Variant report

Variant rs6674287
Chromosome Location chr1:92382494-92382495
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:92378400-92391400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr1:92379000-92389400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr1:92379200-92383600 Enhancers Placenta Placenta
4 chr1:92379400-92384200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr1:92379800-92383000 Weak transcription Placenta Amnion Placenta Amnion
6 chr1:92381400-92385400 Weak transcription Hela-S3 cervix
7 chr1:92381600-92389800 Weak transcription HepG2 liver
8 chr1:92381800-92382600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr1:92381800-92383000 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr1:92382400-92383000 Enhancers HUES64 Cell Line embryonic stem cell
11 chr1:92382400-92383000 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr1:92382400-92383200 Enhancers Fetal Heart heart

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