Variant report

Variant rs3846931
Chromosome Location chr6:56123834-56123835
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:56120800-56129800 Weak transcription Aorta Aorta
2 chr6:56122200-56124400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr6:56123000-56124800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
4 chr6:56123000-56125200 Enhancers Muscle Satellite Cultured Cells --
5 chr6:56123000-56125200 Enhancers Fetal Muscle Leg muscle
6 chr6:56123200-56125000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr6:56123200-56125200 Enhancers Fetal Lung lung
8 chr6:56123200-56125200 Enhancers HSMMtube muscle
9 chr6:56123400-56124400 Weak transcription Osteobl bone
10 chr6:56123400-56124600 Weak transcription NHLF lung
11 chr6:56123400-56124800 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr6:56123600-56124000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr6:56123600-56124600 Enhancers Fetal Brain Male brain
14 chr6:56123800-56124000 Enhancers Fetal Kidney kidney
15 chr6:56123800-56124200 Enhancers H9 Cell Line embryonic stem cell
16 chr6:56123800-56124600 Enhancers HUES48 Cell Line embryonic stem cell
17 chr6:56123800-56124800 Weak transcription iPS-15b Cell Line embryonic stem cell
18 chr6:56123800-56125000 Enhancers HSMM muscle
19 chr6:56123800-56126200 Enhancers Fetal Stomach stomach

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