Variant report

Variant rs6911583
Chromosome Location chr6:29963521-29963522
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29945600-29966400 Weak transcription Pancreas Pancrea
2 chr6:29961400-29963800 Weak transcription Fetal Intestine Small intestine
3 chr6:29962400-29968400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:29962800-29964200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr6:29963000-29963600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
6 chr6:29963000-29963600 Enhancers HMEC breast
7 chr6:29963000-29964200 Enhancers Fetal Intestine Large intestine
8 chr6:29963000-29964400 Enhancers Hela-S3 cervix
9 chr6:29963200-29963800 Enhancers HUVEC blood vessel

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