Variant report

Variant rs11804941
Chromosome Location chr1:174593212-174593213
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174572800-174606200 Weak transcription Primary T cells fromperipheralblood blood
2 chr1:174582800-174606400 Weak transcription Primary T helper cells PMA-I stimulated --
3 chr1:174587600-174594600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:174587600-174606600 Weak transcription Primary B cells from cord blood blood
5 chr1:174587600-174609200 Weak transcription Pancreas Pancrea
6 chr1:174592400-174593400 Enhancers HepG2 liver
7 chr1:174592400-174594000 Enhancers Fetal Intestine Large intestine
8 chr1:174593000-174593600 Enhancers Fetal Intestine Small intestine

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