Variant report

Variant rs58382191
Chromosome Location chr8:119890479-119890480
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:119888200-119890600 Enhancers Fetal Intestine Small intestine
2 chr8:119888200-119891800 Enhancers Fetal Intestine Large intestine
3 chr8:119889000-119895200 Enhancers Hela-S3 cervix
4 chr8:119889600-119890600 Enhancers Stomach Mucosa stomach
5 chr8:119889600-119891600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr8:119889600-119892000 Enhancers HUVEC blood vessel
7 chr8:119889600-119892400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr8:119889600-119895000 Enhancers NHDF-Ad bronchial
9 chr8:119889600-119895200 Enhancers NHLF lung
10 chr8:119889800-119891800 Enhancers Osteobl bone
11 chr8:119889800-119893200 Weak transcription Aorta Aorta
12 chr8:119890000-119891400 Enhancers Muscle Satellite Cultured Cells --
13 chr8:119890000-119892400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr8:119890200-119890600 Enhancers HMEC breast
15 chr8:119890200-119891000 Enhancers A549 lung
16 chr8:119890200-119891000 Enhancers NHEK skin
17 chr8:119890200-119891200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
18 chr8:119890400-119891000 Weak transcription Duodenum Mucosa Duodenum
19 chr8:119890400-119891200 Enhancers Rectal Mucosa Donor 31 rectum
20 chr8:119890400-119891200 Enhancers NH-A brain
21 chr8:119890400-119891600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
22 chr8:119890400-119892600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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