Variant report

Variant rs138987719
Chromosome Location chr6:162479552-162479553
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:162474400-162479600 Weak transcription Left Ventricle heart
2 chr6:162478000-162482600 Weak transcription Psoas Muscle Psoas
3 chr6:162478200-162479600 Enhancers Liver Liver
4 chr6:162478200-162479600 Enhancers Pancreatic Islets Pancreatic Islet
5 chr6:162478600-162482000 Weak transcription Fetal Heart heart
6 chr6:162478800-162483400 Weak transcription Fetal Adrenal Gland Adrenal Gland
7 chr6:162479000-162480000 Enhancers Fetal Intestine Small intestine
8 chr6:162479200-162479600 Flanking Active TSS A549 lung
9 chr6:162479200-162479600 Flanking Active TSS HepG2 liver
10 chr6:162479200-162479600 Enhancers HMEC breast
11 chr6:162479200-162480000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr6:162479200-162480000 Enhancers Pancreas Pancrea
13 chr6:162479200-162480000 Enhancers Stomach Mucosa stomach
14 chr6:162479400-162479600 Enhancers Ovary ovary
15 chr6:162479400-162479600 Enhancers Right Atrium heart
16 chr6:162479400-162479800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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