C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135799239 | |||||||
chr2:135799337 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4867-1199A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135799337 | |||||||
chr2:135799581 | T | C | 1 | a0002c0002t0001g0182 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.4866+1026A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135799581 | |||||||
chr2:135799749 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
127 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.4866+858G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135799749 | |||||||
chr2:135799974 | A | G | 2 | a0002c0002t0003g0108 a0002c0002t0003g0112 |
2 | HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.4866+633T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135799974 | |||||||
chr2:135800261 | G | A | 2 | a0003c0004t0001g0208 a0003c0004t0001g0213 |
2 | NA18981.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.4866+346C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135800261 | |||||||
chr2:135800538 | A | G | 3 | a0002c0002t0001g0121 a0002c0002t0001g0143 a0002c0002t0001g0169 |
3 | NA18963.hp2 NA19058.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.4866+69T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135800538 | |||||||
chr2:135800587 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
127 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.4866+20G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 12/16 | chr2 | 135800587 | |||||||
chr2:135800883 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4664-74G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135800883 | |||||||
chr2:135801161 | G | A | 16 | a0002c0048t0001g0237 a0003c0004t0001g0004 a0003c0004t0001g0013 others(13): Show |
22 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.4664-352C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135801161 | |||||||
chr2:135801437 | A | G | 3 | a0005c0012t0004g0022 a0005c0012t0004g0023 a0005c0012t0004g0025 |
3 | HG02896.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4664-628T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135801437 | |||||||
chr2:135801718 | C | G | 1 | a0003c0003t0002g0072 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4664-909G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135801718 | |||||||
chr2:135801869 | C | T | 2 | a0009c0018t0001g0214 a0009c0018t0001g0215 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4664-1060G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135801869 | |||||||
chr2:135802028 | T | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.4664-1219A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802028 | |||||||
chr2:135802169 | G | A | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4664-1360C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802169 | |||||||
chr2:135802271 | T | G | 14 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(11): Show |
14 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.4664-1462A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802271 | |||||||
chr2:135802433 | T | C | 96 | a0001c0038t0001g0166 a0001c0039t0001g0172 a0002c0002t0001g0117 others(93): Show |
98 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(95): Show |
intron_variant | MODIFIER | c.4663+1497A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802433 | |||||||
chr2:135802556 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4663+1374G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802556 | |||||||
chr2:135802578 | G | A | 16 | a0002c0048t0001g0237 a0003c0004t0001g0004 a0003c0004t0001g0013 others(13): Show |
22 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.4663+1352C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802578 | |||||||
chr2:135802676 | A | C | 1 | a0002c0002t0003g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4663+1254T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802676 | |||||||
chr2:135802726 | G | A | 1 | a0005c0012t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4663+1204C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802726 | |||||||
chr2:135802747 | C | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
360 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(357): Show |
intron_variant | MODIFIER | c.4663+1183G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802747 | |||||||
chr2:135802796 | G | T | 1 | a0002c0002t0001g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4663+1134C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802796 | |||||||
chr2:135802882 | C | T | 2 | a0002c0008t0001g0132 a0002c0008t0001g0133 |
2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.4663+1048G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802882 | |||||||
chr2:135802886 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4663+1044G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802886 | |||||||
chr2:135802894 | C | T | 64 | a0003c0003t0001g0074 a0003c0003t0002g0005 a0003c0003t0002g0008 others(61): Show |
71 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.4663+1036G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802894 | |||||||
chr2:135802896 | G | A | 3 | a0005c0017t0001g0020 a0005c0017t0001g0021 a0005c0017t0001g0031 |
3 | HG02559.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.4663+1034C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135802896 | |||||||
chr2:135803048 | G | A | 2 | a0005c0020t0001g0027 a0005c0020t0001g0029 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4663+882C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135803048 | |||||||
chr2:135803191 | C | G | 88 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(85): Show |
97 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.4663+739G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135803191 | |||||||
chr2:135803191 | C | T | 1 | a0005c0017t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4663+739G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135803191 | |||||||
chr2:135803627 | C | T | 6 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0240 others(3): Show |
6 | HG02895.hp2 HG02897.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.4663+303G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135803627 | |||||||
chr2:135803641 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4663+289C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135803641 | |||||||
chr2:135803908 | A | G | 1 | a0002c0002t0005g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4663+22T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 11/16 | chr2 | 135803908 | |||||||
chr2:135804165 | G | A | 88 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(85): Show |
97 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.4465-37C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 10/16 | chr2 | 135804165 | |||||||
chr2:135804604 | C | T | 3 | a0002c0002t0001g0117 a0002c0002t0001g0126 a0002c0002t0001g0152 |
3 | HG01261.hp1 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4464+163G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 10/16 | chr2 | 135804604 | |||||||
chr2:135804634 | C | T | 1 | a0005c0026t0002g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4464+133G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 10/16 | chr2 | 135804634 | |||||||
chr2:135804709 | C | G | 7 | a0006c0010t0002g0054 a0006c0010t0002g0056 a0006c0010t0002g0060 others(4): Show |
7 | HG00735.hp1 HG01358.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.4464+58G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 10/16 | chr2 | 135804709 | |||||||
chr2:135804750 | G | T | 1 | a0001c0001t0001g0287 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4464+17C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 10/16 | chr2 | 135804750 | |||||||
chr2:135805087 | G | A | 1 | a0002c0048t0001g0237 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4174-30C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135805087 | |||||||
chr2:135805146 | C | T | 9 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.4174-89G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135805146 | |||||||
chr2:135805239 | C | T | 4 | a0005c0012t0004g0022 a0005c0012t0004g0023 a0005c0012t0004g0025 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.4174-182G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135805239 | |||||||
chr2:135805243 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.4174-186A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135805243 | |||||||
chr2:135805306 | C | A | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.4174-249G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135805306 | |||||||
chr2:135805358 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
361 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(358): Show |
intron_variant | MODIFIER | c.4174-301A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135805358 | |||||||
chr2:135805360 | C | T | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4174-303G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135805360 | |||||||
chr2:135805613 | C | G | 1 | a0001c0001t0001g0274 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.4174-556G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135805613 | |||||||
chr2:135805678 | G | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
263 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.4174-621C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135805678 | |||||||
chr2:135805713 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.4174-656G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135805713 | |||||||
chr2:135805714 | A | T | 27 | a0002c0002t0001g0118 a0002c0002t0001g0120 a0002c0002t0001g0124 others(24): Show |
27 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.4174-657T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135805714 | |||||||
chr2:135806085 | G | A | 1 | a0005c0012t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4174-1028C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135806085 | |||||||
chr2:135806155 | T | G | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.4173+973A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135806155 | |||||||
chr2:135806218 | C | T | 1 | a0003c0004t0001g0204 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4173+910G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135806218 | |||||||
chr2:135806242 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.4173+886T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135806242 | |||||||
chr2:135806552 | AGTACCC | A | 7 | a0005c0012t0001g0030 a0005c0017t0001g0020 a0005c0017t0001g0021 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.4173+570_4173+575d others(8): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135806552 | |||||||
chr2:135806709 | G | A | 2 | a0005c0020t0001g0027 a0005c0020t0001g0029 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4173+419C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135806709 | |||||||
chr2:135806866 | C | T | 1 | a0003c0004t0001g0013 | 2 | NA18957.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.4173+262G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135806866 | |||||||
chr2:135806924 | G | A | 16 | a0002c0048t0001g0237 a0003c0004t0001g0004 a0003c0004t0001g0013 others(13): Show |
22 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.4173+204C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135806924 | |||||||
chr2:135807030 | TC | T | 14 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(11): Show |
14 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.4173+97delG | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135807030 | |||||||
chr2:135807033 | C | T | 14 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(11): Show |
14 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.4173+95G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135807033 | |||||||
chr2:135807119 | ACTC | A | 3 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 |
3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
splice_region_variant&intron_variant | LOW | c.4173+6_4173+8delGA others(1): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 9/16 | chr2 | 135807119 | |||||||
chr2:135807458 | C | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.3905-62G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/16 | chr2 | 135807458 | |||||||
chr2:135807758 | G | A | 100 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 others(97): Show |
102 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(99): Show |
intron_variant | MODIFIER | c.3905-362C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/16 | chr2 | 135807758 | |||||||
chr2:135807787 | C | T | 1 | a0001c0019t0004g0032 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3905-391G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/16 | chr2 | 135807787 | |||||||
chr2:135807806 | CA | C | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
363 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(360): Show |
intron_variant | MODIFIER | c.3905-411delT | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/16 | chr2 | 135807806 | |||||||
