Variant report

Variant	rs12974676
Chromosome Location	chr19:43692265-43692266
allele	G/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	chr19:43692220-43692370	HAc	cerebellar:	n/a	n/a
2	CTCF	chr19:43692240-43692390	SAEC	small airway:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
3	FOSL2	chr19:43692191-43692492	HepG2	liver:	n/a	n/a
4	CTCF	chr19:43692066-43692505	SK-N-SH	brain:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
5	CTCF	chr19:43692220-43692370	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr19:43692260-43692410	GM12867	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
7	CTCF	chr19:43692180-43692330	HRE	kidney:	n/a	n/a
8	CTCF	chr19:43692240-43692390	HPAF	blood vessel:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
9	CTCF	chr19:43692260-43692410	GM12871	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
10	CTCF	chr19:43692260-43692410	NHLF	lung:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
11	CTCF	chr19:43692240-43692390	HEK293	kidney:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
12	CTCF	chr19:43692240-43692390	AG04449	skin:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
13	CTCF	chr19:43692260-43692410	GM12866	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
14	CTCF	chr19:43692240-43692390	HBMEC	blood vessel:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
15	CTCF	chr19:43692240-43692390	AG10803	skin:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
16	CTCF	chr19:43692240-43692390	BJ	skin:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
17	CTCF	chr19:43692256-43692469	HepG2	liver:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
18	RAD21	chr19:43692236-43692441	SK-N-SH_RA	brain:	n/a	chr19:43692368-43692387
19	CTCF	chr19:43692240-43692390	GM12874	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
20	CTCF	chr19:43692192-43692552	NHEK	skin:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
21	RAD21	chr19:43692182-43692474	HepG2	liver:	n/a	chr19:43692368-43692387
22	CTCF	chr19:43692240-43692390	AG09309	skin:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
23	CTCF	chr19:43692240-43692390	HPF	lung:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
24	CTCF	chr19:43692140-43692290	HCM	heart:	n/a	n/a
25	CTCF	chr19:43692195-43692560	K562	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
26	CTCF	chr19:43692240-43692390	GM12864	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
27	RAD21	chr19:43692169-43692435	HCT-116	colon:	n/a	chr19:43692368-43692387
28	RAD21	chr19:43692212-43692426	K562	blood:	n/a	chr19:43692368-43692387
29	CTCF	chr19:43692260-43692410	GM12870	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
30	CTCF	chr19:43692255-43692492	GM12891	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
31	CTCF	chr19:43692192-43692568	K562	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
32	CTCF	chr19:43692240-43692390	HMEC	breast:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
33	CTCF	chr19:43692260-43692410	MCF-7	breast:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
34	SMC3	chr19:43692009-43692487	SK-N-SH	brain:	n/a	chr19:43692372-43692386
35	CTCF	chr19:43692240-43692390	GM12870	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
36	CTCF	chr19:43692260-43692410	HVMF	connective:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
37	CTCF	chr19:43692240-43692390	GM12867	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
38	CTCF	chr19:43692260-43692410	GM12873	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
39	CTCF	chr19:43692240-43692390	HCPEpiC	choroid plexus:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
40	POLR2A	chr19:43692214-43692482	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr19:43692200-43692350	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr19:43692256-43692523	MCF-7	breast:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
43	CTCF	chr19:43692260-43692410	GM12865	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
44	CTCF	chr19:43692240-43692390	HFF-Myc	foreskin:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
45	CTCF	chr19:43692120-43692270	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr19:43692240-43692390	GM12875	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
47	CTCF	chr19:43692240-43692390	GM12868	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
48	CTCF	chr19:43692078-43692669	K562	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
49	PAX5	chr19:43692241-43692504	GM12878	blood:	n/a	n/a
50	SMC3	chr19:43692235-43692489	K562	blood:	n/a	chr19:43692372-43692386

