Variant report

Variant rs377642656
Chromosome Location chr8:111861018-111861019
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:111860000-111861400 Enhancers HUVEC blood vessel
2 chr8:111860200-111861200 Weak transcription Fetal Intestine Large intestine
3 chr8:111860200-111862800 Enhancers Fetal Intestine Small intestine
4 chr8:111860600-111861200 Enhancers Hela-S3 cervix
5 chr8:111860600-111861200 Enhancers HSMMtube muscle
6 chr8:111860600-111861400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr8:111860600-111861400 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr8:111860600-111861400 Enhancers HepG2 liver
9 chr8:111860600-111861400 Enhancers NH-A brain
10 chr8:111860600-111861400 Enhancers NHDF-Ad bronchial
11 chr8:111860800-111861400 Flanking Active TSS A549 lung
12 chr8:111861000-111861200 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr8:111861000-111861400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr8:111861000-111861400 Enhancers Muscle Satellite Cultured Cells --
15 chr8:111861000-111861400 Enhancers HSMM muscle

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