chr2:135808052 | G | T | 3 | a0002c0002t0001g0117 a0002c0002t0001g0126 a0002c0002t0001g0152 |
3 | HG01261.hp1 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3904+391C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/16 | chr2 | 135808052 | |||||||
chr2:135808331 | C | A | 4 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3904+112G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 8/16 | chr2 | 135808331 | |||||||
chr2:135810063 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.2354-70T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135810063 | |||||||
chr2:135810143 | C | A | 1 | a0001c0005t0001g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2354-150G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135810143 | |||||||
chr2:135810171 | A | C | 1 | a0001c0005t0001g0042 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2354-178T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135810171 | |||||||
chr2:135810230 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2354-237A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135810230 | |||||||
chr2:135810271 | G | A | 16 | a0002c0048t0001g0237 a0003c0004t0001g0004 a0003c0004t0001g0013 others(13): Show |
22 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.2354-278C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135810271 | |||||||
chr2:135810572 | T | G | 3 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 |
3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2354-579A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135810572 | |||||||
chr2:135810728 | G | GA | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
311 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.2354-736dupT | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135810728 | |||||||
chr2:135810728 | G | GAA | 17 | a0002c0002t0005g0116 a0002c0048t0001g0237 a0003c0004t0001g0004 others(14): Show |
23 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.2354-737_2354-736d others(4): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135810728 | |||||||
chr2:135810888 | G | A | 3 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 |
3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2354-895C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135810888 | |||||||
chr2:135811125 | G | C | 1 | a0002c0002t0001g0122 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2354-1132C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135811125 | |||||||
chr2:135811209 | T | A | 1 | a0003c0003t0002g0008 | 2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2353+1102A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135811209 | |||||||
chr2:135811249 | T | C | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2353+1062A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135811249 | |||||||
chr2:135811701 | TA | T | 64 | a0001c0001t0001g0250 a0001c0001t0001g0253 a0001c0001t0001g0289 others(61): Show |
72 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2353+609delT | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135811701 | |||||||
chr2:135811747 | G | A | 10 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2353+564C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135811747 | |||||||
chr2:135811766 | T | C | 22 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.2353+545A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135811766 | |||||||
chr2:135811788 | TAAG | T | 15 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(12): Show |
15 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2353+520_2353+522d others(5): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135811788 | |||||||
chr2:135811816 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2353+495G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135811816 | |||||||
chr2:135812278 | C | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(80): Show |
116 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.2353+33G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 7/16 | chr2 | 135812278 | |||||||
chr2:135813043 | A | T | 95 | a0001c0038t0001g0166 a0001c0039t0001g0172 a0002c0002t0001g0117 others(92): Show |
97 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.1708-87T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135813043 | |||||||
chr2:135813180 | T | C | 8 | a0004c0006t0001g0015 a0004c0006t0001g0016 a0004c0006t0001g0221 others(5): Show |
10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1708-224A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135813180 | |||||||
chr2:135813226 | TAACAATG others(10): Show |
T | 16 | a0002c0048t0001g0237 a0003c0004t0001g0004 a0003c0004t0001g0013 others(13): Show |
22 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1708-287_1708-271d others(19): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135813226 | |||||||
chr2:135813391 | G | T | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1708-435C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135813391 | |||||||
chr2:135813554 | T | C | 1 | a0005c0026t0002g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1708-598A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135813554 | |||||||
chr2:135813973 | C | T | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1708-1017G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135813973 | |||||||
chr2:135814143 | C | T | 1 | a0003c0004t0001g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1708-1187G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814143 | |||||||
chr2:135814235 | T | C | 1 | a0003c0004t0001g0210 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1708-1279A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814235 | |||||||
chr2:135814246 | C | A | 3 | a0002c0002t0001g0156 a0002c0002t0001g0158 a0002c0002t0001g0159 |
3 | NA18972.hp1 NA18982.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1708-1290G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814246 | |||||||
chr2:135814252 | T | C | 22 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1708-1296A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814252 | |||||||
chr2:135814261 | T | C | 1 | a0003c0003t0002g0090 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1708-1305A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814261 | |||||||
chr2:135814282 | G | T | 81 | a0002c0037t0002g0123 a0003c0003t0001g0074 a0003c0003t0002g0005 others(78): Show |
88 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.1708-1326C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814282 | |||||||
chr2:135814306 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1708-1350A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814306 | |||||||
chr2:135814389 | T | A | 1 | a0003c0007t0001g0053 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1708-1433A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814389 | |||||||
chr2:135814412 | T | A | 95 | a0001c0038t0001g0166 a0001c0039t0001g0172 a0002c0002t0001g0117 others(92): Show |
97 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.1708-1456A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814412 | |||||||
chr2:135814427 | T | A | 1 | a0003c0007t0001g0053 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1708-1471A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814427 | |||||||
chr2:135814521 | C | CT | 10 | a0005c0012t0001g0030 a0005c0012t0004g0022 a0005c0012t0004g0023 others(7): Show |
10 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1708-1566dupA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814521 | |||||||
chr2:135814548 | C | T | 19 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 others(16): Show |
25 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1708-1592G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814548 | |||||||
chr2:135814549 | G | T | 2 | a0005c0020t0001g0027 a0005c0020t0001g0029 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1708-1593C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814549 | |||||||
chr2:135814572 | A | C | 1 | a0003c0007t0001g0053 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1708-1616T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814572 | |||||||
chr2:135814578 | G | A | 1 | a0013c0031t0002g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1708-1622C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814578 | |||||||
chr2:135814715 | C | G | 65 | a0002c0037t0002g0123 a0003c0003t0001g0074 a0003c0003t0002g0005 others(62): Show |
72 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1708-1759G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814715 | |||||||
chr2:135814744 | T | C | 1 | a0016c0028t0002g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1708-1788A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814744 | |||||||
chr2:135814758 | G | A | 1 | a0003c0004t0001g0211 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1708-1802C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135814758 | |||||||
chr2:135815300 | G | T | 19 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 others(16): Show |
25 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1707+2041C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135815300 | |||||||
chr2:135815376 | TACA | T | 10 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1707+1962_1707+196 others(7): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135815376 | |||||||
chr2:135815634 | G | A | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1707+1707C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135815634 | |||||||
chr2:135815682 | G | GTAT | 77 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 others(74): Show |
79 | HG01261.hp1 HG01346.hp1 HG01358.hp1 others(76): Show |
intron_variant | MODIFIER | c.1707+1656_1707+165 others(7): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135815682 | |||||||
chr2:135815682 | G | GTATTAT | 22 | a0002c0002t0001g0118 a0002c0002t0001g0120 a0002c0002t0001g0150 others(19): Show |
22 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1707+1653_1707+165 others(10): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135815682 | |||||||
chr2:135815694 | T | A | 1 | a0016c0028t0002g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1707+1647A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135815694 | |||||||
chr2:135815824 | C | T | 22 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1707+1517G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135815824 | |||||||
chr2:135815840 | C | T | 3 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 |
3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1707+1501G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135815840 | |||||||
chr2:135815845 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.1707+1496T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135815845 | |||||||
chr2:135815996 | C | T | 3 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0160 |
3 | HG01952.hp1 HG01978.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1707+1345G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135815996 | |||||||
chr2:135816001 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1707+1340C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816001 | |||||||
chr2:135816059 | A | G | 13 | a0002c0002t0003g0106 a0002c0002t0003g0107 a0002c0002t0003g0108 others(10): Show |
13 | HG01358.hp1 HG01993.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.1707+1282T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816059 | |||||||
chr2:135816252 | C | T | 1 | a0016c0028t0002g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1707+1089G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816252 | |||||||
chr2:135816253 | T | C | 1 | a0016c0028t0002g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1707+1088A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816253 | |||||||
chr2:135816464 | G | A | 1 | a0016c0028t0002g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1707+877C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816464 | |||||||
chr2:135816599 | A | G | 1 | a0002c0037t0002g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1707+742T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816599 | |||||||
chr2:135816689 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1707+652T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816689 | |||||||
chr2:135816735 | A | G | 95 | a0001c0038t0001g0166 a0001c0039t0001g0172 a0002c0002t0001g0117 others(92): Show |
97 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.1707+606T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816735 | |||||||
chr2:135816778 | C | T | 1 | a0002c0002t0001g0146 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1707+563G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816778 | |||||||
chr2:135816844 | G | T | 1 | a0003c0003t0002g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1707+497C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816844 | |||||||
chr2:135816871 | A | AT | 21 | a0002c0048t0001g0237 a0003c0004t0001g0004 a0003c0004t0001g0013 others(18): Show |
27 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1707+469dupA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816871 | |||||||
chr2:135816871 | AT | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(70): Show |