Variant related genes	Relation type
PSG5	TF binding region

Extended variants
information (count: 510 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10409139	1.00[ASN][1000 genomes]
rs1058259	0.83[EUR][1000 genomes]
rs1135901	0.83[EUR][1000 genomes]
rs1136228	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11666130	0.85[EUR][1000 genomes]
rs11671015	0.81[EUR][1000 genomes]
rs12973688	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12982679	0.80[EUR][1000 genomes]
rs2190835	1.00[ASN][1000 genomes]
rs2190836	0.83[EUR][1000 genomes]
rs2355419	0.80[EUR][1000 genomes]
rs3170216	0.82[EUR][1000 genomes]
rs34123927	0.91[EUR][1000 genomes]
rs34370347	0.83[EUR][1000 genomes]
rs35352398	0.83[EUR][1000 genomes]
rs35669325	0.89[EUR][1000 genomes]
rs35958981	0.83[EUR][1000 genomes]
rs36073871	0.82[EUR][1000 genomes]
rs4028464	0.83[EUR][1000 genomes]
rs56022011	0.91[EUR][1000 genomes]
rs62112085	1.00[ASN][1000 genomes]
rs62115021	1.00[ASN][1000 genomes]
rs62115023	1.00[ASN][1000 genomes]
rs62115024	1.00[ASN][1000 genomes]
rs62115025	1.00[ASN][1000 genomes]
rs71350644	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7249880	0.88[EUR][1000 genomes]
rs7250101	0.91[EUR][1000 genomes]
rs7251927	0.85[EUR][1000 genomes]
rs7253651	0.82[EUR][1000 genomes]
rs73033532	1.00[ASN][1000 genomes]
rs73050262	1.00[ASN][1000 genomes]
rs8102104	0.84[EUR][1000 genomes]
rs8104735	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8107382	0.86[EUR][1000 genomes]
rs8108484	0.80[EUR][1000 genomes]
rs8109606	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	nsv1061798	chr19:43141984-43741311	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv544008	chr19:43141984-43741311	Enhancers Weak transcription Strong transcription Flanking Active TSS 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	20 gene(s)	inside rSNPs	diseases
6	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
7	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
8	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
9	nsv544011	chr19:43173814-43741311	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	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
11	nsv869571	chr19:43203105-43802656	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
12	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
13	nsv963056	chr19:43203249-43798708	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	nsv9730	chr19:43203459-43802656	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription 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	esv1812820	chr19:43203937-43803388	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription 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
16	esv1808074	chr19:43214215-43805847	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
17	esv1813803	chr19:43214415-43805651	Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
18	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
19	esv1846846	chr19:43225921-43774853	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
20	esv1805299	chr19:43227458-43790318	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
21	esv2760524	chr19:43237611-43805328	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
22	esv2751788	chr19:43240379-43711592	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
23	nsv432049	chr19:43240379-43711592	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
24	esv2751789	chr19:43240379-43731159	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
25	nsv432050	chr19:43240379-43777571	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS 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	18 gene(s)	inside rSNPs	diseases
26	esv2751790	chr19:43240379-43805328	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
27	nsv1067715	chr19:43242795-43741310	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
28	nsv529386	chr19:43242795-43741310	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
29	nsv497975	chr19:43242811-43741714	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
30	nsv911811	chr19:43247348-43806559	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
31	nsv544013	chr19:43260648-43741450	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
32	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
33	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
34	nsv544020	chr19:43260848-43741311	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
35	nsv1062869	chr19:43262970-43703492	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
36	esv1811423	chr19:43282955-43779007	Strong transcription Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
37	nsv470143	chr19:43284119-43695839	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
38	nsv458590	chr19:43284120-43792307	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
39	nsv458591	chr19:43284120-43792307	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
40	nsv579656	chr19:43286127-43738340	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
41	esv2751791	chr19:43287237-43731159	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
42	nsv432052	chr19:43287237-43753478	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
43	nsv432053	chr19:43287237-43777571	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
44	nsv911841	chr19:43290263-43711592	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
45	nsv579657	chr19:43290263-43726895	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
46	nsv911842	chr19:43290263-43806559	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
47	nsv1064608	chr19:43290773-43694918	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
48	nsv1066912	chr19:43290773-43777275	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
49	nsv1065396	chr19:43294378-43697321	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
50	nsv1060961	chr19:43294378-43740953	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43690600-43692600	Enhancers	Placenta	Placenta
2	chr19:43691000-43694200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr19:43691000-43705000	Weak transcription	NHLF	lung
4	chr19:43692000-43692400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr19:43692000-43692600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr19:43692200-43692800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr19:43692200-43705000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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