Variant report

Variant rs113609892
Chromosome Location chr8:130213862-130213863
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:130205400-130214600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:130208200-130241600 Weak transcription Thymus Thymus
3 chr8:130209600-130214600 Weak transcription Fetal Stomach stomach
4 chr8:130209800-130214600 Weak transcription Ovary ovary
5 chr8:130210000-130215000 Genic enhancers Dnd41 blood
6 chr8:130210000-130216600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr8:130211400-130215400 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr8:130211800-130214400 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr8:130213400-130214400 Weak transcription NHDF-Ad bronchial
10 chr8:130213400-130215000 Enhancers K562 blood
11 chr8:130213600-130215600 Enhancers Fetal Muscle Leg muscle
12 chr8:130213800-130214000 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr8:130213800-130214200 Genic enhancers Fetal Thymus thymus
14 chr8:130213800-130215600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
15 chr8:130213800-130215600 Enhancers Fetal Adrenal Gland Adrenal Gland

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