Variant report

Variant rs1611753
Chromosome Location chr1:152956381-152956382
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:152954200-152966200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:152954400-152969200 Weak transcription Pancreas Pancrea
3 chr1:152955000-152956400 Weak transcription Ovary ovary
4 chr1:152955600-152956400 Enhancers Esophagus oesophagus
5 chr1:152955600-152956400 Enhancers Placenta Amnion Placenta Amnion
6 chr1:152955600-152956600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:152955600-152956800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:152955600-152956800 Enhancers NHEK skin
9 chr1:152955800-152956800 Enhancers HMEC breast
10 chr1:152956000-152956400 Enhancers Stomach Mucosa stomach
11 chr1:152956000-152956800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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