Variant report

Variant rs4815529
Chromosome Location chr20:26295461-26295462
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:26293800-26295600 Weak transcription Primary T helper cells fromperipheralblood blood
2 chr20:26293800-26295600 Weak transcription HUVEC blood vessel
3 chr20:26293800-26295800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
4 chr20:26293800-26296600 Weak transcription Primary T helper naive cells from peripheral blood blood
5 chr20:26293800-26297800 Weak transcription K562 blood
6 chr20:26293800-26300000 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
7 chr20:26293800-26300000 Weak transcription Colon Smooth Muscle Colon
8 chr20:26293800-26300000 Weak transcription Fetal Kidney kidney
9 chr20:26293800-26300000 Weak transcription Left Ventricle heart
10 chr20:26293800-26304400 Weak transcription NH-A brain
11 chr20:26293800-26309600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr20:26294000-26300000 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
13 chr20:26295400-26296000 Enhancers Primary T helper cells PMA-I stimulated --
14 chr20:26295400-26296000 Enhancers Primary T killer naive cells fromperipheralblood blood
15 chr20:26295400-26296000 Enhancers Primary T killer memory cells from peripheral blood blood
16 chr20:26295400-26296400 ZNF genes & repeats Dnd41 blood
17 chr20:26295400-26297000 Enhancers Primary T helper naive cells fromperipheralblood blood

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