Variant report

Variant rs2638260
Chromosome Location chr12:40548963-40548964
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:40547200-40558600 Weak transcription Liver Liver
2 chr12:40547600-40551800 Weak transcription NHEK skin
3 chr12:40547800-40549600 Weak transcription Primary B cells from peripheral blood blood
4 chr12:40547800-40549600 Weak transcription GM12878-XiMat blood
5 chr12:40547800-40551200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr12:40547800-40551200 Weak transcription HMEC breast
7 chr12:40547800-40551800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr12:40547800-40552200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr12:40548000-40549800 Weak transcription Primary B cells from cord blood blood
10 chr12:40548400-40549200 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr12:40548400-40549400 Enhancers HUES48 Cell Line embryonic stem cell
12 chr12:40548400-40549400 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr12:40548400-40549600 Weak transcription Primary monocytes fromperipheralblood blood
14 chr12:40548400-40549800 Weak transcription Primary neutrophils fromperipheralblood blood
15 chr12:40548400-40551200 Weak transcription Breast Myoepithelial Primary Cells Breast
16 chr12:40548600-40549000 Enhancers iPS-15b Cell Line embryonic stem cell
17 chr12:40548600-40550200 Enhancers HUES64 Cell Line embryonic stem cell
18 chr12:40548800-40549200 Weak transcription Monocytes-CD14+_RO01746 blood
19 chr12:40548800-40553800 Weak transcription H1 Cell Line embryonic stem cell

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