106 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1707+469delA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816871 | |||||||
chr2:135816872 | T | A | 1 | a0003c0007t0001g0053 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1707+469A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816872 | |||||||
chr2:135816886 | T | G | 22 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1707+455A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816886 | |||||||
chr2:135816893 | G | C | 22 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1707+448C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816893 | |||||||
chr2:135816993 | T | A | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1707+348A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135816993 | |||||||
chr2:135817043 | AT | A | 95 | a0001c0038t0001g0166 a0001c0039t0001g0172 a0002c0002t0001g0117 others(92): Show |
97 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.1707+297delA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135817043 | |||||||
chr2:135817068 | G | A | 1 | a0001c0005t0001g0041 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1707+273C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135817068 | |||||||
chr2:135817090 | C | T | 1 | a0015c0027t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1707+251G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 6/16 | chr2 | 135817090 | |||||||
chr2:135818104 | C | T | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.987-43G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135818104 | |||||||
chr2:135818178 | A | C | 9 | a0003c0003t0002g0005 a0003c0003t0002g0011 a0003c0003t0002g0057 others(6): Show |
12 | HG00738.hp1 HG01496.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.987-117T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135818178 | |||||||
chr2:135818317 | C | A | 22 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.987-256G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135818317 | |||||||
chr2:135818483 | C | G | 3 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0018c0032t0001g0217 |
3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.987-422G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135818483 | |||||||
chr2:135818533 | G | A | 1 | a0001c0045t0001g0234 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.987-472C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135818533 | |||||||
chr2:135818575 | C | T | 1 | a0005c0012t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.987-514G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135818575 | |||||||
chr2:135818596 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
205 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.987-535A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135818596 | |||||||
chr2:135818793 | C | T | 23 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(20): Show |
25 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.987-732G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135818793 | |||||||
chr2:135818829 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.987-768G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135818829 | |||||||
chr2:135818855 | G | A | 10 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.987-794C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135818855 | |||||||
chr2:135819007 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(81): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.987-946A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819007 | |||||||
chr2:135819009 | C | G | 10 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.987-948G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819009 | |||||||
chr2:135819102 | C | G | 1 | a0001c0001t0001g0250 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.987-1041G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819102 | |||||||
chr2:135819122 | A | C | 1 | a0016c0028t0002g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.987-1061T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819122 | |||||||
chr2:135819172 | T | A | 1 | a0001c0005t0001g0041 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.987-1111A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819172 | |||||||
chr2:135819615 | C | T | 1 | a0001c0005t0001g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.987-1554G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819615 | |||||||
chr2:135819700 | G | A | 1 | a0001c0045t0001g0234 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.987-1639C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819700 | |||||||
chr2:135819740 | G | A | 11 | a0005c0012t0001g0030 a0005c0012t0004g0022 a0005c0012t0004g0023 others(8): Show |
11 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.987-1679C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819740 | |||||||
chr2:135819753 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.987-1692C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819753 | |||||||
chr2:135819761 | G | A | 1 | a0002c0002t0001g0142 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.987-1700C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819761 | |||||||
chr2:135819776 | C | T | 5 | a0002c0037t0002g0123 a0003c0003t0002g0066 a0003c0003t0002g0072 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.987-1715G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819776 | |||||||
chr2:135819992 | G | T | 1 | a0002c0002t0001g0181 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.987-1931C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135819992 | |||||||
chr2:135820082 | G | A | 1 | a0002c0048t0001g0237 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.986+1938C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820082 | |||||||
chr2:135820147 | T | C | 26 | a0003c0003t0002g0005 a0003c0003t0002g0009 a0003c0003t0002g0011 others(23): Show |
31 | HG00738.hp1 HG01433.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.986+1873A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820147 | |||||||
chr2:135820241 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.986+1779A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820241 | |||||||
chr2:135820274 | C | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.986+1746G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820274 | |||||||
chr2:135820340 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.986+1680G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820340 | |||||||
chr2:135820470 | A | G | 95 | a0001c0038t0001g0166 a0001c0039t0001g0172 a0002c0002t0001g0117 others(92): Show |
97 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.986+1550T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820470 | |||||||
chr2:135820624 | A | C | 95 | a0001c0038t0001g0166 a0001c0039t0001g0172 a0002c0002t0001g0117 others(92): Show |
97 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.986+1396T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820624 | |||||||
chr2:135820783 | T | C | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.986+1237A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820783 | |||||||
chr2:135820882 | A | G | 1 | a0002c0048t0001g0237 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.986+1138T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820882 | |||||||
chr2:135820883 | A | AT | 9 | a0002c0002t0001g0167 a0002c0002t0001g0181 a0003c0003t0002g0009 others(6): Show |
10 | HG02083.hp1 HG02818.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.986+1136dupA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820883 | |||||||
chr2:135820963 | C | A | 2 | a0003c0013t0002g0194 a0003c0013t0002g0195 |
2 | NA18943.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.986+1057G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820963 | |||||||
chr2:135820966 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
118 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.986+1054A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135820966 | |||||||
chr2:135821102 | C | T | 1 | a0003c0004t0001g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.986+918G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821102 | |||||||
chr2:135821117 | G | A | 2 | a0003c0003t0002g0069 a0003c0003t0002g0086 |
2 | NA18968.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.986+903C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821117 | |||||||
chr2:135821125 | C | T | 4 | a0003c0003t0002g0051 a0003c0003t0002g0052 a0010c0024t0002g0304 others(1): Show |
4 | HG02109.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.986+895G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821125 | |||||||
chr2:135821133 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.986+887T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821133 | |||||||
chr2:135821202 | C | T | 15 | a0003c0004t0001g0004 a0003c0004t0001g0013 a0003c0004t0001g0014 others(12): Show |
21 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.986+818G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821202 | |||||||
chr2:135821274 | C | A | 1 | a0003c0003t0002g0012 | 2 | NA18998.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.986+746G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821274 | |||||||
chr2:135821296 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.986+724T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821296 | |||||||
chr2:135821319 | A | G | 4 | a0003c0003t0002g0051 a0003c0003t0002g0052 a0010c0024t0002g0304 others(1): Show |
4 | HG02109.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.986+701T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821319 | |||||||
chr2:135821549 | C | T | 1 | a0003c0030t0002g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.986+471G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821549 | |||||||
chr2:135821638 | G | A | 4 | a0007c0016t0003g0313 a0007c0016t0003g0314 a0007c0016t0003g0315 others(1): Show |
4 | HG02258.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.986+382C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821638 | |||||||
chr2:135821803 | G | A | 1 | a0002c0002t0001g0143 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.986+217C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821803 | |||||||
chr2:135821838 | C | G | 3 | a0002c0002t0001g0125 a0002c0002t0001g0168 a0002c0002t0001g0170 |
3 | NA18939.hp1 NA18959.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.986+182G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821838 | |||||||
chr2:135821840 | A | G | 16 | a0005c0012t0001g0030 a0005c0012t0004g0022 a0005c0012t0004g0023 others(13): Show |
16 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.986+180T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821840 | |||||||
chr2:135821939 | CTATAAGA others(1): Show |
C | 15 | a0003c0004t0001g0004 a0003c0004t0001g0013 a0003c0004t0001g0014 others(12): Show |
21 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.986+73_986+80delAT others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 5/16 | chr2 | 135821939 | |||||||
chr2:135822279 | A | C | 3 | a0002c0002t0001g0153 a0002c0002t0001g0154 a0002c0002t0001g0155 |
3 | HG02451.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.908-181T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135822279 | |||||||
chr2:135822670 | G | A | 1 | a0002c0002t0002g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.908-572C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135822670 | |||||||
chr2:135822671 | G | T | 1 | a0002c0002t0002g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.908-573C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135822671 | |||||||
chr2:135822672 | C | A | 1 | a0002c0002t0002g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.908-574G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135822672 | |||||||
chr2:135822674 | C | A | 1 | a0002c0002t0002g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.908-576G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135822674 | |||||||
chr2:135822679 | G | A | 1 | a0002c0002t0002g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.908-581C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135822679 | |||||||
chr2:135822680 | A | T | 1 | a0002c0002t0002g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.908-582T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135822680 | |||||||
chr2:135822684 | A | T | 1 | a0002c0002t0002g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.908-586T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135822684 | |||||||
chr2:135822690 | T | A | 222 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(219): Show |
239 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.908-592A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135822690 | |||||||
chr2:135822717 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
118 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.908-619A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135822717 | |||||||
chr2:135822828 | G | A | 95 | a0001c0038t0001g0166 a0001c0039t0001g0172 a0002c0002t0001g0117 others(92): Show |
