Variant report

Variant rs11680486
Chromosome Location chr2:187211472-187211473
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:187188600-187216200 Weak transcription Primary hematopoietic stem cells blood
2 chr2:187192400-187211600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:187207600-187213800 Weak transcription Small Intestine intestine
4 chr2:187207800-187212600 Weak transcription HepG2 liver
5 chr2:187207800-187214200 Weak transcription Fetal Stomach stomach
6 chr2:187208200-187213000 Weak transcription Fetal Intestine Small intestine
7 chr2:187208200-187219600 Weak transcription Right Atrium heart
8 chr2:187209400-187213400 Weak transcription Duodenum Mucosa Duodenum
9 chr2:187210400-187211600 Weak transcription Psoas Muscle Psoas
10 chr2:187210400-187211800 Weak transcription Fetal Lung lung
11 chr2:187210400-187212400 Enhancers GM12878-XiMat blood
12 chr2:187210600-187212400 Weak transcription HUVEC blood vessel
13 chr2:187210600-187214400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr2:187211000-187211800 Weak transcription Colon Smooth Muscle Colon
15 chr2:187211000-187212000 Enhancers Rectal Smooth Muscle rectum
16 chr2:187211000-187212600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr2:187211200-187213000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
18 chr2:187211200-187214600 Enhancers NHEK skin
19 chr2:187211400-187211800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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