Variant report

Variant	nsv834590
Chromosome Location	chr3:526216-703999
allele	n/a
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	ARID3A	chr3:534692-534822	HepG2	liver:	n/a	n/a
2	BACH1	chr3:541423-541496	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:577662-577951	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:599827-600084	GM12878	blood:	n/a	chr3:599953-599962
5	BATF	chr3:638972-639242	GM12878	blood:	n/a	chr3:639093-639102
6	BATF	chr3:599789-600089	GM12878	blood:	n/a	chr3:599953-599962
7	BCLAF1	chr3:599656-600200	GM12878	blood:	n/a	chr3:599779-599788 chr3:599826-599835
8	BHLHE40	chr3:543200-543216	GM12878	blood:	n/a	n/a
9	BRCA1	chr3:638578-639330	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr3:649451-649478	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr3:674381-674581	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr3:639591-639851	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:638934-639824	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:700997-701241	H1-hESC	embryonic stem cell:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
15	CEBPB	chr3:674328-674574	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:560575-560880	HepG2	liver:	n/a	chr3:560731-560742
17	CEBPB	chr3:672472-672697	A549	lung:	n/a	chr3:672554-672567 chr3:672555-672566
18	CEBPB	chr3:545112-545116	K562	blood:	n/a	n/a
19	CEBPB	chr3:700965-701296	IMR90	lung:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
20	CEBPB	chr3:591255-591764	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:534354-535027	Hela-S3	cervix:	n/a	chr3:534767-534778
22	CEBPB	chr3:650039-650244	HepG2	liver:	n/a	chr3:650073-650084 chr3:650075-650084
23	CEBPB	chr3:526427-526685	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:697395-697928	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:637765-638119	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr3:560581-560882	A549	lung:	n/a	chr3:560731-560742
27	CEBPB	chr3:700968-701307	HepG2	liver:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
28	CEBPB	chr3:700961-701300	Hela-S3	cervix:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
29	CEBPB	chr3:650024-650224	A549	lung:	n/a	chr3:650073-650084 chr3:650075-650084
30	CEBPB	chr3:701078-701278	A549	lung:	n/a	chr3:701126-701139 chr3:701128-701137 chr3:701128-701137 chr3:701128-701137
31	CEBPB	chr3:672488-672700	HepG2	liver:	n/a	chr3:672554-672567 chr3:672555-672566
32	CEBPB	chr3:575781-576057	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr3:544910-545217	Hela-S3	cervix:	n/a	chr3:545063-545076 chr3:545064-545075
34	CEBPB	chr3:534600-534964	HepG2	liver:	n/a	chr3:534767-534778
35	CEBPB	chr3:544957-545231	H1-hESC	embryonic stem cell:	n/a	chr3:545063-545076 chr3:545064-545075
36	CEBPB	chr3:544919-545200	A549	lung:	n/a	chr3:545063-545076 chr3:545064-545075
37	CEBPB	chr3:649124-649464	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr3:555007-555386	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:526407-526558	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr3:544911-545212	IMR90	lung:	n/a	chr3:545063-545076 chr3:545064-545075
41	CEBPB	chr3:544942-545225	HepG2	liver:	n/a	chr3:545063-545076 chr3:545064-545075
42	CEBPB	chr3:649955-650248	IMR90	lung:	n/a	chr3:650073-650084 chr3:650075-650084
43	CEBPB	chr3:611097-611344	HepG2	liver:	n/a	chr3:611201-611212
44	CHD1	chr3:660628-660658	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr3:577375-577868	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr3:639101-639345	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr3:674360-674510	HMF	breast:	n/a	chr3:674455-674465 chr3:674451-674467 chr3:674453-674466 chr3:674453-674462 chr3:674453-674466 chr3:674450-674468 chr3:674452-674473
48	CTCF	chr3:674380-674530	GM12801	blood:	n/a	chr3:674455-674465 chr3:674451-674467 chr3:674453-674466 chr3:674453-674462 chr3:674453-674466 chr3:674450-674468 chr3:674452-674473
49	CTCF	chr3:577760-577910	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr3:577787-577953	Lung_OC	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:577964-578014	GM19239	blood:	n/a
2	chr3:577964-578014	GM19239	blood:	n/a
3	chr3:577964-578014	GM12891	blood:	n/a
4	chr3:577821-577871	HNPCEpiC	eye:	n/a
5	chr3:577821-577871	HRE	kidney:	n/a
6	chr3:577964-578014	NB4	blood:	n/a
7	chr3:577629-577679	IMR90	lung:	fetal
8	chr3:577964-578014	HMEC	breast:	n/a
9	chr3:577629-577679	AG04450	lung:	fetal
10	chr3:577821-577871	HUVEC	blood vessel:	n/a
11	chr3:577964-578014	HepG2	liver:	n/a
12	chr3:577629-577679	PFSK-1	brain:	n/a
13	chr3:577821-577871	Jurkat	blood:	n/a
14	chr3:577964-578014	HUVEC	blood vessel:	n/a
15	chr3:577821-577871	NHDF-neo	bronchial:	n/a
16	chr3:577964-578014	HPAEpiC	pulmonary alveolar:	n/a
17	chr3:577821-577871	ProgFib	skin:	n/a
18	chr3:577964-578014	BJ	skin:	n/a
19	chr3:577629-577679	HUVEC	blood vessel:	n/a
20	chr3:577821-577871	HAEpiC	amniotic membrane:	n/a
21	chr3:577629-577679	LNCaP	prostate:	n/a
22	chr3:577629-577679	AG09309	skin:	n/a
