Variant report

Variant	nsv1010887
Chromosome Location	chr3:191418384-191775026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1352)
CpG islands
(count:734)
Chromatin interactive
region (count:29)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1352 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:191527176-191527375	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:191479890-191480846	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:191445136-191445516	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:191459594-191460185	HepG2	liver:	n/a	n/a
5	ATF2	chr3:191759698-191760457	GM12878	blood:	n/a	n/a
6	ATF2	chr3:191645728-191646232	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr3:191645274-191646194	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:191759859-191760398	GM12878	blood:	n/a	n/a
9	ATF3	chr3:191492123-191492784	HCT-116	colon:	n/a	n/a
10	BACH1	chr3:191581715-191581880	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:191446042-191446336	H1-hESC	embryonic stem cell:	n/a	chr3:191446165-191446179
12	BACH1	chr3:191446031-191446343	K562	blood:	n/a	chr3:191446165-191446179
13	BACH1	chr3:191756561-191756830	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:191420009-191420174	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:191480062-191480634	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:191757324-191757787	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr3:191759930-191760352	GM12878	blood:	n/a	n/a
18	BATF	chr3:191681014-191681263	GM12878	blood:	n/a	chr3:191681142-191681153
19	BATF	chr3:191759976-191760325	GM12878	blood:	n/a	n/a
20	BATF	chr3:191680972-191681345	GM12878	blood:	n/a	chr3:191681142-191681153
21	BCL11A	chr3:191681123-191681282	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL11A	chr3:191759912-191760278	GM12878	blood:	n/a	chr3:191760069-191760078
23	BCL11A	chr3:191759902-191760327	GM12878	blood:	n/a	chr3:191760069-191760078
24	BCL11A	chr3:191715522-191715941	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCLAF1	chr3:191759889-191760283	GM12878	blood:	n/a	chr3:191760069-191760078
26	BCLAF1	chr3:191759846-191760367	GM12878	blood:	n/a	chr3:191760069-191760078
27	BHLHE40	chr3:191462896-191462914	GM12878	blood:	n/a	n/a
28	BHLHE40	chr3:191759692-191760345	GM12878	blood:	n/a	n/a
29	BRCA1	chr3:191492425-191492773	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr3:191492143-191492799	HCT-116	colon:	n/a	n/a
31	CCNT2	chr3:191670465-191670665	K562	blood:	n/a	n/a
32	CEBPB	chr3:191492213-191492775	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr3:191772662-191772994	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr3:191480071-191480532	HepG2	liver:	n/a	n/a
35	CEBPB	chr3:191439007-191439776	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr3:191644969-191645326	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr3:191567964-191568164	HepG2	liver:	n/a	chr3:191568037-191568050 chr3:191568037-191568048
38	CEBPB	chr3:191675948-191676126	HepG2	liver:	n/a	chr3:191676012-191676023
39	CEBPB	chr3:191459609-191459782	HepG2	liver:	n/a	n/a
40	CEBPB	chr3:191512929-191513417	ECC-1	luminal epithelium:	n/a	chr3:191513150-191513161
41	CEBPB	chr3:191513019-191513296	HepG2	liver:	n/a	chr3:191513150-191513161
42	CEBPB	chr3:191492182-191492867	HCT-116	colon:	n/a	n/a
43	CEBPB	chr3:191601936-191602235	MCF-7	breast:	n/a	chr3:191602068-191602081 chr3:191602068-191602081
44	CEBPB	chr3:191546520-191546623	H1-hESC	embryonic stem cell:	n/a	chr3:191546571-191546582
45	CEBPB	chr3:191445203-191445571	HepG2	liver:	n/a	chr3:191445385-191445396
46	CEBPB	chr3:191502362-191502464	H1-hESC	embryonic stem cell:	n/a	chr3:191502435-191502446
47	CEBPB	chr3:191662605-191662823	H1-hESC	embryonic stem cell:	n/a	chr3:191662724-191662735
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	chr3:191492160-191492637	A549	lung:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:191585219-191585269	SK-N-SH_RA	brain:	n/a
2	chr3:191670257-191670307	HCT-116	colon:	n/a
3	chr3:191585219-191585269	SK-N-SH_RA	brain:	n/a
4	chr3:191670257-191670307	HCT-116	colon:	n/a
5	chr3:191715823-191715873	Hepatocyte	liver:	n/a
6	chr3:191670642-191670692	U87	brain:	n/a
7	chr3:191579258-191579308	AG04450	lung:	fetal
8	chr3:191578720-191578770	Hepatocyte	liver:	n/a
9	chr3:191585219-191585269	BJ	skin:	n/a
10	chr3:191670165-191670215	A549	lung:	n/a
11	chr3:191579258-191579308	NHBE	bronchial:	n/a
12	chr3:191578720-191578770	HEK293	kidney:	embryo
