Variant report

Variant	rs1160588
Chromosome Location	chr19:43809947-43809948
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	RAD21	chr19:43809886-43810071	HepG2	liver:	n/a	chr19:43809960-43809973 chr19:43809993-43810007 chr19:43809962-43809972 chr19:43809957-43809976
2	CTCF	chr19:43809920-43810070	HRPEpiC	eye:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
3	CTCF	chr19:43809920-43810070	SK-N-SH_RA	brain:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
4	CTCF	chr19:43809900-43810050	HFF-Myc	foreskin:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
5	CTCF	chr19:43809874-43810036	A549	lung:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
6	CTCF	chr19:43809929-43810063	A549	lung:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
7	CTCF	chr19:43809902-43810064	GM12878	blood:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
8	CTCF	chr19:43809900-43810050	GM12864	blood:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
9	CTCF	chr19:43809939-43810026	Gliobla	brain:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
10	CTCF	chr19:43809920-43810070	HEEpiC	esophagus:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
11	CTCF	chr19:43809940-43810090	HMEC	breast:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
12	CTCF	chr19:43809719-43810327	MCF-7	breast:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
13	CTCF	chr19:43809935-43810031	Spleen_OC	spleen:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
14	MYC	chr19:43809849-43810101	K562	blood:	n/a	n/a
15	CTCF	chr19:43809900-43810050	HepG2	liver:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
16	CTCF	chr19:43809880-43810030	Hela-S3	cervix:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
17	CTCF	chr19:43809760-43810197	K562	blood:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
18	ESRRA	chr19:43809801-43810198	HepG2	liver:	n/a	chr19:43810032-43810050 chr19:43810032-43810048 chr19:43810031-43810041 chr19:43809847-43809860 chr19:43810031-43810041 chr19:43810032-43810048
19	CTCF	chr19:43809858-43810101	MCF-7	breast:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
20	CTCF	chr19:43809909-43810012	LNCaP	prostate:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
21	SMC3	chr19:43809849-43810179	Hela-S3	cervix:	n/a	chr19:43809962-43809972 chr19:43809958-43809972
22	CTCF	chr19:43809803-43810186	K562	blood:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
23	HCFC1	chr19:43809875-43810141	K562	blood:	n/a	n/a
24	CTCF	chr19:43809940-43810090	AG09309	skin:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
25	CTCF	chr19:43809934-43810053	GM12878	blood:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
26	CTCF	chr19:43809761-43810162	K562	blood:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
27	CTCF	chr19:43809765-43810173	HepG2	liver:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
28	CTCF	chr19:43809820-43809970	NHEK	skin:	n/a	n/a
29	CTCF	chr19:43809860-43810010	GM12864	blood:	n/a	chr19:43809996-43810004 chr19:43809959-43809972
30	CTCF	chr19:43809923-43810056	GM12892	blood:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
31	CTCF	chr19:43809851-43810135	MCF-7	breast:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
32	CTCF	chr19:43809900-43810050	K562	blood:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
33	RAD21	chr19:43809923-43810086	HepG2	liver:	n/a	chr19:43809960-43809973 chr19:43809993-43810007 chr19:43809962-43809972 chr19:43809957-43809976
34	CTCF	chr19:43809860-43810010	A549	lung:	n/a	chr19:43809996-43810004 chr19:43809959-43809972
35	CTCF	chr19:43809900-43810050	HFF	foreskin:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
36	CTCF	chr19:43809861-43810090	A549	lung:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
37	CTCF	chr19:43809864-43810109	Hela-S3	cervix:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
38	CTCF	chr19:43809846-43810082	HepG2	liver:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
39	CTCF	chr19:43809920-43810070	HMEC	breast:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
40	CTCF	chr19:43809940-43810090	AG10803	skin:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
41	RAD21	chr19:43809891-43810011	K562	blood:	n/a	chr19:43809960-43809973 chr19:43809993-43810007 chr19:43809962-43809972 chr19:43809957-43809976
42	CTCF	chr19:43809723-43810268	MCF-7	breast:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
43	CTCF	chr19:43809625-43810339	HCT-116	colon:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
44	CTCF	chr19:43809770-43810266	A549	lung:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
45	CTCF	chr19:43809880-43810030	SAEC	small airway:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
46	CTCF	chr19:43809770-43810167	A549	lung:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
47	CTCF	chr19:43809900-43810050	Hela-S3	cervix:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
48	CTCF	chr19:43809920-43810070	HCFaa	heart:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972
49	CTCF	chr19:43809860-43810010	GM12865	blood:	n/a	chr19:43809996-43810004 chr19:43809959-43809972
50	CTCF	chr19:43809879-43810070	HepG2	liver:	n/a	chr19:43809996-43810004 chr19:43809993-43810011 chr19:43809959-43809972

No.	Distal block	Cell Line	Cell type
1	chr19:43809493..43810365-chr19:43820777..43821441,3	MCF-7	breast:
2	chr19:43809519..43810435-chr19:43820572..43821543,3	K562	blood:
3	chr19:43809862..43810443-chr19:43929397..43930009,2	MCF-7	breast:

