Variant report

Variant rs60615122
Chromosome Location chr1:246195885-246195886
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246176400-246198400 Weak transcription K562 blood
2 chr1:246193200-246202200 Weak transcription Aorta Aorta
3 chr1:246195000-246196200 Enhancers HepG2 liver
4 chr1:246195200-246196000 Enhancers Fetal Intestine Small intestine
5 chr1:246195200-246196000 Enhancers Pancreatic Islets Pancreatic Islet
6 chr1:246195200-246196200 Enhancers Fetal Kidney kidney
7 chr1:246195200-246196600 Enhancers Fetal Lung lung
8 chr1:246195400-246196000 Enhancers Fetal Heart heart
9 chr1:246195400-246196000 Enhancers Fetal Intestine Large intestine
10 chr1:246195400-246198600 Weak transcription Left Ventricle heart
11 chr1:246195600-246196000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr1:246195600-246196000 Enhancers Fetal Brain Male brain
13 chr1:246195600-246196400 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr1:246195800-246197800 Weak transcription Fetal Stomach stomach
15 chr1:246195800-246198000 Weak transcription Lung lung
16 chr1:246195800-246198400 Weak transcription Placenta Placenta
17 chr1:246195800-246198400 Weak transcription Ovary ovary
18 chr1:246195800-246198600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
19 chr1:246195800-246203000 Weak transcription Pancreas Pancrea

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