Variant report

Variant	rs9307347
Chromosome Location	chr4:110882460-110882461
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:110875646..110878215-chr4:110881372..110883545,2	K562	blood:
2	chr4:110736083..110738603-chr4:110880229..110882607,2	K562	blood:

Variant related genes	Relation type
ENSG00000272795	Chromatin interaction
ENSG00000109534	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10002971	0.87[EUR][1000 genomes]
rs10011112	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10014383	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10017261	0.87[EUR][1000 genomes]
rs10023272	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10029105	0.96[EUR][1000 genomes]
rs10029654	0.95[EUR][1000 genomes]
rs10213531	0.95[EUR][1000 genomes]
rs1024600	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10470911	0.96[EUR][1000 genomes]
rs10488881	0.97[EUR][1000 genomes]
rs11098056	0.91[EUR][1000 genomes]
rs11568903	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11568905	0.81[EUR][1000 genomes]
rs11568950	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11568972	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11568994	0.86[EUR][1000 genomes]
rs17238095	0.87[ASN][1000 genomes]
rs17253063	0.88[EUR][1000 genomes]
rs17316633	0.87[ASN][1000 genomes]
rs2024114	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2067004	0.95[EUR][1000 genomes]
rs2190909	0.94[EUR][1000 genomes]
rs2237041	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2237045	0.95[EUR][1000 genomes]
rs2250616	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2282785	0.96[EUR][1000 genomes]
rs2298977	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2347136	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28437404	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28535066	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28540029	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28564978	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28629923	0.95[EUR][1000 genomes]
rs28672708	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28734982	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3764861	0.95[EUR][1000 genomes]
rs3775967	0.95[EUR][1000 genomes]
rs3796945	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3796946	0.96[EUR][1000 genomes]
rs3822288	0.96[EUR][1000 genomes]
rs4279279	0.93[EUR][1000 genomes]
rs4698755	0.96[EUR][1000 genomes]
rs4698756	0.95[EUR][1000 genomes]
rs4698800	0.96[EUR][1000 genomes]
rs4698801	0.96[EUR][1000 genomes]
rs62327602	0.87[ASN][1000 genomes]
rs62327604	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6533481	0.96[EUR][1000 genomes]
rs6837717	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7655579	0.95[EUR][1000 genomes]
rs7668520	0.95[EUR][1000 genomes]
rs7680062	0.80[EUR][1000 genomes]
rs881878	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9992755	0.96[EUR][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	nsv530156	chr4:110721397-110911297	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv820232	chr4:110882124-110883098	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110860600-110906600	Weak transcription	Psoas Muscle	Psoas
2	chr4:110869600-110888000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:110872000-110883600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr4:110872000-110885200	Weak transcription	Left Ventricle	heart
5	chr4:110874400-110889000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr4:110875600-110909800	Weak transcription	Pancreas	Pancrea
7	chr4:110879400-110883000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:110880200-110883600	Strong transcription	Skeletal Muscle Female	skeletal muscle

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