Variant report

Variant	rs6002080
Chromosome Location	chr22:22734848-22734849
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	CTCF	chr22:22734770-22734992	MCF-7	breast:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
2	RAD21	chr22:22734691-22735074	H1-hESC	embryonic stem cell:	n/a	chr22:22734901-22734920 chr22:22734906-22734916
3	CTCF	chr22:22734780-22734930	HMF	breast:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
4	CTCF	chr22:22734800-22734950	Hela-S3	cervix:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
5	CTCF	chr22:22734804-22734954	Fibrobl	skin:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
6	CTCF	chr22:22734840-22734990	HepG2	liver:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
7	CTCF	chr22:22734800-22734950	HUVEC	blood vessel:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
8	CTCF	chr22:22734820-22734970	K562	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
9	MAZ	chr22:22734729-22735087	K562	blood:	n/a	n/a
10	CTCF	chr22:22734743-22735016	H1-hESC	embryonic stem cell:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
11	CTCF	chr22:22734841-22734947	Kidney_OC	kidney:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
12	CTCF	chr22:22734836-22734949	NHEK	skin:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
13	CTCF	chr22:22734820-22734970	GM12864	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
14	CTCF	chr22:22734800-22734950	HPAF	blood vessel:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
15	RAD21	chr22:22734810-22735050	GM12878	blood:	n/a	chr22:22734901-22734920 chr22:22734906-22734916
16	CTCF	chr22:22734760-22734910	GM12873	blood:	n/a	n/a
17	CTCF	chr22:22734780-22734930	HBMEC	blood vessel:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
18	CTCF	chr22:22734780-22734930	K562	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
19	CTCF	chr22:22734740-22734890	GM12869	blood:	n/a	n/a
20	CTCF	chr22:22734643-22735112	K562	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
21	RAD21	chr22:22734784-22735012	K562	blood:	n/a	chr22:22734901-22734920 chr22:22734906-22734916
22	CTCF	chr22:22734805-22735008	MCF-7	breast:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
23	CTCF	chr22:22734820-22734970	GM12871	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
24	CTCF	chr22:22734784-22735119	H1-hESC	embryonic stem cell:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
25	CTCF	chr22:22734800-22734950	BE2_C	brain:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
26	CTCF	chr22:22734787-22734969	MCF-7	breast:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
27	CTCF	chr22:22734780-22734930	HepG2	liver:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
28	CTCF	chr22:22734718-22735154	HCT-116	colon:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
29	CTCF	chr22:22734820-22734970	GM12866	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
30	CTCF	chr22:22734840-22734990	Caco-2	colon:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
31	CTCF	chr22:22734753-22735003	A549	lung:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
32	RAD21	chr22:22734747-22735080	ECC-1	luminal epithelium:	n/a	chr22:22734901-22734920 chr22:22734906-22734916
33	RAD21	chr22:22734708-22735061	A549	lung:	n/a	chr22:22734901-22734920 chr22:22734906-22734916
34	CTCF	chr22:22734780-22734930	HPF	lung:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
35	CTCF	chr22:22734788-22734986	MCF-7	breast:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
36	CTCF	chr22:22734840-22734990	GM12872	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
37	CTCF	chr22:22734800-22734950	GM12865	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
38	CTCF	chr22:22734840-22734990	HCT-116	colon:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
39	SMC3	chr22:22734711-22735034	HepG2	liver:	n/a	chr22:22734902-22734916 chr22:22734906-22734916
40	CTCF	chr22:22734797-22734980	A549	lung:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
41	CTCF	chr22:22734800-22734950	RPTEC	kidney:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
42	CTCF	chr22:22734788-22734966	GM13977	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
43	CTCF	chr22:22734739-22735045	GM12891	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
44	CTCF	chr22:22734840-22734990	NHEK	skin:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
45	CTCF	chr22:22734780-22734930	AG09319	gingival:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
46	CTCF	chr22:22734800-22734950	GM12875	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
47	CTCF	chr22:22734840-22734990	GM12864	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
48	CTCF	chr22:22734830-22734933	LNCaP	prostate:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
49	CTCF	chr22:22734800-22734950	GM12873	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923
50	CTCF	chr22:22734800-22734950	GM12869	blood:	n/a	chr22:22734905-22734915 chr22:22734901-22734917 chr22:22734900-22734918 chr22:22734902-22734923

No.	Distal block	Cell Line	Cell type
1	chr22:22734086..22737664-chr22:22750261..22752211,3	K562	blood:
2	chr22:22711677..22712315-chr22:22734391..22735319,2	K562	blood:
3	chr22:22734112..22734934-chr22:22958434..22959274,2	K562	blood:
4	chr22:22732728..22735140-chr22:22752978..22754604,2	K562	blood:

Variant related genes	Relation type
IGLV1-44	TF binding region
ENSG00000254073	Chromatin interaction
ENSG00000211648	Chromatin interaction
ENSG00000254175	Chromatin interaction

