Variant report

Variant rs855695
Chromosome Location chr7:149486726-149486727
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:149473800-149534800 Weak transcription Right Atrium heart
2 chr7:149480800-149486800 Weak transcription Primary hematopoietic stem cells short term culture blood
3 chr7:149484800-149486800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr7:149485000-149487200 Weak transcription Pancreas Pancrea
5 chr7:149485200-149486800 Weak transcription A549 lung
6 chr7:149485200-149487200 Enhancers Liver Liver
7 chr7:149485200-149487200 Weak transcription Gastric stomach
8 chr7:149485200-149489200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr7:149485400-149487400 Weak transcription Primary T helper naive cells from peripheral blood blood
10 chr7:149486200-149487000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr7:149486200-149487800 Bivalent Enhancer Fetal Muscle Trunk muscle
12 chr7:149486400-149486800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
13 chr7:149486400-149486800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
14 chr7:149486600-149488200 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell

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