Variant report

Variant rs2973770
Chromosome Location chr5:177714109-177714110
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177703600-177728800 Weak transcription Right Atrium heart
2 chr5:177707800-177715200 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr5:177713200-177714200 Bivalent Enhancer Fetal Stomach stomach
4 chr5:177713400-177715000 Weak transcription Primary hematopoietic stem cells short term culture blood
5 chr5:177713400-177715000 Weak transcription Fetal Thymus thymus
6 chr5:177713400-177715200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr5:177713400-177715200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr5:177713400-177715200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
9 chr5:177713400-177715600 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr5:177713400-177717000 Bivalent Enhancer Fetal Muscle Trunk muscle
11 chr5:177713400-177719000 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr5:177713800-177714600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
13 chr5:177714000-177714200 Bivalent Enhancer HSMMtube muscle
14 chr5:177714000-177715600 Bivalent Enhancer NHEK skin

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