Variant report

Variant rs73038099
Chromosome Location chr1:172712469-172712470
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172711400-172714000 Weak transcription Primary T cells from cord blood blood
2 chr1:172712000-172712600 Enhancers Hela-S3 cervix
3 chr1:172712000-172712800 Enhancers Muscle Satellite Cultured Cells --
4 chr1:172712000-172712800 Enhancers NHLF lung
5 chr1:172712000-172714000 Weak transcription Primary T helper naive cells from peripheral blood blood
6 chr1:172712000-172714000 Weak transcription Primary T helper cells PMA-I stimulated --
7 chr1:172712000-172716400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
8 chr1:172712000-172716400 Enhancers HMEC breast
9 chr1:172712000-172717000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr1:172712200-172712600 Enhancers HUVEC blood vessel
11 chr1:172712200-172712800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr1:172712200-172712800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr1:172712200-172716400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:172712400-172712600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr1:172712400-172714000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr1:172712400-172714400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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