Variant report

Variant	nsv1007883
Chromosome Location	chr3:191413126-191786869
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1507)
CpG islands
(count:855)
Chromatin interactive
region (count:31)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1507 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:191459594-191460185	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:191445136-191445516	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:191479890-191480846	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:191527176-191527375	HepG2	liver:	n/a	n/a
5	ATF2	chr3:191786156-191787084	GM12878	blood:	n/a	n/a
6	ATF2	chr3:191645274-191646194	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr3:191759859-191760398	GM12878	blood:	n/a	n/a
8	ATF2	chr3:191645728-191646232	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr3:191759698-191760457	GM12878	blood:	n/a	n/a
10	ATF3	chr3:191492123-191492784	HCT-116	colon:	n/a	n/a
11	BACH1	chr3:191756561-191756830	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:191480062-191480634	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:191446042-191446336	H1-hESC	embryonic stem cell:	n/a	chr3:191446165-191446179
14	BACH1	chr3:191420009-191420174	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:191581715-191581880	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:191446031-191446343	K562	blood:	n/a	chr3:191446165-191446179
17	BACH1	chr3:191757324-191757787	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr3:191759930-191760352	GM12878	blood:	n/a	n/a
19	BATF	chr3:191681014-191681263	GM12878	blood:	n/a	chr3:191681142-191681153
20	BATF	chr3:191759976-191760325	GM12878	blood:	n/a	n/a
21	BATF	chr3:191786659-191786998	GM12878	blood:	n/a	n/a
22	BATF	chr3:191680972-191681345	GM12878	blood:	n/a	chr3:191681142-191681153
23	BCL11A	chr3:191759912-191760278	GM12878	blood:	n/a	chr3:191760069-191760078
24	BCL11A	chr3:191759902-191760327	GM12878	blood:	n/a	chr3:191760069-191760078
25	BCL11A	chr3:191681123-191681282	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr3:191715522-191715941	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCLAF1	chr3:191759846-191760367	GM12878	blood:	n/a	chr3:191760069-191760078
28	BCLAF1	chr3:191759889-191760283	GM12878	blood:	n/a	chr3:191760069-191760078
29	BCLAF1	chr3:191785967-191786464	GM12878	blood:	n/a	n/a
30	BHLHE40	chr3:191759692-191760345	GM12878	blood:	n/a	n/a
31	BHLHE40	chr3:191462896-191462914	GM12878	blood:	n/a	n/a
32	BRCA1	chr3:191492425-191492773	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr3:191492143-191492799	HCT-116	colon:	n/a	n/a
34	CCNT2	chr3:191670465-191670665	K562	blood:	n/a	n/a
35	CEBPB	chr3:191546390-191546626	A549	lung:	n/a	chr3:191546571-191546582
36	CEBPB	chr3:191600171-191600371	HepG2	liver:	n/a	n/a
37	CEBPB	chr3:191492197-191492583	A549	lung:	n/a	n/a
38	CEBPB	chr3:191662605-191662823	H1-hESC	embryonic stem cell:	n/a	chr3:191662724-191662735
39	CEBPB	chr3:191543987-191544290	IMR90	lung:	n/a	n/a
40	CEBPB	chr3:191772591-191773214	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr3:191632247-191632587	IMR90	lung:	n/a	chr3:191632399-191632410
42	CEBPB	chr3:191500819-191501411	HepG2	liver:	n/a	chr3:191500951-191500962
43	CEBPB	chr3:191459609-191459782	HepG2	liver:	n/a	n/a
44	CEBPB	chr3:191502284-191502484	HepG2	liver:	n/a	chr3:191502435-191502446
45	CEBPB	chr3:191546520-191546623	H1-hESC	embryonic stem cell:	n/a	chr3:191546571-191546582
46	CEBPB	chr3:191567964-191568164	HepG2	liver:	n/a	chr3:191568037-191568050 chr3:191568037-191568048
47	CEBPB	chr3:191778072-191778672	ECC-1	luminal epithelium:	n/a	chr3:191778408-191778425
48	CEBPB	chr3:191681654-191681823	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr3:191493185-191494098	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr3:191601936-191602235	MCF-7	breast:	n/a	chr3:191602068-191602081 chr3:191602068-191602081

