Variant report

Variant rs10029464
Chromosome Location chr4:186960726-186960727
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:186959200-186960800 Enhancers Rectal Smooth Muscle rectum
2 chr4:186959200-186960800 Weak transcription Right Ventricle heart
3 chr4:186959200-186961200 Enhancers Fetal Heart heart
4 chr4:186959400-186960800 Weak transcription ES-WA7 Cell Line embryonic stem cell
5 chr4:186959600-186961400 Enhancers Placenta Placenta
6 chr4:186959800-186960800 Weak transcription Ovary ovary
7 chr4:186960200-186961000 Flanking Active TSS Stomach Smooth Muscle stomach
8 chr4:186960400-186960800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr4:186960400-186960800 Enhancers Fetal Stomach stomach
10 chr4:186960400-186961000 Enhancers HUES48 Cell Line embryonic stem cell
11 chr4:186960600-186960800 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr4:186960600-186960800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr4:186960600-186960800 Flanking Active TSS Colon Smooth Muscle Colon
14 chr4:186960600-186960800 Flanking Active TSS Duodenum Smooth Muscle Duodenum
15 chr4:186960600-186961400 Active TSS Aorta Aorta
16 chr4:186960600-186961400 Enhancers Placenta Amnion Placenta Amnion
17 chr4:186960600-186961400 Bivalent/Poised TSS A549 lung
18 chr4:186960600-186961600 Flanking Bivalent TSS/Enh Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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