Variant report

Variant	rs10739780
Chromosome Location	chr9:102139975-102139976
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr9:102139943-102140582	HepG2	liver:	n/a	chr9:102140237-102140251
2	POLR2A	chr9:102138326-102140784	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:102137069..102139229-chr9:102139414..102141097,2	MCF-7	breast:

Variant related genes	Relation type
NAMA	TF binding region
ENSG00000271086	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10491654	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10760680	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10819657	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1323470	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1555572	0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1555573	0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1626179	0.88[ASN][1000 genomes]
rs1648636	0.84[ASN][1000 genomes]
rs16918536	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs170461	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1746153	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs192965	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2281728	0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2586563	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs323723	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs323724	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs323725	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs323726	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs323734	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs323735	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs398150	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs398676	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs417512	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs439733	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4742768	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs696875	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs696876	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs701343	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs701344	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs701347	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs701349	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs701350	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7023945	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7024065	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7029079	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7030379	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7037489	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7038667	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7871334	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs988245	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]

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	nsv893620	chr9:102029791-102194921	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv831667	chr9:102068047-102285691	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1046898	chr9:102111890-102163313	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:102131600-102140200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr9:102131800-102140200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr9:102131800-102140600	Weak transcription	Brain Substantia Nigra	brain
4	chr9:102132400-102148000	Weak transcription	Psoas Muscle	Psoas
5	chr9:102136600-102140000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:102136600-102140600	Weak transcription	Brain Angular Gyrus	brain
7	chr9:102139200-102146000	Enhancers	HepG2	liver
8	chr9:102139400-102140000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr9:102139400-102141600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr9:102139400-102142000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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