97 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.908-730C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135822828 | |||||||
chr2:135823084 | C | T | 4 | a0002c0002t0001g0140 a0002c0002t0001g0141 a0002c0002t0001g0145 others(1): Show |
4 | HG02280.hp2 HG02486.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.907+817G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135823084 | |||||||
chr2:135823158 | C | T | 15 | a0003c0004t0001g0004 a0003c0004t0001g0013 a0003c0004t0001g0014 others(12): Show |
21 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.907+743G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135823158 | |||||||
chr2:135823174 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.907+727G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135823174 | |||||||
chr2:135823234 | G | A | 11 | a0005c0012t0001g0030 a0005c0012t0004g0022 a0005c0012t0004g0023 others(8): Show |
11 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.907+667C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135823234 | |||||||
chr2:135823303 | T | C | 1 | a0001c0005t0001g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.907+598A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135823303 | |||||||
chr2:135823380 | A | C | 3 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 |
3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.907+521T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135823380 | |||||||
chr2:135823413 | C | T | 1 | a0017c0043t0001g0038 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.907+488G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135823413 | |||||||
chr2:135823486 | C | G | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.907+415G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135823486 | |||||||
chr2:135823502 | A | T | 1 | a0003c0003t0002g0067 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.907+399T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135823502 | |||||||
chr2:135823784 | T | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.907+117A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 4/16 | chr2 | 135823784 | |||||||
chr2:135824115 | G | C | 25 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(22): Show |
27 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.805-112C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824115 | |||||||
chr2:135824152 | C | G | 1 | a0001c0001t0001g0018 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.805-149G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824152 | |||||||
chr2:135824205 | C | T | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-202G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824205 | |||||||
chr2:135824247 | C | T | 4 | a0003c0003t0002g0051 a0003c0003t0002g0052 a0010c0024t0002g0304 others(1): Show |
4 | HG02109.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-244G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824247 | |||||||
chr2:135824278 | A | G | 182 | a0001c0038t0001g0166 a0001c0039t0001g0172 a0002c0002t0001g0117 others(179): Show |
191 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(188): Show |
intron_variant | MODIFIER | c.805-275T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824278 | |||||||
chr2:135824456 | G | A | 1 | a0002c0002t0001g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.805-453C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824456 | |||||||
chr2:135824624 | T | C | 1 | a0002c0002t0001g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.805-621A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824624 | |||||||
chr2:135824828 | C | T | 4 | a0001c0011t0001g0131 a0001c0011t0001g0190 a0002c0023t0001g0161 others(1): Show |
4 | NA18945.hp2 NA18957.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-825G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824828 | |||||||
chr2:135824922 | G | A | 2 | a0003c0003t0002g0066 a0003c0003t0002g0084 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.805-919C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824922 | |||||||
chr2:135824952 | G | A | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.805-949C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824952 | |||||||
chr2:135824992 | CA | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
237 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.805-990delT | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824992 | |||||||
chr2:135824992 | CAA | C | 6 | a0001c0001t0001g0266 a0002c0023t0001g0161 a0002c0023t0001g0174 others(3): Show |
6 | HG02895.hp1 HG02896.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-991_805-990del others(2): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135824992 | |||||||
chr2:135825012 | AAAAG | A | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-1013_805-1010d others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825012 | |||||||
chr2:135825090 | T | C | 3 | a0002c0002t0001g0156 a0002c0002t0001g0158 a0002c0002t0001g0159 |
3 | NA18972.hp1 NA18982.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.805-1087A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825090 | |||||||
chr2:135825124 | T | C | 65 | a0002c0037t0002g0123 a0003c0003t0001g0074 a0003c0003t0002g0005 others(62): Show |
72 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.805-1121A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825124 | |||||||
chr2:135825155 | G | T | 25 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(22): Show |
27 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.805-1152C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825155 | |||||||
chr2:135825198 | T | C | 1 | a0003c0003t0002g0089 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.805-1195A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825198 | |||||||
chr2:135825239 | A | G | 60 | a0003c0003t0001g0074 a0003c0003t0002g0005 a0003c0003t0002g0008 others(57): Show |
67 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.805-1236T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825239 | |||||||
chr2:135825355 | G | A | 2 | a0003c0003t0002g0085 a0003c0003t0002g0097 |
2 | HG00733.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.805-1352C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825355 | |||||||
chr2:135825588 | A | G | 11 | a0005c0012t0001g0030 a0005c0012t0004g0022 a0005c0012t0004g0023 others(8): Show |
11 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.805-1585T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825588 | |||||||
chr2:135825597 | TG | T | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-1595delC | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825597 | |||||||
chr2:135825610 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.805-1607G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825610 | |||||||
chr2:135825622 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
118 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.805-1619C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825622 | |||||||
chr2:135825706 | G | A | 1 | a0003c0004t0001g0213 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.805-1703C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825706 | |||||||
chr2:135825823 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.805-1820G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825823 | |||||||
chr2:135825827 | C | T | 6 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-1824G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825827 | |||||||
chr2:135825946 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.805-1943A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135825946 | |||||||
chr2:135826037 | G | A | 6 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-2034C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135826037 | |||||||
chr2:135826296 | G | A | 2 | a0003c0007t0001g0098 a0003c0007t0001g0099 |
2 | NA18941.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.805-2293C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135826296 | |||||||
chr2:135826388 | A | C | 222 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(219): Show |
239 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.805-2385T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135826388 | |||||||
chr2:135826402 | C | CA | 102 | a0001c0001t0001g0281 a0001c0005t0001g0041 a0001c0038t0001g0166 others(99): Show |
106 | HG00639.hp1 HG00673.hp1 HG00741.hp1 others(103): Show |
intron_variant | MODIFIER | c.805-2400dupT | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135826402 | |||||||
chr2:135826402 | C | CAA | 21 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(18): Show |
21 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.805-2401_805-2400d others(4): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135826402 | |||||||
chr2:135826402 | CA | C | 73 | a0002c0037t0002g0123 a0003c0003t0001g0074 a0003c0003t0001g0218 others(70): Show |
80 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.805-2400delT | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135826402 | |||||||
chr2:135826515 | G | A | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.805-2512C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135826515 | |||||||
chr2:135826806 | G | A | 10 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.804+2787C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135826806 | |||||||
chr2:135826968 | A | T | 64 | a0003c0003t0001g0074 a0003c0003t0002g0005 a0003c0003t0002g0008 others(61): Show |
71 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.804+2625T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135826968 | |||||||
chr2:135826976 | T | C | 4 | a0001c0001t0001g0239 a0001c0001t0001g0248 a0001c0001t0001g0252 others(1): Show |
4 | HG00673.hp2 HG01993.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+2617A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135826976 | |||||||
chr2:135827053 | A | G | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+2540T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135827053 | |||||||
chr2:135827144 | A | G | 10 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.804+2449T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135827144 | |||||||
chr2:135827225 | T | A | 15 | a0003c0004t0001g0004 a0003c0004t0001g0013 a0003c0004t0001g0014 others(12): Show |
21 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.804+2368A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135827225 | |||||||
chr2:135827309 | A | G | 22 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+2284T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135827309 | |||||||
chr2:135827528 | C | T | 8 | a0004c0006t0001g0015 a0004c0006t0001g0016 a0004c0006t0001g0221 others(5): Show |
10 | HG01175.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.804+2065G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135827528 | |||||||
chr2:135827572 | G | C | 1 | a0002c0002t0001g0151 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.804+2021C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135827572 | |||||||
chr2:135827664 | C | T | 1 | a0002c0002t0001g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.804+1929G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135827664 | |||||||
chr2:135827753 | C | T | 65 | a0002c0037t0002g0123 a0003c0003t0001g0074 a0003c0003t0002g0005 others(62): Show |
72 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.804+1840G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135827753 | |||||||
chr2:135828457 | G | A | 76 | a0002c0002t0001g0130 a0002c0037t0002g0123 a0003c0003t0001g0074 others(73): Show |
83 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.804+1136C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135828457 | |||||||
chr2:135828488 | G | A | 22 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+1105C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135828488 | |||||||
chr2:135828613 | C | T | 75 | a0002c0037t0002g0123 a0003c0003t0001g0074 a0003c0003t0001g0218 others(72): Show |
82 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.804+980G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135828613 | |||||||
chr2:135828752 | C | G | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+841G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135828752 | |||||||
chr2:135828789 | G | C | 3 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 |
3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.804+804C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135828789 | |||||||
chr2:135828810 | G | A | 1 | a0015c0027t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.804+783C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135828810 | |||||||
chr2:135828840 | G | A | 40 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(37): Show |
48 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.804+753C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135828840 | |||||||
chr2:135828871 | A | T | 6 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+722T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135828871 | |||||||
chr2:135828928 | C | T | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804+665G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135828928 | |||||||
