Variant report

Variant rs6675980
Chromosome Location chr1:224898863-224898864
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:224862400-224902000 Weak transcription Pancreas Pancrea
2 chr1:224885000-224920200 Weak transcription Right Atrium heart
3 chr1:224896000-224902000 Weak transcription Dnd41 blood
4 chr1:224896200-224914000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr1:224896400-224910600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr1:224896400-224913800 Weak transcription NHLF lung
7 chr1:224896400-224914000 Weak transcription NH-A brain
8 chr1:224896600-224899400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:224896600-224902600 Weak transcription NHDF-Ad bronchial
10 chr1:224896800-224899400 Weak transcription HMEC breast
11 chr1:224897000-224901200 Genic enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr1:224897200-224899600 Weak transcription Cortex derived primary cultured neurospheres brain
13 chr1:224897200-224900600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
14 chr1:224897400-224900200 Weak transcription Breast Myoepithelial Primary Cells Breast
15 chr1:224898000-224899000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr1:224898000-224901600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
17 chr1:224898400-224904400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr1:224898600-224902000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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