Item | Value |
---|---|
geneid | 9654 |
ensemblid | ENSG00000135912.11 |
hgncid | 28976 |
symbol | TTLL4 |
name | tubulin tyrosine ligase like 4 |
refseq_nuc | NM_014640.5 |
refseq_prot | NP_055455.3 |
ensembl_nuc | ENST00000392102.6 |
ensembl_prot | ENSP00000375951.1 |
mane_status | MANE Select |
chr | chr2 |
start | 218710835 |
end | 218755416 |
strand | + |
ver | v1.2 |
region | chr2:218710835-218755416 |
region5000 | chr2:218705835-218760416 |
regionname0 | TTLL4_chr2_218710835_218755416 |
regionname5000 | TTLL4_chr2_218705835_218760416 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1199 | 114 | 43 | 23 | 30 | 4 | 14 | 25 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0002 | 1/1 | 1199 | 99 | 13 | 17 | 45 | 5 | 17 | 30 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0003 | 0/0 | 1199 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0004 | 0/0 | 1199 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0005 | 0/0 | 1199 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0006 | 0/0 | 1199 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0007 | 0/0 | 1199 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0008 | 0/0 | 1199 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0009 | 0/0 | 1199 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0010 | 0/0 | 1199 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0011 | 0/0 | 1199 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0012 | 0/0 | 1199 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0013 | 0/0 | 1199 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0014 | 0/0 | 1199 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0015 | 0/0 | 1199 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0016 | 0/0 | 1199 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0017 | 0/0 | 1199 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0018 | 0/0 | 1199 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0019 | 0/0 | 1199 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
a0020 | 0/0 | 1199 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | MASAG others(1194): Show |
chr2 | 218705835 | 218760416 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3597 | 113 | 42 | 23 | 30 | 4 | 14 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0001c0016 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0002c0002 | 1/1 | 3597 | 89 | 5 | 16 | 44 | 5 | 17 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0002c0007 | 0/0 | 3597 | 4 | 3 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0002c0011 | 0/0 | 3597 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0002c0013 | 0/0 | 3597 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0002c0023 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0002c0025 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0003c0003 | 0/0 | 3597 | 13 | 13 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0004c0004 | 0/0 | 3597 | 6 | 6 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0005c0005 | 0/0 | 3597 | 5 | 5 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0006c0006 | 0/0 | 3597 | 4 | 0 | 0 | 4 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0007c0009 | 0/0 | 3597 | 3 | 3 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0008c0008 | 0/0 | 3597 | 3 | 3 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0009c0012 | 0/0 | 3597 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0010c0014 | 0/0 | 3597 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0011c0010 | 0/0 | 3597 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0012c0019 | 0/0 | 3597 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0013c0026 | 0/0 | 3597 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0014c0015 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0015c0024 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0016c0021 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0017c0018 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0018c0017 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0019c0022 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 | ||
a0020c0020 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | ATGGC others(3592): Show |
chr2 | 218705835 | 218760416 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5007 | 103 | 34 | 21 | 30 | 4 | 14 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0001c0001t0003 | 0/0 | 5007 | 6 | 6 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0001c0001t0007 | 0/0 | 5007 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0001c0001t0009 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0001c0001t0012 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | GTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0001c0016t0001 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0002c0002t0002 | 1/1 | 5007 | 87 | 5 | 15 | 44 | 5 | 16 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0002c0002t0008 | 0/0 | 5007 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0002c0002t0011 | 0/0 | 5007 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0002c0007t0002 | 0/0 | 5007 | 4 | 3 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0002c0011t0006 | 0/0 | 5007 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0002c0013t0002 | 0/0 | 5007 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0002c0023t0002 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0002c0025t0002 | 0/0 | 5007 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0003c0003t0004 | 0/0 | 5007 | 8 | 8 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | GTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0003c0003t0005 | 0/0 | 5007 | 5 | 5 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0004c0004t0001 | 0/0 | 5007 | 5 | 5 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0004c0004t0003 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0005c0005t0001 | 0/0 | 5007 | 5 | 5 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0006c0006t0001 | 0/0 | 5007 | 4 | 0 | 0 | 4 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0007c0009t0002 | 0/0 | 5007 | 3 | 3 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0008c0008t0001 | 0/0 | 5007 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0008c0008t0003 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0009c0012t0002 | 0/0 | 5007 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0010c0014t0002 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0010c0014t0010 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0011c0010t0001 | 0/0 | 5007 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0012c0019t0001 | 0/0 | 5007 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0013c0026t0002 | 0/0 | 5007 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0014c0015t0001 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0015c0024t0002 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0016c0021t0001 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0017c0018t0001 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0018c0017t0001 | 0/0 | 5007 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0019c0022t0002 | 0/0 | 5007 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
a0020c0020t0001 | 0/0 | 5007 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | CTCTT others(5002): Show |
chr2 | 218705835 | 218760416 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0007g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0016t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0001 | 0/0 | 8 | 0 | 4 | 2 | 1 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0003 | 1/0 | 3 | 1 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0008g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0011g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0007t0002g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0007t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0007t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0011t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0011t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0013t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0013t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0023t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0025t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0005g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0005c0005t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0005c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0005c0005t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0005c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0006c0006t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0006c0006t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0006c0006t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0006c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0007c0009t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0007c0009t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0007c0009t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0008c0008t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0008c0008t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0008c0008t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0009c0012t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0009c0012t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0010c0014t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0010c0014t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0011c0010t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0011c0010t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0012c0019t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0013c0026t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0014c0015t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0015c0024t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0016c0021t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0017c0018t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0018c0017t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0019c0022t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0020c0020t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0008 | EUR | GBR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0088 | EUR | GBR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0076 | EUR | FIN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | FIN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0092 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01109 | hp2 | a0012 | c0019 | t0001 | g0023 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0133 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01256 | hp2 | a0001 | c0001 | t0007 | g0020 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01261 | hp1 | a0001 | c0001 | t0007 | g0020 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01261 | hp2 | a0013 | c0026 | t0002 | g0102 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01891 | hp2 | a0014 | c0015 | t0001 | g0183 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0116 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01975 | hp1 | a0002 | c0007 | t0002 | g0011 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01993 | hp2 | a0002 | c0002 | t0008 | g0001 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02055 | hp2 | a0003 | c0003 | t0005 | g0209 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02145 | hp1 | a0001 | c0016 | t0001 | g0182 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02145 | hp2 | a0004 | c0004 | t0001 | g0171 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | CDX | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | CDX | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02257 | hp2 | a0002 | c0011 | t0006 | g0200 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02280 | hp1 | a0016 | c0021 | t0001 | g0184 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02293 | hp1 | a0009 | c0012 | t0002 | g0110 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02451 | hp1 | a0002 | c0011 | t0006 | g0199 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02451 | hp2 | a0002 | c0013 | t0002 | g0118 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02572 | hp2 | a0004 | c0004 | t0001 | g0144 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02615 | hp1 | a0003 | c0003 | t0004 | g0204 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02615 | hp2 | a0010 | c0014 | t0002 | g0112 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02622 | hp1 | a0003 | c0003 | t0004 | g0208 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02622 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02630 | hp1 | a0002 | c0023 | t0002 | g0119 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02630 | hp2 | a0003 | c0003 | t0005 | g0025 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02647 | hp2 | a0017 | c0018 | t0001 | g0063 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0075 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0082 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02698 | hp2 | a0002 | c0002 | t0011 | g0099 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0201 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02717 | hp2 | a0007 | c0009 | t0002 | g0131 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02818 | hp1 | a0003 | c0003 | t0005 | g0207 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02818 | hp2 | a0004 | c0004 | t0003 | g0026 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02886 | hp1 | a0011 | c0010 | t0001 | g0191 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02886 | hp2 | a0007 | c0009 | t0002 | g0130 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02897 | hp2 | a0005 | c0005 | t0001 | g0014 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02922 | hp1 | a0010 | c0014 | t0010 | g0017 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02922 | hp2 | a0005 | c0005 | t0001 | g0053 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02965 | hp2 | a0002 | c0007 | t0002 | g0011 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02970 | hp1 | a0004 | c0004 | t0001 | g0152 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02976 | hp1 | a0007 | c0009 | t0002 | g0132 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0027 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03041 | hp1 | a0003 | c0003 | t0004 | g0202 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03041 | hp2 | a0002 | c0007 | t0002 | g0135 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03139 | hp1 | a0008 | c0008 | t0001 | g0186 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03195 | hp2 | a0003 | c0003 | t0005 | g0212 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03209 | hp2 | a0003 | c0003 | t0005 | g0025 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0094 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03453 | hp1 | a0011 | c0010 | t0001 | g0192 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03486 | hp2 | a0002 | c0013 | t0002 | g0128 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0125 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0113 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03516 | hp1 | a0008 | c0008 | t0003 | g0188 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03540 | hp1 | a0008 | c0008 | t0001 | g0187 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03540 | hp2 | a0005 | c0005 | t0001 | g0014 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03579 | hp2 | a0003 | c0003 | t0004 | g0203 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03654 | hp2 | a0018 | c0017 | t0001 | g0044 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0078 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | STU | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0126 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0095 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0108 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0087 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0032 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0072 | SAS | STU | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18906 | hp1 | a0003 | c0003 | t0004 | g0211 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18950 | hp1 | a0006 | c0006 | t0001 | g0178 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18950 | hp2 | a0019 | c0022 | t0002 | g0008 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18953 | hp2 | a0006 | c0006 | t0001 | g0179 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18963 | hp1 | a0006 | c0006 | t0001 | g0166 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18984 | hp1 | a0006 | c0006 | t0001 | g0167 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19030 | hp1 | a0003 | c0003 | t0004 | g0206 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0114 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19076 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19084 | hp2 | a0002 | c0025 | t0002 | g0101 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0103 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | ASW | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20129 | hp2 | a0005 | c0005 | t0001 | g0054 | AFR | ASW | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20805 | hp1 | a0020 | c0020 | t0001 | g0005 | EUR | TSI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0115 | EUR | TSI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | GIH | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01123 | hp2 | a0009 | c0012 | t0002 | g0003 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02109 | hp1 | a0004 | c0004 | t0001 | g0146 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02109 | hp2 | a0015 | c0024 | t0002 | g0120 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02486 | hp1 | a0003 | c0003 | t0004 | g0210 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03471 | hp1 | a0002 | c0007 | t0002 | g0028 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03471 | hp2 | a0004 | c0004 | t0001 | g0145 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | USA | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG06807 | hp2 | a0003 | c0003 | t0004 | g0205 | AFR | USA | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | USA | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20300 | hp2 | a0005 | c0005 | t0001 | g0055 | AFR | USA | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0083 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0071 | REF | REF | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0003 | REF | REF | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218737776 | G | C | 12 | a0001 a0004 a0005 others(9): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
missense_variant | MODERATE | c.100G>C | p.Glu34Gln | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 480/5007 | 100/3600 | 34/1199 | chr2 | 218737776 | |||
chr2:218737817 | G | T | 2 | a0008 a0016 |
4 | HG02280.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
missense_variant | MODERATE | c.141G>T | p.Gln47His | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 521/5007 | 141/3600 | 47/1199 | chr2 | 218737817 | |||
chr2:218738014 | A | G | 1 | a0020 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.338A>G | p.Asn113Ser | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 718/5007 | 338/3600 | 113/1199 | chr2 | 218738014 | |||
chr2:218738031 | C | T | 1 | a0013 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.355C>T | p.Arg119Cys | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 735/5007 | 355/3600 | 119/1199 | chr2 | 218738031 | |||
chr2:218738089 | C | T | 1 | a0010 | 2 | HG02615.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.413C>T | p.Ser138Leu | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 793/5007 | 413/3600 | 138/1199 | chr2 | 218738089 | |||
chr2:218738544 | G | A | 1 | a0019 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.868G>A | p.Ala290Thr | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1248/5007 | 868/3600 | 290/1199 | chr2 | 218738544 | |||
chr2:218738731 | C | T | 1 | a0012 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1055C>T | p.Pro352Leu | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1435/5007 | 1055/3600 | 352/1199 | chr2 | 218738731 | |||
chr2:218738808 | C | T | 1 | a0017 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1132C>T | p.Arg378Trp | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1512/5007 | 1132/3600 | 378/1199 | chr2 | 218738808 | |||
chr2:218738834 | G | T | 1 | a0011 | 2 | HG02886.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.1158G>T | p.Gln386His | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1538/5007 | 1158/3600 | 386/1199 | chr2 | 218738834 | |||
chr2:218738929 | G | A | 1 | a0003 | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
missense_variant | MODERATE | c.1253G>A | p.Arg418His | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1633/5007 | 1253/3600 | 418/1199 | chr2 | 218738929 | |||
chr2:218739067 | A | G | 1 | a0017 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1391A>G | p.Asn464Ser | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1771/5007 | 1391/3600 | 464/1199 | chr2 | 218739067 | |||
chr2:218740102 | C | T | 1 | a0006 | 4 | NA18950.hp1 NA18953.hp2 NA18963.hp1 others(1): Show |
missense_variant | MODERATE | c.1532C>T | p.Thr511Ile | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 4/20 | 1912/5007 | 1532/3600 | 511/1199 | chr2 | 218740102 | |||
chr2:218745155 | G | A | 1 | a0007 | 3 | HG02717.hp2 HG02886.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.1708G>A | p.Val570Ile | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 6/20 | 2088/5007 | 1708/3600 | 570/1199 | chr2 | 218745155 | |||
chr2:218747148 | G | A | 1 | a0014 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2120G>A | p.Arg707His | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 9/20 | 2500/5007 | 2120/3600 | 707/1199 | chr2 | 218747148 | |||
chr2:218747171 | C | T | 1 | a0015 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2143C>T | p.Arg715Cys | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 9/20 | 2523/5007 | 2143/3600 | 715/1199 | chr2 | 218747171 | |||
chr2:218750050 | A | G | 1 | a0018 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2777A>G | p.Gln926Arg | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/20 | 3157/5007 | 2777/3600 | 926/1199 | chr2 | 218750050 | |||
chr2:218753659 | A | G | 1 | a0009 | 2 | HG01123.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.3334A>G | p.Ser1112Gly | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 19/20 | 3714/5007 | 3334/3600 | 1112/1199 | chr2 | 218753659 | |||
chr2:218754202 | C | T | 1 | a0004 | 6 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
missense_variant | MODERATE | c.3413C>T | p.Thr1138Ile | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 3793/5007 | 3413/3600 | 1138/1199 | chr2 | 218754202 | |||
chr2:218754357 | A | T | 1 | a0005 | 5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
missense_variant | MODERATE | c.3568A>T | p.Ile1190Phe | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 3948/5007 | 3568/3600 | 1190/1199 | chr2 | 218754357 | |||
chr2:218754376 | C | A | 1 | a0016 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.3587C>A | p.Ala1196Asp | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 3967/5007 | 3587/3600 | 1196/1199 | chr2 | 218754376 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218737787 | G | A | 1 | a0002c0011 | 2 | HG02257.hp2 HG02451.hp1 |
synonymous_variant | LOW | c.111G>A | p.Ser37Ser | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 491/5007 | 111/3600 | 37/1199 | chr2 | 218737787 | |||
chr2:218738096 | G | A | 17 | a0001c0001 a0001c0016 a0002c0007 others(14): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
synonymous_variant | LOW | c.420G>A | p.Pro140Pro | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 800/5007 | 420/3600 | 140/1199 | chr2 | 218738096 | |||
chr2:218738567 | C | T | 1 | a0002c0025 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.891C>T | p.Thr297Thr | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1271/5007 | 891/3600 | 297/1199 | chr2 | 218738567 | |||
chr2:218745710 | A | G | 20 | a0001c0001 a0001c0016 a0002c0007 others(17): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): Show |
synonymous_variant | LOW | c.1806A>G | p.Glu602Glu | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 7/20 | 2186/5007 | 1806/3600 | 602/1199 | chr2 | 218745710 | |||
chr2:218752852 | G | A | 1 | a0002c0023 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.3066G>A | p.Gln1022Gln | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 17/20 | 3446/5007 | 3066/3600 | 1022/1199 | chr2 | 218752852 | |||
chr2:218754293 | G | A | 1 | a0001c0016 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.3504G>A | p.Thr1168Thr | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 3884/5007 | 3504/3600 | 1168/1199 | chr2 | 218754293 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218710835 | C | G | 2 | a0001c0001t0012 a0003c0003t0004 |
9 | HG02486.hp1 HG02615.hp1 HG02622.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-380C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/20 | 26842 | chr2 | 218710835 | ||||||
chr2:218710849 | T | C | 7 | a0001c0001t0003 a0001c0001t0012 a0002c0011t0006 others(4): Show |
24 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-366T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/20 | 26828 | chr2 | 218710849 | ||||||
chr2:218710964 | C | A | 1 | a0002c0002t0008 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-251C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/20 | 26713 | chr2 | 218710964 | ||||||
chr2:218727278 | C | T | 1 | a0002c0011t0006 | 2 | HG02257.hp2 HG02451.hp1 |
5_prime_UTR_variant | MODIFIER | c.-168C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/20 | 10399 | chr2 | 218727278 | ||||||
chr2:218727320 | T | C | 2 | a0003c0003t0004 a0003c0003t0005 |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-126T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/20 | 10357 | chr2 | 218727320 | ||||||
chr2:218737666 | G | A | 1 | a0001c0001t0009 | 1 | HG02976.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-11G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | chr2 | 218737666 | |||||||
chr2:218754404 | A | G | 1 | a0002c0002t0011 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 15 | chr2 | 218754404 | ||||||
chr2:218754552 | C | T | 1 | a0010c0014t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*163C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 163 | chr2 | 218754552 | ||||||
chr2:218754827 | C | T | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(17): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*438C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 438 | chr2 | 218754827 | ||||||
chr2:218755043 | T | C | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(17): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*654T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 654 | chr2 | 218755043 | ||||||
chr2:218755100 | G | T | 1 | a0001c0001t0007 | 2 | HG01256.hp2 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*711G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 711 | chr2 | 218755100 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218711069 | C | T | 22 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(19): Show |
23 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-178+32C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711069 | |||||||
chr2:218711120 | T | C | 1 | a0001c0001t0009g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-178+83T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711120 | |||||||
chr2:218711161 | C | A | 2 | a0002c0007t0002g0011 a0002c0007t0002g0028 |
3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-178+124C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711161 | |||||||
chr2:218711249 | C | T | 2 | a0002c0007t0002g0011 a0002c0007t0002g0028 |
3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-178+212C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711249 | |||||||
chr2:218711323 | A | G | 1 | a0001c0001t0009g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-178+286A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711323 | |||||||
chr2:218711400 | C | G | 4 | a0001c0001t0003g0026 a0001c0001t0003g0213 a0001c0001t0003g0214 others(1): Show |
4 | HG02257.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+363C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711400 | |||||||
chr2:218711434 | C | CT | 15 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0024 others(12): Show |
21 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-178+402dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711434 | ||||||
