Variant report

Variant rs4244199
Chromosome Location chr3:196064644-196064645
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:196054600-196091000 Weak transcription ES-WA7 Cell Line embryonic stem cell
2 chr3:196062600-196065000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr3:196062800-196075000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr3:196063000-196064800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr3:196063200-196065600 Enhancers HSMMtube muscle
6 chr3:196063800-196064800 Weak transcription Muscle Satellite Cultured Cells --
7 chr3:196063800-196064800 Weak transcription HSMM muscle
8 chr3:196063800-196065000 Weak transcription Esophagus oesophagus
9 chr3:196064000-196065000 Active TSS Primary Natural Killer cells fromperipheralblood blood
10 chr3:196064200-196065000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr3:196064200-196065600 Flanking Active TSS A549 lung
12 chr3:196064200-196065600 Enhancers HepG2 liver
13 chr3:196064400-196064800 Flanking Active TSS Skeletal Muscle Male skeletal muscle
14 chr3:196064400-196065000 Enhancers HMEC breast
15 chr3:196064400-196065800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr3:196064400-196065800 Flanking Active TSS NHEK skin
17 chr3:196064400-196066000 Flanking Active TSS Hela-S3 cervix
18 chr3:196064600-196064800 Active TSS ES-I3 Cell Line embryonic stem cell
19 chr3:196064600-196064800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr3:196064600-196065200 Flanking Active TSS K562 blood
21 chr3:196064600-196065600 Bivalent/Poised TSS Primary T cells fromperipheralblood blood
22 chr3:196064600-196070200 Enhancers Primary monocytes fromperipheralblood blood

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