Variant report

Variant rs17376659
Chromosome Location chr12:25151624-25151625
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:25141000-25152000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr12:25150200-25152000 Enhancers HSMMtube muscle
3 chr12:25150200-25152200 Enhancers HSMM muscle
4 chr12:25150400-25151800 Enhancers Rectal Mucosa Donor 29 rectum
5 chr12:25150400-25152000 Enhancers Osteobl bone
6 chr12:25150400-25152200 Enhancers Fetal Lung lung
7 chr12:25150600-25151800 Enhancers HUVEC blood vessel
8 chr12:25150600-25152400 Enhancers Colon Smooth Muscle Colon
9 chr12:25150800-25151800 Flanking Active TSS Muscle Satellite Cultured Cells --
10 chr12:25150800-25154200 Weak transcription Fetal Thymus thymus
11 chr12:25151000-25151800 Enhancers Dnd41 blood
12 chr12:25151000-25152400 Enhancers Primary hematopoietic stem cells blood
13 chr12:25151200-25154200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr12:25151200-25155200 Enhancers Primary B cells from peripheral blood blood
15 chr12:25151400-25151800 Flanking Active TSS GM12878-XiMat blood
16 chr12:25151400-25152000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr12:25151600-25152000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
18 chr12:25151600-25152200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
19 chr12:25151600-25152200 Enhancers NH-A brain
20 chr12:25151600-25152200 Enhancers NHLF lung
21 chr12:25151600-25154800 Enhancers Primary B cells from cord blood blood

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