Variant report

Variant rs11176777
Chromosome Location chr12:67935513-67935514
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:67930400-67935600 Weak transcription Fetal Intestine Large intestine
2 chr12:67933200-67935600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr12:67933600-67935800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr12:67933800-67935800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr12:67933800-67935800 Enhancers HMEC breast
6 chr12:67933800-67936600 Enhancers NHEK skin
7 chr12:67934400-67936200 Enhancers Primary T helper cells PMA-I stimulated --
8 chr12:67934600-67936200 Enhancers Primary T helper naive cells from peripheral blood blood
9 chr12:67934800-67935600 Enhancers Gastric stomach
10 chr12:67934800-67936000 Enhancers Primary T helper naive cells fromperipheralblood blood
11 chr12:67934800-67936400 Enhancers Primary T helper memory cells from peripheral blood 2 blood
12 chr12:67934800-67937800 Enhancers Fetal Intestine Small intestine
13 chr12:67935000-67935600 Enhancers Primary T cells from cord blood blood
14 chr12:67935000-67935600 Enhancers Primary T helper 17 cells PMA-I stimulated --
15 chr12:67935000-67935800 Enhancers Primary T killer memory cells from peripheral blood blood
16 chr12:67935000-67935800 Enhancers Stomach Mucosa stomach
17 chr12:67935000-67936000 Enhancers Primary T killer naive cells fromperipheralblood blood
18 chr12:67935000-67936400 Enhancers Primary T helper cells fromperipheralblood blood
19 chr12:67935400-67935600 Weak transcription Fetal Kidney kidney
20 chr12:67935400-67935600 Flanking Active TSS GM12878-XiMat blood

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