Variant report

Variant rs4073398
Chromosome Location chr2:10161891-10161892
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:10159200-10163400 Enhancers Placenta Placenta
2 chr2:10159800-10167600 Weak transcription Right Atrium heart
3 chr2:10160200-10168000 Weak transcription Spleen Spleen
4 chr2:10160400-10175000 Weak transcription Liver Liver
5 chr2:10161600-10162000 Enhancers NHEK skin
6 chr2:10161600-10162200 Bivalent Enhancer HepG2 liver
7 chr2:10161800-10162400 Enhancers K562 blood
8 chr2:10161800-10162600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr2:10161800-10162600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr2:10161800-10163600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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