chr2:135828966 | G | A | 11 | a0005c0012t0001g0030 a0005c0012t0004g0022 a0005c0012t0004g0023 others(8): Show |
11 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.804+627C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135828966 | |||||||
chr2:135829015 | T | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.804+578A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829015 | |||||||
chr2:135829052 | G | A | 3 | a0002c0002t0001g0142 a0002c0002t0001g0147 a0002c0002t0001g0163 |
3 | HG03688.hp2 HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.804+541C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829052 | |||||||
chr2:135829062 | G | T | 22 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+531C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829062 | |||||||
chr2:135829114 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.804+479G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829114 | |||||||
chr2:135829151 | A | G | 22 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+442T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829151 | |||||||
chr2:135829255 | C | T | 60 | a0003c0003t0001g0074 a0003c0003t0002g0005 a0003c0003t0002g0008 others(57): Show |
67 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.804+338G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829255 | |||||||
chr2:135829258 | T | C | 95 | a0001c0038t0001g0166 a0001c0039t0001g0172 a0002c0002t0001g0117 others(92): Show |
97 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.804+335A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829258 | |||||||
chr2:135829270 | A | C | 76 | a0002c0037t0002g0123 a0003c0003t0001g0074 a0003c0003t0001g0218 others(73): Show |
83 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.804+323T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829270 | |||||||
chr2:135829274 | C | A | 1 | a0002c0002t0002g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.804+319G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829274 | |||||||
chr2:135829275 | C | T | 1 | a0002c0002t0002g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.804+318G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829275 | |||||||
chr2:135829277 | T | G | 1 | a0002c0002t0002g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.804+316A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829277 | |||||||
chr2:135829285 | T | C | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+308A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829285 | |||||||
chr2:135829388 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
118 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.804+205G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 3/16 | chr2 | 135829388 | |||||||
chr2:135829727 | T | A | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-51A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135829727 | |||||||
chr2:135829801 | C | T | 5 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-125G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135829801 | |||||||
chr2:135829830 | A | AGT | 18 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 others(15): Show |
24 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.721-156_721-155dup others(2): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135829830 | |||||||
chr2:135829830 | A | AGTGT | 30 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0240 others(27): Show |
31 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.721-158_721-155dup others(4): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135829830 | |||||||
chr2:135829830 | A | AGTGTGT | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(70): Show |
107 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.721-160_721-155dup others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135829830 | |||||||
chr2:135829830 | A | AGTGTGTG others(1): Show |
97 | a0001c0001t0001g0241 a0001c0011t0001g0046 a0001c0011t0001g0131 others(94): Show |
99 | HG00408.hp1 HG00673.hp1 HG00741.hp1 others(96): Show |
intron_variant | MODIFIER | c.721-162_721-155dup others(8): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135829830 | |||||||
chr2:135829830 | A | AGTGTGTG others(3): Show |
77 | a0001c0038t0001g0166 a0002c0002t0001g0124 a0002c0002t0001g0156 others(74): Show |
84 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.721-164_721-155dup others(10): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135829830 | |||||||
chr2:135829830 | A | AGTGTGTG others(5): Show |
12 | a0001c0044t0001g0286 a0002c0002t0001g0158 a0002c0002t0001g0159 others(9): Show |
12 | HG02735.hp1 HG02818.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.721-166_721-155dup others(12): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135829830 | |||||||
chr2:135829830 | A | AGTGTGTG others(7): Show |
5 | a0005c0017t0001g0021 a0007c0016t0003g0313 a0007c0016t0003g0314 others(2): Show |
5 | HG02258.hp1 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-168_721-155dup others(14): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135829830 | |||||||
chr2:135829949 | C | T | 1 | a0001c0005t0001g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.721-273G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135829949 | |||||||
chr2:135829973 | G | T | 5 | a0002c0002t0003g0106 a0002c0002t0003g0107 a0002c0002t0003g0110 others(2): Show |
5 | NA18952.hp2 NA18966.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-297C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135829973 | |||||||
chr2:135830028 | C | G | 11 | a0005c0012t0001g0030 a0005c0012t0004g0022 a0005c0012t0004g0023 others(8): Show |
11 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.721-352G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135830028 | |||||||
chr2:135830108 | T | C | 1 | a0001c0011t0001g0046 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.721-432A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135830108 | |||||||
chr2:135830246 | C | A | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.721-570G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135830246 | |||||||
chr2:135830461 | C | A | 110 | a0002c0037t0002g0123 a0003c0003t0001g0074 a0003c0003t0001g0218 others(107): Show |
125 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.721-785G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135830461 | |||||||
chr2:135830554 | T | A | 15 | a0003c0004t0001g0004 a0003c0004t0001g0013 a0003c0004t0001g0014 others(12): Show |
21 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.721-878A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135830554 | |||||||
chr2:135830810 | A | T | 4 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-1134T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135830810 | |||||||
chr2:135830908 | T | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
115 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.721-1232A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135830908 | |||||||
chr2:135830913 | T | C | 1 | a0003c0004t0001g0014 | 2 | HG00544.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.721-1237A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135830913 | |||||||
chr2:135831168 | G | A | 4 | a0009c0018t0001g0214 a0009c0018t0001g0215 a0009c0018t0001g0216 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-1492C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831168 | |||||||
chr2:135831371 | G | A | 1 | a0002c0002t0002g0179 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.721-1695C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831371 | |||||||
chr2:135831388 | CAGAG | C | 104 | a0002c0037t0002g0123 a0003c0003t0001g0074 a0003c0003t0001g0218 others(101): Show |
121 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.721-1716_721-1713d others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831388 | |||||||
chr2:135831398 | G | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.720+1713C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831398 | |||||||
chr2:135831439 | C | T | 1 | a0003c0033t0002g0092 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.720+1672G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831439 | |||||||
chr2:135831512 | T | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.720+1599A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831512 | |||||||
chr2:135831562 | A | T | 1 | a0002c0002t0001g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.720+1549T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831562 | |||||||
chr2:135831566 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.720+1545T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831566 | |||||||
chr2:135831575 | A | T | 1 | a0002c0002t0001g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.720+1536T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831575 | |||||||
chr2:135831583 | TTTGGTCT others(17): Show |
T | 1 | a0002c0002t0001g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.720+1504_720+1527d others(26): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831583 | |||||||
chr2:135831595 | C | T | 1 | a0001c0045t0001g0234 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.720+1516G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831595 | |||||||
chr2:135831635 | T | A | 1 | a0002c0002t0001g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.720+1476A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831635 | |||||||
chr2:135831653 | C | A | 1 | a0002c0002t0001g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.720+1458G>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831653 | |||||||
chr2:135831655 | T | C | 1 | a0002c0002t0001g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.720+1456A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831655 | |||||||
chr2:135831680 | C | T | 1 | a0002c0002t0001g0118 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.720+1431G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831680 | |||||||
chr2:135831708 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
224 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.720+1403C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831708 | |||||||
chr2:135831772 | G | A | 4 | a0007c0016t0003g0313 a0007c0016t0003g0314 a0007c0016t0003g0315 others(1): Show |
4 | HG02258.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+1339C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831772 | |||||||
chr2:135831809 | G | A | 121 | a0002c0037t0002g0123 a0003c0003t0001g0074 a0003c0003t0001g0218 others(118): Show |
138 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.720+1302C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831809 | |||||||
chr2:135831877 | G | T | 3 | a0003c0003t0002g0008 a0003c0003t0002g0058 a0003c0007t0001g0059 |
4 | HG02717.hp2 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+1234C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831877 | |||||||
chr2:135831942 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.720+1169G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831942 | |||||||
chr2:135831943 | G | A | 2 | a0003c0007t0001g0006 a0003c0007t0001g0101 |
4 | NA18970.hp1 NA19056.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+1168C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831943 | |||||||
chr2:135831944 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.720+1167A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831944 | |||||||
chr2:135831951 | T | C | 8 | a0007c0016t0003g0313 a0007c0016t0003g0314 a0007c0016t0003g0315 others(5): Show |
8 | HG02258.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+1160A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831951 | |||||||
chr2:135831970 | A | T | 15 | a0003c0004t0001g0004 a0003c0004t0001g0013 a0003c0004t0001g0014 others(12): Show |
21 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.720+1141T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135831970 | |||||||
chr2:135832042 | C | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
112 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.720+1069G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135832042 | |||||||
chr2:135832072 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.720+1039G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135832072 | |||||||
chr2:135832130 | C | T | 2 | a0003c0013t0002g0194 a0003c0013t0002g0195 |
2 | NA18943.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.720+981G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135832130 | |||||||
chr2:135832131 | A | G | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
363 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(360): Show |
intron_variant | MODIFIER | c.720+980T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135832131 | |||||||
chr2:135832171 | G | A | 120 | a0003c0003t0001g0074 a0003c0003t0001g0218 a0003c0003t0001g0219 others(117): Show |
137 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.720+940C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135832171 | |||||||
chr2:135832291 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.720+820C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135832291 | |||||||