chr2:218711486 | C | T | 1 | a0014c0015t0001g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-178+449C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711486 | |||||||
chr2:218711772 | A | T | 13 | a0001c0001t0012g0201 a0003c0003t0004g0202 a0003c0003t0004g0203 others(10): Show |
14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-178+735A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711772 | |||||||
chr2:218711870 | C | CAAATCAC others(309): Show |
2 | a0001c0001t0001g0136 a0001c0001t0007g0020 |
3 | HG01256.hp2 HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-178+849_-178+850i others(318): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | ||||||
chr2:218711870 | C | CAAATCAC others(315): Show |
2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-178+849_-178+850i others(324): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | ||||||
chr2:218711870 | C | CAAATCAC others(318): Show |
1 | a0001c0001t0001g0139 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-178+849_-178+850i others(327): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | ||||||
chr2:218711870 | C | CAAATCAC others(319): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02896.hp2 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-178+849_-178+850i others(328): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | ||||||
chr2:218711870 | C | CAAATCAC others(323): Show |
1 | a0001c0001t0001g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-178+849_-178+850i others(332): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | ||||||
chr2:218711870 | C | CAAATCAC others(324): Show |
5 | a0001c0001t0001g0021 a0001c0001t0001g0147 a0004c0004t0001g0144 others(2): Show |
6 | HG00280.hp2 HG00741.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-178+849_-178+850i others(333): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | ||||||
chr2:218711870 | C | CAAATCAC others(325): Show |
24 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0148 others(21): Show |
27 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-178+849_-178+850i others(334): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | ||||||
chr2:218711870 | C | CAAATCAC others(326): Show |
15 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0169 others(12): Show |
17 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.-178+849_-178+850i others(335): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | ||||||
chr2:218711870 | C | CAAATCAC others(327): Show |
1 | a0001c0001t0001g0181 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-178+849_-178+850i others(336): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | ||||||
chr2:218711870 | C | CAAATCAC others(335): Show |
1 | a0001c0016t0001g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-178+849_-178+850i others(344): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | ||||||
chr2:218711880 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
7 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+843A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711880 | |||||||
chr2:218711902 | T | G | 13 | a0001c0001t0012g0201 a0003c0003t0004g0202 a0003c0003t0004g0203 others(10): Show |
14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-178+865T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711902 | |||||||
chr2:218712018 | A | G | 9 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(6): Show |
9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-178+981A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712018 | |||||||
chr2:218712026 | C | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-178+989C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712026 | |||||||
chr2:218712101 | G | A | 2 | a0002c0002t0002g0029 a0002c0002t0002g0030 |
2 | HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-178+1064G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712101 | |||||||
chr2:218712243 | C | T | 1 | a0002c0007t0002g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-178+1206C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712243 | |||||||
chr2:218712388 | CT | C | 23 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(20): Show |
24 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-178+1367delT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218712388 | ||||||
chr2:218712422 | C | G | 9 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(6): Show |
9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-178+1385C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712422 | |||||||
chr2:218712633 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-178+1596C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712633 | |||||||
chr2:218712650 | A | G | 22 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(19): Show |
23 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-178+1613A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712650 | |||||||
chr2:218712702 | T | G | 1 | a0002c0002t0002g0032 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-178+1665T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712702 | |||||||
chr2:218712961 | G | A | 1 | a0001c0001t0003g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-178+1924G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712961 | |||||||
chr2:218713025 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-178+1988G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713025 | |||||||
chr2:218713130 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-178+2093A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713130 | |||||||
chr2:218713244 | G | C | 2 | a0002c0002t0002g0033 a0002c0002t0002g0034 |
2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-178+2207G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713244 | |||||||
chr2:218713321 | A | C | 22 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(19): Show |
23 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-178+2284A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713321 | |||||||
chr2:218713426 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-178+2389C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713426 | |||||||
chr2:218713627 | C | G | 2 | a0011c0010t0001g0191 a0011c0010t0001g0192 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-178+2590C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713627 | |||||||
chr2:218713638 | T | G | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(132): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-178+2601T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713638 | |||||||
chr2:218714309 | A | G | 2 | a0003c0003t0005g0025 a0003c0003t0005g0212 |
3 | HG02630.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-178+3272A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714309 | |||||||
chr2:218714429 | C | G | 2 | a0011c0010t0001g0191 a0011c0010t0001g0192 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-178+3392C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714429 | |||||||
chr2:218714530 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | NA18971.hp1 NA19012.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-178+3493T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714530 | |||||||
chr2:218714622 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-178+3585T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714622 | |||||||
chr2:218714645 | C | G | 1 | a0002c0002t0002g0133 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-178+3608C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714645 | |||||||
chr2:218714797 | T | TG | 5 | a0001c0001t0001g0006 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
8 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-178+3764dupG | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218714797 | ||||||
chr2:218714844 | AACAG | A | 4 | a0002c0007t0002g0135 a0007c0009t0002g0130 a0007c0009t0002g0131 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+3808_-178+381 others(8): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714844 | |||||||
chr2:218714848 | G | A | 213 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(210): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-178+3811G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714848 | |||||||
chr2:218714912 | AATATT | A | 21 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(18): Show |
22 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-178+3882_-178+388 others(9): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218714912 | ||||||
chr2:218714958 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-178+3921A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714958 | |||||||
chr2:218715019 | AAGTT | A | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-178+3988_-178+399 others(8): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218715019 | ||||||
chr2:218715185 | CAT | C | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(7): Show |
10 | NA18939.hp2 NA18968.hp2 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.-178+4151_-178+415 others(6): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218715185 | ||||||
chr2:218715216 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-178+4179T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715216 | |||||||
chr2:218715323 | A | G | 21 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(18): Show |
22 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-178+4286A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715323 | |||||||
chr2:218715586 | A | G | 1 | a0002c0002t0002g0129 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-178+4549A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715586 | |||||||
chr2:218715690 | C | T | 1 | a0017c0018t0001g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-178+4653C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715690 | |||||||
chr2:218715699 | G | C | 2 | a0002c0007t0002g0011 a0002c0007t0002g0028 |
3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-178+4662G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715699 | |||||||
chr2:218715724 | C | T | 21 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(18): Show |
22 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-178+4687C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715724 | |||||||
chr2:218715947 | G | A | 1 | a0002c0002t0002g0072 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-178+4910G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715947 | |||||||
chr2:218715968 | A | G | 1 | a0002c0013t0002g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-178+4931A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715968 | |||||||
chr2:218715975 | G | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0170 |
2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-178+4938G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715975 | |||||||
chr2:218716099 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-178+5062C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716099 | |||||||
chr2:218716262 | A | C | 1 | a0002c0002t0002g0072 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-178+5225A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716262 | |||||||
chr2:218716442 | CAG | C | 21 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(18): Show |
22 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-178+5407_-178+540 others(6): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218716442 | ||||||
chr2:218716554 | C | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0185 others(9): Show |
17 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-178+5517C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716554 | |||||||
chr2:218716555 | C | T | 2 | a0002c0002t0002g0127 a0007c0009t0002g0132 |
2 | HG02976.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-178+5518C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716555 | |||||||
chr2:218716606 | G | A | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-178+5569G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716606 | |||||||
chr2:218716862 | A | G | 2 | a0011c0010t0001g0191 a0011c0010t0001g0192 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-178+5825A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716862 | |||||||
chr2:218716920 | G | A | 28 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0035 others(25): Show |
30 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-178+5883G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716920 | |||||||
chr2:218716981 | A | G | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-178+5944A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716981 | |||||||
chr2:218717074 | C | G | 4 | a0006c0006t0001g0166 a0006c0006t0001g0167 a0006c0006t0001g0178 others(1): Show |
4 | NA18950.hp1 NA18953.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+6037C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717074 | |||||||
chr2:218717098 | C | T | 21 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(18): Show |
22 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-178+6061C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717098 | |||||||
chr2:218717253 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-178+6216C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717253 | |||||||
chr2:218717260 | G | C | 6 | a0001c0001t0001g0151 a0004c0004t0001g0144 a0004c0004t0001g0145 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-178+6223G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717260 | |||||||
chr2:218717295 | T | C | 1 | a0002c0007t0002g0028 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-178+6258T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717295 | |||||||
chr2:218717339 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-178+6302G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717339 | |||||||
chr2:218717578 | C | A | 2 | a0002c0007t0002g0011 a0002c0007t0002g0028 |
3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-178+6541C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717578 | |||||||
chr2:218717801 | C | CT | 4 | a0001c0001t0001g0024 a0001c0001t0001g0190 a0011c0010t0001g0191 others(1): Show |
5 | HG02886.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-178+6778dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218717801 | ||||||
