Variant report

Variant rs2973760
Chromosome Location chr5:177703387-177703388
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:5 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177700400-177704200 Bivalent Enhancer Fetal Stomach stomach
2 chr5:177701400-177705200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr5:177702200-177706800 Weak transcription Fetal Heart heart
4 chr5:177702800-177703400 ZNF genes & repeats Spleen Spleen
5 chr5:177703200-177703400 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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