Variant report

Variant rs17289507
Chromosome Location chr8:131493326-131493327
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:131486600-131493600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr8:131490000-131494200 Weak transcription Placenta Placenta
3 chr8:131490200-131495600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr8:131490400-131495200 Weak transcription NHLF lung
5 chr8:131490400-131495200 Weak transcription Osteobl bone
6 chr8:131490600-131495800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr8:131490800-131493600 Enhancers Fetal Intestine Large intestine
8 chr8:131491200-131495200 Enhancers A549 lung
9 chr8:131491200-131495400 Weak transcription Fetal Adrenal Gland Adrenal Gland
10 chr8:131491400-131498000 Weak transcription Lung lung
11 chr8:131491600-131494400 Weak transcription HUVEC blood vessel
12 chr8:131491600-131495200 Weak transcription Muscle Satellite Cultured Cells --
13 chr8:131492800-131495400 Weak transcription Fetal Intestine Small intestine
14 chr8:131492800-131495800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr8:131492800-131498000 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr8:131493000-131493600 Enhancers Fetal Brain Male brain
17 chr8:131493000-131493800 Enhancers Fetal Brain Female brain
18 chr8:131493200-131493400 Enhancers Pancreatic Islets Pancreatic Islet

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