Variant report

Variant rs7938656
Chromosome Location chr11:121740615-121740616
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:121735600-121740800 Weak transcription Aorta Aorta
2 chr11:121738800-121744600 Weak transcription Psoas Muscle Psoas
3 chr11:121740000-121741000 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr11:121740200-121740800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr11:121740200-121741000 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr11:121740200-121741000 Enhancers H1 Cell Line embryonic stem cell
7 chr11:121740200-121741000 Enhancers HUES6 Cell Line embryonic stem cell
8 chr11:121740200-121741000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr11:121740200-121741000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr11:121740200-121741400 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr11:121740200-121741600 Enhancers Ovary ovary
12 chr11:121740200-121741600 Enhancers Pancreas Pancrea
13 chr11:121740200-121741800 Enhancers Adipose Nuclei Adipose
14 chr11:121740200-121741800 Enhancers Stomach Smooth Muscle stomach
15 chr11:121740200-121745000 Enhancers Skeletal Muscle Female skeletal muscle
16 chr11:121740400-121741400 Enhancers HepG2 liver
17 chr11:121740400-121741800 Enhancers Right Atrium heart
18 chr11:121740600-121741600 Enhancers Colon Smooth Muscle Colon
19 chr11:121740600-121741600 Enhancers Fetal Brain Male brain

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