Variant report

Variant rs11760159
Chromosome Location chr6:113983034-113983035
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:113976000-113990800 Weak transcription Psoas Muscle Psoas
2 chr6:113979600-113983800 Enhancers GM12878-XiMat blood
3 chr6:113981000-113983400 Enhancers Fetal Intestine Large intestine
4 chr6:113981000-113983400 Enhancers Fetal Intestine Small intestine
5 chr6:113981200-113983600 Enhancers Primary monocytes fromperipheralblood blood
6 chr6:113981600-113983800 Weak transcription Duodenum Mucosa Duodenum
7 chr6:113982000-113983800 Enhancers Monocytes-CD14+_RO01746 blood
8 chr6:113982200-113983800 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr6:113982400-113983800 Weak transcription Primary B cells from cord blood blood
10 chr6:113982400-113983800 Weak transcription HepG2 liver
11 chr6:113982400-113993600 Weak transcription Placenta Placenta
12 chr6:113982600-113983200 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr6:113982800-113983200 Enhancers HUVEC blood vessel
14 chr6:113982800-113984000 Enhancers Adipose Nuclei Adipose
15 chr6:113982800-113984400 Enhancers Stomach Mucosa stomach
16 chr6:113983000-113983400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr6:113983000-113993800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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