Variant report

Variant rs17136070
Chromosome Location chr7:102802681-102802682
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:102790200-102803200 Weak transcription Gastric stomach
2 chr7:102794800-102803200 Weak transcription Fetal Intestine Large intestine
3 chr7:102801600-102803400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr7:102801800-102803200 Weak transcription Skeletal Muscle Female skeletal muscle
5 chr7:102802000-102803200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr7:102802000-102804800 Enhancers Muscle Satellite Cultured Cells --
7 chr7:102802200-102802800 Weak transcription K562 blood
8 chr7:102802200-102803200 Enhancers Osteobl bone
9 chr7:102802200-102803600 Enhancers Fetal Intestine Small intestine
10 chr7:102802400-102803600 Enhancers Skeletal Muscle Male skeletal muscle
11 chr7:102802400-102804600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr7:102802400-102804600 Enhancers NH-A brain
13 chr7:102802600-102802800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr7:102802600-102803800 Enhancers NHEK skin

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