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:191579258-191579308	HNPCEpiC	eye:	n/a
2	chr3:191579258-191579308	HNPCEpiC	eye:	n/a
3	chr3:191715823-191715873	HUVEC	blood vessel:	n/a
4	chr3:191781655-191781705	IMR90	lung:	fetal
5	chr3:191781581-191781631	Caco-2	colon:	n/a
6	chr3:191579258-191579308	SKMC	muscle:	n/a
7	chr3:191588392-191588442	HCM	heart:	n/a
8	chr3:191585219-191585269	K562	blood:	n/a
9	chr3:191781581-191781631	HepG2	liver:	n/a
10	chr3:191670485-191670535	GM12891	blood:	n/a
11	chr3:191670165-191670215	SK-N-SH_RA	brain:	n/a
12	chr3:191581259-191581309	HL-60	blood:	n/a
13	chr3:191670642-191670692	GM06990	blood:	n/a
14	chr3:191578720-191578770	RPTEC	kidney:	n/a
15	chr3:191578720-191578770	AG09319	gingival:	n/a
16	chr3:191715823-191715873	Hela-S3	cervix:	n/a
17	chr3:191585219-191585269	Hepatocyte	liver:	n/a
18	chr3:191670485-191670535	Caco-2	colon:	n/a
19	chr3:191781655-191781705	HMEC	breast:	n/a
20	chr3:191680064-191680114	U87	brain:	n/a
21	chr3:191670637-191670687	CMK	blood:	n/a
22	chr3:191680064-191680114	MCF-7	breast:	n/a
23	chr3:191579258-191579308	U87	brain:	n/a
24	chr3:191781655-191781705	Hepatocyte	liver:	n/a
25	chr3:191579258-191579308	AG09309	skin:	n/a
26	chr3:191680064-191680114	ovcar-3	ovarian:	n/a
27	chr3:191670485-191670535	GM12892	blood:	n/a
28	chr3:191670485-191670535	AG04449	skin:	fetal
29	chr3:191670165-191670215	GM12878	blood:	n/a
30	chr3:191715823-191715873	HIPEpiC	eye:	n/a
31	chr3:191680064-191680114	HRCEpiC	kidney:	n/a
32	chr3:191670165-191670215	Caco-2	colon:	n/a
33	chr3:191588392-191588442	HRE	kidney:	n/a
34	chr3:191670642-191670692	Jurkat	blood:	n/a
35	chr3:191588392-191588442	BE2_C	brain:	n/a
36	chr3:191588392-191588442	SKMC	muscle:	n/a
37	chr3:191670642-191670692	SK-N-SH_RA	brain:	n/a
38	chr3:191680064-191680114	K562	blood:	n/a
39	chr3:191680064-191680114	GM12878	blood:	n/a
40	chr3:191715823-191715873	HMEC	breast:	n/a
41	chr3:191581259-191581309	PFSK-1	brain:	n/a
42	chr3:191579258-191579308	PFSK-1	brain:	n/a
43	chr3:191680064-191680114	HL-60	blood:	n/a
44	chr3:191715823-191715873	HAEpiC	amniotic membrane:	n/a
45	chr3:191670165-191670215	SAEC	small airway:	n/a
46	chr3:191680064-191680114	ProgFib	skin:	n/a
47	chr3:191670637-191670687	SKMC	muscle:	n/a
48	chr3:191715823-191715873	HRCEpiC	kidney:	n/a
49	chr3:191585219-191585269	BJ	skin:	n/a
50	chr3:191581259-191581309	HRPEpiC	eye:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:191543102..191545359-chr3:191547187..191548804,2	K562	blood:
2	chr3:191474938..191477385-chr3:191479227..191481235,2	K562	blood:
3	chr3:191642414..191643940-chr3:191650422..191652499,2	K562	blood:
4	chr3:191586534..191587250-chr3:191604791..191605375,2	MCF-7	breast:
5	chr3:191636417..191637147-chr9:139422447..139423366,2	MCF-7	breast:
6	chr3:191474938..191477385-chr3:191479227..191481235,2	K562	blood:
7	chr3:191414615..191416798-chr3:191418714..191420918,2	K562	blood:
8	chr3:191655366..191657510-chr3:191658751..191661236,3	MCF-7	breast:
