Variant report

Variant rs571272660
Chromosome Location chr7:3197300-3197301
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:3178400-3204600 Weak transcription Right Atrium heart
2 chr7:3196800-3197600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr7:3196800-3197600 Enhancers Primary B cells from peripheral blood blood
4 chr7:3197000-3197400 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr7:3197000-3197600 Enhancers Esophagus oesophagus
6 chr7:3197000-3197800 Enhancers ES-WA7 Cell Line embryonic stem cell
7 chr7:3197000-3197800 Enhancers H1 Cell Line embryonic stem cell
8 chr7:3197000-3197800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr7:3197000-3198200 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr7:3197200-3197400 Enhancers Primary T helper cells fromperipheralblood blood
11 chr7:3197200-3197600 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr7:3197200-3197600 Bivalent Enhancer Fetal Muscle Trunk muscle
13 chr7:3197200-3197600 Bivalent Enhancer Fetal Muscle Leg muscle
14 chr7:3197200-3197800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr7:3197200-3197800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
16 chr7:3197200-3197800 Enhancers Primary B cells from cord blood blood
17 chr7:3197200-3197800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
18 chr7:3197200-3197800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr7:3197200-3197800 Enhancers NH-A brain

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