Variant report

Variant rs3755956
Chromosome Location chr4:994356-994357
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:990600-994400 Bivalent Enhancer Spleen Spleen
2 chr4:991600-1002800 Weak transcription Right Atrium heart
3 chr4:992000-995800 Weak transcription Liver Liver
4 chr4:992400-994400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
5 chr4:992400-995400 Weak transcription Gastric stomach
6 chr4:992400-995600 Weak transcription Pancreas Pancrea
7 chr4:993000-994600 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
8 chr4:993000-997800 Bivalent Enhancer Fetal Muscle Trunk muscle
9 chr4:993200-994600 Bivalent Enhancer Primary B cells from peripheral blood blood
10 chr4:993800-995000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin

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