Variant report

Variant	rs76780019
Chromosome Location	chr2:110829699-110829700
allele	C/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	CTCF	chr2:110829594-110829842	H1-hESC	embryonic stem cell:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
2	CTCF	chr2:110829483-110829860	K562	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
3	JUND	chr2:110829572-110829881	HepG2	liver:	n/a	n/a
4	CTCF	chr2:110829573-110829852	Gliobla	brain:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
5	MYC	chr2:110829653-110829740	K562	blood:	n/a	n/a
6	POU2F2	chr2:110829500-110829901	GM12891	blood:	n/a	chr2:110829790-110829802
7	CTCF	chr2:110829575-110829860	GM12891	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
8	JUND	chr2:110829527-110829960	A549	lung:	n/a	n/a
9	POLR2A	chr2:110829564-110829822	PANC-1	pancreas:	n/a	n/a
10	FOXA1	chr2:110829506-110829886	HepG2	liver:	n/a	n/a
11	CTCF	chr2:110829564-110829870	GM13976	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
12	CTCF	chr2:110829640-110829875	LNCaP	prostate:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
13	USF1	chr2:110829523-110829886	A549	lung:	n/a	n/a
14	RXRA	chr2:110829535-110829901	HepG2	liver:	n/a	n/a
15	SP1	chr2:110829545-110829931	A549	lung:	n/a	chr2:110829790-110829799 chr2:110829565-110829572 chr2:110829789-110829803 chr2:110829789-110829798
16	FOXA2	chr2:110829229-110829894	A549	lung:	n/a	n/a
17	POLR2A	chr2:110829394-110829739	A549	lung:	n/a	n/a
18	CTCF	chr2:110829573-110829856	GM12892	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
19	CTCF	chr2:110829583-110829851	NHEK	skin:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
20	CTCF	chr2:110829593-110829882	Pancreas_OC	pancreas:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
21	EBF1	chr2:110829581-110829830	GM12878	blood:	n/a	n/a
22	CTCF	chr2:110829585-110829848	ProgFib	skin:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
23	CTCF	chr2:110829668-110829843	GM20000	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
24	USF1	chr2:110829527-110829842	HepG2	liver:	n/a	n/a
25	IRF4	chr2:110829497-110829840	GM12878	blood:	n/a	n/a
26	USF1	chr2:110829518-110829942	A549	lung:	n/a	n/a
27	POLR2A	chr2:110829452-110829747	A549	lung:	n/a	n/a
28	USF1	chr2:110829463-110829927	A549	lung:	n/a	n/a
29	CTCF	chr2:110829620-110829884	GM10266	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
30	CTCF	chr2:110829604-110829827	MCF-7	breast:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
31	CTCF	chr2:110829618-110829875	LNCaP	prostate:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
32	CTCF	chr2:110829568-110829860	GM12878	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
33	POU2F2	chr2:110829487-110829925	GM12878	blood:	n/a	chr2:110829790-110829802
34	CTCF	chr2:110829570-110829865	GM19238	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
35	CTCF	chr2:110829588-110829846	Fibrobl	skin:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
36	CTCF	chr2:110829617-110829877	Medullo	brain:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
37	CTCF	chr2:110829459-110829873	A549	lung:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
38	CTCF	chr2:110829606-110829879	Kidney_OC	kidney:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
39	CTCF	chr2:110829577-110829863	K562	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
40	USF1	chr2:110829601-110829798	HepG2	liver:	n/a	n/a
41	CTCF	chr2:110829593-110829842	HepG2	liver:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
42	CTCF	chr2:110829488-110829922	K562	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
43	TCF12	chr2:110829645-110829816	GM12878	blood:	n/a	n/a
44	CTCF	chr2:110829503-110829833	A549	lung:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
45	SIN3AK20	chr2:110829605-110829789	HepG2	liver:	n/a	n/a
46	JUND	chr2:110829504-110829833	HepG2	liver:	n/a	n/a
47	CTCF	chr2:110829650-110829844	GM10248	blood:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
48	BATF	chr2:110829579-110829796	GM12878	blood:	n/a	n/a
49	CTCF	chr2:110829590-110829859	HUVEC	blood vessel:	n/a	chr2:110829740-110829753 chr2:110829733-110829754 chr2:110829792-110829805 chr2:110829739-110829755 chr2:110829738-110829756 chr2:110829795-110829808
50	POU2F2	chr2:110829646-110829825	GM12878	blood:	n/a	chr2:110829790-110829802

