Variant report

Variant	rs9893752
Chromosome Location	chr17:66563374-66563375
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:66508241..66510455-chr17:66561114..66563780,2	K562	blood:
2	chr17:66549645..66553348-chr17:66560847..66563979,4	MCF-7	breast:
3	chr17:66561395..66563836-chr17:66567665..66570201,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000108946	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833524	chr17:66524030-66705194	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	esv3315393	chr17:66562992-66565471	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	esv3315394	chr17:66562992-66565471	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66538800-66575800	Weak transcription	Spleen	Spleen
2	chr17:66539200-66588000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr17:66540200-66563400	Weak transcription	Placenta	Placenta
4	chr17:66544800-66563600	Weak transcription	Stomach Mucosa	stomach
5	chr17:66551800-66567400	Weak transcription	Fetal Stomach	stomach
6	chr17:66551800-66570600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr17:66551800-66572000	Weak transcription	Gastric	stomach
8	chr17:66551800-66587800	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr17:66552000-66584200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr17:66552000-66585200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr17:66554600-66566400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr17:66558800-66566800	Weak transcription	Fetal Heart	heart
13	chr17:66560200-66563400	Weak transcription	Aorta	Aorta
14	chr17:66560200-66564000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr17:66561000-66563400	Weak transcription	Esophagus	oesophagus
16	chr17:66561000-66568200	Weak transcription	Lung	lung
17	chr17:66561200-66563400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr17:66561800-66563400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr17:66562000-66563600	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr17:66562000-66563800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr17:66562000-66564000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr17:66562000-66564200	Enhancers	Liver	Liver
23	chr17:66562400-66564000	Enhancers	Osteobl	bone
24	chr17:66562400-66564400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr17:66562600-66564200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr17:66562600-66564200	Enhancers	HepG2	liver
27	chr17:66562800-66566800	Weak transcription	Fetal Lung	lung
28	chr17:66563000-66563400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr17:66563200-66563600	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr17:66563200-66563800	Enhancers	Ovary	ovary

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