Variant report

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873179	chr1:217056893-217112871	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

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Chromatin state (count:20 , 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	chr1:217056800-217058400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr1:217056800-217058800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr1:217057000-217058800	Enhancers	Fetal Intestine Small	intestine
5	chr1:217057000-217061200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr1:217057400-217058400	Enhancers	Small Intestine	intestine
7	chr1:217057400-217058600	Enhancers	HMEC	breast
8	chr1:217057600-217058400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:217057600-217058600	Enhancers	NHEK	skin
10	chr1:217057600-217058800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:217057600-217058800	Enhancers	Duodenum Mucosa	Duodenum
12	chr1:217057800-217058400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:217057800-217058400	Enhancers	Fetal Intestine Large	intestine
14	chr1:217057800-217058400	Enhancers	Stomach Mucosa	stomach
15	chr1:217057800-217058400	Enhancers	Stomach Smooth Muscle	stomach
16	chr1:217057800-217058600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:217057800-217058600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:217058000-217058400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr1:217058000-217058600	Enhancers	Fetal Kidney	kidney
20	chr1:217058000-217062200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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