Variant report

Variant rs73286605
Chromosome Location chr12:11729918-11729919
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:11728000-11730400 ZNF genes & repeats GM12878-XiMat blood
2 chr12:11728800-11731000 Enhancers HMEC breast
3 chr12:11728800-11731200 Enhancers NHEK skin
4 chr12:11728800-11731600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr12:11728800-11734000 Enhancers Monocytes-CD14+_RO01746 blood
6 chr12:11729000-11730000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr12:11729000-11730000 Enhancers Primary monocytes fromperipheralblood blood
8 chr12:11729000-11731800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr12:11729000-11732000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr12:11729200-11730000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr12:11729200-11730600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr12:11729200-11732600 Weak transcription NH-A brain
13 chr12:11729200-11733200 Weak transcription Thymus Thymus
14 chr12:11729400-11730600 Weak transcription Rectal Smooth Muscle rectum
15 chr12:11729400-11730600 Weak transcription Osteobl bone
16 chr12:11729400-11732400 Weak transcription Aorta Aorta
17 chr12:11729600-11733000 Weak transcription Colon Smooth Muscle Colon
18 chr12:11729600-11733200 Weak transcription HUVEC blood vessel
19 chr12:11729800-11733400 Weak transcription Esophagus oesophagus

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