chr2:135832757 | T | A | 1 | a0001c0001t0001g0249 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.720+354A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135832757 | |||||||
chr2:135832791 | C | T | 1 | a0002c0002t0003g0110 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.720+320G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135832791 | |||||||
chr2:135832988 | C | T | 95 | a0001c0011t0001g0131 a0001c0011t0001g0180 a0001c0011t0001g0190 others(92): Show |
95 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.720+123G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 2/16 | chr2 | 135832988 | |||||||
chr2:135833211 | G | A | 9 | a0007c0016t0003g0313 a0007c0016t0003g0314 a0007c0016t0003g0315 others(6): Show |
9 | HG02258.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-21C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833211 | |||||||
chr2:135833225 | C | G | 3 | a0003c0003t0002g0008 a0003c0003t0002g0058 a0003c0007t0001g0059 |
4 | HG02717.hp2 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-35G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833225 | |||||||
chr2:135833225 | C | T | 15 | a0003c0004t0001g0004 a0003c0004t0001g0013 a0003c0004t0001g0014 others(12): Show |
21 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.641-35G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833225 | |||||||
chr2:135833278 | A | T | 1 | a0001c0001t0001g0268 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.641-88T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833278 | |||||||
chr2:135833409 | A | C | 1 | a0001c0001t0001g0265 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.641-219T>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833409 | |||||||
chr2:135833441 | C | CT | 6 | a0005c0012t0001g0030 a0005c0012t0004g0022 a0005c0012t0004g0023 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-252dupA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833441 | |||||||
chr2:135833441 | CT | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
290 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.641-252delA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833441 | |||||||
chr2:135833483 | G | A | 15 | a0003c0004t0001g0004 a0003c0004t0001g0013 a0003c0004t0001g0014 others(12): Show |
21 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.641-293C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833483 | |||||||
chr2:135833516 | G | A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0300 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.641-326C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833516 | |||||||
chr2:135833525 | A | AAAGCTCC others(3955): Show |
2 | a0003c0003t0002g0103 a0003c0003t0002g0104 |
2 | NA19057.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.641-336_641-335ins others(3962): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833525 | |||||||
chr2:135833525 | A | AAAGCTCC others(3956): Show |
1 | a0003c0003t0002g0102 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.641-336_641-335ins others(3963): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833525 | |||||||
chr2:135833532 | C | CGCCTCCT others(3944): Show |
1 | a0003c0007t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.641-343_641-342ins others(3951): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3944): Show |
1 | a0015c0027t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.641-343_641-342ins others(3951): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3943): Show |
1 | a0002c0002t0001g0159 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.641-343_641-342ins others(3950): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3943): Show |
1 | a0002c0002t0005g0115 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.641-343_641-342ins others(3950): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3943): Show |
1 | a0002c0002t0001g0164 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.641-343_641-342ins others(3950): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3943): Show |
1 | a0002c0002t0001g0124 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3950): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3942): Show |
7 | a0002c0002t0003g0106 a0002c0002t0003g0107 a0002c0002t0003g0108 others(4): Show |
7 | HG03704.hp1 HG04184.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-343_641-342ins others(3949): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3943): Show |
42 | a0001c0038t0001g0166 a0001c0039t0001g0172 a0002c0002t0001g0121 others(39): Show |
42 | HG01346.hp1 HG01358.hp1 HG01981.hp2 others(39): Show |
intron_variant | MODIFIER | c.641-343_641-342ins others(3950): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3943): Show |
3 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0160 |
3 | HG01952.hp1 HG01978.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.641-343_641-342ins others(3950): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3944): Show |
2 | a0002c0002t0001g0142 a0002c0002t0001g0157 |
2 | HG02300.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.641-343_641-342ins others(3951): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3944): Show |
28 | a0001c0011t0001g0131 a0001c0011t0001g0180 a0001c0011t0001g0190 others(25): Show |
28 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.641-343_641-342ins others(3951): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3946): Show |
1 | a0002c0023t0001g0174 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3953): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3945): Show |
2 | a0002c0008t0001g0132 a0002c0009t0001g0312 |
2 | HG01192.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.641-343_641-342ins others(3952): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3943): Show |
1 | a0002c0002t0003g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3950): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3944): Show |
3 | a0002c0002t0001g0117 a0002c0002t0001g0126 a0002c0002t0001g0152 |
3 | HG01261.hp1 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.641-343_641-342ins others(3951): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3945): Show |
1 | a0002c0009t0001g0311 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3952): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3944): Show |
1 | a0002c0002t0001g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.641-343_641-342ins others(3951): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3954): Show |
1 | a0003c0003t0002g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.641-343_641-342ins others(3961): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3954): Show |
2 | a0005c0012t0004g0022 a0005c0012t0004g0023 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.641-343_641-342ins others(3961): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3954): Show |
7 | a0005c0012t0001g0030 a0005c0017t0001g0020 a0005c0017t0001g0021 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-343_641-342ins others(3961): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3954): Show |
1 | a0014c0025t0004g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3961): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3955): Show |
1 | a0004c0014t0002g0087 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3962): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3951): Show |
1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.641-343_641-342ins others(3958): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3954): Show |
1 | a0003c0003t0002g0088 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3961): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3954): Show |
2 | a0003c0003t0001g0218 a0003c0003t0001g0229 |
2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.641-343_641-342ins others(3961): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3955): Show |
57 | a0003c0003t0001g0074 a0003c0003t0001g0226 a0003c0003t0002g0005 others(54): Show |
65 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.641-343_641-342ins others(3962): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3956): Show |
6 | a0003c0003t0001g0219 a0003c0003t0002g0008 a0003c0003t0002g0058 others(3): Show |
7 | HG01069.hp1 HG02055.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-343_641-342ins others(3963): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3956): Show |
1 | a0003c0003t0002g0065 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.641-343_641-342ins others(3963): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3951): Show |
1 | a0001c0019t0004g0032 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3958): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3952): Show |
2 | a0001c0019t0004g0033 a0001c0019t0004g0184 |
2 | HG03491.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.641-343_641-342ins others(3959): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3956): Show |
2 | a0009c0018t0001g0214 a0009c0018t0001g0215 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.641-343_641-342ins others(3963): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3950): Show |
13 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0039 others(10): Show |
13 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-343_641-342ins others(3957): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3951): Show |
1 | a0001c0005t0001g0037 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3958): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3959): Show |
13 | a0003c0004t0001g0004 a0003c0004t0001g0013 a0003c0004t0001g0014 others(10): Show |
19 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.641-343_641-342ins others(3966): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3955): Show |
1 | a0005c0012t0004g0025 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.641-343_641-342ins others(3962): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3957): Show |
1 | a0018c0032t0001g0217 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3964): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3956): Show |
4 | a0007c0016t0003g0314 a0007c0016t0003g0315 a0007c0016t0003g0316 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-343_641-342ins others(3963): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3957): Show |
1 | a0007c0016t0003g0313 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3964): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3956): Show |
10 | a0003c0003t0001g0228 a0004c0006t0001g0015 a0004c0006t0001g0016 others(7): Show |
12 | HG01175.hp2 HG01884.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-343_641-342ins others(3963): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3951): Show |
1 | a0001c0005t0001g0036 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.641-343_641-342ins others(3958): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3960): Show |
2 | a0003c0004t0001g0204 a0003c0004t0001g0205 |
2 | HG00423.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.641-343_641-342ins others(3967): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833532 | C | CGCCTCCT others(3957): Show |
1 | a0004c0006t0001g0221 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.641-343_641-342ins others(3964): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833532 | |||||||
chr2:135833540 | G | A | 1 | a0003c0003t0002g0089 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.641-350C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833540 | |||||||
chr2:135833608 | G | A | 233 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(230): Show |
250 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.641-418C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833608 | |||||||
chr2:135833645 | A | T | 1 | a0008c0022t0003g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.641-455T>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833645 | |||||||
chr2:135833686 | T | A | 3 | a0002c0002t0001g0153 a0002c0002t0001g0154 a0002c0002t0001g0155 |
3 | HG02451.hp1 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.641-496A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833686 | |||||||
chr2:135833688 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.641-498A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833688 | |||||||
chr2:135833689 | G | A | 1 | a0002c0002t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.641-499C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833689 | |||||||
chr2:135833697 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.641-507A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833697 | |||||||
chr2:135833712 | T | C | 2 | a0005c0020t0001g0027 a0005c0020t0001g0029 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.641-522A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833712 | |||||||
chr2:135833735 | C | G | 1 | a0015c0027t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.641-545G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833735 | |||||||
chr2:135833738 | G | A | 3 | a0001c0019t0004g0032 a0001c0019t0004g0033 a0001c0019t0004g0184 |
3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.641-548C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833738 | |||||||
chr2:135833967 | G | A | 1 | a0005c0017t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.641-777C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135833967 | |||||||