13	chr3:191670485-191670535	HEEpiC	esophagus:	n/a
14	chr3:191715823-191715873	GM19239	blood:	n/a
15	chr3:191670637-191670687	HCT-116	colon:	n/a
16	chr3:191670485-191670535	A549	lung:	n/a
17	chr3:191578720-191578770	GM12892	blood:	n/a
18	chr3:191578720-191578770	PANC-1	pancreas:	n/a
19	chr3:191579258-191579308	HRE	kidney:	n/a
20	chr3:191670642-191670692	Jurkat	blood:	n/a
21	chr3:191715823-191715873	NT2-D1	testis:	n/a
22	chr3:191670642-191670692	HCM	heart:	n/a
23	chr3:191670642-191670692	H1-hESC	embryonic stem cell:	embryo
24	chr3:191588392-191588442	SK-N-MC	brain:	n/a
25	chr3:191680064-191680114	PANC-1	pancreas:	n/a
26	chr3:191578720-191578770	HEEpiC	esophagus:	n/a
27	chr3:191715823-191715873	HCM	heart:	n/a
28	chr3:191578720-191578770	SK-N-MC	brain:	n/a
29	chr3:191585219-191585269	PrEC	prostate:	n/a
30	chr3:191670642-191670692	Caco-2	colon:	n/a
31	chr3:191680064-191680114	NT2-D1	testis:	n/a
32	chr3:191588392-191588442	AG04450	lung:	fetal
33	chr3:191581259-191581309	NT2-D1	testis:	n/a
34	chr3:191670165-191670215	HMEC	breast:	n/a
35	chr3:191588392-191588442	SKMC	muscle:	n/a
36	chr3:191670165-191670215	LNCaP	prostate:	n/a
37	chr3:191588392-191588442	K562	blood:	n/a
38	chr3:191670637-191670687	HNPCEpiC	eye:	n/a
39	chr3:191670642-191670692	GM06990	blood:	n/a
40	chr3:191579258-191579308	SK-N-SH	brain:	n/a
41	chr3:191715823-191715873	HepG2	liver:	n/a
42	chr3:191579258-191579308	AoSMC	blood vessel:	n/a
43	chr3:191581259-191581309	LNCaP	prostate:	n/a
44	chr3:191578720-191578770	HMEC	breast:	n/a
45	chr3:191588392-191588442	HEK293	kidney:	embryo
46	chr3:191581259-191581309	AG04449	skin:	fetal
47	chr3:191680064-191680114	HUVEC	blood vessel:	n/a
48	chr3:191581259-191581309	AG09319	gingival:	n/a
49	chr3:191680064-191680114	HEEpiC	esophagus:	n/a
50	chr3:191715823-191715873	SK-N-SH_RA	brain:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:191699562..191701581-chr3:191755371..191757226,2	MCF-7	breast:
2	chr3:191543102..191545359-chr3:191547187..191548804,2	K562	blood:
3	chr3:191642414..191643940-chr3:191650422..191652499,2	K562	blood:
4	chr3:191655366..191657510-chr3:191658751..191661236,3	MCF-7	breast:
5	chr3:191673185..191674856-chr3:191675139..191678048,2	MCF-7	breast:
6	chr15:71423988..71424731-chr3:191581561..191582555,2	MCF-7	breast:
7	chr3:191427154..191429836-chr3:191435371..191438311,2	MCF-7	breast:
8	chr3:191655366..191657510-chr3:191658751..191661236,3	MCF-7	breast:
9	chr3:191543102..191545359-chr3:191547187..191548804,2	K562	blood:
10	chr3:191474938..191477385-chr3:191479227..191481235,2	K562	blood:
11	chr3:191699997..191702549-chr3:191705897..191708844,2	K562	blood:
12	chr3:191474938..191477385-chr3:191479227..191481235,2	K562	blood:
13	chr3:191742888..191745500-chr3:191747337..191750200,2	K562	blood:
14	chr12:14927202..14927710-chr3:191649972..191650753,2	MCF-7	breast:
15	chr3:191220103..191221050-chr3:191527147..191528017,3	MCF-7	breast:
16	chr3:191636417..191637147-chr9:139422447..139423366,2	MCF-7	breast:
17	chr3:191586534..191587250-chr3:191604791..191605375,2	MCF-7	breast:
18	chr3:191642414..191643940-chr3:191650422..191652499,2	K562	blood:
19	chr3:191467984..191470316-chr3:191474260..191476654,2	MCF-7	breast:
20	chr3:191427154..191429836-chr3:191435371..191438311,2	MCF-7	breast:
21	chr3:191673185..191674856-chr3:191675139..191678048,2	MCF-7	breast:
22	chr3:191415298..191416937-chr3:191418603..191420214,2	K562	blood:
23	chr3:191586534..191587250-chr3:191604791..191605375,2	MCF-7	breast:
24	chr3:191666453..191669153-chr3:191669731..191672462,2	K562	blood:
25	chr3:191467984..191470316-chr3:191474260..191476654,2	MCF-7	breast:
26	chr3:191134537..191135165-chr3:191527181..191527753,2	MCF-7	breast:
27	chr3:191699562..191701581-chr3:191755371..191757226,2	MCF-7	breast:
28	chr3:191414615..191416798-chr3:191418714..191420918,2	K562	blood:
29	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-FGF12-3	chr3:191632977-191633333	NONHSAT093987
2	lnc-PYDC2-3	chr3:191753807-191754031	XLOC_002970
3	lnc-FGF12-1	chr3:191500507-191500590	XLOC_003375
4	lnc-FGF12-1	chr3:191469931-191470131	XLOC_003375
5	lnc-PYDC2-3	chr3:191753807-191754346	XLOC_002970
6	lnc-FGF12-3	chr3:191634462-191635275	NONHSAT093987
7	lnc-PYDC2-3	chr3:191749998-191750200	XLOC_002970
8	lnc-FGF12-2	chr3:191466402-191466767	XLOC_003374
9	lnc-PYDC2-3	chr3:191749997-191750200	NONHSAT093989
10	lnc-FGF12-1	chr3:191469930-191470131	NONHSAT093983
11	lnc-PYDC2-3	chr3:191753806-191754346	NONHSAT093989
12	lnc-PYDC2-2	chr3:191470957-191471124	XLOC_002969
