Variant report

Variant rs10217231
Chromosome Location chr9:16840472-16840473
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:16829200-16852800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr9:16829800-16864200 Weak transcription NH-A brain
3 chr9:16831000-16859600 Weak transcription HSMM muscle
4 chr9:16831200-16852600 Weak transcription Fetal Lung lung
5 chr9:16831200-16863400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr9:16831200-16864400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr9:16833800-16863800 Weak transcription NHLF lung
8 chr9:16834600-16852600 Weak transcription Fetal Stomach stomach
9 chr9:16835200-16848400 Weak transcription HUES48 Cell Line embryonic stem cell
10 chr9:16836200-16864400 Weak transcription NHDF-Ad bronchial
11 chr9:16838200-16842400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr9:16838800-16852000 Weak transcription Muscle Satellite Cultured Cells --
13 chr9:16839200-16846400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr9:16839800-16842200 Enhancers Colon Smooth Muscle Colon
15 chr9:16840200-16840600 Enhancers Ovary ovary
16 chr9:16840200-16841600 Enhancers Rectal Smooth Muscle rectum
17 chr9:16840200-16842600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
18 chr9:16840400-16840600 Enhancers Fetal Intestine Large intestine
19 chr9:16840400-16841000 Enhancers iPS-15b Cell Line embryonic stem cell
20 chr9:16840400-16852000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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