Variant report

Variant rs4845430
Chromosome Location chr1:152225378-152225379
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:152219400-152230200 Weak transcription Ovary ovary
2 chr1:152220800-152230400 Weak transcription Brain Angular Gyrus brain
3 chr1:152222200-152225600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:152223200-152230400 Weak transcription Stomach Smooth Muscle stomach
5 chr1:152223400-152228400 Weak transcription Fetal Adrenal Gland Adrenal Gland
6 chr1:152223600-152225400 Enhancers HMEC breast
7 chr1:152223600-152229600 Weak transcription Duodenum Smooth Muscle Duodenum
8 chr1:152224000-152225400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:152224400-152226200 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr1:152224600-152225400 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr1:152224600-152230400 Weak transcription Fetal Kidney kidney
12 chr1:152224800-152225800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr1:152225000-152225400 Enhancers Esophagus oesophagus
14 chr1:152225200-152225600 ZNF genes & repeats Aorta Aorta
15 chr1:152225200-152225600 Enhancers NHEK skin

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