Variant report

Variant rs2799535
Chromosome Location chr1:92379448-92379449
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:92378400-92379600 Enhancers A549 lung
2 chr1:92378400-92379600 Enhancers HUVEC blood vessel
3 chr1:92378400-92391400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr1:92379000-92389400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr1:92379200-92380200 Flanking Active TSS Hela-S3 cervix
6 chr1:92379200-92383600 Enhancers Placenta Placenta
7 chr1:92379400-92379800 Enhancers Placenta Amnion Placenta Amnion
8 chr1:92379400-92379800 Enhancers HepG2 liver
9 chr1:92379400-92379800 Enhancers K562 blood
10 chr1:92379400-92384200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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