Variant report

Variant rs10152647
Chromosome Location chr15:31384185-31384186
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:31376200-31384800 Weak transcription Gastric stomach
2 chr15:31376200-31389000 Weak transcription Right Atrium heart
3 chr15:31376200-31390800 Weak transcription Brain Substantia Nigra brain
4 chr15:31379800-31388600 Weak transcription Placenta Placenta
5 chr15:31382200-31385800 Enhancers HepG2 liver
6 chr15:31383000-31385000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr15:31383000-31385000 Enhancers HSMMtube muscle
8 chr15:31383200-31384800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr15:31383200-31385000 Transcr. at gene 5' and 3' Foreskin Melanocyte Primary Cells skin03 Skin
10 chr15:31383400-31384200 Enhancers Muscle Satellite Cultured Cells --
11 chr15:31383400-31384600 Enhancers Esophagus oesophagus
12 chr15:31383400-31384800 Enhancers NH-A brain
13 chr15:31383400-31385000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr15:31383400-31385000 Enhancers HSMM muscle
15 chr15:31383600-31384200 Flanking Active TSS Foreskin Melanocyte Primary Cells skin01 Skin
16 chr15:31383800-31384400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
17 chr15:31383800-31384600 Enhancers A549 lung
18 chr15:31383800-31384800 Weak transcription Stomach Mucosa stomach
19 chr15:31383800-31384800 Enhancers Osteobl bone
20 chr15:31383800-31385000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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