Variant report

Variant rs12688014
Chromosome Location chrX:138955180-138955181
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:138927400-138960200 Weak transcription Liver Liver
2 chrX:138934000-138964600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chrX:138935600-138967600 Weak transcription Primary neutrophils fromperipheralblood blood
4 chrX:138937000-138964200 Weak transcription HUES64 Cell Line embryonic stem cell
5 chrX:138938800-138960200 Weak transcription HUES6 Cell Line embryonic stem cell
6 chrX:138939400-138962400 Weak transcription HUES48 Cell Line embryonic stem cell
7 chrX:138941600-138964200 Weak transcription Primary T cells from cord blood blood
8 chrX:138941800-138988200 Weak transcription Primary T cells fromperipheralblood blood
9 chrX:138942800-138963000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chrX:138946600-138958400 Weak transcription K562 blood
11 chrX:138949000-138978800 Weak transcription Fetal Intestine Small intestine
12 chrX:138949600-138964600 Weak transcription Duodenum Smooth Muscle Duodenum
13 chrX:138950800-138959200 Weak transcription Primary Natural Killer cells fromperipheralblood blood
14 chrX:138951400-138966600 Weak transcription GM12878-XiMat blood
15 chrX:138952800-138957200 Weak transcription HUVEC blood vessel
16 chrX:138953400-138957600 Weak transcription Fetal Adrenal Gland Adrenal Gland
17 chrX:138954400-138965600 Weak transcription Primary mononuclear cells fromperipheralblood Blood

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