Variant report

Variant rs568710297
Chromosome Location chr1:217058767-217058768
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:217055600-217062200 Weak transcription H9 Cell Line embryonic stem cell
2 chr1:217056800-217058800 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr1:217057000-217058800 Enhancers Fetal Intestine Small intestine
4 chr1:217057000-217061200 Weak transcription HUES64 Cell Line embryonic stem cell
5 chr1:217057600-217058800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr1:217057600-217058800 Enhancers Duodenum Mucosa Duodenum
7 chr1:217058000-217062200 Weak transcription Fetal Adrenal Gland Adrenal Gland
8 chr1:217058200-217058800 Enhancers Cortex derived primary cultured neurospheres brain
9 chr1:217058200-217067600 Weak transcription iPS-20b Cell Line embryonic stem cell
10 chr1:217058400-217061600 Weak transcription Fetal Intestine Large intestine
11 chr1:217058400-217061800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr1:217058400-217062000 Weak transcription Stomach Mucosa stomach
13 chr1:217058400-217065200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:217058400-217067800 Weak transcription Small Intestine intestine
15 chr1:217058600-217061400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
16 chr1:217058600-217062000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr1:217058600-217067800 Weak transcription Fetal Kidney kidney

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