Variant report

Variant rs17137282
Chromosome Location chr7:17184870-17184871
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17178600-17188800 Weak transcription Aorta Aorta
2 chr7:17182000-17185200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr7:17182600-17185000 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
4 chr7:17182800-17185000 Enhancers Primary T helper memory cells from peripheral blood 2 blood
5 chr7:17182800-17185000 Enhancers Primary T helper cells fromperipheralblood blood
6 chr7:17183000-17185000 Enhancers Dnd41 blood
7 chr7:17183200-17185200 Enhancers Primary T helper naive cells from peripheral blood blood
8 chr7:17183200-17185400 Enhancers Primary T helper 17 cells PMA-I stimulated --
9 chr7:17183200-17185600 Enhancers Primary T helper cells PMA-I stimulated --
10 chr7:17183400-17185000 Enhancers Monocytes-CD14+_RO01746 blood
11 chr7:17183400-17186400 Weak transcription Ovary ovary
12 chr7:17184200-17186000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
13 chr7:17184200-17188000 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr7:17184400-17185200 Active TSS Liver Liver
15 chr7:17184400-17186800 Weak transcription NHDF-Ad bronchial
16 chr7:17184400-17188200 Weak transcription Gastric stomach
17 chr7:17184600-17185200 Enhancers Primary T helper memory cells from peripheral blood 1 blood
18 chr7:17184600-17187000 Weak transcription Osteobl bone
19 chr7:17184600-17188000 Weak transcription HepG2 liver
20 chr7:17184600-17189000 Weak transcription Primary monocytes fromperipheralblood blood
21 chr7:17184600-17189000 Weak transcription GM12878-XiMat blood
22 chr7:17184800-17185000 Enhancers Small Intestine intestine

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