Variant report

Variant rs2817027
Chromosome Location chr6:35778719-35778720
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:35773000-35791400 Weak transcription Right Atrium heart
2 chr6:35773400-35778800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr6:35773800-35778800 Weak transcription Pancreas Pancrea
4 chr6:35776200-35785000 Weak transcription Brain Anterior Caudate brain
5 chr6:35777000-35778800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr6:35777000-35778800 Weak transcription Esophagus oesophagus
7 chr6:35777000-35782400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr6:35777000-35801400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr6:35777800-35779800 Enhancers Primary neutrophils fromperipheralblood blood
10 chr6:35778600-35778800 Enhancers Muscle Satellite Cultured Cells --
11 chr6:35778600-35778800 Enhancers A549 lung
12 chr6:35778600-35779400 Enhancers NH-A brain
13 chr6:35778600-35779800 Flanking Active TSS Hela-S3 cervix
14 chr6:35778600-35779800 Enhancers HMEC breast
15 chr6:35778600-35779800 Enhancers HUVEC blood vessel
16 chr6:35778600-35780200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr6:35778600-35780400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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