Variant report

Variant rs145751686
Chromosome Location chr20:52784704-52784705
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:52768800-52790200 Transcr. at gene 5' and 3' A549 lung
2 chr20:52769200-52789400 Weak transcription Esophagus oesophagus
3 chr20:52769600-52785800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr20:52771200-52786000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr20:52777800-52784800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr20:52784200-52786200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr20:52784200-52786200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr20:52784400-52785200 Enhancers HMEC breast
9 chr20:52784400-52786400 Enhancers NHEK skin
10 chr20:52784600-52784800 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
11 chr20:52784600-52784800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
12 chr20:52784600-52784800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
13 chr20:52784600-52785000 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
14 chr20:52784600-52785200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
15 chr20:52784600-52785200 Enhancers Hela-S3 cervix
16 chr20:52784600-52787200 Enhancers HepG2 liver

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