Variant report

Variant rs72948653
Chromosome Location chr2:114563911-114563912
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:114554600-114564400 Weak transcription Small Intestine intestine
2 chr2:114563200-114565800 Genic enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr2:114563600-114564800 Enhancers Rectal Mucosa Donor 31 rectum
4 chr2:114563800-114564000 Enhancers HepG2 liver
5 chr2:114563800-114564200 Enhancers A549 lung
6 chr2:114563800-114564200 Enhancers K562 blood
7 chr2:114563800-114564400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
8 chr2:114563800-114564600 Enhancers Fetal Intestine Small intestine
9 chr2:114563800-114564600 Enhancers Rectal Mucosa Donor 29 rectum
10 chr2:114563800-114564600 Enhancers Sigmoid Colon Sigmoid Colon
11 chr2:114563800-114564800 Enhancers Fetal Intestine Large intestine
12 chr2:114563800-114565400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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