chr2:135834289 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
112 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.641-1099C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834289 | |||||||
chr2:135834325 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.641-1135T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834325 | |||||||
chr2:135834407 | G | C | 8 | a0007c0016t0003g0313 a0007c0016t0003g0314 a0007c0016t0003g0315 others(5): Show |
8 | HG02258.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-1217C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834407 | |||||||
chr2:135834480 | T | C | 12 | a0005c0012t0001g0030 a0005c0012t0004g0022 a0005c0012t0004g0023 others(9): Show |
12 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-1290A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834480 | |||||||
chr2:135834510 | G | A | 19 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(16): Show |
21 | HG01175.hp2 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.641-1320C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834510 | |||||||
chr2:135834739 | G | A | 96 | a0001c0011t0001g0131 a0001c0011t0001g0180 a0001c0011t0001g0190 others(93): Show |
96 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.641-1549C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834739 | |||||||
chr2:135834787 | C | CAA | 8 | a0001c0001t0001g0235 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
8 | HG01975.hp1 HG02897.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.641-1599_641-1598d others(4): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834787 | |||||||
chr2:135834787 | C | CAAA | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
114 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(111): Show |
intron_variant | MODIFIER | c.641-1600_641-1598d others(5): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834787 | |||||||
chr2:135834787 | C | CAAAA | 90 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0265 others(87): Show |
98 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.641-1601_641-1598d others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834787 | |||||||
chr2:135834787 | C | CAAAAA | 8 | a0001c0011t0001g0180 a0002c0002t0001g0159 a0002c0008t0001g0165 others(5): Show |
8 | HG01109.hp2 HG02074.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.641-1602_641-1598d others(7): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834787 | |||||||
chr2:135834787 | C | CAAAAAA | 11 | a0002c0002t0001g0167 a0002c0002t0001g0178 a0002c0002t0001g0183 others(8): Show |
12 | HG01175.hp1 HG01243.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-1603_641-1598d others(8): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834787 | |||||||
chr2:135834787 | C | CAAAAAAA others(3): Show |
30 | a0003c0003t0001g0074 a0003c0003t0002g0005 a0003c0003t0002g0009 others(27): Show |
36 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.641-1607_641-1598d others(12): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834787 | |||||||
chr2:135834787 | C | CAAAAAAA others(4): Show |
15 | a0003c0003t0002g0090 a0003c0003t0002g0093 a0003c0003t0002g0094 others(12): Show |
17 | HG01255.hp1 HG01433.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.641-1608_641-1598d others(13): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834787 | |||||||
chr2:135834787 | C | CAAAAAAA others(5): Show |
5 | a0003c0003t0002g0100 a0003c0003t0002g0102 a0003c0003t0002g0103 others(2): Show |
5 | HG02080.hp1 NA19057.hp2 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-1609_641-1598d others(14): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834787 | |||||||
chr2:135834787 | C | CAAAAAAA others(6): Show |
1 | a0016c0028t0002g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.641-1610_641-1598d others(15): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834787 | |||||||
chr2:135834787 | CAAAAAAA others(3): Show |
C | 9 | a0002c0037t0002g0123 a0007c0016t0003g0313 a0007c0016t0003g0314 others(6): Show |
9 | HG02258.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-1607_641-1598d others(12): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834787 | |||||||
chr2:135834808 | A | AAAAAAAA others(1): Show |
16 | a0001c0005t0001g0035 a0001c0005t0001g0037 a0001c0005t0001g0039 others(13): Show |
16 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.641-1619_641-1618i others(10): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834808 | |||||||
chr2:135834808 | A | AAAAAAAG | 22 | a0001c0019t0004g0184 a0001c0038t0001g0166 a0001c0039t0001g0172 others(19): Show |
22 | HG02698.hp2 HG03654.hp1 HG03688.hp2 others(19): Show |
intron_variant | MODIFIER | c.641-1619_641-1618i others(9): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834808 | |||||||
chr2:135834808 | A | AAAAG | 7 | a0001c0005t0001g0034 a0001c0005t0001g0036 a0001c0005t0001g0040 others(4): Show |
7 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-1619_641-1618i others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834808 | |||||||
chr2:135834817 | G | A | 17 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(14): Show |
17 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.641-1627C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834817 | |||||||
chr2:135834957 | T | G | 5 | a0003c0003t0002g0051 a0003c0003t0002g0052 a0003c0007t0001g0050 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+1573A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135834957 | |||||||
chr2:135835130 | G | GT | 9 | a0003c0003t0003g0105 a0007c0016t0003g0313 a0007c0016t0003g0314 others(6): Show |
9 | HG00639.hp1 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+1399dupA | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835130 | |||||||
chr2:135835156 | T | A | 1 | a0002c0009t0001g0311 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.640+1374A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835156 | |||||||
chr2:135835242 | T | C | 1 | a0002c0009t0001g0308 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.640+1288A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835242 | |||||||
chr2:135835379 | C | T | 1 | a0002c0009t0001g0311 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.640+1151G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835379 | |||||||
chr2:135835394 | G | A | 1 | a0018c0032t0001g0217 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.640+1136C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835394 | |||||||
chr2:135835409 | G | A | 9 | a0003c0003t0003g0105 a0007c0016t0003g0313 a0007c0016t0003g0314 others(6): Show |
9 | HG00639.hp1 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+1121C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835409 | |||||||
chr2:135835482 | G | GTA | 43 | a0001c0001t0001g0003 a0001c0001t0001g0287 a0001c0001t0001g0288 others(40): Show |
51 | HG00738.hp2 HG01099.hp1 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.640+1046_640+1047d others(4): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | G | GTATA | 5 | a0001c0001t0001g0302 a0001c0039t0001g0172 a0002c0002t0001g0170 others(2): Show |
5 | HG01358.hp1 HG04204.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+1044_640+1047d others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | G | GTATATA | 4 | a0001c0001t0001g0019 a0002c0002t0001g0160 a0002c0046t0001g0303 others(1): Show |
5 | HG01952.hp1 HG02698.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.640+1042_640+1047d others(8): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | G | GTATATAT others(5): Show |
2 | a0002c0002t0001g0173 a0002c0002t0005g0116 |
2 | HG04184.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.640+1036_640+1047d others(14): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTA | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0252 others(36): Show |
52 | HG00280.hp1 HG00673.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.640+1046_640+1047d others(4): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATA | G | 25 | a0001c0001t0001g0007 a0001c0001t0001g0241 a0001c0001t0001g0242 others(22): Show |
27 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.640+1044_640+1047d others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATA | G | 8 | a0001c0001t0001g0240 a0001c0005t0001g0034 a0001c0005t0001g0045 others(5): Show |
8 | HG00558.hp2 HG00741.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.640+1042_640+1047d others(8): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(1): Show |
G | 8 | a0001c0001t0001g0233 a0001c0001t0001g0238 a0001c0001t0001g0239 others(5): Show |
8 | HG00735.hp2 HG01070.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+1040_640+1047d others(10): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(3): Show |
G | 1 | a0001c0001t0001g0017 | 2 | HG02165.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.640+1038_640+1047d others(12): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(7): Show |
G | 1 | a0002c0002t0003g0113 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.640+1034_640+1047d others(16): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(9): Show |
G | 3 | a0001c0011t0001g0190 a0002c0002t0001g0120 a0002c0048t0001g0237 |
3 | HG01433.hp2 HG02683.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.640+1032_640+1047d others(18): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(11): Show |
G | 3 | a0001c0011t0001g0131 a0002c0023t0001g0161 a0002c0023t0001g0174 |
3 | NA18957.hp2 NA18972.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.640+1030_640+1047d others(20): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(13): Show |
G | 5 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0002c0002t0001g0118 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+1028_640+1047d others(22): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(17): Show |
G | 6 | a0001c0045t0001g0234 a0005c0012t0001g0030 a0005c0017t0001g0020 others(3): Show |
6 | HG00733.hp1 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+1024_640+1047d others(26): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(19): Show |
G | 17 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(14): Show |
19 | HG01175.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.640+1022_640+1047d others(28): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(21): Show |
G | 90 | a0003c0003t0001g0074 a0003c0003t0002g0005 a0003c0003t0002g0008 others(87): Show |
105 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.640+1020_640+1047d others(30): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(25): Show |
G | 1 | a0002c0002t0001g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.640+1016_640+1047d others(34): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(27): Show |
G | 1 | a0002c0002t0001g0153 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.640+1014_640+1047d others(36): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835482 | GTATATAT others(31): Show |
G | 8 | a0007c0016t0003g0313 a0007c0016t0003g0314 a0007c0016t0003g0315 others(5): Show |
8 | HG02258.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+1010_640+1047d others(40): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835482 | |||||||
chr2:135835486 | A | G | 1 | a0001c0005t0001g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.640+1044T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835486 | |||||||
chr2:135835566 | T | A | 9 | a0003c0003t0003g0105 a0007c0016t0003g0313 a0007c0016t0003g0314 others(6): Show |
9 | HG00639.hp1 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+964A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835566 | |||||||
chr2:135835604 | T | TGATTCTC others(3): Show |
1 | a0002c0023t0001g0174 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.640+916_640+925dup others(10): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835604 | |||||||
chr2:135835613 | A | G | 1 | a0002c0002t0001g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.640+917T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835613 | |||||||
chr2:135835683 | A | G | 1 | a0001c0011t0001g0190 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.640+847T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835683 | |||||||
chr2:135835887 | G | C | 1 | a0002c0002t0001g0152 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.640+643C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835887 | |||||||
chr2:135835928 | C | T | 80 | a0003c0003t0001g0074 a0003c0003t0002g0005 a0003c0003t0002g0008 others(77): Show |
95 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.640+602G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835928 | |||||||
chr2:135835955 | G | T | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.640+575C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835955 | |||||||
chr2:135835965 | A | G | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
363 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(360): Show |
intron_variant | MODIFIER | c.640+565T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835965 | |||||||
chr2:135835970 | A | AAG | 27 | a0001c0011t0001g0131 a0002c0002t0001g0139 a0002c0002t0001g0140 others(24): Show |