chr2:218717885 | G | A | 14 | a0002c0011t0006g0199 a0002c0011t0006g0200 a0003c0003t0004g0202 others(11): Show |
15 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-178+6848G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717885 | |||||||
chr2:218717938 | G | A | 14 | a0002c0011t0006g0199 a0002c0011t0006g0200 a0003c0003t0004g0202 others(11): Show |
15 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-178+6901G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717938 | |||||||
chr2:218718174 | T | C | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(133): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-178+7137T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718174 | |||||||
chr2:218718247 | T | G | 4 | a0002c0002t0002g0075 a0002c0002t0002g0076 a0002c0002t0002g0077 others(1): Show |
4 | HG00280.hp1 HG01255.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+7210T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718247 | |||||||
chr2:218718285 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-178+7248G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718285 | |||||||
chr2:218718409 | A | C | 1 | a0002c0002t0002g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-178+7372A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718409 | |||||||
chr2:218718418 | G | A | 14 | a0002c0011t0006g0199 a0002c0011t0006g0200 a0003c0003t0004g0202 others(11): Show |
15 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-178+7381G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718418 | |||||||
chr2:218718533 | C | T | 7 | a0001c0001t0003g0026 a0001c0001t0003g0196 a0001c0001t0003g0197 others(4): Show |
7 | HG02257.hp1 HG02818.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-178+7496C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718533 | |||||||
chr2:218718542 | C | T | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-178+7505C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718542 | |||||||
chr2:218718669 | C | G | 1 | a0001c0001t0001g0189 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-178+7632C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718669 | |||||||
chr2:218718789 | C | G | 4 | a0002c0002t0002g0121 a0002c0002t0002g0122 a0002c0002t0002g0123 others(1): Show |
4 | HG02083.hp1 HG02132.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+7752C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718789 | |||||||
chr2:218718915 | A | G | 14 | a0002c0011t0006g0199 a0002c0011t0006g0200 a0003c0003t0004g0202 others(11): Show |
15 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-178+7878A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718915 | |||||||
chr2:218719067 | G | A | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-178+8030G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719067 | |||||||
chr2:218719135 | C | T | 3 | a0008c0008t0001g0186 a0008c0008t0001g0187 a0008c0008t0003g0188 |
3 | HG03139.hp1 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-178+8098C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719135 | |||||||
chr2:218719182 | C | T | 14 | a0002c0011t0006g0199 a0002c0011t0006g0200 a0003c0003t0004g0202 others(11): Show |
15 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-8087C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719182 | |||||||
chr2:218719300 | G | C | 1 | a0016c0021t0001g0184 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-177-7969G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719300 | |||||||
chr2:218719302 | A | G | 3 | a0002c0013t0002g0118 a0002c0023t0002g0119 a0015c0024t0002g0120 |
3 | HG02109.hp2 HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-177-7967A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719302 | |||||||
chr2:218719355 | G | A | 1 | a0002c0002t0002g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-177-7914G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719355 | |||||||
chr2:218719534 | A | G | 1 | a0002c0002t0002g0117 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-177-7735A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719534 | |||||||
chr2:218719570 | T | TA | 39 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(36): Show |
46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.-177-7682dupA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218719570 | ||||||
chr2:218719570 | TA | T | 17 | a0001c0001t0001g0050 a0001c0001t0001g0062 a0001c0001t0001g0142 others(14): Show |
18 | HG00099.hp1 HG01943.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-177-7682delA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218719570 | ||||||
chr2:218720000 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-177-7269C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720000 | |||||||
chr2:218720199 | C | T | 40 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(37): Show |
43 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.-177-7070C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720199 | |||||||
chr2:218720252 | G | C | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(79): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-177-7017G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720252 | |||||||
chr2:218720266 | G | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-177-7003G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720266 | |||||||
chr2:218720530 | C | T | 2 | a0005c0005t0001g0014 a0005c0005t0001g0055 |
3 | HG02897.hp2 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-177-6739C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720530 | |||||||
chr2:218720668 | C | T | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-177-6601C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720668 | |||||||
chr2:218720674 | C | CA | 9 | a0001c0001t0001g0052 a0002c0002t0002g0016 a0002c0002t0002g0080 others(6): Show |
10 | HG02886.hp1 HG03041.hp1 HG03453.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177-6578dupA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218720674 | ||||||
chr2:218720674 | CA | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0069 a0001c0001t0001g0161 others(2): Show |
6 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.-177-6578delA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218720674 | ||||||
chr2:218720690 | A | G | 1 | a0002c0002t0002g0113 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-177-6579A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720690 | |||||||
chr2:218720707 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0185 a0001c0001t0001g0189 |
5 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-6562T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720707 | |||||||
chr2:218720756 | G | A | 2 | a0002c0007t0002g0011 a0002c0007t0002g0028 |
3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-177-6513G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720756 | |||||||
chr2:218720786 | A | G | 1 | a0010c0014t0002g0112 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-177-6483A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720786 | |||||||
chr2:218720865 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0070 |
2 | NA18939.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-177-6404G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720865 | |||||||
chr2:218720888 | C | T | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-177-6381C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720888 | |||||||
chr2:218721132 | A | G | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-177-6137A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721132 | |||||||
chr2:218721235 | CAAT | C | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-177-6033_-177-603 others(7): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721235 | |||||||
chr2:218721235 | CAATT | C | 133 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(130): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-177-6011_-177-600 others(8): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218721235 | ||||||
chr2:218721239 | T | C | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-177-6030T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721239 | |||||||
chr2:218721359 | C | T | 1 | a0002c0002t0002g0117 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-177-5910C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721359 | |||||||
chr2:218721624 | C | T | 1 | a0017c0018t0001g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-177-5645C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721624 | |||||||
chr2:218721667 | A | G | 1 | a0016c0021t0001g0184 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-177-5602A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721667 | |||||||
chr2:218721750 | G | T | 2 | a0002c0002t0002g0018 a0002c0002t0002g0111 |
3 | HG00438.hp1 HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-177-5519G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721750 | |||||||
chr2:218721837 | A | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0176 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177-5432A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721837 | |||||||
chr2:218721867 | A | T | 1 | a0009c0012t0002g0110 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-177-5402A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721867 | |||||||
chr2:218721899 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-177-5370G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721899 | |||||||
chr2:218721962 | TA | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0062 others(10): Show |
16 | HG01943.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-177-5296delA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218721962 | ||||||
chr2:218722022 | C | T | 4 | a0005c0005t0001g0014 a0005c0005t0001g0053 a0005c0005t0001g0054 others(1): Show |
5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177-5247C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218722022 | |||||||
chr2:218722356 | C | CT | 119 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(116): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-177-4901dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218722356 | ||||||
chr2:218722356 | C | CTT | 6 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177-4902_-177-490 others(6): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218722356 | ||||||
chr2:218722568 | A | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-4701A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218722568 | |||||||
chr2:218722617 | G | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0193 a0001c0001t0001g0194 others(9): Show |
15 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-4652G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218722617 | |||||||
chr2:218722698 | A | G | 1 | a0002c0002t0002g0109 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-177-4571A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218722698 | |||||||
chr2:218722754 | C | T | 1 | a0002c0002t0002g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-177-4515C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218722754 | |||||||
chr2:218723015 | A | G | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-177-4254A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218723015 | |||||||
chr2:218723051 | T | C | 1 | a0002c0002t0002g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-177-4218T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218723051 | |||||||
chr2:218723411 | A | G | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-177-3858A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218723411 | |||||||
chr2:218723974 | A | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-3295A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218723974 | |||||||
chr2:218724167 | G | T | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(134): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-177-3102G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724167 | |||||||
chr2:218724245 | T | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0193 a0001c0001t0001g0194 others(10): Show |
16 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-177-3024T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724245 | |||||||
chr2:218724441 | C | T | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-177-2828C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724441 | |||||||
chr2:218724452 | T | C | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-2817T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724452 | |||||||
chr2:218724525 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-177-2744A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724525 | |||||||
chr2:218724535 | C | T | 1 | a0008c0008t0003g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-177-2734C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724535 | |||||||
chr2:218724557 | T | A | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-2712T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724557 | |||||||
chr2:218724699 | A | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0193 a0001c0001t0001g0194 others(9): Show |
15 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-2570A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724699 | |||||||
chr2:218724871 | T | C | 124 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(121): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-177-2398T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724871 | |||||||
chr2:218724872 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-177-2397A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724872 | |||||||
chr2:218724901 | G | A | 1 | a0002c0002t0002g0085 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-177-2368G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724901 | |||||||
chr2:218725052 | A | G | 1 | a0002c0002t0002g0107 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-177-2217A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725052 | |||||||
chr2:218725077 | T | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0007g0020 |
4 | HG00741.hp2 HG01256.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177-2192T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725077 | |||||||
chr2:218725107 | A | G | 4 | a0002c0007t0002g0135 a0007c0009t0002g0130 a0007c0009t0002g0131 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177-2162A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725107 | |||||||
