Variant report

Variant	rs5759664
Chromosome Location	chr22:23591723-23591724
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	TEAD4	chr22:23591609-23594640	K562	blood:	n/a	n/a
2	MAX	chr22:23591576-23594666	K562	blood:	n/a	chr22:23594366-23594375 chr22:23593934-23593943 chr22:23594161-23594168 chr22:23594157-23594170 chr22:23591995-23592005 chr22:23594261-23594271 chr22:23594159-23594166
3	ATF3	chr22:23591609-23594592	K562	blood:	n/a	chr22:23593950-23593964 chr22:23593948-23593961 chr22:23593948-23593959 chr22:23593951-23593958 chr22:23593951-23593959 chr22:23593948-23593961 chr22:23593950-23593958 chr22:23593947-23593962 chr22:23593949-23593960 chr22:23593951-23593962 chr22:23593950-23593961
4	ELF1	chr22:23591579-23594644	K562	blood:	n/a	chr22:23591881-23591892
5	CBX3	chr22:23591625-23594653	K562	blood:	n/a	n/a
6	JUN	chr22:23591468-23594706	K562	blood:	n/a	chr22:23593949-23593962 chr22:23594364-23594376 chr22:23592067-23592078 chr22:23594366-23594373 chr22:23593950-23593959 chr22:23591938-23591950 chr22:23593935-23593946 chr22:23594366-23594374 chr22:23594366-23594374 chr22:23593933-23593942 chr22:23593158-23593167 chr22:23593933-23593943 chr22:23593932-23593944
7	NR2F2	chr22:23591603-23594685	K562	blood:	n/a	n/a
8	HDAC2	chr22:23591537-23594616	K562	blood:	n/a	chr22:23592407-23592415
9	CEBPB	chr22:23591669-23594678	K562	blood:	n/a	n/a
10	NR2F2	chr22:23591443-23594707	K562	blood:	n/a	n/a
11	FOSL1	chr22:23591622-23594584	K562	blood:	n/a	chr22:23594364-23594376 chr22:23592067-23592078 chr22:23594366-23594373 chr22:23593950-23593959 chr22:23591938-23591950 chr22:23593935-23593946 chr22:23594366-23594374 chr22:23594366-23594374 chr22:23593933-23593942 chr22:23593158-23593167 chr22:23593933-23593943 chr22:23593932-23593944
12	STAT5A	chr22:23591631-23594717	K562	blood:	n/a	chr22:23593662-23593674 chr22:23593656-23593668 chr22:23593933-23593942

No.	Distal block	Cell Line	Cell type
1	chr22:23522061..23524722-chr22:23589297..23592350,3	MCF-7	breast:
2	chr22:23522033..23525900-chr22:23589634..23593895,5	MCF-7	breast:
3	chr22:23583747..23587100-chr22:23587236..23592263,6	MCF-7	breast:
4	chr22:23583033..23586852-chr22:23588137..23592281,4	MCF-7	breast:
5	chr22:23590317..23592486-chr22:23595692..23597693,3	MCF-7	breast:

