Variant report

Variant rs185754674
Chromosome Location chr4:69522780-69522781
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69513000-69522800 Weak transcription Pancreas Pancrea
2 chr4:69519800-69523000 Enhancers HMEC breast
3 chr4:69520400-69523000 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr4:69520400-69523000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr4:69521200-69522800 Enhancers H9 Cell Line embryonic stem cell
6 chr4:69521200-69522800 Enhancers HUES48 Cell Line embryonic stem cell
7 chr4:69521200-69522800 Enhancers Fetal Intestine Large intestine
8 chr4:69521400-69522800 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr4:69521600-69522800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr4:69521800-69522800 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr4:69521800-69523000 Enhancers HUES64 Cell Line embryonic stem cell
12 chr4:69522000-69523200 Weak transcription Fetal Intestine Small intestine
13 chr4:69522000-69525400 Enhancers Liver Liver
14 chr4:69522200-69527400 Weak transcription iPS-18 Cell Line embryonic stem cell
15 chr4:69522400-69523000 Weak transcription Duodenum Mucosa Duodenum
16 chr4:69522600-69523000 Flanking Active TSS HepG2 liver
17 chr4:69522600-69523200 Weak transcription Stomach Mucosa stomach
18 chr4:69522600-69523600 Weak transcription Rectal Mucosa Donor 31 rectum
19 chr4:69522600-69523600 Enhancers A549 lung
20 chr4:69522600-69523600 Enhancers GM12878-XiMat blood

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