Variant report

Variant	rs527244532
Chromosome Location	chr16:32876870-32876871
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	USF2	chr16:32876754-32876912	HepG2	liver:	n/a	chr16:32876834-32876850
2	CTCF	chr16:32876820-32876970	GM12874	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
3	HCFC1	chr16:32876766-32876920	K562	blood:	n/a	n/a
4	CTCF	chr16:32876760-32876910	BE2_C	brain:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
5	CTCF	chr16:32876780-32876930	HEK293	kidney:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
6	RAD21	chr16:32876733-32876988	GM12878	blood:	n/a	chr16:32876831-32876850 chr16:32876868-32876878 chr16:32876836-32876848
7	RAD21	chr16:32876686-32876990	Hela-S3	cervix:	n/a	chr16:32876831-32876850 chr16:32876868-32876878 chr16:32876836-32876848
8	CTCF	chr16:32876708-32876937	Spleen_OC	spleen:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
9	CTCF	chr16:32876679-32876966	MCF-7	breast:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
10	RAD21	chr16:32876738-32876929	H1-hESC	embryonic stem cell:	n/a	chr16:32876831-32876850 chr16:32876868-32876878 chr16:32876836-32876848
11	SMC3	chr16:32876697-32877224	SK-N-SH	brain:	n/a	chr16:32876836-32876846 chr16:32876832-32876846
12	USF1	chr16:32876588-32876912	HepG2	liver:	n/a	chr16:32876726-32876737 chr16:32876834-32876850
13	CTCF	chr16:32876668-32876982	LNCaP	prostate:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
14	RAD21	chr16:32876566-32877280	SK-N-SH	brain:	n/a	chr16:32876831-32876850 chr16:32876868-32876878 chr16:32876836-32876848
15	CTCF	chr16:32876733-32876931	GM12878	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
16	CTCF	chr16:32876780-32876930	GM12875	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
17	CTCF	chr16:32876780-32876930	GM12864	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
18	CTCF	chr16:32876697-32876941	Gliobla	brain:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
19	RAD21	chr16:32876718-32876911	IMR90	lung:	n/a	chr16:32876831-32876850 chr16:32876868-32876878 chr16:32876836-32876848
20	CTCF	chr16:32876725-32876954	ECC-1	luminal epithelium:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
21	CTCF	chr16:32876725-32877031	MCF-7	breast:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
22	CTCF	chr16:32876550-32877229	SK-N-SH	brain:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
23	CTCF	chr16:32876682-32876962	MCF-7	breast:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
24	CTCF	chr16:32876727-32876923	SK-N-SH_RA	brain:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
25	CTCF	chr16:32876780-32876930	GM12865	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
26	CTCF	chr16:32876672-32876994	K562	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
27	CTCF	chr16:32876760-32876910	GM12866	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
28	CTCF	chr16:32876698-32876937	A549	lung:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
29	FOSL2	chr16:32876534-32877024	HepG2	liver:	n/a	n/a
30	CTCF	chr16:32876780-32876930	K562	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
31	CTCF	chr16:32876760-32876910	Caco-2	colon:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
32	CTCF	chr16:32876733-32876933	Pancreas_OC	pancreas:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
33	MYC	chr16:32876784-32877056	HepG2	liver:	n/a	n/a
34	RAD21	chr16:32876747-32877022	MCF-7	breast:	n/a	chr16:32876831-32876850 chr16:32876868-32876878 chr16:32876836-32876848
35	CTCF	chr16:32876800-32876950	WERI-Rb-1	eye:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
36	CTCF	chr16:32876724-32876929	GM13977	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
37	RAD21	chr16:32876710-32876980	SK-N-SH_RA	brain:	n/a	chr16:32876831-32876850 chr16:32876868-32876878 chr16:32876836-32876848
38	RCOR1	chr16:32876769-32876969	K562	blood:	n/a	n/a
39	CTCF	chr16:32876809-32876879	GM13976	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
40	SMC3	chr16:32876683-32876993	Hela-S3	cervix:	n/a	chr16:32876836-32876846 chr16:32876832-32876846
41	CTCF	chr16:32876760-32876910	GM12867	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
42	CTCF	chr16:32876684-32876972	K562	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
43	JUND	chr16:32876834-32876913	K562	blood:	n/a	n/a
44	CTCF	chr16:32876714-32876907	Fibrobl	skin:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
45	CTCF	chr16:32876693-32876959	MCF-7	breast:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
46	RCOR1	chr16:32876722-32876899	HepG2	liver:	n/a	n/a
47	CTCF	chr16:32876712-32876976	GM19239	blood:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
48	CTCF	chr16:32876780-32876930	HCT-116	colon:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
49	CTCF	chr16:32876649-32876965	ECC-1	luminal epithelium:	n/a	chr16:32876831-32876847 chr16:32876832-32876853 chr16:32876830-32876848 chr16:32876833-32876846
50	CTCF	chr16:32876860-32877010	GM12865	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:32876380..32877212-chr16:32951315..32951834,2	MCF-7	breast:
2	chr16:32876653..32877208-chr16:33618895..33619446,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000260047	TF binding region

Extended variants
