Variant report

Variant rs13403743
Chromosome Location chr2:172972197-172972198
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:172968000-172974800 Weak transcription Gastric stomach
2 chr2:172970600-172973000 Enhancers Pancreas Pancrea
3 chr2:172970600-172973400 Bivalent Enhancer Fetal Muscle Leg muscle
4 chr2:172970600-172973600 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
5 chr2:172970800-172973200 Bivalent Enhancer Fetal Stomach stomach
6 chr2:172971000-172972600 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
7 chr2:172971200-172973600 Bivalent Enhancer Primary T cells fromperipheralblood blood
8 chr2:172971400-172973400 Bivalent Enhancer Fetal Muscle Trunk muscle
9 chr2:172971600-172972600 Bivalent Enhancer Primary neutrophils fromperipheralblood blood
10 chr2:172971600-172973400 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
11 chr2:172971600-172973600 Bivalent Enhancer Primary monocytes fromperipheralblood blood
12 chr2:172971600-172975200 Bivalent Enhancer Fetal Thymus thymus
13 chr2:172971800-172972400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
14 chr2:172971800-172972400 Weak transcription NHDF-Ad bronchial
15 chr2:172971800-172972600 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr2:172971800-172972600 Bivalent Enhancer Monocytes-CD14+_RO01746 blood
17 chr2:172971800-172974200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr2:172971800-172974200 Weak transcription NHEK skin
19 chr2:172971800-172974400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr2:172971800-172974600 Weak transcription HMEC breast

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