Variant report

Variant rs35211425
Chromosome Location chr5:150960306-150960307
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:150951200-150960400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr5:150951600-150960400 Genic enhancers NHEK skin
3 chr5:150957200-150960400 Genic enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr5:150958000-150960800 Weak transcription Fetal Thymus thymus
5 chr5:150959400-150965600 Weak transcription Pancreas Pancrea
6 chr5:150959600-150960800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr5:150959600-150961200 Genic enhancers HMEC breast
8 chr5:150959600-150962000 Enhancers Placenta Placenta
9 chr5:150959600-150967400 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr5:150959800-150960600 Enhancers Adipose Nuclei Adipose
11 chr5:150960000-150961600 Enhancers Esophagus oesophagus
12 chr5:150960000-150962000 Enhancers Fetal Muscle Leg muscle
13 chr5:150960000-150962600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr5:150960200-150961400 Transcr. at gene 5' and 3' Foreskin Keratinocyte Primary Cells skin03 Skin

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