Variant report

Variant rs1035707
Chromosome Location chr15:31384797-31384798
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 chr15:31383400-31384800 Enhancers NH-A brain
11 chr15:31383400-31385000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr15:31383400-31385000 Enhancers HSMM muscle
13 chr15:31383800-31384800 Weak transcription Stomach Mucosa stomach
14 chr15:31383800-31384800 Enhancers Osteobl bone
15 chr15:31383800-31385000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr15:31384200-31388800 Active TSS Foreskin Melanocyte Primary Cells skin01 Skin
17 chr15:31384600-31385000 Enhancers Primary hematopoietic stem cells short term culture blood
18 chr15:31384600-31385000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
19 chr15:31384600-31385200 Flanking Active TSS A549 lung
20 chr15:31384600-31389800 Weak transcription Esophagus oesophagus

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