Variant report

Variant rs115615011
Chromosome Location chr1:172836950-172836951
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172820600-172840200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr1:172828600-172840600 Weak transcription A549 lung
3 chr1:172828800-172840200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:172831200-172844000 Weak transcription HUVEC blood vessel
5 chr1:172836000-172837600 Enhancers Primary T helper memory cells from peripheral blood 1 blood
6 chr1:172836000-172837600 Enhancers Primary T helper cells PMA-I stimulated --
7 chr1:172836400-172837000 Enhancers Primary T helper memory cells from peripheral blood 2 blood
8 chr1:172836400-172837000 Enhancers Primary T helper cells fromperipheralblood blood
9 chr1:172836400-172837000 Enhancers Dnd41 blood
10 chr1:172836400-172837400 Enhancers Primary T cells from cord blood blood
11 chr1:172836400-172837400 Enhancers Primary T helper naive cells from peripheral blood blood
12 chr1:172836600-172837200 Weak transcription Primary T helper 17 cells PMA-I stimulated --
13 chr1:172836800-172837200 Weak transcription Primary T helper naive cells fromperipheralblood blood

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