Variant report

Variant rs9382699
Chromosome Location chr6:57169715-57169716
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:26 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:57164200-57171600 Enhancers Rectal Smooth Muscle rectum
2 chr6:57168000-57170600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
3 chr6:57168200-57169800 Enhancers NHDF-Ad bronchial
4 chr6:57168200-57170200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
5 chr6:57168200-57171600 Enhancers Fetal Stomach stomach
6 chr6:57168400-57170200 Enhancers Ovary ovary
7 chr6:57168400-57171800 Enhancers NHLF lung
8 chr6:57168600-57169800 Enhancers Fetal Adrenal Gland Adrenal Gland
9 chr6:57168600-57171400 Enhancers Colon Smooth Muscle Colon
10 chr6:57168600-57171400 Enhancers HSMM muscle
11 chr6:57168600-57171800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr6:57168800-57170000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr6:57168800-57170400 Enhancers Adipose Nuclei Adipose
14 chr6:57168800-57171000 Enhancers Osteobl bone
15 chr6:57168800-57171200 Enhancers HSMMtube muscle
16 chr6:57169000-57170800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr6:57169200-57169800 Flanking Active TSS Stomach Smooth Muscle stomach
18 chr6:57169400-57170200 Enhancers Skeletal Muscle Female skeletal muscle
19 chr6:57169400-57170400 Enhancers Fetal Lung lung
20 chr6:57169400-57170600 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
21 chr6:57169400-57171600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
22 chr6:57169600-57169800 Enhancers Fetal Kidney kidney
23 chr6:57169600-57170000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
24 chr6:57169600-57170000 Enhancers Muscle Satellite Cultured Cells --
25 chr6:57169600-57170200 Weak transcription Fetal Muscle Leg muscle
26 chr6:57169600-57170400 Active TSS Duodenum Smooth Muscle Duodenum

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