Variant related genes	Relation type
BCR	TF binding region
ENSG00000236794	Chromatin interaction
ENSG00000186716	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1004040	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11090226	0.92[ASN][1000 genomes]
rs2267018	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2267019	0.96[ASN][1000 genomes]
rs2283805	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5751613	0.94[ASN][1000 genomes]
rs5751614	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5759660	0.92[ASN][1000 genomes]
rs5759662	0.95[ASN][1000 genomes]
rs5759663	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5759667	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs5996505	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9620232	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915235	chr22:22971768-23650987	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
2	esv3388845	chr22:22973346-23652447	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	100 gene(s)	inside rSNPs	diseases
3	nsv531799	chr22:22993679-23642142	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
4	nsv1061433	chr22:22997799-23649107	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
5	nsv521695	chr22:22998337-23648009	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
6	nsv915236	chr22:22998337-23650987	Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
7	nsv588512	chr22:22998337-23667731	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
8	nsv531800	chr22:23002708-23648163	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
9	nsv916593	chr22:23002709-23648790	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers 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	97 gene(s)	inside rSNPs	diseases
10	nsv993496	chr22:23002709-23654222	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
11	nsv1067002	chr22:23007167-23643363	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
12	nsv1067324	chr22:23007367-23654223	Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
13	nsv533839	chr22:23012013-23643223	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
14	nsv916933	chr22:23012069-23654237	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
15	nsv531801	chr22:23028586-23657804	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS 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	92 gene(s)	inside rSNPs	diseases
16	nsv531802	chr22:23046186-23627391	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	85 gene(s)	inside rSNPs	diseases
17	nsv1060509	chr22:23055148-23648719	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	83 gene(s)	inside rSNPs	diseases
18	nsv1056324	chr22:23055148-23750989	Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS 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 miRNA target site	88 gene(s)	inside rSNPs	diseases
19	nsv1062780	chr22:23060449-23648719	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
20	nsv948942	chr22:23063178-23645718	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
21	nsv1063200	chr22:23097177-23643224	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	80 gene(s)	inside rSNPs	diseases
22	nsv949250	chr22:23157485-23645718	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
23	nsv1057659	chr22:23400739-24138788	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
24	nsv588598	chr22:23530168-23638025	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
25	nsv9876	chr22:23563331-23923059	Strong transcription Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
26	nsv482557	chr22:23584948-23741799	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
27	nsv531550	chr22:23589667-24012550	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23573800-23593400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr22:23583800-23596000	Weak transcription	Colonic Mucosa	Colon
3	chr22:23585200-23595000	Weak transcription	Dnd41	blood
4	chr22:23585200-23595800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr22:23585400-23593800	Weak transcription	Fetal Heart	heart
6	chr22:23585600-23595800	Weak transcription	Fetal Brain Female	brain
7	chr22:23585800-23591800	Weak transcription	Placenta	Placenta
8	chr22:23585800-23592800	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr22:23585800-23592800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr22:23585800-23593400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr22:23585800-23594200	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr22:23585800-23594400	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr22:23585800-23594400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr22:23585800-23594600	Enhancers	Primary T cells fromperipheralblood	blood
15	chr22:23585800-23596000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr22:23585800-23605600	Weak transcription	Fetal Lung	lung
17	chr22:23587000-23593600	Weak transcription	A549	lung
18	chr22:23587200-23591800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr22:23587400-23592800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr22:23587400-23597400	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr22:23587600-23593000	Weak transcription	Esophagus	oesophagus
22	chr22:23587600-23593800	Weak transcription	NHLF	lung
23	chr22:23587600-23596000	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr22:23587800-23593800	Weak transcription	NHDF-Ad	bronchial
25	chr22:23587800-23595600	Weak transcription	Duodenum Mucosa	Duodenum
26	chr22:23587800-23595800	Weak transcription	Brain Germinal Matrix	brain
27	chr22:23587800-23598000	Weak transcription	Colon Smooth Muscle	Colon
28	chr22:23588000-23592000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr22:23588200-23596000	Weak transcription	Brain Cingulate Gyrus	brain
30	chr22:23588400-23593200	Weak transcription	Stomach Smooth Muscle	stomach
31	chr22:23588400-23593400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr22:23588400-23594400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr22:23588400-23595800	Weak transcription	Aorta	Aorta
34	chr22:23588400-23596400	Weak transcription	HSMMtube	muscle
35	chr22:23588800-23591800	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr22:23588800-23594200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr22:23588800-23594400	Enhancers	Stomach Mucosa	stomach
38	chr22:23588800-23598800	Weak transcription	HSMM	muscle
39	chr22:23589000-23592600	Enhancers	Lung	lung
40	chr22:23589200-23591800	Enhancers	Primary T cells from cord blood	blood
41	chr22:23589200-23594400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr22:23589400-23594600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr22:23589600-23592000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr22:23589600-23592000	Enhancers	Primary B cells from cord blood	blood
45	chr22:23589800-23591800	Genic enhancers	K562	blood
46	chr22:23589800-23592200	Weak transcription	Fetal Intestine Small	intestine
47	chr22:23589800-23593000	Enhancers	HepG2	liver
48	chr22:23589800-23593400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr22:23589800-23595200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr22:23589800-23596000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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