Variant report

Variant rs6712113
Chromosome Location chr2:171600254-171600255
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171574000-171620800 Weak transcription Pancreas Pancrea
2 chr2:171593600-171600800 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr2:171596200-171601200 Weak transcription HSMMtube muscle
4 chr2:171597600-171603800 Weak transcription HMEC breast
5 chr2:171597800-171604000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:171598000-171603800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr2:171598400-171600600 Enhancers Fetal Intestine Small intestine
8 chr2:171599800-171600400 Enhancers HepG2 liver
9 chr2:171599800-171601800 Enhancers Stomach Mucosa stomach
10 chr2:171600000-171600600 Weak transcription Duodenum Mucosa Duodenum
11 chr2:171600200-171600400 Enhancers Hela-S3 cervix
12 chr2:171600200-171600400 Active TSS Monocytes-CD14+_RO01746 blood
13 chr2:171600200-171600600 Enhancers Primary monocytes fromperipheralblood blood
14 chr2:171600200-171600600 Weak transcription Fetal Intestine Large intestine
15 chr2:171600200-171600800 Enhancers iPS-18 Cell Line embryonic stem cell
16 chr2:171600200-171601200 Flanking Active TSS K562 blood
17 chr2:171600200-171601600 Enhancers Gastric stomach

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