chr2:218725396 | G | GT | 7 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0001g0190 others(4): Show |
7 | HG00621.hp2 HG03098.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.-177-1863dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218725396 | ||||||
chr2:218725415 | A | G | 1 | a0002c0002t0002g0105 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-177-1854A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725415 | |||||||
chr2:218725461 | G | C | 1 | a0002c0002t0002g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-177-1808G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725461 | |||||||
chr2:218725544 | A | G | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-177-1725A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725544 | |||||||
chr2:218725546 | A | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0193 a0001c0001t0001g0194 others(9): Show |
15 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-1723A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725546 | |||||||
chr2:218725584 | C | T | 1 | a0002c0002t0002g0104 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-177-1685C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725584 | |||||||
chr2:218725602 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0137 others(4): Show |
9 | HG00733.hp2 HG01070.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.-177-1667C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725602 | |||||||
chr2:218725625 | G | A | 2 | a0002c0002t0002g0087 a0002c0002t0002g0088 |
2 | HG00140.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-177-1644G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725625 | |||||||
chr2:218725696 | T | C | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-1573T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725696 | |||||||
chr2:218726148 | A | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-1121A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726148 | |||||||
chr2:218726152 | C | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0185 others(8): Show |
14 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-177-1117C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726152 | |||||||
chr2:218726481 | C | T | 1 | a0001c0016t0001g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-177-788C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726481 | |||||||
chr2:218726498 | C | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-177-771C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726498 | |||||||
chr2:218726568 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0185 a0001c0001t0001g0189 others(4): Show |
9 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-177-701C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726568 | |||||||
chr2:218726759 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0176 a0001c0016t0001g0182 |
3 | HG02145.hp1 HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177-510G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726759 | |||||||
chr2:218726898 | G | A | 2 | a0003c0003t0005g0025 a0003c0003t0005g0212 |
3 | HG02630.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-177-371G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726898 | |||||||
chr2:218727008 | C | T | 10 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177-261C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218727008 | |||||||
chr2:218727060 | C | T | 1 | a0003c0003t0004g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-177-209C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218727060 | |||||||
chr2:218727261 | A | G | 2 | a0002c0002t0002g0123 a0002c0002t0002g0124 |
2 | HG02083.hp1 NA19087.hp1 |
splice_region_variant&intron_variant | LOW | c.-177-8A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218727261 | |||||||
chr2:218727395 | A | G | 1 | a0002c0002t0002g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-99+48A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727395 | |||||||
chr2:218727419 | C | G | 28 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0035 others(25): Show |
30 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-99+72C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727419 | |||||||
chr2:218727503 | C | T | 3 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0001c0001t0003g0198 |
3 | NA19030.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-99+156C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727503 | |||||||
chr2:218727504 | A | G | 127 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(124): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.-99+157A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727504 | |||||||
chr2:218727599 | G | A | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-99+252G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727599 | |||||||
chr2:218727864 | T | C | 2 | a0002c0002t0002g0018 a0002c0002t0002g0111 |
3 | HG00438.hp1 HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-99+517T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727864 | |||||||
chr2:218727908 | C | A | 2 | a0002c0007t0002g0011 a0002c0007t0002g0028 |
3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-99+561C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727908 | |||||||
chr2:218727925 | A | T | 1 | a0002c0002t0002g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-99+578A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727925 | |||||||
chr2:218728136 | A | G | 2 | a0002c0002t0002g0032 a0013c0026t0002g0102 |
2 | HG01261.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-99+789A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728136 | |||||||
chr2:218728480 | T | C | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(134): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-99+1133T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728480 | |||||||
chr2:218728508 | C | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+1161C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728508 | |||||||
chr2:218728606 | G | A | 23 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0035 others(20): Show |
25 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-99+1259G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728606 | |||||||
chr2:218728701 | C | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+1354C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728701 | |||||||
chr2:218728921 | A | AT | 32 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0029 others(29): Show |
34 | HG01123.hp2 HG01192.hp2 HG01975.hp1 others(31): Show |
intron_variant | MODIFIER | c.-99+1594dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218728921 | ||||||
chr2:218728942 | G | T | 14 | a0001c0001t0001g0067 a0001c0001t0001g0150 a0001c0001t0001g0151 others(11): Show |
14 | HG01192.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-99+1595G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728942 | |||||||
chr2:218728943 | GC | G | 8 | a0001c0001t0001g0067 a0001c0001t0001g0150 a0001c0001t0001g0158 others(5): Show |
8 | HG01192.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-99+1597delC | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728943 | |||||||
chr2:218728944 | C | G | 6 | a0001c0001t0001g0151 a0001c0016t0001g0182 a0004c0004t0001g0145 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-99+1597C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728944 | |||||||
chr2:218728944 | CGG | C | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(102): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-99+1605_-99+1606d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218728944 | ||||||
chr2:218728945 | G | A | 1 | a0002c0002t0002g0072 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-99+1598G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728945 | |||||||
chr2:218728945 | G | C | 6 | a0001c0001t0001g0151 a0001c0016t0001g0182 a0004c0004t0001g0145 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-99+1598G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728945 | |||||||
chr2:218728946 | G | C | 8 | a0001c0001t0001g0067 a0001c0001t0001g0150 a0001c0001t0001g0158 others(5): Show |
8 | HG01192.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-99+1599G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728946 | |||||||
chr2:218728950 | G | A | 1 | a0002c0002t0002g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-99+1603G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728950 | |||||||
chr2:218728952 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-99+1605G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728952 | |||||||
chr2:218728986 | G | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+1639G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728986 | |||||||
chr2:218728987 | C | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+1640C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728987 | |||||||
chr2:218729497 | C | G | 6 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+2150C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729497 | |||||||
chr2:218729511 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-99+2164A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729511 | |||||||
chr2:218729689 | A | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-99+2342A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729689 | |||||||
chr2:218729747 | T | TAAA | 4 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0185 others(1): Show |
6 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-99+2400_-99+2401i others(5): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729747 | |||||||
chr2:218729747 | TTAAAAAA others(3): Show |
T | 2 | a0008c0008t0001g0186 a0008c0008t0003g0188 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-99+2401_-99+2410d others(12): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729747 | |||||||
chr2:218729747 | TTAAAAAA others(9): Show |
T | 1 | a0001c0001t0001g0037 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-99+2401_-99+2416d others(18): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729747 | |||||||
chr2:218729748 | T | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
9 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-99+2401T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729748 | |||||||
chr2:218729748 | T | TAAAA | 12 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0048 others(9): Show |
13 | HG00621.hp2 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-99+2412_-99+2415d others(6): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729748 | ||||||
chr2:218729748 | T | TAAAAA | 11 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0041 others(8): Show |
12 | HG00558.hp2 HG02074.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.-99+2411_-99+2415d others(7): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729748 | ||||||
chr2:218729748 | T | TAAAAAAA | 5 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
5 | HG02559.hp1 HG03130.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+2409_-99+2415d others(9): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729748 | ||||||
chr2:218729756 | A | AAC | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-99+2410_-99+2411i others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729756 | ||||||
chr2:218729756 | A | C | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-99+2409A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729756 | |||||||
chr2:218729759 | A | AAC | 6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0143 others(3): Show |
6 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+2413_-99+2414i others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729759 | ||||||
chr2:218729759 | A | AC | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(60): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-99+2412_-99+2413i others(3): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729759 | |||||||
chr2:218729759 | A | C | 1 | a0001c0001t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-99+2412A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729759 | |||||||
chr2:218729759 | A | G | 1 | a0002c0002t0002g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-99+2412A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729759 | |||||||
chr2:218729760 | A | C | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-99+2413A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729760 | |||||||
chr2:218729762 | A | C | 1 | a0002c0025t0002g0101 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-99+2415A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729762 | |||||||
chr2:218729762 | AC | A | 3 | a0001c0001t0009g0027 a0002c0011t0006g0199 a0002c0011t0006g0200 |
3 | HG02257.hp2 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-99+2416delC | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729762 | |||||||
chr2:218729763 | C | A | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(134): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-99+2416C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729763 | |||||||
chr2:218729764 | A | C | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-99+2417A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729764 | |||||||
chr2:218729766 | A | AAC | 4 | a0005c0005t0001g0014 a0005c0005t0001g0053 a0005c0005t0001g0054 others(1): Show |
5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+2420_-99+2421i others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729766 | ||||||
chr2:218729766 | A | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(67): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.-99+2419A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729766 | |||||||
chr2:218729767 | A | C | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+2420A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729767 | |||||||
chr2:218729769 | A | C | 4 | a0005c0005t0001g0014 a0005c0005t0001g0053 a0005c0005t0001g0054 others(1): Show |
5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+2422A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729769 | |||||||
chr2:218729947 | T | C | 1 | a0014c0015t0001g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-99+2600T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729947 | |||||||
