The 2.0 version of rSNPBase

Variant report

Variant rs10798130
Chromosome Location chr1:172620101-172620102
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172608800-172624000 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr1:172613200-172620200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:172613200-172620200 Weak transcription HMEC breast
4 chr1:172613600-172623400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr1:172613800-172623400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr1:172616800-172623600 Weak transcription NH-A brain
7 chr1:172616800-172627400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
8 chr1:172617200-172622400 Weak transcription Primary T helper cells PMA-I stimulated --
9 chr1:172617400-172622400 Weak transcription Primary T helper naive cells from peripheral blood blood
10 chr1:172617400-172626800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
11 chr1:172617600-172623800 Weak transcription Osteobl bone
12 chr1:172617600-172626800 Weak transcription Primary T killer memory cells from peripheral blood blood
13 chr1:172617800-172621400 Weak transcription Dnd41 blood
14 chr1:172619800-172620400 Enhancers NHEK skin
15 chr1:172620000-172620400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
16 chr1:172620000-172620400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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Last update: Aug 31, 2015