27 | HG01070.hp1 HG01192.hp2 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.640+559_640+560ins others(2): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835970 | |||||||
chr2:135835970 | A | AAGTG | 25 | a0001c0019t0004g0184 a0001c0038t0001g0166 a0001c0039t0001g0172 others(22): Show |
25 | HG00741.hp1 HG01109.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.640+559_640+560ins others(4): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835970 | |||||||
chr2:135835970 | A | AAGTGTG | 18 | a0001c0011t0001g0180 a0002c0002t0001g0156 a0002c0002t0001g0157 others(15): Show |
18 | HG00673.hp1 HG01952.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.640+559_640+560ins others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835970 | |||||||
chr2:135835971 | T | A | 24 | a0001c0011t0001g0190 a0002c0002t0001g0117 a0002c0002t0001g0118 others(21): Show |
24 | HG01261.hp1 HG01433.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.640+559A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835971 | |||||||
chr2:135835976 | G | A | 19 | a0001c0011t0001g0180 a0001c0019t0004g0184 a0002c0002t0001g0177 others(16): Show |
19 | HG00673.hp1 HG01346.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.640+554C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTA | 7 | a0001c0005t0001g0042 a0001c0005t0001g0043 a0001c0005t0001g0045 others(4): Show |
7 | HG00408.hp1 HG00735.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.640+552_640+553dup others(2): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTATATAA others(1): Show |
5 | a0003c0003t0001g0228 a0003c0003t0001g0229 a0004c0006t0001g0227 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+553_640+554ins others(8): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTATATAA others(3): Show |
5 | a0003c0003t0001g0226 a0004c0006t0001g0016 a0004c0006t0001g0225 others(2): Show |
6 | HG01175.hp2 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+553_640+554ins others(10): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTATATAA others(5): Show |
8 | a0003c0003t0002g0052 a0004c0006t0001g0015 a0004c0006t0001g0221 others(5): Show |
9 | HG01884.hp2 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+553_640+554ins others(12): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTATATAA others(7): Show |
4 | a0003c0003t0001g0219 a0005c0012t0004g0022 a0005c0012t0004g0023 others(1): Show |
4 | HG02055.hp2 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+553_640+554ins others(14): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTATATAA others(9): Show |
2 | a0003c0003t0001g0218 a0010c0024t0002g0304 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.640+553_640+554ins others(16): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTATATAA others(11): Show |
1 | a0003c0003t0002g0051 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.640+553_640+554ins others(18): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTATATAA others(15): Show |
1 | a0003c0007t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.640+553_640+554ins others(22): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTGTATA | 4 | a0002c0002t0003g0113 a0002c0002t0005g0114 a0002c0002t0005g0115 others(1): Show |
4 | HG01993.hp1 HG02293.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+553_640+554ins others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTGTGTAT others(1): Show |
3 | a0002c0002t0001g0188 a0002c0002t0005g0189 a0002c0009t0001g0312 |
3 | HG01928.hp2 NA19077.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.640+553_640+554ins others(8): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTGTGTAT others(5): Show |
1 | a0001c0011t0001g0190 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.640+553_640+554ins others(12): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTGTGTAT others(7): Show |
2 | a0002c0002t0001g0191 a0002c0002t0005g0192 |
2 | NA18954.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.640+553_640+554ins others(14): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835976 | G | GTGTGTGT others(3): Show |
1 | a0002c0002t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.640+553_640+554ins others(10): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835976 | |||||||
chr2:135835978 | A | G | 42 | a0001c0011t0001g0131 a0001c0019t0004g0032 a0001c0019t0004g0033 others(39): Show |
42 | HG01070.hp1 HG01192.hp2 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.640+552T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835978 | |||||||
chr2:135835980 | A | G | 10 | a0002c0002t0001g0117 a0002c0002t0001g0118 a0002c0002t0001g0120 others(7): Show |
10 | HG01261.hp1 HG01433.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.640+550T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835980 | |||||||
chr2:135835983 | T | A | 90 | a0003c0003t0001g0074 a0003c0003t0002g0005 a0003c0003t0002g0008 others(87): Show |
105 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.640+547A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835983 | |||||||
chr2:135835994 | ATATATAT others(15): Show |
A | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.640+514_640+535del others(22): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835994 | |||||||
chr2:135835998 | ATATATAT others(11): Show |
A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
108 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.640+514_640+531del others(18): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135835998 | |||||||
chr2:135836000 | ATATATAT others(9): Show |
A | 4 | a0001c0001t0001g0239 a0001c0001t0001g0276 a0001c0011t0001g0200 others(1): Show |
4 | HG00642.hp1 HG01433.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+514_640+529del others(16): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836000 | |||||||
chr2:135836002 | ATATATAT others(7): Show |
A | 1 | a0002c0002t0001g0122 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.640+514_640+527del others(14): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836002 | |||||||
chr2:135836003 | T | C | 1 | a0001c0001t0001g0003 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.640+527A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836003 | |||||||
chr2:135836004 | ATATATAT others(5): Show |
A | 62 | a0001c0005t0001g0037 a0003c0003t0001g0074 a0003c0003t0002g0005 others(59): Show |
69 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.640+514_640+525del others(12): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836004 | |||||||
chr2:135836005 | T | C | 1 | a0003c0007t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.640+525A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836005 | |||||||
chr2:135836006 | ATATATAT others(3): Show |
A | 5 | a0003c0003t0002g0010 a0003c0003t0002g0012 a0003c0003t0002g0072 others(2): Show |
6 | HG00642.hp2 HG01515.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+514_640+523del others(10): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836006 | |||||||
chr2:135836007 | TATATATA others(10): Show |
T | 1 | a0001c0001t0001g0003 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.640+506_640+522del others(17): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836007 | |||||||
chr2:135836008 | ATATATAT others(1): Show |
A | 5 | a0007c0016t0003g0315 a0009c0018t0001g0214 a0009c0018t0001g0215 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+514_640+521del others(8): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836008 | |||||||
chr2:135836009 | T | C | 2 | a0001c0019t0004g0032 a0001c0019t0004g0033 |
2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.640+521A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836009 | |||||||
chr2:135836010 | ATATATG | A | 6 | a0002c0002t0001g0125 a0003c0004t0001g0014 a0005c0012t0001g0030 others(3): Show |
6 | HG00544.hp2 HG02258.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+514_640+519del others(6): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836010 | |||||||
chr2:135836012 | ATATG | A | 15 | a0001c0005t0001g0041 a0002c0002t0001g0153 a0002c0002t0001g0154 others(12): Show |
18 | HG00408.hp2 HG00423.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.640+514_640+517del others(4): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836012 | |||||||
chr2:135836012 | ATATGTAT others(6): Show |
A | 2 | a0001c0019t0004g0032 a0001c0019t0004g0033 |
2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.640+505_640+517del others(13): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836012 | |||||||
chr2:135836014 | ATG | A | 8 | a0002c0002t0001g0117 a0002c0002t0001g0124 a0002c0002t0001g0126 others(5): Show |
9 | HG00558.hp1 HG01261.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.640+514_640+515del others(2): Show |
LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836014 | |||||||
chr2:135836016 | G | A | 130 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(127): Show |
132 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.640+514C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836016 | |||||||
chr2:135836018 | A | G | 1 | a0003c0030t0002g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.640+512T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836018 | |||||||
chr2:135836019 | T | C | 7 | a0005c0012t0001g0030 a0005c0017t0001g0020 a0005c0017t0001g0021 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+511A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836019 | |||||||
chr2:135836023 | TA | T | 15 | a0003c0004t0001g0004 a0003c0004t0001g0013 a0003c0004t0001g0014 others(12): Show |
21 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+506delT | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836023 | |||||||
chr2:135836057 | C | T | 3 | a0005c0017t0001g0020 a0005c0017t0001g0021 a0005c0017t0001g0031 |
3 | HG02559.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.640+473G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836057 | |||||||
chr2:135836066 | T | A | 1 | a0003c0003t0003g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.640+464A>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836066 | |||||||
chr2:135836074 | A | G | 11 | a0002c0002t0003g0106 a0002c0002t0003g0107 a0002c0002t0003g0108 others(8): Show |
11 | HG01358.hp1 HG01993.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.640+456T>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836074 | |||||||
chr2:135836108 | T | C | 120 | a0003c0003t0001g0074 a0003c0003t0001g0218 a0003c0003t0001g0219 others(117): Show |
137 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.640+422A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836108 | |||||||
chr2:135836124 | T | C | 96 | a0001c0011t0001g0131 a0001c0011t0001g0180 a0001c0011t0001g0190 others(93): Show |
96 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.640+406A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836124 | |||||||
chr2:135836130 | T | C | 5 | a0003c0013t0002g0194 a0003c0013t0002g0195 a0003c0013t0002g0196 others(2): Show |
5 | HG02135.hp2 NA18943.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+400A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836130 | |||||||
chr2:135836132 | C | G | 12 | a0005c0012t0001g0030 a0005c0012t0004g0022 a0005c0012t0004g0023 others(9): Show |
12 | HG02559.hp1 HG02615.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.640+398G>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836132 | |||||||
chr2:135836190 | G | T | 233 | a0001c0005t0001g0034 a0001c0005t0001g0035 a0001c0005t0001g0036 others(230): Show |
250 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.640+340C>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836190 | |||||||
chr2:135836195 | T | G | 1 | a0005c0017t0001g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.640+335A>C | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836195 | |||||||
chr2:135836206 | AC | A | 15 | a0003c0004t0001g0004 a0003c0004t0001g0013 a0003c0004t0001g0014 others(12): Show |
21 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+323delG | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836206 | |||||||
chr2:135836239 | G | C | 8 | a0007c0016t0003g0313 a0007c0016t0003g0314 a0007c0016t0003g0315 others(5): Show |
8 | HG02258.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+291C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836239 | |||||||
chr2:135836285 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0233 |
3 | HG02129.hp2 HG02165.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.640+245G>A | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836285 | |||||||
chr2:135836390 | T | C | 14 | a0003c0003t0001g0218 a0003c0003t0001g0219 a0003c0003t0001g0226 others(11): Show |
16 | HG01175.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.640+140A>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836390 | |||||||
chr2:135836474 | G | C | 2 | a0002c0002t0001g0230 a0002c0002t0001g0231 |
2 | NA18979.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.640+56C>G | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836474 | |||||||
chr2:135836479 | G | A | 1 | a0003c0004t0001g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.640+51C>T | LCT | ENSG00000115850.10 | transcript | ENST00000264162.7 | protein_coding | 1/16 | chr2 | 135836479 |