Variant report

Variant rs10810609
Chromosome Location chr9:16755346-16755347
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:16745400-16758000 Weak transcription Ovary ovary
2 chr9:16745400-16774800 Weak transcription Osteobl bone
3 chr9:16745600-16766200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr9:16750000-16756000 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr9:16750000-16756600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr9:16753200-16757200 Enhancers Fetal Intestine Large intestine
7 chr9:16754000-16766600 Weak transcription NHDF-Ad bronchial
8 chr9:16754000-16787000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr9:16754200-16755600 Weak transcription Colon Smooth Muscle Colon
10 chr9:16754200-16755600 Weak transcription Rectal Smooth Muscle rectum
11 chr9:16754400-16755400 Weak transcription Fetal Intestine Small intestine
12 chr9:16754400-16767200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr9:16755000-16756000 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr9:16755200-16755800 Enhancers HUES48 Cell Line embryonic stem cell
15 chr9:16755200-16756200 Enhancers iPS-18 Cell Line embryonic stem cell

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