9	chr3:191414615..191416798-chr3:191418714..191420918,2	K562	blood:
10	chr3:191673185..191674856-chr3:191675139..191678048,2	MCF-7	breast:
11	chr3:191415298..191416937-chr3:191418603..191420214,2	K562	blood:
12	chr3:191220103..191221050-chr3:191527147..191528017,3	MCF-7	breast:
13	chr3:191699997..191702549-chr3:191705897..191708844,2	K562	blood:
14	chr3:191586534..191587250-chr3:191604791..191605375,2	MCF-7	breast:
15	chr3:191415298..191416937-chr3:191418603..191420214,2	K562	blood:
16	chr3:191642414..191643940-chr3:191650422..191652499,2	K562	blood:
17	chr3:191467984..191470316-chr3:191474260..191476654,2	MCF-7	breast:
18	chr3:191673185..191674856-chr3:191675139..191678048,2	MCF-7	breast:
19	chr3:191467984..191470316-chr3:191474260..191476654,2	MCF-7	breast:
20	chr3:191134537..191135165-chr3:191527181..191527753,2	MCF-7	breast:
21	chr12:14927202..14927710-chr3:191649972..191650753,2	MCF-7	breast:
22	chr3:191699562..191701581-chr3:191755371..191757226,2	MCF-7	breast:
23	chr3:191666453..191669153-chr3:191669731..191672462,2	K562	blood:
24	chr3:191655366..191657510-chr3:191658751..191661236,3	MCF-7	breast:
25	chr3:191427154..191429836-chr3:191435371..191438311,2	MCF-7	breast:
26	chr3:191543102..191545359-chr3:191547187..191548804,2	K562	blood:
27	chr3:191742888..191745500-chr3:191747337..191750200,2	K562	blood:
28	chr3:191427154..191429836-chr3:191435371..191438311,2	MCF-7	breast:
29	chr3:191699562..191701581-chr3:191755371..191757226,2	MCF-7	breast:
30	chr15:71423988..71424731-chr3:191581561..191582555,2	MCF-7	breast:
31	chr3:191699997..191702549-chr3:191705897..191708844,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGF12-2	chr3:191466402-191466767	XLOC_003374
2	lnc-PYDC2-3	chr3:191747668-191747828	NONHSAT093989
3	lnc-FGF12-1	chr3:191469930-191470131	NONHSAT093983
4	lnc-FGF12-3	chr3:191634462-191635275	NONHSAT093987
5	lnc-PYDC2-2	chr3:191477302-191477492	NONHSAT093985
6	lnc-PYDC2-2	chr3:191470957-191471124	XLOC_002969
7	lnc-FGF12-1	chr3:191500506-191500590	NONHSAT093983
8	lnc-FGF12-1	chr3:191500507-191500590	XLOC_003375
9	lnc-PYDC2-3	chr3:191750096-191750200	XLOC_002970
10	lnc-PYDC2-2	chr3:191470956-191471124	NONHSAT093985
11	lnc-PYDC2-3	chr3:191747669-191747695	XLOC_002970
12	lnc-FGF12-2	chr3:191467745-191467882	XLOC_003374
13	lnc-PYDC2-3	chr3:191753807-191754346	XLOC_002970
14	lnc-PYDC2-3	chr3:191753806-191754346	NONHSAT093989
15	lnc-PYDC2-3	chr3:191753807-191754178	XLOC_002970
16	lnc-FGF12-1	chr3:191469931-191470131	XLOC_003375
17	lnc-PYDC2-3	chr3:191753807-191754031	XLOC_002970
18	lnc-PYDC2-3	chr3:191749997-191750200	NONHSAT093989
19	lnc-PYDC2-3	chr3:191750096-191750200	XLOC_002970
20	lnc-PYDC2-3	chr3:191749998-191750200	XLOC_002970
21	lnc-FGF12-3	chr3:191644766-191645225	NONHSAT093987
22	lnc-PYDC2-3	chr3:191747669-191747828	XLOC_002970
23	lnc-PYDC2-2	chr3:191477303-191477492	XLOC_002969
24	lnc-FGF12-3	chr3:191632977-191633333	NONHSAT093987

