Variant report

Variant rs6433240
Chromosome Location chr2:171590224-171590225
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171574000-171620800 Weak transcription Pancreas Pancrea
2 chr2:171580800-171590400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr2:171584800-171590600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:171586400-171592200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr2:171586800-171590800 Weak transcription HMEC breast
6 chr2:171590000-171590400 Flanking Active TSS Fetal Intestine Small intestine
7 chr2:171590000-171591600 Enhancers NHEK skin
8 chr2:171590200-171590400 Flanking Active TSS Fetal Intestine Large intestine
9 chr2:171590200-171591000 Enhancers Duodenum Mucosa Duodenum
10 chr2:171590200-171591400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr2:171590200-171591600 Enhancers Placenta Placenta

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