Variant report

Variant	rs9610199
Chromosome Location	chr22:22091957-22091958
allele	C/T
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	CEBPB	chr22:22091712-22092046	K562	blood:	n/a	chr22:22091854-22091865
2	USF1	chr22:22091854-22092977	K562	blood:	n/a	chr22:22092584-22092595
3	STAT5A	chr22:22091765-22092752	K562	blood:	n/a	n/a
4	CEBPB	chr22:22091781-22091986	HepG2	liver:	n/a	chr22:22091854-22091865

No.	Distal block	Cell Line	Cell type
1	chr22:22087956..22092439-chr22:22291559..22296073,7	K562	blood:
2	chr22:22088248..22093129-chr22:22216287..22223699,14	K562	blood:
3	chr22:21995824..21997937-chr22:22089395..22092110,2	MCF-7	breast:
4	chr22:22019023..22020752-chr22:22089369..22093678,3	K562	blood:
5	chr22:22091591..22094874-chr22:22098707..22104176,4	MCF-7	breast:
6	chr22:22089106..22092560-chr22:22306070..22309716,3	K562	blood:
7	chr22:22090396..22092560-chr22:22305855..22308907,4	K562	blood:

Variant related genes	Relation type
YPEL1	TF binding region
ENSG00000100030	Chromatin interaction
ENSG00000224086	Chromatin interaction
ENSG00000100023	Chromatin interaction
ENSG00000100034	Chromatin interaction
ENSG00000128228	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11089745	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11703350	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11703624	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11704433	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11704597	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs12172215	1.00[AFR][1000 genomes]
rs12172286	0.85[EUR][1000 genomes]
rs12172360	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs13058633	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs2040167	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2040168	1.00[AFR][1000 genomes]
rs2266968	1.00[AFR][1000 genomes]
rs2276005	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs2276006	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs2298434	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs3827303	0.82[EUR][1000 genomes]
rs4820146	0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4821263	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs4821336	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs4821367	0.82[EUR][1000 genomes]
rs4821369	0.82[EUR][1000 genomes]
rs5749769	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5749779	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs5749792	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs5749811	0.96[EUR][1000 genomes]
rs5749939	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs5749984	0.82[EUR][1000 genomes]
rs5754916	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs5754927	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs5754932	0.80[ASN][1000 genomes]
rs5754944	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs5754947	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs5754968	0.89[EUR][1000 genomes]
rs5754970	0.89[EUR][1000 genomes]
rs5755008	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs5755040	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs5755074	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs61757967	1.00[AFR][1000 genomes]
rs71314794	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9607207	0.81[EUR][1000 genomes]
rs9607209	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs9607210	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs9607274	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs9607286	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs9610174	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs9610181	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs9610219	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9610228	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs9610355	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1823866	chr22:21928916-22131125	Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	374 gene(s)	inside rSNPs	diseases
2	nsv948603	chr22:21928916-22601814	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	422 gene(s)	inside rSNPs	diseases
3	nsv948902	chr22:21928916-22657900	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	426 gene(s)	inside rSNPs	diseases
4	nsv1063962	chr22:21939722-22934593	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	477 gene(s)	inside rSNPs	diseases
5	nsv1058617	chr22:21939922-22934454	Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	477 gene(s)	inside rSNPs	diseases
6	nsv529694	chr22:21957411-22905068	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	474 gene(s)	inside rSNPs	diseases
7	nsv531797	chr22:21977700-22959729	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	476 gene(s)	inside rSNPs	diseases
8	nsv1066403	chr22:22010822-22352262	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
9	nsv510804	chr22:22024531-22132764	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
10	nsv1066964	chr22:22055123-22228745	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
11	nsv544604	chr22:22055123-22228745	Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
12	nsv1063134	chr22:22067645-22129322	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
13	nsv544605	chr22:22067645-22129322	Genic enhancers Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
14	esv3423141	chr22:22074283-22135439	Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
15	nsv1060548	chr22:22079163-22126826	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
16	nsv531549	chr22:22082380-22116681	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
17	nsv588322	chr22:22086373-22186479	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:22090800-22092000	Enhancers	Primary B cells from cord blood	blood
2	chr22:22090800-22092000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr22:22090800-22092000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr22:22090800-22092200	Weak transcription	Dnd41	blood
5	chr22:22090800-22111000	Weak transcription	Primary T cells from cord blood	blood
6	chr22:22090800-22115800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr22:22091000-22092200	Enhancers	Primary B cells from peripheral blood	blood
8	chr22:22091000-22092800	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr22:22091000-22093200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr22:22091000-22093200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr22:22091000-22093200	Weak transcription	Fetal Thymus	thymus
12	chr22:22091000-22093200	Weak transcription	Right Atrium	heart
13	chr22:22091000-22093600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr22:22091000-22095400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr22:22091000-22102800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr22:22091000-22107600	Weak transcription	Spleen	Spleen
17	chr22:22091000-22110000	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr22:22091000-22110800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr22:22091000-22111200	Weak transcription	Pancreas	Pancrea
20	chr22:22091000-22112600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr22:22091000-22116600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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