13	lnc-PYDC2-3	chr3:191747669-191747695	XLOC_002970
14	lnc-PYDC2-3	chr3:191750096-191750200	XLOC_002970
15	lnc-FGF12-1	chr3:191500506-191500590	NONHSAT093983
16	lnc-PYDC2-3	chr3:191747668-191747828	NONHSAT093989
17	lnc-FGF12-2	chr3:191467745-191467882	XLOC_003374
18	lnc-PYDC2-2	chr3:191477302-191477492	NONHSAT093985
19	lnc-PYDC2-3	chr3:191747669-191747828	XLOC_002970
20	lnc-PYDC2-2	chr3:191477303-191477492	XLOC_002969
21	lnc-FGF12-3	chr3:191644766-191645225	NONHSAT093987
22	lnc-PYDC2-3	chr3:191753807-191754178	XLOC_002970
23	lnc-PYDC2-2	chr3:191470956-191471124	NONHSAT093985
24	lnc-PYDC2-3	chr3:191750096-191750200	XLOC_002970

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
ENSG00000237653	chromatin interactions
ENSG00000232353	chromatin interactions
ENSG00000246705	chromatin interactions
ZEB1	miRNA target sites

Extended variants
information (count: 10415 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:10415 , 50 per page) page: 1 2 3 4 5 6 7 ... 209

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181254508	chr3:191418405-191418406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs77228569	chr3:191418425-191418426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186307436	chr3:191418448-191418449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139315738	chr3:191418449-191418450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs62289104	chr3:191418460-191418461	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs142558754	chr3:191418484-191418485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530107951	chr3:191418527-191418528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550315566	chr3:191418622-191418623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79208536	chr3:191418690-191418691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563513141	chr3:191418722-191418723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570026248	chr3:191418750-191418751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532554030	chr3:191418760-191418761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552651875	chr3:191418762-191418763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115393566	chr3:191418794-191418795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535365129	chr3:191418840-191418841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371140983	chr3:191418887-191418888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568661830	chr3:191418896-191418897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536706106	chr3:191418914-191418915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191149749	chr3:191418949-191418950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576573630	chr3:191418957-191418958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs180848470	chr3:191418962-191418963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552967250	chr3:191418984-191418985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs779503	chr3:191418993-191418994	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs114662297	chr3:191419016-191419017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561696850	chr3:191419040-191419041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533443748	chr3:191419062-191419063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146099650	chr3:191419095-191419096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543892025	chr3:191419189-191419190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77004239	chr3:191419204-191419205	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62289105	chr3:191419207-191419208	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528566495	chr3:191419240-191419241	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563640244	chr3:191419300-191419301	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532694852	chr3:191419346-191419347	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74287911	chr3:191419348-191419349	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74315718	chr3:191419379-191419380	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148739534	chr3:191419399-191419400	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4687253	chr3:191419488-191419489	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs568511973	chr3:191419527-191419528	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142308674	chr3:191419538-191419539	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539037558	chr3:191419581-191419582	