Variant report

Variant	rs61893074
Chromosome Location	chr11:50257839-50257840
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:50257343-50257882	K562	blood:	n/a	n/a
2	HEY1	chr11:50257283-50258041	K562	blood:	n/a	chr11:50257372-50257387
3	CREB1	chr11:50257411-50258094	K562	blood:	n/a	chr11:50257724-50257737
4	POLR2A	chr11:50257344-50257944	K562	blood:	n/a	n/a
5	POLR2A	chr11:50257397-50257987	SK-N-SH	brain:	n/a	n/a
6	HCFC1	chr11:50257575-50257898	K562	blood:	n/a	n/a
7	CREB1	chr11:50257549-50258023	K562	blood:	n/a	chr11:50257724-50257737
8	NFYB	chr11:50257522-50257909	K562	blood:	n/a	chr11:50257668-50257682 chr11:50257667-50257682 chr11:50257667-50257682
9	RCOR1	chr11:50257475-50257923	K562	blood:	n/a	n/a
10	PML	chr11:50257474-50257948	K562	blood:	n/a	n/a
11	GATA2	chr11:50257172-50257867	SH-SY5Y	brain:	n/a	n/a
12	YY1	chr11:50257449-50258228	SK-N-SH	brain:	n/a	chr11:50257925-50257936
13	POLR2A	chr11:50257290-50258099	K562	blood:	n/a	n/a
14	EGR1	chr11:50257540-50257866	K562	blood:	n/a	chr11:50257600-50257610
15	MAZ	chr11:50257485-50257951	K562	blood:	n/a	n/a
16	POLR2A	chr11:50257376-50258019	K562	blood:	n/a	n/a
17	POLR2A	chr11:50257396-50257977	K562	blood:	n/a	n/a
18	MAX	chr11:50257439-50257850	K562	blood:	n/a	n/a
19	MAX	chr11:50257310-50258002	SK-N-SH	brain:	n/a	n/a
20	TAF1	chr11:50257356-50257947	K562	blood:	n/a	n/a
21	MYC	chr11:50257417-50257987	K562	blood:	n/a	n/a
22	ATF1	chr11:50257555-50257921	K562	blood:	n/a	n/a
23	NFYA	chr11:50257563-50257911	K562	blood:	n/a	chr11:50257668-50257682 chr11:50257663-50257681 chr11:50257667-50257682 chr11:50257667-50257682
24	TBP	chr11:50257416-50257953	K562	blood:	n/a	n/a
25	IRF1	chr11:50257606-50257858	K562	blood:	n/a	n/a
26	POLR2A	chr11:50257752-50257863	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr11:50257398-50257886	SK-N-SH	brain:	n/a	n/a
28	YY1	chr11:50257392-50258171	NT2-D1	testis:	n/a	chr11:50257925-50257936
29	JUND	chr11:50257422-50257919	K562	blood:	n/a	chr11:50257669-50257678
30	POLR2A	chr11:50257163-50258013	K562	blood:	n/a	n/a
31	POLR2A	chr11:50257237-50258009	K562	blood:	n/a	n/a
32	TAF1	chr11:50257387-50257844	SK-N-SH	brain:	n/a	n/a
33	E2F6	chr11:50257236-50257997	K562	blood:	n/a	chr11:50257626-50257635 chr11:50257377-50257387 chr11:50257671-50257680
34	ZMIZ1	chr11:50257630-50257894	K562	blood:	n/a	n/a
35	POLR2A	chr11:50257316-50258064	K562	blood:	n/a	n/a
36	POLR2A	chr11:50257381-50257996	K562	blood:	n/a	n/a
37	MAX	chr11:50257279-50257958	K562	blood:	n/a	n/a
38	MYC	chr11:50257770-50257866	K562	blood:	n/a	n/a
39	POLR2A	chr11:50257463-50257930	K562	blood:	n/a	n/a
40	YY1	chr11:50257485-50257997	K562	blood:	n/a	chr11:50257925-50257936
41	MAX	chr11:50257284-50257858	SK-N-SH	brain:	n/a	n/a
42	YY1	chr11:50257467-50258074	SK-N-SH_RA	brain:	n/a	chr11:50257925-50257936
43	YY1	chr11:50257346-50258108	SK-N-SH_RA	brain:	n/a	chr11:50257386-50257400 chr11:50257376-50257390 chr11:50257370-50257381 chr11:50257925-50257936