Variant related genes	Relation type
CEACAMP4	TF binding region

Extended variants
information (count: 141 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10420322	0.88[EUR][1000 genomes]
rs1135863	0.81[EUR][1000 genomes]
rs1160589	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1160590	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12459792	0.88[EUR][1000 genomes]
rs12462090	0.81[EUR][1000 genomes]
rs12462669	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs12463367	0.81[EUR][1000 genomes]
rs17655130	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs17711503	1.00[EUR][1000 genomes]
rs1972531	0.81[EUR][1000 genomes]
rs2098020	1.00[EUR][1000 genomes]
rs2190835	1.00[CEU][hapmap]
rs55869533	0.88[EUR][1000 genomes]
rs56272829	0.98[EUR][1000 genomes]
rs56313579	0.81[EUR][1000 genomes]
rs56360135	0.88[EUR][1000 genomes]
rs56372966	0.81[EUR][1000 genomes]
rs56408078	0.85[EUR][1000 genomes]
rs62113680	1.00[EUR][1000 genomes]
rs62113681	1.00[EUR][1000 genomes]
rs62113682	1.00[EUR][1000 genomes]
rs62113684	1.00[EUR][1000 genomes]
rs62113685	1.00[EUR][1000 genomes]
rs62113686	1.00[EUR][1000 genomes]
rs62113687	1.00[EUR][1000 genomes]
rs62113688	1.00[EUR][1000 genomes]
rs62113689	1.00[EUR][1000 genomes]
rs62113690	1.00[EUR][1000 genomes]
rs62113692	0.87[EUR][1000 genomes]
rs62113694	0.94[EUR][1000 genomes]
rs62113713	0.87[EUR][1000 genomes]
rs62113714	0.84[EUR][1000 genomes]
rs62115869	0.81[EUR][1000 genomes]
rs62115870	0.81[EUR][1000 genomes]
rs62115878	0.86[EUR][1000 genomes]
rs62115906	0.85[EUR][1000 genomes]
rs62115907	0.85[EUR][1000 genomes]
rs62115908	0.88[EUR][1000 genomes]
rs62115910	0.88[EUR][1000 genomes]
rs62115916	0.88[EUR][1000 genomes]
rs62115917	0.88[EUR][1000 genomes]
rs62115918	0.88[EUR][1000 genomes]
rs62115920	0.88[EUR][1000 genomes]
rs62115953	0.88[EUR][1000 genomes]
rs62117062	1.00[EUR][1000 genomes]
rs7251430	0.82[EUR][1000 genomes]
rs73037743	1.00[EUR][1000 genomes]
rs73037764	1.00[EUR][1000 genomes]
rs73037775	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:91 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758501	chr19:43042747-43899053	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	esv2758763	chr19:43042747-43899053	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	nsv428023	chr19:43042747-43899053	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
4	esv2757697	chr19:43164418-43870887	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS 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	24 gene(s)	inside rSNPs	diseases
5	nsv1055872	chr19:43173614-44075193	Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	nsv544009	chr19:43173614-44075193	Enhancers ZNF genes & repeats Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS 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 target site	43 gene(s)	inside rSNPs	diseases
7	nsv516973	chr19:43202770-43866823	Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	nsv869565	chr19:43203105-43810421	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
9	esv2763121	chr19:43215328-43846394	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
10	nsv1067126	chr19:43260649-44075194	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
11	nsv544015	chr19:43260649-44075194	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers 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	41 gene(s)	inside rSNPs	diseases
12	nsv1057657	chr19:43302497-44076564	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
13	nsv1064999	chr19:43315599-43811811	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
14	nsv544023	chr19:43316778-43842582	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	nsv544029	chr19:43316978-43842443	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
16	nsv1059631	chr19:43316978-44075054	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
17	nsv544030	chr19:43316978-44075054	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers 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 target site	40 gene(s)	inside rSNPs	diseases
18	nsv470145	chr19:43322065-43840088	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
19	nsv544035	chr19:43354258-43842443	Flanking Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
20	nsv579728	chr19:43390362-43838753	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
21	nsv432064	chr19:43467860-43819360	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
22	nsv432065	chr19:43538941-43819404	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
23	esv2754667	chr19:43559330-43819404	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
24	nsv579779	chr19:43559330-43848797	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
25	esv2751795	chr19:43559330-43870887	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription 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	12 gene(s)	inside rSNPs	diseases
26	nsv1061385	chr19:43642540-43846382	Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
27	nsv1056122	chr19:43647978-43846382	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
28	nsv1061772	chr19:43652661-43846382	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
29	nsv1056183	chr19:43652661-43852695	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
30	nsv1055952	chr19:43652661-43856672	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
31	nsv1060310	chr19:43654209-43846382	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
32	nsv1063262	chr19:43658826-43824942	Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
33	nsv1066677	chr19:43658826-43838753	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
34	nsv1060137	chr19:43658826-43839699	Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
35	nsv1056910	chr19:43658826-43842906	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
36	nsv1062110	chr19:43658826-43846238	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
37	nsv1063021	chr19:43658826-43846382	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
38	nsv1058727	chr19:43658826-43852695	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
39	nsv1061582	chr19:43660795-43817862	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
40	nsv1060224	chr19:43660795-43839699	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
41	nsv1064467	chr19:43660795-43846382	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
42	nsv1064002	chr19:43660795-43876534	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Strong transcription 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	10 gene(s)	inside rSNPs	diseases
43	nsv458705	chr19:43663086-43840088	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
44	nsv579816	chr19:43663086-43840088	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
45	nsv817848	chr19:43663086-43840088	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
46	nsv579817	chr19:43663086-43845593	Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
47	nsv579818	chr19:43663086-43848797	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
48	nsv579819	chr19:43663086-43853505	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
49	nsv1057430	chr19:43663357-43838753	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
50	nsv1061779	chr19:43663357-43842906	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43804800-43810200	Weak transcription	HMEC	breast
2	chr19:43805600-43810200	Weak transcription	NHEK	skin
3	chr19:43805800-43810200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr19:43809600-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr19:43809800-43811000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr19:43809800-43811200	Enhancers	Primary neutrophils fromperipheralblood	blood

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