Variant report

Variant rs6696098
Chromosome Location chr1:224267958-224267959
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:224266800-224268200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr1:224267400-224268600 Enhancers HUVEC blood vessel
3 chr1:224267600-224268400 Enhancers Right Atrium heart
4 chr1:224267600-224268600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
5 chr1:224267600-224270000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr1:224267800-224268400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr1:224267800-224268400 Enhancers Muscle Satellite Cultured Cells --
8 chr1:224267800-224268600 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr1:224267800-224268600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:224267800-224268600 Flanking Active TSS K562 blood
11 chr1:224267800-224268800 Enhancers Fetal Lung lung
12 chr1:224267800-224268800 Enhancers NH-A brain
13 chr1:224267800-224269200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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