44	YY1	chr11:50257535-50258145	SK-N-SH	brain:	n/a	chr11:50257925-50257936
45	HEY1	chr11:50257344-50257945	K562	blood:	n/a	chr11:50257372-50257387
46	CCNT2	chr11:50257299-50257888	K562	blood:	n/a	n/a
47	MYC	chr11:50257351-50257923	K562	blood:	n/a	n/a
48	SIN3AK20	chr11:50257557-50257902	K562	blood:	n/a	n/a
49	IRF1	chr11:50257596-50257970	K562	blood:	n/a	n/a
50	MAX	chr11:50257417-50257935	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50257830-50257880	PrEC	prostate:	n/a
2	chr11:50257830-50257880	HNPCEpiC	eye:	n/a
3	chr11:50257830-50257880	AG04450	lung:	fetal
4	chr11:50257830-50257880	Caco-2	colon:	n/a
5	chr11:50257830-50257880	GM06990	blood:	n/a
6	chr11:50257830-50257880	ovcar-3	ovarian:	n/a
7	chr11:50257830-50257880	HepG2	liver:	n/a
8	chr11:50257830-50257880	HAEpiC	amniotic membrane:	n/a
9	chr11:50257830-50257880	NB4	blood:	n/a
10	chr11:50257830-50257880	HCM	heart:	n/a
11	chr11:50257830-50257880	HRE	kidney:	n/a
12	chr11:50257830-50257880	IMR90	lung:	fetal
13	chr11:50257830-50257880	ECC-1	luminal epithelium:	n/a
14	chr11:50257830-50257880	SK-N-SH	brain:	n/a
15	chr11:50257830-50257880	A549	lung:	n/a
16	chr11:50257830-50257880	GM12891	blood:	n/a
17	chr11:50257830-50257880	HEK293	kidney:	embryo
18	chr11:50257830-50257880	AoSMC	blood vessel:	n/a
19	chr11:50257830-50257880	HMEC	breast:	n/a
20	chr11:50257830-50257880	SAEC	small airway:	n/a
21	chr11:50257830-50257880	HRCEpiC	kidney:	n/a
22	chr11:50257830-50257880	HL-60	blood:	n/a
23	chr11:50257830-50257880	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:50257830-50257880	AG10803	skin:	n/a
25	chr11:50257830-50257880	HCT-116	colon:	n/a
26	chr11:50257830-50257880	SK-N-MC	brain:	n/a
27	chr11:50257830-50257880	T-47D	breast:	n/a
28	chr11:50257830-50257880	HRPEpiC	eye:	n/a
29	chr11:50257830-50257880	MCF-7	breast:	n/a
30	chr11:50257830-50257880	K562	blood:	n/a
31	chr11:50257830-50257880	H1-hESC	embryonic stem cell:	embryo
32	chr11:50257830-50257880	AG09309	skin:	n/a
33	chr11:50257830-50257880	BJ	skin:	n/a
34	chr11:50257830-50257880	PANC-1	pancreas:	n/a
35	chr11:50257830-50257880	MCF10A-Er-Src	breast:	n/a
36	chr11:50257830-50257880	Hepatocyte	liver:	n/a
37	chr11:50257830-50257880	HEEpiC	esophagus:	n/a
38	chr11:50257830-50257880	BE2_C	brain:	n/a
39	chr11:50257830-50257880	HCF	heart:	n/a
40	chr11:50257830-50257880	SKMC	muscle:	n/a
41	chr11:50257830-50257880	PFSK-1	brain:	n/a
42	chr11:50257830-50257880	NH-A	brain:	n/a
43	chr11:50257830-50257880	GM19239	blood:	n/a
44	chr11:50257830-50257880	NT2-D1	testis:	n/a
45	chr11:50257830-50257880	NHDF-neo	bronchial:	n/a
46	chr11:50257830-50257880	SK-N-SH_RA	brain:	n/a
47	chr11:50257830-50257880	HUVEC	blood vessel:	n/a
48	chr11:50257830-50257880	HCPEpiC	choroid plexus:	n/a
49	chr11:50257830-50257880	CMK	blood:	n/a
50	chr11:50257830-50257880	AG09319	gingival:	n/a

