Variant report

Variant rs56981802
Chromosome Location chr1:94297335-94297336
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94279600-94302800 Weak transcription Stomach Smooth Muscle stomach
2 chr1:94283400-94310000 Weak transcription Skeletal Muscle Male skeletal muscle
3 chr1:94284200-94306200 Weak transcription Fetal Muscle Trunk muscle
4 chr1:94284200-94311200 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
5 chr1:94290200-94311400 Weak transcription Aorta Aorta
6 chr1:94292600-94303200 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr1:94294000-94302200 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr1:94294200-94297800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr1:94294200-94305400 Weak transcription A549 lung
10 chr1:94295000-94297400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr1:94295000-94298400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:94295400-94310000 Weak transcription ES-WA7 Cell Line embryonic stem cell
13 chr1:94296200-94302000 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
14 chr1:94296600-94297400 Enhancers Lung lung
15 chr1:94296800-94297800 Weak transcription H1 Cell Line embryonic stem cell
16 chr1:94297200-94298600 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
17 chr1:94297200-94299000 ZNF genes & repeats Placenta Placenta

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