Variant report

Variant rs55710308
Chromosome Location chr6:423988-423989
allele A/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:422000-424200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr6:422800-428000 Weak transcription Primary T helper cells fromperipheralblood blood
3 chr6:423000-424200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr6:423200-424000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
5 chr6:423200-424000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
6 chr6:423200-425200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr6:423400-424000 Enhancers A549 lung
8 chr6:423600-424200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr6:423600-428000 Weak transcription Primary B cells from peripheral blood blood
10 chr6:423800-424800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
11 chr6:423800-425000 Weak transcription HepG2 liver
12 chr6:423800-425200 Weak transcription Primary T helper 17 cells PMA-I stimulated --
13 chr6:423800-427800 Weak transcription Primary T helper cells PMA-I stimulated --
14 chr6:423800-434400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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