23	chr3:577964-578014	T-47D	breast:	n/a
24	chr3:577964-578014	HEK293	kidney:	embryo
25	chr3:577964-578014	PANC-1	pancreas:	n/a
26	chr3:577821-577871	PFSK-1	brain:	n/a
27	chr3:577964-578014	AG10803	skin:	n/a
28	chr3:577964-578014	LNCaP	prostate:	n/a
29	chr3:577629-577679	AoSMC	blood vessel:	n/a
30	chr3:577629-577679	SAEC	small airway:	n/a
31	chr3:577821-577871	GM06990	blood:	n/a
32	chr3:577821-577871	AG09309	skin:	n/a
33	chr3:577629-577679	GM19239	blood:	n/a
34	chr3:577964-578014	PrEC	prostate:	n/a
35	chr3:577821-577871	Hepatocyte	liver:	n/a
36	chr3:577821-577871	CMK	blood:	n/a
37	chr3:577821-577871	BE2_C	brain:	n/a
38	chr3:577629-577679	GM12892	blood:	n/a
39	chr3:577629-577679	HEEpiC	esophagus:	n/a
40	chr3:577964-578014	MCF-7	breast:	n/a
41	chr3:577821-577871	SK-N-MC	brain:	n/a
42	chr3:577629-577679	GM06990	blood:	n/a
43	chr3:577821-577871	HMEC	breast:	n/a
44	chr3:577964-578014	SK-N-MC	brain:	n/a
45	chr3:577821-577871	AG04449	skin:	fetal
46	chr3:577629-577679	Jurkat	blood:	n/a
47	chr3:577629-577679	HRE	kidney:	n/a
48	chr3:577964-578014	Hepatocyte	liver:	n/a
49	chr3:577964-578014	AoSMC	blood vessel:	n/a
50	chr3:577629-577679	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:554700..557337-chr3:557649..560284,2	K562	blood:
2	chr3:674217..674800-chr3:1123463..1123990,2	MCF-7	breast:
3	chr3:556350..557928-chr3:558208..559835,2	MCF-7	breast:
4	chr3:554700..557337-chr3:557649..560284,2	K562	blood:
5	chr3:565796..568589-chr3:571178..572728,2	K562	blood:
6	chr3:674203..674975-chr3:2197712..2198482,2	MCF-7	breast:
7	chr21:9517250..9519290-chr3:632442..635070,2	MCF-7	breast:
8	chr3:571404..573075-chr3:573790..576325,2	MCF-7	breast:
9	chr3:512741..514299-chr3:528430..530623,2	K562	blood:
10	chr21:9533639..9536328-chr3:614645..617390,2	MCF-7	breast:
11	chr21:9537493..9539688-chr3:612236..614804,2	MCF-7	breast:
12	chr3:703062..705164-chr3:828470..830008,2	K562	blood:
13	chr3:571404..573075-chr3:573790..576325,2	MCF-7	breast:
14	chr3:522873..523625-chr3:674344..674995,2	MCF-7	breast:
15	chr3:556350..557928-chr3:558208..559835,2	MCF-7	breast:
16	chr3:565796..568589-chr3:571178..572728,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHL1-3	chr3:577936-578010	ENSG00000224957
2	lnc-CHL1-6	chr3:608788-608866	ucscGeneNc_uc003boy_1
3	lnc-CHL1-6	chr3:552914-553010	ucscGeneNc_uc003boy_1
4	lnc-CHL1-3	chr3:633788-633866	NR_110118
5	lnc-CHL1-3	chr3:633788-633866	ENSG00000224957
6	lnc-IL5RA-14	chr3:659472-659997	NONHSAT087571
7	lnc-CHL1-3	chr3:577941-579275	NONHSAT087570

Variant related genes	Relation type
ENSG00000224957	TF binding region
ENSG00000238075	TF binding region
ENSG00000224957	CpG island
ENSG00000238075	CpG island
DCBLD2	miRNA target sites

Extended variants
information (count: 3308 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3308 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567983761	chr3:526226-526227	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538222173	chr3:526231-526232	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549944381	chr3:526244-526245	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569489911	chr3:526264-526265	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551067833	chr3:526274-526275	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535518443	chr3:526329-526330	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184422291	chr3:526363-526364	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76652842	chr3:526463-526464	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571869481	chr3:526494-526495	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189199452	chr3:526537-526538	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554421107	chr3:526579-526580	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141922857	chr3:526595-526596	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72985314	chr3:526601-526602	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558314647	chr3:526643-526644	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571008876	chr3:526722-526723	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576772981	chr3:526756-526757	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181110611	chr3:526763-526764	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559412312	chr3:526786-526787	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111975219	chr3:526841-526842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75962948	chr3:526850-526851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561551927	chr3:526864-526865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145651692	chr3:526867-526868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186470007	chr3:526905-526906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138633945	chr3:526922-526923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149334153	chr3:526962-526963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35983981	chr3:526982-526983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547540730	chr3:527013-527014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139474899	