Extended variants
information (count: 438 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs13055161	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1477442	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16987792	1.00[ASN][1000 genomes]
rs1862933	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1985918	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4821946	1.00[ASN][1000 genomes]
rs55802730	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55917206	0.94[EUR][1000 genomes]
rs56413433	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58009851	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59717931	1.00[ASN][1000 genomes]
rs5995896	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5995897	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5995900	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5995931	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5995942	1.00[ASN][1000 genomes]
rs6002024	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6002026	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6002028	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6002029	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6002030	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6002074	1.00[ASN][1000 genomes]
rs6002106	1.00[ASN][1000 genomes]
rs6002112	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6002248	1.00[ASN][1000 genomes]
rs6519258	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6519259	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6519260	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6519263	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68171706	1.00[ASN][1000 genomes]
rs7284345	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7284647	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7286936	1.00[ASN][1000 genomes]
rs7289376	1.00[ASN][1000 genomes]
rs7290362	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73878444	1.00[ASN][1000 genomes]
rs8137544	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8139459	1.00[ASN][1000 genomes]
rs8140324	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8140331	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9607987	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	nsv948580	chr22:22100718-22839559	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic 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 target site	97 gene(s)	inside rSNPs	diseases
6	esv2422403	chr22:22152248-23112582	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
7	esv2422390	chr22:22157964-23112582	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer 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 miRNA target site	145 gene(s)	inside rSNPs	diseases
8	esv2422362	chr22:22198357-23125553	Enhancers Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS 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 miRNA target site	145 gene(s)	inside rSNPs	diseases
9	esv2422446	chr22:22198357-23127963	Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
10	esv2422217	chr22:22217341-23120076	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
11	esv2422343	chr22:22298025-23112582	Bivalent Enhancer Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
12	nsv432178	chr22:22307519-23222208	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers 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 miRNA target site	160 gene(s)	inside rSNPs	diseases
13	nsv432179	chr22:22307519-23288012	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
14	nsv9875	chr22:22312880-23277895	Strong transcription Bivalent Enhancer Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers 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	167 gene(s)	inside rSNPs	diseases
15	nsv1063653	chr22:22312927-23087293	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS 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	129 gene(s)	inside rSNPs	diseases
16	nsv1061533	chr22:22312927-23097377	Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Flanking 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	132 gene(s)	inside rSNPs	diseases
17	nsv1063119	chr22:22313127-23087154	Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	129 gene(s)	inside rSNPs	diseases
18	nsv1060418	chr22:22313127-23097238	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
19	nsv1060595	chr22:22313127-23122548	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	133 gene(s)	inside rSNPs	diseases
20	nsv1057610	chr22:22313127-23245889	Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
21	nsv1066111	chr22:22315077-23099160	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised 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 target site	130 gene(s)	inside rSNPs	diseases
22	esv2755411	chr22:22322138-23149622	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
23	esv2756590	chr22:22322138-23222208	Bivalent Enhancer Bivalent/Poised TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
24	nsv432183	chr22:22322138-23222208	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
25	nsv526328	chr22:22328391-22911060	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
26	esv2755870	chr22:22332876-23222208	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers 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	157 gene(s)	inside rSNPs	diseases
27	nsv459421	chr22:22336512-22911060	Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
28	nsv588348	chr22:22336512-22911060	Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
29	esv2753191	chr22:22343054-23157485	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers 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	142 gene(s)	inside rSNPs	diseases
30	esv2755227	chr22:22343336-23157485	Bivalent Enhancer Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	142 gene(s)	inside rSNPs	diseases
31	esv2754921	chr22:22353066-23278593	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
32	nsv3567	chr22:22375862-23272265	Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
33	esv2752535	chr22:22379067-22952239	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
34	esv2753011	chr22:22381768-23157485	Strong transcription Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	142 gene(s)	inside rSNPs	diseases
35	nsv588355	chr22:22384041-23111861	Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	129 gene(s)	inside rSNPs	diseases
36	nsv459426	chr22:22384041-23240027	Enhancers Strong transcription Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
37	nsv459427	chr22:22384041-23240027	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
38	nsv588356	chr22:22384041-23240027	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
39	esv3449995	chr22:22384825-23247356	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
40	nsv1055761	chr22:22386434-23035233	Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
41	esv2755658	chr22:22386434-23222208	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
42	esv2756635	chr22:22386434-23222208	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats 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	156 gene(s)	inside rSNPs	diseases
43	nsv1060460	chr22:22386434-23222279	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
44	nsv1061057	chr22:22386434-23223233	Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS 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 miRNA target site	156 gene(s)	inside rSNPs	diseases
45	nsv459430	chr22:22386617-23127585	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
46	nsv459431	chr22:22386617-23224835	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
47	nsv588359	chr22:22386617-23224835	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
48	nsv459432	chr22:22386617-23234792	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
49	nsv459433	chr22:22386617-23240027	Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
50	nsv588360	chr22:22386617-23240027	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:22725800-22735600	Weak transcription	Pancreas	Pancrea
2	chr22:22728200-22737400	Enhancers	Primary B cells from cord blood	blood
3	chr22:22728400-22737000	Enhancers	Primary B cells from peripheral blood	blood
4	chr22:22730800-22736000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr22:22734400-22735200	Enhancers	HSMMtube	muscle
6	chr22:22734400-22736000	Enhancers	Fetal Muscle Leg	muscle
7	chr22:22734600-22735000	Enhancers	Fetal Muscle Trunk	muscle
8	chr22:22734600-22735200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr22:22734600-22735200	Enhancers	Fetal Thymus	thymus
10	chr22:22734600-22736000	Enhancers	GM12878-XiMat	blood
11	chr22:22734600-22736200	Strong transcription	Right Atrium	heart
12	chr22:22734800-22735000	Enhancers	Thymus	Thymus

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