Variant report

Variant rs145116311
Chromosome Location chr4:9965928-9965929
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:25 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9911400-9979800 Weak transcription Duodenum Smooth Muscle Duodenum
2 chr4:9944000-9979400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
3 chr4:9949800-9979400 Weak transcription Liver Liver
4 chr4:9950000-9966600 Weak transcription Psoas Muscle Psoas
5 chr4:9958600-9984800 Weak transcription Aorta Aorta
6 chr4:9963400-9996400 Weak transcription Adipose Nuclei Adipose
7 chr4:9964000-9966000 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr4:9964000-9966800 Strong transcription Monocytes-CD14+_RO01746 blood
9 chr4:9964200-9966000 Strong transcription NHEK skin
10 chr4:9964200-9966600 Strong transcription Breast Myoepithelial Primary Cells Breast
11 chr4:9964200-9967000 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr4:9964200-9967000 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr4:9964200-9968600 Strong transcription Fetal Intestine Large intestine
14 chr4:9964200-9986600 Weak transcription Ovary ovary
15 chr4:9964400-9968800 Strong transcription HMEC breast
16 chr4:9964400-9980800 Weak transcription Esophagus oesophagus
17 chr4:9964800-9966000 Strong transcription Fetal Intestine Small intestine
18 chr4:9964800-9979200 Weak transcription Duodenum Mucosa Duodenum
19 chr4:9965200-9967000 Enhancers Brain Germinal Matrix brain
20 chr4:9965400-9971600 Strong transcription Primary monocytes fromperipheralblood blood
21 chr4:9965600-9966200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
22 chr4:9965600-9966800 Genic enhancers HepG2 liver
23 chr4:9965800-9966200 Enhancers HUES48 Cell Line embryonic stem cell
24 chr4:9965800-9966800 Enhancers Fetal Brain Male brain
25 chr4:9965800-9969800 Weak transcription GM12878-XiMat blood

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