chr3:527046-527047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565858926	chr3:527055-527056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533982006	chr3:527106-527107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536022417	chr3:527135-527136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555830789	chr3:527163-527164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144544708	chr3:527181-527182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148442660	chr3:527204-527205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6442890	chr3:527223-527224	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs141738757	chr3:527249-527250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10617674	chr3:527263-527264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78708516	chr3:527273-527274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs398051474	chr3:527274-527275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544497227	chr3:527319-527320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188942379	chr3:527344-527345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541041498	chr3:527358-527359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147157105	chr3:527361-527362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181550987	chr3:527378-527379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140422621	chr3:527385-527386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561515801	chr3:527433-527434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531946215	chr3:527450-527451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186206044	chr3:527484-527485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191028863	chr3:527514-527515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144178409	chr3:527565-527566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:525200-526800	Active TSS	Aorta	Aorta
2	chr3:525800-526600	Enhancers	Fetal Muscle Leg	muscle
3	chr3:525800-529200	Weak transcription	Ovary	ovary
4	chr3:526000-526800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr3:526000-527200	Weak transcription	NHLF	lung
6	chr3:526200-526800	Enhancers	Hela-S3	cervix
7	chr3:526200-527000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr3:526800-533800	Weak transcription	Hela-S3	cervix
9	chr3:526800-543200	Weak transcription	Aorta	Aorta
10	chr3:527000-528200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr3:528000-528800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr3:528200-528600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr3:528200-528800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr3:528200-529000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr3:528800-534000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr3:528800-534200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr3:529000-534200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr3:529200-529800	Enhancers	Ovary	ovary
19	chr3:533000-534200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr3:533800-534200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr3:533800-534200	Enhancers	Hela-S3	cervix
22	chr3:533800-535000	Enhancers	Fetal Intestine Large	intestine
23	chr3:534000-534200	Enhancers	GM12878-XiMat	blood
24	chr3:534000-534400	Enhancers	Liver	Liver
25	chr3:534000-534600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr3:534000-535000	Enhancers	H9 Cell Line	embryonic stem cell
27	chr3:534000-535000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr3:534200-534600	Enhancers	Fetal Intestine Small	intestine
29	chr3:534200-534600	Active TSS	GM12878-XiMat	blood
30	chr3:534200-534800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr3:534200-534800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr3:534200-534800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr3:534200-535000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr3:534200-535000	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr3:534200-535000	Flanking Active TSS	Hela-S3	cervix
36	chr3:534400-534800	Flanking Active TSS	Liver	Liver
37	chr3:534400-534800	Enhancers	Fetal Kidney	kidney
38	chr3:534400-535000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr3:534600-534800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr3:534600-534800	Enhancers	GM12878-XiMat	blood
41	chr3:534800-535000	Enhancers	Liver	Liver
42	chr3:534800-540600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr3:535000-535200	Enhancers	Hela-S3	cervix
44	chr3:540600-540800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr3:543600-543800	Enhancers	Aorta	Aorta
46	chr3:554600-556200	Enhancers	Hela-S3	cervix
47	chr3:554600-556400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr3:554800-556400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr3:555400-556400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr3:556000-556400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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