Variant report

Variant rs28538252
Chromosome Location chr4:79606620-79606621
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:79604200-79610000 Weak transcription Fetal Intestine Large intestine
2 chr4:79605600-79609000 Weak transcription Placenta Placenta
3 chr4:79605800-79607400 Enhancers Fetal Heart heart
4 chr4:79605800-79609000 Weak transcription NHEK skin
5 chr4:79605800-79612200 Weak transcription Fetal Intestine Small intestine
6 chr4:79606000-79609600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr4:79606000-79609800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr4:79606000-79610200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr4:79606000-79611800 Weak transcription Fetal Adrenal Gland Adrenal Gland
10 chr4:79606200-79609200 Weak transcription Muscle Satellite Cultured Cells --
11 chr4:79606200-79609600 Weak transcription NHLF lung
12 chr4:79606400-79607200 Enhancers K562 blood
13 chr4:79606600-79609000 Weak transcription NHDF-Ad bronchial
14 chr4:79606600-79609600 Weak transcription HSMM muscle
15 chr4:79606600-79612200 Weak transcription HSMMtube muscle

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