No data

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C13-1	chr11:50257750-50258088	ENSG00000254518
2	lnc-OR4C13-1	chr11:50257789-50258088	ENSG00000254518
3	lnc-OR4C13-1	chr11:50257750-50258210	NONHSAT021336

No data

Variant related genes	Relation type
ENSG00000255042	TF binding region
ENSG00000255042	CpG island

Extended variants
information (count: 138 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs17489472	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs17568903	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3904265	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4066577	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4096596	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs479037	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs497028	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs514030	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs514031	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55880405	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56019961	1.00[AFR][1000 genomes]
rs56136311	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56294529	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61891485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61891486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61891487	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61891488	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61891490	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61891521	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61891528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61891961	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61891966	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61892000	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61892001	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61892002	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61892003	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61892005	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61892025	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61892033	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61892034	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61892037	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61892038	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61892039	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61892040	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61892044	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs61892045	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs61893067	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61893068	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61893069	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61893071	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61893072	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61893076	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61893105	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61893158	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61893159	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61893390	1.00[AFR][1000 genomes]
rs61893391	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61893393	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs61894060	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs61894061	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs61894062	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs61894063	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs61894064	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs61894067	0.80[EUR][1000 genomes]
rs61894560	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61894564	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61894565	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61894566	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7105925	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7120107	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7128387	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7293947	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7294073	1.00[AFR][1000 genomes]
rs7936183	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8188850	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8189244	0.80[EUR][1000 genomes]
rs8189421	0.80[EUR][1000 genomes]
rs8189424	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:70 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051021	chr11:49692184-50658777	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv1048074	chr11:49823455-50302232	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1036701	chr11:49846590-50769305	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv897498	chr11:49997431-50325741	Strong transcription ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv554395	chr11:50008258-50642550	ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1047235	chr11:50012174-50769305	ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1051699	chr11:50013671-50769305	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv1037403	chr11:50019556-50751358	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv1044792	chr11:50019556-50769305	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	esv2758270	chr11:50056424-50447563	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	esv2759827	chr11:50056424-50449192	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	nsv467877	chr11:50057854-50642550	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	nsv554396	chr11:50057854-50642550	Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
14	esv3693389	chr11:50058095-50713402	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	nsv897504	chr11:50121285-50275257	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
16	nsv469594	chr11:50121285-50285880	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
17	nsv482621	chr11:50121285-50285880	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
18	nsv897505	chr11:50121285-50292520	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
19	nsv1035439	chr11:50121285-50524009	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
20	nsv1049947	chr11:50121285-50524009	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
21	nsv1035641	chr11:50121285-50573214	ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
22	nsv1041731	chr11:50121285-50590065	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
23	nsv1053769	chr11:50121285-50613401	ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
24	nsv1042046	chr11:50121285-50637245	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
25	nsv1051675	chr11:50121285-50637245	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
26	nsv554397	chr11:50121285-50642550	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
27	nsv554402	chr11:50121285-50642550	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
28	nsv897506	chr11:50121285-50642550	ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
29	nsv1047502	chr11:50121285-50651567	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
30	nsv1051055	chr11:50121285-50658777	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
31	nsv554400	chr11:50121285-50736106	Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
32	nsv554398	chr11:50121285-50738763	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
33	nsv554399	chr11:50121285-50766308	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
34	nsv554401	chr11:50121285-50766308	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
35	nsv1035727	chr11:50121285-50769305	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
36	nsv1036371	chr11:50121285-50769305	ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
37	nsv1042993	chr11:50121285-50769305	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
38	nsv1045083	chr11:50121285-50769305	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
39	nsv1051800	chr11:50121285-50769305	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
40	nsv1051873	chr11:50121285-50769305	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
41	nsv897507	chr11:50121285-51093950	ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
42	nsv1040407	chr11:50121285-51095992	Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
43	esv2760366	chr11:50138650-50524009	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
44	nsv832149	chr11:50142116-50316451	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
45	nsv897508	chr11:50152718-50304124	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
46	nsv897509	chr11:50152718-50440270	ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
47	nsv554403	chr11:50164027-50766308	ZNF genes & repeats Active TSS Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
48	esv2757444	chr11:50171877-50449192	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
49	nsv897511	chr11:50182364-50304124	ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
50	nsv897512	chr11:50185153-50258453	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50256200-50258600	Active TSS	K562	blood
2	chr11:50257000-50258200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
3	chr11:50257200-50258000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:50257200-50258000	ZNF genes & repeats	Gastric	stomach
5	chr11:50257200-50258000	ZNF genes & repeats	Pancreas	Pancrea
6	chr11:50257200-50258200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:50257400-50258000	Active TSS	Fetal Lung	lung
8	chr11:50257400-50258800	ZNF genes & repeats	Placenta	Placenta

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