information (count: 198 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:198 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063872	chr16:31974698-32956058	Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
2	nsv1067090	chr16:31998170-32907428	ZNF genes & repeats Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv1057254	chr16:32027966-32915501	ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
4	nsv1059261	chr16:32033374-32879772	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
5	nsv1058855	chr16:32033374-32915501	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
6	nsv1064461	chr16:32033374-32956058	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
7	esv3401400	chr16:32054167-32993916	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
8	nsv1056990	chr16:32058483-33013850	Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
9	nsv1062667	chr16:32058483-33035996	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
10	nsv1065533	chr16:32058483-33054646	ZNF genes & repeats Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
11	nsv1060799	chr16:32080861-32879772	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
12	nsv1067067	chr16:32080861-32915501	Bivalent/Poised TSS Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
13	nsv1060944	chr16:32080861-32954713	Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
14	nsv1064268	chr16:32080861-32956058	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
15	nsv1063680	chr16:32080861-33054646	Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
16	nsv1061474	chr16:32092822-32907428	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
17	nsv1061520	chr16:32092822-32915501	Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
18	nsv1060168	chr16:32092822-32950241	Bivalent/Poised TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
19	nsv1063122	chr16:32092822-32954713	Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
20	nsv1056741	chr16:32092822-32956058	ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
21	nsv1058069	chr16:32092822-33054646	ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
22	esv3337080	chr16:32100987-33041130	Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
23	esv3394991	chr16:32103119-33044376	ZNF genes & repeats Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
24	esv3529103	chr16:32104939-33041147	ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
25	esv3529104	chr16:32104939-33041147	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
26	nsv1058970	chr16:32113670-33054646	Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
27	nsv1063843	chr16:32113670-33097410	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
28	nsv1067445	chr16:32146874-32915501	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
29	nsv1062792	chr16:32146874-32954713	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
30	nsv1058432	chr16:32146874-33097410	ZNF genes & repeats Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
31	nsv1058508	chr16:32158595-32879772	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
32	nsv1062199	chr16:32158595-32950241	Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
33	nsv1065801	chr16:32158595-32956058	Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
34	nsv1057931	chr16:32158595-33013850	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
35	nsv1060058	chr16:32158595-33097410	ZNF genes & repeats Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
36	nsv1056746	chr16:32180774-32915501	ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
37	nsv1065083	chr16:32180774-32950241	Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
38	nsv1059272	chr16:32180774-33054646	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
39	nsv1067109	chr16:32180774-33097410	ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
40	nsv1064661	chr16:32208734-32915501	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
41	nsv1061635	chr16:32208734-32950241	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
42	nsv1064517	chr16:32208734-33097410	ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
43	nsv1061105	chr16:32228980-32879772	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
44	nsv1065879	chr16:32228980-32956058	Bivalent/Poised TSS ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
45	nsv1055377	chr16:32228980-33097410	ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
46	nsv1066270	chr16:32244461-32879772	ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
47	nsv1062844	chr16:32244461-32905866	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
48	nsv1059129	chr16:32244461-32915501	ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
49	nsv1064815	chr16:32244461-33054646	Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
50	nsv1058349	chr16:32244461-33097410	Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:32876800-32877000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr16:32876800-32877000	Enhancers	Skeletal Muscle Male	skeletal muscle
3	chr16:32876800-32877200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
4	chr16:32876800-32881000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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