Variant report

Variant rs1165671
Chromosome Location chr12:104318984-104318985
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:104306200-104320800 Weak transcription Psoas Muscle Psoas
2 chr12:104317200-104322600 Weak transcription Aorta Aorta
3 chr12:104317400-104322200 Weak transcription Brain Anterior Caudate brain
4 chr12:104318000-104322400 Weak transcription Brain Substantia Nigra brain
5 chr12:104318200-104321400 Weak transcription Primary B cells from peripheral blood blood
6 chr12:104318200-104322200 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr12:104318400-104319000 Enhancers GM12878-XiMat blood
8 chr12:104318600-104319200 Enhancers Primary T regulatory cells fromperipheralblood blood
9 chr12:104318600-104319800 Enhancers Primary T cells fromperipheralblood blood
10 chr12:104318800-104319400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr12:104318800-104319400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr12:104318800-104319400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
13 chr12:104318800-104319600 Enhancers Primary T helper cells PMA-I stimulated --
14 chr12:104318800-104319600 Enhancers Primary T helper 17 cells PMA-I stimulated --
15 chr12:104318800-104319600 Enhancers Muscle Satellite Cultured Cells --
16 chr12:104318800-104319600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
17 chr12:104318800-104319600 Enhancers NHEK skin
18 chr12:104318800-104319800 Enhancers NH-A brain
19 chr12:104318800-104322000 Weak transcription NHLF lung

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