Variant report

Variant rs2481712
Chromosome Location chr1:93351477-93351478
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:93339000-93352600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
2 chr1:93340800-93351600 Weak transcription Small Intestine intestine
3 chr1:93348800-93352400 Weak transcription Rectal Mucosa Donor 31 rectum
4 chr1:93349000-93354800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:93349200-93352800 Enhancers HepG2 liver
6 chr1:93349600-93352400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr1:93349600-93352400 Weak transcription Sigmoid Colon Sigmoid Colon
8 chr1:93349800-93351600 Weak transcription Primary B cells from peripheral blood blood
9 chr1:93350000-93351600 Weak transcription Primary T cells fromperipheralblood blood
10 chr1:93350000-93366400 Weak transcription Thymus Thymus
11 chr1:93350400-93352200 Weak transcription Liver Liver
12 chr1:93350800-93351600 Weak transcription Primary T helper cells PMA-I stimulated --
13 chr1:93350800-93352000 Weak transcription Primary T helper 17 cells PMA-I stimulated --

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