Variant report

Variant rs61767367
Chromosome Location chr1:57744592-57744593
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:57735200-57747200 Weak transcription Esophagus oesophagus
2 chr1:57737400-57746800 Weak transcription Fetal Brain Female brain
3 chr1:57741800-57749400 Enhancers Fetal Intestine Small intestine
4 chr1:57742000-57749200 Enhancers Liver Liver
5 chr1:57742200-57755400 Weak transcription Fetal Brain Male brain
6 chr1:57743200-57745600 Enhancers NHEK skin
7 chr1:57743400-57745400 Weak transcription Duodenum Mucosa Duodenum
8 chr1:57743800-57745000 Weak transcription HMEC breast
9 chr1:57743800-57745200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr1:57743800-57745200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr1:57743800-57745400 Enhancers HepG2 liver
12 chr1:57744000-57745200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:57744200-57744600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr1:57744200-57744600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr1:57744400-57749600 Enhancers Fetal Intestine Large intestine

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