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79715220	chr3:191419592-191419593	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539174970	chr3:191419635-191419636	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552665649	chr3:191419665-191419666	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534854067	chr3:191419693-191419694	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs151253143	chr3:191419743-191419744	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555640158	chr3:191419794-191419795	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558988420	chr3:191419795-191419796	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187646102	chr3:191419803-191419804	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs564310869	chr3:191419819-191419820	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs61039969	chr3:191419846-191419847	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:658 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:191412000-191420400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:191419200-191420000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
3	chr3:191419600-191419800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
4	chr3:191419800-191420400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr3:191420000-191420400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr3:191420200-191420600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr3:191420200-191421800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr3:191420400-191420600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:191420400-191420600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr3:191420600-191421000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr3:191421000-191422000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr3:191421200-191421400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr3:191421400-191422000	ZNF genes & repeats	Gastric	stomach
14	chr3:191421400-191422200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
15	chr3:191421800-191422000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr3:191422000-191425600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr3:191425600-191425800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr3:191425800-191426200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:191425800-191426200	Enhancers	HepG2	liver
20	chr3:191426200-191426600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr3:191431600-191431800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
22	chr3:191431800-191433800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr3:191432400-191434400	Enhancers	Fetal Heart	heart
24	chr3:191433200-191433600	Enhancers	Right Ventricle	heart
25	chr3:191433200-191434200	Enhancers	Left Ventricle	heart
26	chr3:191433200-191434400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr3:191433400-191434400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:191434200-191439800	Weak transcription	Left Ventricle	heart
29	chr3:191434400-191439800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:191438800-191439400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr3:191439000-191439400	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr3:191439000-191440200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr3:191439000-191440200	Enhancers	HUVEC	blood vessel
34	chr3:191439000-191440400	Enhancers	Fetal Heart	heart
35	chr3:191439000-191440400	Enhancers	HepG2	liver
36	chr3:191439200-191440000	Enhancers	Fetal Lung	lung
37	chr3:191439200-191440200	Enhancers	HMEC	breast
38	chr3:191439400-191439800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr3:191439800-191440200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:191439800-191440200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr3:191439800-191440200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr3:191439800-191440200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr3:191439800-191440200	Enhancers	Left Ventricle	heart
44	chr3:191440000-191440400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr3:191440400-191444200	Weak transcription	HepG2	liver
46	chr3:191444200-191446600	Enhancers	HepG2	liver
47	chr3:191444200-191447000	Enhancers	Liver	Liver
48	chr3:191446200-191452600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr3:191447000-191448400	Weak transcription	Liver	Liver
50	chr3:191448400-191448600	Enhancers	Liver	Liver

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