Variant report

Variant rs2913834
Chromosome Location chr5:177713888-177713889
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr5:177712600-177714000 Enhancers Right Ventricle heart
4 chr5:177713200-177714200 Bivalent Enhancer Fetal Stomach stomach
5 chr5:177713400-177715000 Weak transcription Primary hematopoietic stem cells short term culture blood
6 chr5:177713400-177715000 Weak transcription Fetal Thymus thymus
7 chr5:177713400-177715200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr5:177713400-177715200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr5:177713400-177715200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
10 chr5:177713400-177715600 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr5:177713400-177717000 Bivalent Enhancer Fetal Muscle Trunk muscle
12 chr5:177713400-177719000 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr5:177713600-177714000 Enhancers Esophagus oesophagus
14 chr5:177713600-177714000 Bivalent Enhancer Fetal Muscle Leg muscle
15 chr5:177713800-177714600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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