Variant report

Variant rs10160437
Chromosome Location chr11:46181739-46181740
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:46180000-46183000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr11:46180800-46182200 Enhancers Hela-S3 cervix
3 chr11:46180800-46182200 Enhancers HMEC breast
4 chr11:46181000-46181800 Enhancers Placenta Amnion Placenta Amnion
5 chr11:46181000-46182000 Flanking Active TSS NHEK skin
6 chr11:46181200-46181800 Enhancers Rectal Mucosa Donor 31 rectum
7 chr11:46181400-46181800 Enhancers H9 Cell Line embryonic stem cell
8 chr11:46181400-46181800 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
9 chr11:46181400-46182000 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr11:46181400-46182000 Enhancers Duodenum Mucosa Duodenum
11 chr11:46181400-46182000 Enhancers Fetal Thymus thymus
12 chr11:46181400-46182000 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
13 chr11:46181400-46182200 Enhancers ES-I3 Cell Line embryonic stem cell
14 chr11:46181400-46182400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr11:46181400-46182400 Bivalent Enhancer Fetal Muscle Leg muscle
16 chr11:46181600-46181800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr11:46181600-46182000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
18 chr11:46181600-46182000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
19 chr11:46181600-46182000 Enhancers Esophagus oesophagus

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