Variant report

Variant rs566987111
Chromosome Location chr3:100354351-100354352
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100352600-100354600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr3:100352800-100354800 Enhancers Fetal Intestine Small intestine
3 chr3:100353400-100354400 Enhancers Primary Natural Killer cells fromperipheralblood blood
4 chr3:100353400-100354600 Enhancers Stomach Mucosa stomach
5 chr3:100353600-100354400 Enhancers Rectal Mucosa Donor 31 rectum
6 chr3:100353600-100354400 Enhancers HMEC breast
7 chr3:100353600-100354400 Enhancers K562 blood
8 chr3:100353800-100354400 Enhancers Pancreas Pancrea
9 chr3:100353800-100354400 Active TSS Rectal Mucosa Donor 29 rectum
10 chr3:100353800-100354400 Flanking Active TSS HepG2 liver
11 chr3:100353800-100354600 Active TSS Liver Liver
12 chr3:100353800-100355200 Weak transcription Primary neutrophils fromperipheralblood blood
13 chr3:100353800-100356200 Enhancers Fetal Intestine Large intestine
14 chr3:100354000-100354400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr3:100354000-100354600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr3:100354000-100357800 Weak transcription Fetal Brain Male brain
17 chr3:100354200-100354400 Enhancers Sigmoid Colon Sigmoid Colon
18 chr3:100354200-100354600 Flanking Active TSS Duodenum Mucosa Duodenum

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