Variant report

Variant rs2708941
Chromosome Location chr2:113673566-113673567
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113664800-113678000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr2:113671600-113674400 Enhancers Primary Natural Killer cells fromperipheralblood blood
3 chr2:113671600-113674800 Enhancers Primary T cells fromperipheralblood blood
4 chr2:113671600-113683000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr2:113671800-113674600 Enhancers Fetal Thymus thymus
6 chr2:113671800-113675000 Enhancers Thymus Thymus
7 chr2:113672000-113674200 Enhancers Primary T killer memory cells from peripheral blood blood
8 chr2:113672000-113674600 Enhancers Primary T helper naive cells from peripheral blood blood
9 chr2:113672200-113674200 Enhancers Primary T killer naive cells fromperipheralblood blood
10 chr2:113672400-113674200 Enhancers Primary T helper memory cells from peripheral blood 2 blood
11 chr2:113672600-113677800 Enhancers Fetal Intestine Small intestine
12 chr2:113672800-113673800 Enhancers Primary T helper memory cells from peripheral blood 1 blood
13 chr2:113672800-113674000 Enhancers Primary T helper cells PMA-I stimulated --
14 chr2:113672800-113677600 Enhancers Fetal Intestine Large intestine
15 chr2:113673000-113674200 Enhancers Primary T helper cells fromperipheralblood blood
16 chr2:113673200-113674000 Enhancers GM12878-XiMat blood

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