chr2:218730054 | A | G | 2 | a0011c0010t0001g0191 a0011c0010t0001g0192 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-99+2707A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730054 | |||||||
chr2:218730249 | C | T | 1 | a0001c0016t0001g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-99+2902C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730249 | |||||||
chr2:218730278 | C | T | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-99+2931C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730278 | |||||||
chr2:218730309 | T | TA | 4 | a0002c0002t0002g0087 a0002c0002t0002g0088 a0002c0002t0002g0090 others(1): Show |
4 | HG00140.hp2 HG03834.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2962_-99+2963i others(3): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCC | T | 31 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0008 others(28): Show |
39 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2964d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCCA | T | 16 | a0002c0002t0002g0001 a0002c0002t0002g0029 a0002c0002t0002g0030 others(13): Show |
23 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2965d others(5): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCCAA | T | 4 | a0002c0002t0002g0017 a0002c0002t0002g0116 a0010c0014t0002g0112 others(1): Show |
4 | HG01943.hp2 HG02615.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2966d others(6): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCCAAA | T | 3 | a0002c0007t0002g0011 a0002c0007t0002g0028 a0007c0009t0002g0130 |
4 | HG01975.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2967d others(7): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCCAAAA | T | 3 | a0002c0007t0002g0135 a0007c0009t0002g0131 a0007c0009t0002g0132 |
3 | HG02717.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-99+2963_-99+2968d others(8): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCCAAAAA others(3): Show |
T | 2 | a0002c0002t0002g0018 a0002c0011t0006g0200 |
3 | HG02074.hp2 HG02257.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-99+2963_-99+2972d others(12): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCCAAAAA others(4): Show |
T | 1 | a0002c0011t0006g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-99+2963_-99+2973d others(13): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCCAAAAA others(5): Show |
T | 1 | a0003c0003t0004g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-99+2963_-99+2974d others(14): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCCAAAAA others(6): Show |
T | 1 | a0003c0003t0004g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-99+2963_-99+2975d others(15): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCCAAAAA others(11): Show |
T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0169 a0008c0008t0003g0188 others(1): Show |
4 | HG01192.hp1 HG02886.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2980d others(20): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCCAAAAA others(12): Show |
T | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(110): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2981d others(21): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730309 | TCCAAAAA others(13): Show |
T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0051 others(3): Show |
8 | HG02280.hp2 HG02896.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2982d others(22): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | |||||||
chr2:218730310 | C | A | 30 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0019 others(27): Show |
36 | HG00438.hp2 HG00621.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-99+2963C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730310 | |||||||
chr2:218730311 | C | A | 4 | a0002c0002t0002g0087 a0002c0002t0002g0088 a0002c0002t0002g0090 others(1): Show |
4 | HG00140.hp2 HG03834.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2964C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730311 | |||||||
chr2:218730311 | C | CAAA | 4 | a0003c0003t0004g0203 a0003c0003t0004g0211 a0003c0003t0005g0025 others(1): Show |
5 | HG02630.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+3000_-99+3002d others(5): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218730311 | ||||||
chr2:218730311 | CA | C | 17 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0019 others(14): Show |
21 | HG00438.hp2 HG00621.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-99+3002delA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218730311 | ||||||
chr2:218730313 | A | C | 31 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0008 others(28): Show |
39 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-99+2966A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730313 | |||||||
chr2:218730314 | A | C | 16 | a0002c0002t0002g0001 a0002c0002t0002g0029 a0002c0002t0002g0030 others(13): Show |
23 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-99+2967A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730314 | |||||||
chr2:218730315 | A | C | 4 | a0002c0002t0002g0017 a0002c0002t0002g0116 a0010c0014t0002g0112 others(1): Show |
4 | HG01943.hp2 HG02615.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2968A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730315 | |||||||
chr2:218730316 | A | C | 3 | a0002c0007t0002g0011 a0002c0007t0002g0028 a0007c0009t0002g0130 |
4 | HG01975.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+2969A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730316 | |||||||
chr2:218730317 | A | C | 3 | a0002c0007t0002g0135 a0007c0009t0002g0131 a0007c0009t0002g0132 |
3 | HG02717.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-99+2970A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730317 | |||||||
chr2:218730320 | A | C | 1 | a0002c0002t0002g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-99+2973A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730320 | |||||||
chr2:218730321 | A | C | 2 | a0002c0002t0002g0018 a0002c0011t0006g0200 |
3 | HG02074.hp2 HG02257.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-99+2974A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730321 | |||||||
chr2:218730322 | A | C | 1 | a0002c0011t0006g0199 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-99+2975A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730322 | |||||||
chr2:218730323 | A | C | 1 | a0003c0003t0004g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-99+2976A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730323 | |||||||
chr2:218730324 | A | C | 1 | a0003c0003t0004g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-99+2977A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730324 | |||||||
chr2:218730329 | A | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0169 a0008c0008t0003g0188 others(1): Show |
4 | HG01192.hp1 HG02886.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2982A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730329 | |||||||
chr2:218730330 | A | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(110): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-99+2983A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730330 | |||||||
chr2:218730331 | A | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0051 others(3): Show |
8 | HG02280.hp2 HG02896.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+2984A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730331 | |||||||
chr2:218730342 | A | G | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+2995A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730342 | |||||||
chr2:218730346 | A | G | 4 | a0005c0005t0001g0014 a0005c0005t0001g0053 a0005c0005t0001g0054 others(1): Show |
5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+2999A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730346 | |||||||
chr2:218730437 | G | A | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-99+3090G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730437 | |||||||
chr2:218730463 | A | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-99+3116A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730463 | |||||||
chr2:218730508 | A | G | 4 | a0002c0007t0002g0135 a0007c0009t0002g0130 a0007c0009t0002g0131 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+3161A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730508 | |||||||
chr2:218730532 | T | A | 7 | a0001c0001t0001g0151 a0004c0004t0001g0144 a0004c0004t0001g0145 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-99+3185T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730532 | |||||||
chr2:218730730 | CA | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+3385delA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218730730 | ||||||
chr2:218730784 | A | G | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-99+3437A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730784 | |||||||
chr2:218730825 | C | T | 1 | a0002c0002t0002g0115 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-99+3478C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730825 | |||||||
chr2:218730895 | A | C | 4 | a0005c0005t0001g0014 a0005c0005t0001g0053 a0005c0005t0001g0054 others(1): Show |
5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+3548A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730895 | |||||||
chr2:218730906 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-99+3559C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730906 | |||||||
chr2:218730987 | T | C | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-99+3640T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730987 | |||||||
chr2:218731072 | G | A | 2 | a0002c0007t0002g0011 a0002c0007t0002g0028 |
3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-99+3725G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731072 | |||||||
chr2:218731121 | A | AAT | 8 | a0001c0001t0001g0151 a0002c0011t0006g0199 a0002c0011t0006g0200 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+3775_-99+3776i others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218731121 | ||||||
chr2:218731121 | A | AT | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(114): Show |
134 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-99+3774_-99+3775i others(3): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731121 | |||||||
chr2:218731209 | G | A | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(67): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.-99+3862G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731209 | |||||||
chr2:218731236 | C | T | 1 | a0002c0002t0002g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-99+3889C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731236 | |||||||
chr2:218731384 | G | C | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(134): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-99+4037G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731384 | |||||||
chr2:218731598 | G | A | 38 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(35): Show |
41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-99+4251G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731598 | |||||||
chr2:218731730 | C | T | 4 | a0002c0007t0002g0135 a0007c0009t0002g0130 a0007c0009t0002g0131 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+4383C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731730 | |||||||
chr2:218731787 | T | C | 1 | a0002c0002t0002g0098 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-99+4440T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731787 | |||||||
chr2:218732298 | A | G | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+4951A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732298 | |||||||
chr2:218732393 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0189 |
2 | HG01175.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-99+5046G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732393 | |||||||
chr2:218732462 | T | C | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-99+5115T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732462 | |||||||
chr2:218732536 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0185 a0001c0001t0001g0189 |
5 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-98-5043G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732536 | |||||||
chr2:218732653 | C | T | 6 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-98-4926C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732653 | |||||||
chr2:218732724 | C | T | 1 | a0002c0002t0002g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-98-4855C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732724 | |||||||
chr2:218733237 | A | G | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-98-4342A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733237 | |||||||
chr2:218733318 | A | T | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-98-4261A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733318 | |||||||
chr2:218733350 | G | A | 1 | a0002c0013t0002g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-98-4229G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733350 | |||||||
chr2:218733355 | G | A | 1 | a0002c0013t0002g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-98-4224G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733355 | |||||||
chr2:218733369 | G | A | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-98-4210G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733369 | |||||||
chr2:218733372 | C | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(121): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-98-4207C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733372 | |||||||
chr2:218733873 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-98-3706A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733873 | |||||||
chr2:218734054 | G | T | 38 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(35): Show |
41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-98-3525G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734054 | |||||||
chr2:218734545 | G | A | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-98-3034G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734545 | |||||||
chr2:218734583 | G | A | 1 | a0016c0021t0001g0184 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-98-2996G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734583 | |||||||
