Variant report

Variant rs2913827
Chromosome Location chr5:177716953-177716954
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177703600-177728800 Weak transcription Right Atrium heart
2 chr5:177713400-177717000 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr5:177713400-177719000 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr5:177714800-177717000 Bivalent Enhancer Fetal Muscle Leg muscle
5 chr5:177714800-177717000 Enhancers Placenta Placenta
6 chr5:177715200-177717000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
7 chr5:177715200-177717400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr5:177715200-177718600 Enhancers Cortex derived primary cultured neurospheres brain
9 chr5:177715400-177717400 Enhancers Esophagus oesophagus
10 chr5:177715800-177717400 Enhancers Skeletal Muscle Female skeletal muscle
11 chr5:177716200-177717600 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
12 chr5:177716600-177717000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr5:177716600-177717000 Enhancers NHEK skin
14 chr5:177716600-177720200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr5:177716800-177717000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr5:177716800-177717800 Weak transcription Fetal Lung lung

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