Variant report

Variant rs295065
Chromosome Location chr6:11598931-11598932
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:11593200-11600800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr6:11593200-11605400 Weak transcription Right Atrium heart
3 chr6:11593600-11604600 Weak transcription Muscle Satellite Cultured Cells --
4 chr6:11593800-11609800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr6:11595200-11602400 Weak transcription HSMMtube muscle
6 chr6:11597400-11599200 Weak transcription Placenta Amnion Placenta Amnion
7 chr6:11597400-11606600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr6:11597600-11599600 Enhancers Ovary ovary
9 chr6:11597600-11599800 Enhancers Fetal Intestine Large intestine
10 chr6:11598000-11599800 Enhancers HepG2 liver
11 chr6:11598000-11600000 Enhancers Primary neutrophils fromperipheralblood blood
12 chr6:11598000-11600000 Enhancers Placenta Placenta
13 chr6:11598600-11599800 Enhancers Primary monocytes fromperipheralblood blood
14 chr6:11598600-11599800 Enhancers Monocytes-CD14+_RO01746 blood
15 chr6:11598800-11599000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
16 chr6:11598800-11599200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr6:11598800-11599200 Enhancers Liver Liver
18 chr6:11598800-11599400 Flanking Active TSS A549 lung
19 chr6:11598800-11599600 Strong transcription HSMM muscle
20 chr6:11598800-11599800 Enhancers Fetal Intestine Small intestine

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