chr2:218734593 | C | T | 1 | a0002c0013t0002g0118 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-98-2986C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734593 | |||||||
chr2:218734713 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-98-2866T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734713 | |||||||
chr2:218734758 | G | A | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-2821G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734758 | |||||||
chr2:218734761 | A | G | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-98-2818A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734761 | |||||||
chr2:218735034 | A | G | 1 | a0002c0002t0002g0115 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-98-2545A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735034 | |||||||
chr2:218735345 | T | G | 5 | a0004c0004t0001g0144 a0004c0004t0001g0145 a0004c0004t0001g0146 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-98-2234T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735345 | |||||||
chr2:218735468 | G | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-98-2111G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735468 | |||||||
chr2:218735514 | C | T | 1 | a0002c0002t0002g0097 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-98-2065C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735514 | |||||||
chr2:218735593 | A | T | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(134): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-98-1986A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735593 | |||||||
chr2:218735712 | A | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-98-1867A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735712 | |||||||
chr2:218735727 | C | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-98-1852C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735727 | |||||||
chr2:218735742 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 |
3 | HG01891.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-98-1837G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735742 | |||||||
chr2:218735967 | C | CT | 44 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0038 others(41): Show |
52 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-98-1589dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218735967 | ||||||
chr2:218735967 | C | CTT | 9 | a0001c0001t0001g0048 a0002c0011t0006g0199 a0002c0011t0006g0200 others(6): Show |
10 | HG00621.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-98-1590_-98-1589d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218735967 | ||||||
chr2:218735967 | CT | C | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(55): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-98-1589delT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218735967 | ||||||
chr2:218735967 | CTT | C | 6 | a0001c0001t0001g0151 a0001c0001t0001g0161 a0001c0001t0001g0193 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-98-1590_-98-1589d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218735967 | ||||||
chr2:218736126 | C | CACCAT | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-1449_-98-1445d others(7): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218736126 | ||||||
chr2:218736147 | G | C | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-1432G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736147 | |||||||
chr2:218736276 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-98-1303C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736276 | |||||||
chr2:218736277 | G | A | 1 | a0002c0002t0002g0095 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-98-1302G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736277 | |||||||
chr2:218736425 | G | C | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-1154G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736425 | |||||||
chr2:218736527 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0070 |
2 | NA18939.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-98-1052G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736527 | |||||||
chr2:218736591 | C | CT | 46 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(43): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.-98-985dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218736591 | ||||||
chr2:218736603 | A | G | 1 | a0002c0002t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-98-976A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736603 | |||||||
chr2:218736609 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-98-970C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736609 | |||||||
chr2:218736669 | A | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-98-910A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736669 | |||||||
chr2:218736849 | C | CT | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-98-714dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218736849 | ||||||
chr2:218736849 | C | CTT | 17 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0049 others(14): Show |
21 | HG01884.hp1 HG02055.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-98-715_-98-714dup others(2): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218736849 | ||||||
chr2:218737030 | C | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-98-549C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737030 | |||||||
chr2:218737135 | G | T | 2 | a0002c0002t0002g0029 a0002c0002t0002g0030 |
2 | HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-98-444G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737135 | |||||||
chr2:218737403 | G | C | 1 | a0016c0021t0001g0184 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-98-176G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737403 | |||||||
chr2:218737515 | C | T | 1 | a0002c0002t0002g0096 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-98-64C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737515 | |||||||
chr2:218737533 | G | A | 2 | a0002c0007t0002g0011 a0002c0007t0002g0028 |
3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-98-46G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737533 | |||||||
chr2:218737540 | T | A | 1 | a0005c0005t0001g0053 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-98-39T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737540 | |||||||
chr2:218739209 | A | G | 1 | a0002c0002t0002g0124 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1487+46A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/19 | chr2 | 218739209 | |||||||
chr2:218739462 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1487+299C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/19 | chr2 | 218739462 | |||||||
chr2:218739603 | T | C | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(55): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.1487+440T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/19 | chr2 | 218739603 | |||||||
chr2:218740395 | G | A | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1598-126G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 4/19 | chr2 | 218740395 | |||||||
chr2:218740809 | C | T | 4 | a0001c0001t0003g0026 a0001c0001t0003g0213 a0001c0001t0003g0214 others(1): Show |
4 | HG02257.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1661+225C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740809 | |||||||
chr2:218740816 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1661+232G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740816 | |||||||
chr2:218740847 | C | T | 12 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(9): Show |
12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1661+263C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740847 | |||||||
chr2:218740852 | C | A | 1 | a0002c0002t0002g0095 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1661+268C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740852 | |||||||
chr2:218740870 | C | G | 38 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(35): Show |
41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1661+286C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740870 | |||||||
chr2:218740918 | T | C | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1661+334T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740918 | |||||||
chr2:218740937 | G | A | 12 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0141 others(9): Show |
12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1661+353G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740937 | |||||||
chr2:218741206 | G | A | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1661+622G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741206 | |||||||
chr2:218741219 | A | C | 1 | a0001c0001t0001g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1661+635A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741219 | |||||||
chr2:218741329 | C | T | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1661+745C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741329 | |||||||
chr2:218741355 | G | C | 1 | a0003c0003t0004g0205 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1661+771G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741355 | |||||||
chr2:218741408 | A | G | 3 | a0002c0002t0002g0031 a0002c0002t0002g0082 a0002c0002t0002g0091 |
3 | HG02698.hp1 NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1661+824A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741408 | |||||||
chr2:218741454 | C | T | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(132): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1661+870C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741454 | |||||||
chr2:218741495 | T | G | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(134): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1661+911T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741495 | |||||||
chr2:218741518 | A | G | 1 | a0001c0001t0009g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1661+934A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741518 | |||||||
chr2:218741537 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1661+953G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741537 | |||||||
chr2:218741729 | T | G | 1 | a0001c0001t0001g0040 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1661+1145T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741729 | |||||||
chr2:218741815 | C | A | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1661+1231C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741815 | |||||||
chr2:218742025 | A | G | 28 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0035 others(25): Show |
30 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1661+1441A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742025 | |||||||
chr2:218742129 | A | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0185 others(12): Show |
19 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1661+1545A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742129 | |||||||
chr2:218742153 | G | A | 1 | a0002c0002t0002g0114 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1661+1569G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742153 | |||||||
chr2:218742208 | A | G | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(134): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1661+1624A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742208 | |||||||
chr2:218742236 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1661+1652C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742236 | |||||||
chr2:218742434 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1661+1850T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742434 | |||||||
chr2:218742638 | C | T | 1 | a0002c0002t0002g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1661+2054C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742638 | |||||||
chr2:218742677 | A | G | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1661+2093A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742677 | |||||||
chr2:218742688 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0185 a0001c0001t0001g0189 others(4): Show |
9 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1661+2104A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742688 | |||||||
chr2:218742750 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1661+2166A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742750 | |||||||
chr2:218743096 | A | G | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1662-2013A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743096 | |||||||
chr2:218743144 | C | CA | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1662-1954dupA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr2 | 218743144 | ||||||
chr2:218743268 | G | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1662-1841G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743268 | |||||||
chr2:218743363 | C | G | 1 | a0001c0001t0001g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1662-1746C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743363 | |||||||
chr2:218743420 | G | A | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1662-1689G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743420 | |||||||
chr2:218743574 | A | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0185 others(8): Show |
14 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1662-1535A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743574 | |||||||
chr2:218743678 | G | GTTTTGT | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1662-1420_1662-141 others(10): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr2 | 218743678 | ||||||
chr2:218743829 | G | A | 1 | a0002c0002t0002g0095 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1662-1280G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743829 | |||||||
chr2:218743854 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1662-1255T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743854 | |||||||
chr2:218743931 | A | G | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1662-1178A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743931 | |||||||
chr2:218744139 | T | A | 1 | a0003c0003t0004g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1662-970T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744139 | |||||||
