Variant report

Variant rs11204952
Chromosome Location chr1:152227321-152227322
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr1:152223200-152230400 Weak transcription Stomach Smooth Muscle stomach
4 chr1:152223400-152228400 Weak transcription Fetal Adrenal Gland Adrenal Gland
5 chr1:152223600-152229600 Weak transcription Duodenum Smooth Muscle Duodenum
6 chr1:152224600-152230400 Weak transcription Fetal Kidney kidney
7 chr1:152225400-152229000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:152225400-152229000 Weak transcription Esophagus oesophagus
9 chr1:152225400-152232200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:152225600-152229000 Weak transcription Aorta Aorta
11 chr1:152225600-152232200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr1:152226400-152228000 ZNF genes & repeats HUES64 Cell Line embryonic stem cell

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