Variant report

Variant rs72952697
Chromosome Location chr6:113976814-113976815
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:113967600-113980600 Weak transcription Placenta Placenta
2 chr6:113970800-113977400 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr6:113971400-113981000 Weak transcription Fetal Intestine Large intestine
4 chr6:113971600-113979000 Weak transcription HepG2 liver
5 chr6:113974800-113977600 Enhancers NHEK skin
6 chr6:113975000-113982000 Weak transcription Monocytes-CD14+_RO01746 blood
7 chr6:113975400-113981200 Weak transcription Duodenum Mucosa Duodenum
8 chr6:113975600-113977600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:113976000-113977000 Enhancers A549 lung
10 chr6:113976000-113980600 Weak transcription Primary monocytes fromperipheralblood blood
11 chr6:113976000-113990800 Weak transcription Psoas Muscle Psoas
12 chr6:113976200-113977000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:113976200-113977200 Weak transcription HMEC breast
14 chr6:113976200-113977400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr6:113976200-113981000 Weak transcription Liver Liver
16 chr6:113976200-113982200 Weak transcription Stomach Mucosa stomach
17 chr6:113976200-113982800 Weak transcription Adipose Nuclei Adipose
18 chr6:113976800-113977400 Enhancers Cortex derived primary cultured neurospheres brain

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