Variant report

Variant rs536801097
Chromosome Location chr2:234725238-234725239
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:234713200-234731400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr2:234723600-234726200 Enhancers HSMMtube muscle
3 chr2:234724400-234727200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr2:234724800-234726600 Enhancers Fetal Brain Male brain
5 chr2:234724800-234727200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr2:234725000-234727600 Enhancers Fetal Intestine Large intestine
7 chr2:234725000-234728000 Enhancers Fetal Intestine Small intestine
8 chr2:234725200-234725600 Bivalent Enhancer Placenta Placenta
9 chr2:234725200-234725800 Enhancers HSMM muscle
10 chr2:234725200-234726600 Enhancers Fetal Muscle Trunk muscle
11 chr2:234725200-234727000 Enhancers A549 lung
12 chr2:234725200-234727200 Enhancers Adipose Nuclei Adipose

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