Variant report

Variant rs147701796
Chromosome Location chr4:78276949-78276950
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:78272000-78277000 Weak transcription HMEC breast
2 chr4:78273800-78277000 Weak transcription Fetal Heart heart
3 chr4:78275400-78277400 Enhancers Fetal Thymus thymus
4 chr4:78276000-78277000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr4:78276400-78281400 Weak transcription Primary B cells from peripheral blood blood
6 chr4:78276600-78277000 Weak transcription Fetal Muscle Leg muscle
7 chr4:78276600-78281200 Weak transcription Fetal Kidney kidney
8 chr4:78276800-78277600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr4:78276800-78277800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr4:78276800-78277800 Enhancers NHEK skin

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