Variant report

Variant	rs10991697
Chromosome Location	chr9:92780180-92780181
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:92779076..92781069-chr9:92783497..92785199,2	MCF-7	breast:
2	chr9:92779670..92782151-chr9:92784242..92786135,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000263967	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10122211	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs10820817	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10820826	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10821471	0.81[CEU][hapmap]
rs10821474	0.83[CEU][hapmap]
rs10821478	0.82[AMR][1000 genomes]
rs10821479	0.82[AMR][1000 genomes]
rs10821505	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10821512	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs10991831	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs10993656	0.86[CEU][hapmap];0.85[AMR][1000 genomes]
rs1348383	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs17361084	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35216191	0.85[AMR][1000 genomes]
rs4743823	0.89[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4743824	0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4743827	0.94[JPT][hapmap]
rs4744020	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4744040	0.89[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4744467	0.83[CEU][hapmap]
rs496129	0.88[AFR][1000 genomes]
rs552128	0.93[YRI][hapmap]
rs586750	0.94[AFR][1000 genomes]
rs6479330	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs652454	0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs661741	0.86[AFR][1000 genomes]
rs7021437	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7025825	0.81[CEU][hapmap]
rs7027342	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7030563	0.89[CHB][hapmap];0.88[JPT][hapmap];0.96[YRI][hapmap];0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs920753	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs980139	0.88[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893561	chr9:92732368-92802101	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv482303	chr9:92752928-92890226	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:92771800-92781400	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr9:92772200-92780800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr9:92773400-92780400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr9:92773800-92780800	Weak transcription	Primary B cells from cord blood	blood
5	chr9:92775600-92780400	Weak transcription	Lung	lung
6	chr9:92775800-92780600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr9:92775800-92780600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr9:92775800-92780800	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr9:92775800-92780800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr9:92775800-92781200	Weak transcription	HSMMtube	muscle
11	chr9:92776800-92787200	Weak transcription	Esophagus	oesophagus
12	chr9:92777800-92782600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr9:92778000-92781400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr9:92778800-92781600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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