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:110829661-110829711	SK-N-SH	brain:	n/a
2	chr2:110829661-110829711	IMR90	lung:	fetal
3	chr2:110829661-110829711	NB4	blood:	n/a
4	chr2:110829661-110829711	Hepatocyte	liver:	n/a
5	chr2:110829661-110829711	AG04450	lung:	fetal
6	chr2:110829661-110829711	Jurkat	blood:	n/a
7	chr2:110829661-110829711	K562	blood:	n/a
8	chr2:110829661-110829711	AG09319	gingival:	n/a
9	chr2:110829661-110829711	NT2-D1	testis:	n/a
10	chr2:110829661-110829711	HMEC	breast:	n/a
11	chr2:110829661-110829711	Hela-S3	cervix:	n/a
12	chr2:110829661-110829711	HRE	kidney:	n/a
13	chr2:110829661-110829711	HNPCEpiC	eye:	n/a
14	chr2:110829661-110829711	GM12891	blood:	n/a
15	chr2:110829661-110829711	SAEC	small airway:	n/a
16	chr2:110829661-110829711	T-47D	breast:	n/a
17	chr2:110829661-110829711	GM06990	blood:	n/a
18	chr2:110829661-110829711	H1-hESC	embryonic stem cell:	embryo
19	chr2:110829661-110829711	SK-N-SH_RA	brain:	n/a
20	chr2:110829661-110829711	GM12892	blood:	n/a
21	chr2:110829661-110829711	AG09309	skin:	n/a
22	chr2:110829661-110829711	PFSK-1	brain:	n/a
23	chr2:110829661-110829711	NH-A	brain:	n/a
24	chr2:110829661-110829711	ovcar-3	ovarian:	n/a
25	chr2:110829661-110829711	MCF10A-Er-Src	breast:	n/a
26	chr2:110829661-110829711	HCT-116	colon:	n/a
27	chr2:110829661-110829711	SK-N-MC	brain:	n/a
28	chr2:110829661-110829711	BE2_C	brain:	n/a
29	chr2:110829661-110829711	HEEpiC	esophagus:	n/a
30	chr2:110829661-110829711	HRCEpiC	kidney:	n/a
31	chr2:110829661-110829711	RPTEC	kidney:	n/a
32	chr2:110829661-110829711	MCF-7	breast:	n/a
33	chr2:110829661-110829711	AG10803	skin:	n/a
34	chr2:110829661-110829711	HRPEpiC	eye:	n/a
35	chr2:110829661-110829711	AoSMC	blood vessel:	n/a
36	chr2:110829661-110829711	HCF	heart:	n/a
37	chr2:110829661-110829711	CMK	blood:	n/a
38	chr2:110829661-110829711	NHDF-neo	bronchial:	n/a
39	chr2:110829661-110829711	ProgFib	skin:	n/a
40	chr2:110829661-110829711	AG04449	skin:	fetal
41	chr2:110829661-110829711	HUVEC	blood vessel:	n/a
42	chr2:110829661-110829711	HAEpiC	amniotic membrane:	n/a
43	chr2:110829661-110829711	SKMC	muscle:	n/a
44	chr2:110829661-110829711	HEK293	kidney:	embryo
45	chr2:110829661-110829711	HIPEpiC	eye:	n/a
46	chr2:110829661-110829711	GM12878	blood:	n/a
47	chr2:110829661-110829711	A549	lung:	n/a
48	chr2:110829661-110829711	BJ	skin:	n/a
49	chr2:110829661-110829711	HL-60	blood:	n/a
50	chr2:110829661-110829711	U87	brain:	n/a

Variant related genes	Relation type
MIR4267	TF binding region
MIR4267	CpG island

Extended variants
information (count: 106 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:106 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011456	chr2:110290958-110980402	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv535861	chr2:110290958-110980402	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv1009367	chr2:110349178-110863354	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv491837	chr2:110381297-110964737	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv999552	chr2:110396395-110978224	Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	esv2751812	chr2:110457214-110980346	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv1011653	chr2:110461521-110978224	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv874782	chr2:110463288-111334482	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
9	nsv874783	chr2:110498943-110886142	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	nsv1013901	chr2:110501500-110983669	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
11	nsv1003103	chr2:110504334-111084885	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
12	nsv874785	chr2:110524250-110843108	Enhancers Weak transcription Active TSS	TF binding region CpG island lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
13	nsv874786	chr2:110524250-110857243	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
14	nsv874787	chr2:110524250-111334482	Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
15	nsv469649	chr2:110663085-110840236	Enhancers Weak transcription Active TSS	TF binding region CpG island lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
16	nsv482634	chr2:110663085-110840236	Enhancers Active TSS Weak transcription	TF binding region CpG island lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
17	esv2757824	chr2:110693356-111123649	Strong transcription Genic enhancers Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
18	esv2759082	chr2:110693356-111123649	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
19	nsv532271	chr2:110694195-111209736	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
20	nsv582654	chr2:110695564-110983320	Flanking Bivalent TSS/Enh Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
21	nsv917407	chr2:110704031-110983669	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
22	nsv918119	chr2:110704031-111084885	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
23	nsv998768	chr2:110704032-110973315	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
24	nsv1010477	chr2:110704032-110983669	Bivalent Enhancer Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
25	nsv1003206	chr2:110704032-111066273	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
26	nsv1010763	chr2:110704032-111084885	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
27	esv2763637	chr2:110704032-111169128	ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
28	nsv1010870	chr2:110704032-111400650	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
29	nsv874788	chr2:110706146-111334482	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
30	nsv1011659	chr2:110710762-110983669	Active TSS Enhancers Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
31	nsv998349	chr2:110710762-111084885	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
32	nsv1005578	chr2:110717078-111084885	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
33	nsv874789	chr2:110727715-110834186	Weak transcription Enhancers Active TSS	TF binding region CpG island lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
34	nsv874790	chr2:110727715-111334482	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
35	esv2830158	chr2:110727715-111419426	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
36	nsv994984	chr2:110732632-110964737	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
37	nsv869158	chr2:110732632-111334482	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
38	nsv915752	chr2:110732649-110964775	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
39	nsv874792	chr2:110732676-110871665	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
40	nsv874793	chr2:110732676-111334482	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
41	nsv834329	chr2:110733609-110892184	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
42	nsv1008374	chr2:110768230-111084885	Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
43	nsv874794	chr2:110772440-111334482	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
44	nsv961858	chr2:110779013-110837772	Weak transcription Enhancers	TF binding region CpG island miRNA	1 gene(s)	inside rSNPs	diseases
45	nsv917668	chr2:110783035-110981045	Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
46	nsv918099	chr2:110783035-111369031	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
47	nsv529084	chr2:110783036-110964878	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	10 gene(s)	inside rSNPs	diseases
48	nsv1067566	chr2:110783236-110964737	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	10 gene(s)	inside rSNPs	diseases
49	nsv491906	chr2:110783236-110964737	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	10 gene(s)	inside rSNPs	diseases
50	nsv529799	chr2:110783236-111128847	ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links