No data

Variant related genes	Relation type
ENSG00000216020	TF binding region
ENSG00000232353	TF binding region
ENSG00000237653	TF binding region
ENSG00000216020	CpG island
ENSG00000232353	CpG island
ENSG00000237653	CpG island
ENSG00000232353	chromatin interactions
ENSG00000237653	chromatin interactions
ENSG00000246705	chromatin interactions
ZEB1	miRNA target sites

Extended variants
information (count: 11062 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:11062 , 50 per page) page: 1 2 3 4 5 6 7 ... 222

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9809440	chr3:191413126-191413127	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117209533	chr3:191413149-191413150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541055625	chr3:191413160-191413161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35266564	chr3:191413162-191413163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542330865	chr3:191413204-191413205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561896665	chr3:191413216-191413217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187143675	chr3:191413274-191413275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554550692	chr3:191413276-191413277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77393246	chr3:191413293-191413294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1083698	chr3:191413314-191413315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
11	rs533487933	chr3:191413317-191413318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543542825	chr3:191413331-191413332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546776328	chr3:191413408-191413409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566754209	chr3:191413443-191413444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149765942	chr3:191413444-191413445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532855509	chr3:191413462-191413463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191591295	chr3:191413465-191413466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78187160	chr3:191413473-191413474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568719452	chr3:191413490-191413491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73204676	chr3:191413512-191413513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375895079	chr3:191413515-191413516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76408160	chr3:191413563-191413564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577986036	chr3:191413648-191413649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534108706	chr3:191413690-191413691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553981089	chr3:191413692-191413693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573794879	chr3:191413807-191413808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541915720	chr3:191413816-191413817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183833169	chr3:191413850-191413851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563099816	chr3:191413903-191413904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189056628	chr3:191413904-191413905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573275432	chr3:191413914-191413915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182444620	chr3:191413915-191413916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564176195	chr3:191413950-191413951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185494537	chr3:191413957-191413958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546913228	chr3:191413992-191413993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531769450	chr3:191414083-191414084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149010309	chr3:191414118-191414119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190347034	chr3:191414122-191414123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548757278	chr3:191414129-191414130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548361972	chr3:191414140-191414141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537576883	chr3:191414148-191414149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143801689	chr3:191414160-191414161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571284651	chr3:191414161-191414162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181540636	chr3:191414196-191414197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554115415	chr3:191414199-191414200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568258215	chr3:191414218-191414219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114451429	chr3:191414233-191414234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142494901	chr3:191414253-191414254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs547620402	chr3:191414295-191414296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544329951	chr3:191414376-191414377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Lung cancer	19547694	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Optic atrophy	21457585	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	16397240	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD

Chromatin state (count:773 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:191411600-191413800	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr3:191411800-191413800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr3:191411800-191416800	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr3:191412000-191420400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:191412400-191413600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr3:191412800-191414600	Enhancers	Fetal Heart	heart
7	chr3:191413200-191413400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr3:191413600-191413800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr3:191419200-191420000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
10	chr3:191419600-191419800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
11	chr3:191419800-191420400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr3:191420000-191420400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr3:191420200-191420600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr3:191420200-191421800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr3:191420400-191420600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr3:191420400-191420600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr3:191420600-191421000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr3:191421000-191422000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:191421200-191421400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr3:191421400-191422000	ZNF genes & repeats	Gastric	stomach
21	chr3:191421400-191422200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
22	chr3:191421800-191422000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr3:191422000-191425600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:191425600-191425800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr3:191425800-191426200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr3:191425800-191426200	Enhancers	HepG2	liver
27	chr3:191426200-191426600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr3:191431600-191431800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
29	chr3:191431800-191433800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr3:191432400-191434400	Enhancers	Fetal Heart	heart
31	chr3:191433200-191433600	Enhancers	Right Ventricle	heart
32	chr3:191433200-191434200	Enhancers	Left Ventricle	heart
33	chr3:191433200-191434400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr3:191433400-191434400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr3:191434200-191439800	Weak transcription	Left Ventricle	heart
36	chr3:191434400-191439800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:191438800-191439400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr3:191439000-191439400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr3:191439000-191440200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr3:191439000-191440200	Enhancers	HUVEC	blood vessel
41	chr3:191439000-191440400	Enhancers	Fetal Heart	heart
42	chr3:191439000-191440400	Enhancers	HepG2	liver
43	chr3:191439200-191440000	Enhancers	Fetal Lung	lung
44	chr3:191439200-191440200	Enhancers	HMEC	breast
45	chr3:191439400-191439800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr3:191439800-191440200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:191439800-191440200	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr3:191439800-191440200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr3:191439800-191440200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr3:191439800-191440200	Enhancers	Left Ventricle	heart

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