Variant report

Variant	rs7753565
Chromosome Location	chr6:26560012-26560013
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	chr6:26552134..26560768-chr6:26592842..26598560,12	K562	blood:
2	chr6:26199265..26202124-chr6:26559313..26562023,2	K562	blood:

Variant related genes	Relation type
ENSG00000197846	Chromatin interaction
ENSG00000146109	Chromatin interaction
ENSG00000196866	Chromatin interaction
ENSG00000197409	Chromatin interaction

Extended variants
information (count: 96 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs1021372	0.93[YRI][hapmap]
rs10214634	0.82[EUR][1000 genomes]
rs1027204	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs10484442	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1056667	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1078679	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[EUR][1000 genomes]
rs10946834	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs10946835	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs10946837	0.81[EUR][1000 genomes]
rs12526680	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs1321479	0.96[CEU][hapmap];0.96[YRI][hapmap]
rs1321481	0.95[CEU][hapmap];1.00[YRI][hapmap];0.80[EUR][1000 genomes]
rs1321482	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs1535276	1.00[CEU][hapmap];0.96[YRI][hapmap]
rs1535277	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1570059	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs1570060	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs1570061	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs1884946	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs1884947	1.00[CEU][hapmap];0.86[CHB][hapmap]
rs1884948	0.81[EUR][1000 genomes]
rs1884949	0.81[EUR][1000 genomes]
rs2172007	0.82[CHB][hapmap]
rs2224380	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2255070	1.00[CEU][hapmap];0.96[YRI][hapmap]
rs2393670	1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs2451711	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs2451741	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs2494692	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs2494701	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs2498380	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs2504565	0.85[JPT][hapmap];0.89[YRI][hapmap]
rs2504566	0.87[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs2504567	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs2504571	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs2504599	1.00[JPT][hapmap];0.96[YRI][hapmap]
rs2504600	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs3736781	1.00[CEU][hapmap];0.96[YRI][hapmap]
rs3736782	1.00[CEU][hapmap];0.96[YRI][hapmap]
rs3800303	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs4368798	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs4573	0.96[CEU][hapmap]
rs4713006	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs4713008	0.96[CEU][hapmap];1.00[YRI][hapmap];0.80[EUR][1000 genomes]
rs4871	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs6456733	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6456734	0.80[EUR][1000 genomes]
rs6456735	0.95[CEU][hapmap];0.90[JPT][hapmap];0.93[YRI][hapmap]
rs6903973	1.00[CEU][hapmap];0.96[YRI][hapmap]
rs6913398	0.83[EUR][1000 genomes]
rs6918360	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6918506	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs6918854	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs6922824	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6924838	0.81[EUR][1000 genomes]
rs6924865	1.00[YRI][hapmap]
rs6925703	1.00[CEU][hapmap]
rs6925895	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[EUR][1000 genomes]
rs6926629	1.00[CEU][hapmap];0.93[YRI][hapmap]
rs6930120	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6932156	0.81[EUR][1000 genomes]
rs6932865	0.83[EUR][1000 genomes]
rs6933176	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs6940053	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6940188	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6941022	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs767471	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7767847	0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs9295695	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs9295698	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9357010	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs9393729	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs9461267	1.00[CEU][hapmap]
rs9461270	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs9461271	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9461272	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs9461273	1.00[JPT][hapmap]
rs9467773	1.00[YRI][hapmap]
rs9467774	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs9467778	0.81[EUR][1000 genomes]
rs9467779	1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs9467782	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs9467783	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs9467784	0.83[EUR][1000 genomes]
rs9467787	0.82[EUR][1000 genomes]
rs9467788	0.90[YRI][hapmap]
rs9467791	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9467796	0.81[EUR][1000 genomes]
rs9467797	0.81[EUR][1000 genomes]
rs9467798	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs9467800	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs9467810	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs9986382	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[EUR][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	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv948921	chr6:26556890-27443957	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	472 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs7753565	HCG11	cis	uninvolved skin	skin_eQTL
rs7753565	HMGN4	cis	brain	BrainEAC
rs7753565	HMGN4	Cis_1M	lymphoblastoid	RTeQTL
rs7753565	ZNF322	cis	Nerve Tibial	GTEx
rs7753565	HMGN4	cis	Whole Blood	GTEx
rs7753565	HCG11	cis	normal skin	skin_eQTL
rs7753565	HCG11	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26555200-26561800	Weak transcription	Aorta	Aorta
2	chr6:26555400-26562000	Weak transcription	Pancreas	Pancrea
3	chr6:26556000-26561400	Weak transcription	Right Atrium	heart
4	chr6:26556800-26561600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:26557400-26568400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:26558000-26560600	Weak transcription	HepG2	liver
7	chr6:26558000-26563000	Weak transcription	K562	blood
8	chr6:26558400-26561200	Weak transcription	A549	lung
9	chr6:26559600-26568200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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