Variant report

Variant rs2068909
Chromosome Location chr11:94458168-94458169
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:94450200-94465000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr11:94454200-94458200 Weak transcription Skeletal Muscle Male skeletal muscle
3 chr11:94455400-94467800 Weak transcription Psoas Muscle Psoas
4 chr11:94455600-94459600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr11:94456200-94458400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr11:94456400-94461000 Weak transcription Hela-S3 cervix
7 chr11:94456600-94459000 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr11:94457000-94458200 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr11:94457200-94460000 Enhancers Skeletal Muscle Female skeletal muscle
10 chr11:94457800-94458800 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr11:94457800-94463000 Weak transcription K562 blood
12 chr11:94458000-94458200 Enhancers Monocytes-CD14+_RO01746 blood
13 chr11:94458000-94459000 Genic enhancers NHEK skin
14 chr11:94458000-94459400 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr11:94458000-94460000 Enhancers Placenta Placenta
16 chr11:94458000-94460200 Enhancers Primary monocytes fromperipheralblood blood
17 chr11:94458000-94460400 Enhancers Primary neutrophils fromperipheralblood blood
18 chr11:94458000-94462400 Enhancers HMEC breast

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