Variant report

Variant rs12293091
Chromosome Location chr11:94411665-94411666
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:94404400-94413000 Enhancers HMEC breast
2 chr11:94405400-94415600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr11:94406600-94412400 Enhancers Psoas Muscle Psoas
4 chr11:94406800-94413000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr11:94407200-94412800 Enhancers Fetal Intestine Large intestine
6 chr11:94407400-94412600 Enhancers Fetal Intestine Small intestine
7 chr11:94408200-94412400 Enhancers Skeletal Muscle Male skeletal muscle
8 chr11:94408800-94413000 Enhancers Esophagus oesophagus
9 chr11:94409600-94413600 Enhancers K562 blood
10 chr11:94410400-94412600 Enhancers Placenta Placenta
11 chr11:94410400-94414000 Enhancers Placenta Amnion Placenta Amnion
12 chr11:94410800-94412600 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr11:94411000-94415400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr11:94411200-94412600 Flanking Active TSS NHEK skin
15 chr11:94411400-94411800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr11:94411400-94412400 Enhancers Hela-S3 cervix
17 chr11:94411600-94412000 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin

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