Variant report

Variant rs2957658
Chromosome Location chr11:10393468-10393469
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:10388400-10393800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr11:10388600-10396200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr11:10388800-10394200 Weak transcription Rectal Smooth Muscle rectum
4 chr11:10388800-10394800 Weak transcription Ovary ovary
5 chr11:10388800-10401400 Weak transcription Esophagus oesophagus
6 chr11:10389000-10394800 Weak transcription Lung lung
7 chr11:10389000-10394800 Weak transcription Psoas Muscle Psoas
8 chr11:10389000-10394800 Weak transcription Spleen Spleen
9 chr11:10389000-10394800 Weak transcription Osteobl bone
10 chr11:10389000-10401400 Weak transcription Duodenum Smooth Muscle Duodenum
11 chr11:10389000-10401600 Weak transcription Right Atrium heart
12 chr11:10389400-10394800 Weak transcription Skeletal Muscle Female skeletal muscle
13 chr11:10389800-10394800 Weak transcription Skeletal Muscle Male skeletal muscle
14 chr11:10390000-10394800 Weak transcription Fetal Adrenal Gland Adrenal Gland
15 chr11:10391800-10396000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr11:10391800-10403800 Enhancers Adipose Nuclei Adipose
17 chr11:10392000-10398000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
18 chr11:10392600-10396200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
19 chr11:10392800-10394200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
20 chr11:10392800-10394200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
21 chr11:10392800-10403000 Enhancers NHLF lung
22 chr11:10393200-10394000 Enhancers NHDF-Ad bronchial
23 chr11:10393400-10395400 Enhancers Liver Liver

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