chr2:218744140 | C | A | 1 | a0003c0003t0004g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1662-969C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744140 | |||||||
chr2:218744246 | A | T | 1 | a0002c0002t0002g0100 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1662-863A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744246 | |||||||
chr2:218744391 | T | C | 1 | a0002c0002t0002g0093 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1662-718T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744391 | |||||||
chr2:218744439 | T | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1662-670T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744439 | |||||||
chr2:218744717 | T | C | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1662-392T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744717 | |||||||
chr2:218744961 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1662-148C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744961 | |||||||
chr2:218745039 | G | A | 28 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0035 others(25): Show |
30 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1662-70G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218745039 | |||||||
chr2:218745053 | G | A | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1662-56G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218745053 | |||||||
chr2:218745272 | G | C | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1786+39G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 6/19 | chr2 | 218745272 | |||||||
chr2:218745395 | A | C | 10 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1786+162A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 6/19 | chr2 | 218745395 | |||||||
chr2:218745560 | G | C | 1 | a0002c0023t0002g0119 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1787-131G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 6/19 | chr2 | 218745560 | |||||||
chr2:218745599 | G | A | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(134): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1787-92G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 6/19 | chr2 | 218745599 | |||||||
chr2:218745930 | A | T | 1 | a0002c0002t0002g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1897+129A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 7/19 | chr2 | 218745930 | |||||||
chr2:218745995 | A | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG00558.hp2 HG00621.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1898-160A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 7/19 | chr2 | 218745995 | |||||||
chr2:218746005 | C | T | 38 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(35): Show |
41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1898-150C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 7/19 | chr2 | 218746005 | |||||||
chr2:218746292 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1974+61A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 8/19 | chr2 | 218746292 | |||||||
chr2:218746711 | T | G | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1975-292T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 8/19 | chr2 | 218746711 | |||||||
chr2:218746742 | A | G | 1 | a0005c0005t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1975-261A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 8/19 | chr2 | 218746742 | |||||||
chr2:218747431 | CCTT | C | 2 | a0002c0007t0002g0011 a0002c0007t0002g0028 |
3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2249+63_2249+65del others(3): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 218747431 | ||||||
chr2:218747559 | A | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(122): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.2250-38A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 10/19 | chr2 | 218747559 | |||||||
chr2:218747904 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2378+179G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 11/19 | chr2 | 218747904 | |||||||
chr2:218748524 | A | G | 38 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(35): Show |
41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2501+297A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 12/19 | chr2 | 218748524 | |||||||
chr2:218748526 | G | A | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.2501+299G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 12/19 | chr2 | 218748526 | |||||||
chr2:218748587 | G | A | 1 | a0009c0012t0002g0110 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2502-249G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 12/19 | chr2 | 218748587 | |||||||
chr2:218748654 | C | CA | 95 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(92): Show |
108 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.2502-161dupA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | 218748654 | ||||||
chr2:218748654 | C | CAA | 14 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0001c0001t0001g0142 others(11): Show |
15 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.2502-162_2502-161d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | 218748654 | ||||||
chr2:218748959 | G | A | 4 | a0005c0005t0001g0014 a0005c0005t0001g0053 a0005c0005t0001g0054 others(1): Show |
5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2600+25G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 13/19 | chr2 | 218748959 | |||||||
chr2:218749049 | A | G | 38 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(35): Show |
41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2600+115A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 13/19 | chr2 | 218749049 | |||||||
chr2:218749143 | C | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0185 others(12): Show |
19 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.2601-110C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 13/19 | chr2 | 218749143 | |||||||
chr2:218749467 | CT | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0185 others(8): Show |
14 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2735+95delT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 218749467 | ||||||
chr2:218749480 | T | C | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2735+93T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749480 | |||||||
chr2:218749483 | C | T | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2735+96C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749483 | |||||||
chr2:218749550 | C | T | 1 | a0002c0002t0002g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2735+163C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749550 | |||||||
chr2:218749706 | A | G | 4 | a0002c0007t0002g0135 a0007c0009t0002g0130 a0007c0009t0002g0131 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2736-303A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749706 | |||||||
chr2:218749718 | C | T | 12 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(9): Show |
13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2736-291C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749718 | |||||||
chr2:218749756 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2736-253C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749756 | |||||||
chr2:218749935 | C | G | 8 | a0003c0003t0004g0202 a0003c0003t0004g0203 a0003c0003t0004g0204 others(5): Show |
8 | HG02486.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2736-74C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749935 | |||||||
chr2:218749936 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2736-73C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749936 | |||||||
chr2:218750541 | T | TA | 29 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0035 others(26): Show |
31 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.2873+407dupA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr2 | 218750541 | ||||||
chr2:218750618 | C | T | 2 | a0002c0007t0002g0011 a0002c0007t0002g0028 |
3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2873+472C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218750618 | |||||||
chr2:218750867 | A | AT | 12 | a0001c0001t0001g0010 a0001c0001t0001g0185 a0001c0001t0001g0189 others(9): Show |
15 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2873+731dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr2 | 218750867 | ||||||
chr2:218751051 | T | C | 2 | a0002c0011t0006g0199 a0002c0011t0006g0200 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2874-653T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751051 | |||||||
chr2:218751076 | A | G | 1 | a0002c0002t0011g0099 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2874-628A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751076 | |||||||
chr2:218751107 | C | G | 2 | a0003c0003t0005g0207 a0003c0003t0005g0209 |
2 | HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2874-597C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751107 | |||||||
chr2:218751132 | CT | C | 5 | a0004c0004t0001g0144 a0004c0004t0001g0145 a0004c0004t0001g0146 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2874-569delT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr2 | 218751132 | ||||||
chr2:218751155 | CTCATGTT others(8): Show |
C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2874-546_2874-532d others(17): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr2 | 218751155 | ||||||
chr2:218751187 | G | T | 147 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(144): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.2874-517G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751187 | |||||||
chr2:218751245 | T | C | 2 | a0002c0002t0002g0079 a0002c0002t0002g0092 |
2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.2874-459T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751245 | |||||||
chr2:218751279 | C | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2874-425C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751279 | |||||||
chr2:218751640 | A | G | 1 | a0002c0002t0002g0095 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2874-64A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751640 | |||||||
chr2:218751887 | C | CT | 4 | a0005c0005t0001g0014 a0005c0005t0001g0053 a0005c0005t0001g0054 others(1): Show |
5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2976+92dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751887 | ||||||
chr2:218751887 | C | CTT | 62 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(59): Show |
68 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.2976+91_2976+92dup others(2): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751887 | ||||||
chr2:218751887 | C | CTTT | 46 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(43): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.2976+90_2976+92dup others(3): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751887 | ||||||
chr2:218751904 | C | CT | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(72): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.2976+103dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751904 | ||||||
chr2:218751904 | C | CTT | 8 | a0001c0001t0001g0154 a0001c0001t0001g0159 a0001c0001t0001g0174 others(5): Show |
8 | HG00642.hp2 HG01993.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2976+102_2976+103d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751904 | ||||||
chr2:218751910 | C | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(121): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.2976+104C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218751910 | |||||||
chr2:218751910 | CT | C | 22 | a0002c0007t0002g0011 a0002c0007t0002g0028 a0002c0007t0002g0135 others(19): Show |
24 | HG01975.hp1 HG02055.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.2976+118delT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751910 | ||||||
chr2:218751958 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2976+152A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218751958 | |||||||
chr2:218752150 | C | T | 38 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(35): Show |
41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2976+344C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218752150 | |||||||
chr2:218752199 | C | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0185 others(8): Show |
14 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2976+393C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218752199 | |||||||
chr2:218752316 | T | C | 1 | a0002c0002t0002g0109 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2977-447T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218752316 | |||||||
chr2:218752372 | C | T | 1 | a0014c0015t0001g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2977-391C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218752372 | |||||||
chr2:218752470 | A | C | 4 | a0005c0005t0001g0014 a0005c0005t0001g0053 a0005c0005t0001g0054 others(1): Show |
5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2977-293A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218752470 | |||||||
chr2:218753093 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3188-22A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 17/19 | chr2 | 218753093 | |||||||
chr2:218753452 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3259-132C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 18/19 | chr2 | 218753452 | |||||||
chr2:218753514 | A | C | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(134): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.3259-70A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 18/19 | chr2 | 218753514 | |||||||
chr2:218753774 | T | G | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.3344+105T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 19/19 | chr2 | 218753774 | |||||||
chr2:218753807 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0170 |
2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3344+138A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 19/19 | chr2 | 218753807 | |||||||
chr2:218753974 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3345-160A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 19/19 | chr2 | 218753974 | |||||||
chr2:218753985 | T | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(43): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.3345-149T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 19/19 | chr2 | 218753985 |