Variant report

Variant rs9994482
Chromosome Location chr4:152391230-152391231
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:152386000-152393600 Weak transcription Skeletal Muscle Male skeletal muscle
2 chr4:152389600-152391800 Enhancers ES-I3 Cell Line embryonic stem cell
3 chr4:152389600-152391800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr4:152389600-152391800 Enhancers HMEC breast
5 chr4:152389600-152392000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr4:152389600-152392200 Enhancers HUES48 Cell Line embryonic stem cell
7 chr4:152389800-152391800 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr4:152389800-152391800 Enhancers NHEK skin
9 chr4:152389800-152392400 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr4:152390000-152396200 Weak transcription iPS-20b Cell Line embryonic stem cell
11 chr4:152390200-152392000 Weak transcription H1 Cell Line embryonic stem cell
12 chr4:152390200-152393600 Weak transcription HUES6 Cell Line embryonic stem cell
13 chr4:152390800-152391600 Enhancers HUES64 Cell Line embryonic stem cell
14 chr4:152390800-152392200 Weak transcription H9 Cell Line embryonic stem cell
15 chr4:152391200-152391400 Enhancers Skeletal Muscle Female skeletal muscle
16 chr4:152391200-152391600 Enhancers iPS-15b Cell Line embryonic stem cell
17 chr4:152391200-152391600 Enhancers Muscle Satellite Cultured Cells --
18 chr4:152391200-152391600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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