Variant report

Variant	nsv834719
Chromosome Location	chr3:67396626-67589852
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1493)
CpG islands
(count:427)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1493 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:67551099-67551461	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:67487581-67487716	K562	blood:	n/a	n/a
3	ARID3A	chr3:67579956-67579992	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:67522493-67522693	K562	blood:	n/a	n/a
5	ARID3A	chr3:67408282-67408518	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:67413206-67413406	K562	blood:	n/a	n/a
7	ARID3A	chr3:67435311-67435486	K562	blood:	n/a	n/a
8	ATF1	chr3:67413144-67413469	K562	blood:	n/a	n/a
9	ATF2	chr3:67439607-67440037	GM12878	blood:	n/a	n/a
10	ATF2	chr3:67527562-67528008	GM12878	blood:	n/a	n/a
11	ATF2	chr3:67436901-67437458	GM12878	blood:	n/a	n/a
12	ATF2	chr3:67439478-67440142	GM12878	blood:	n/a	n/a
13	ATF3	chr3:67427795-67428091	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr3:67427779-67428115	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr3:67413084-67413465	K562	blood:	n/a	n/a
16	ATF3	chr3:67427781-67428040	K562	blood:	n/a	n/a
17	ATF3	chr3:67427812-67428056	GM12878	blood:	n/a	n/a
18	BATF	chr3:67527534-67527950	GM12878	blood:	n/a	chr3:67527760-67527771
19	BATF	chr3:67439580-67439991	GM12878	blood:	n/a	n/a
20	BATF	chr3:67399912-67400336	GM12878	blood:	n/a	n/a
21	BATF	chr3:67527590-67527892	GM12878	blood:	n/a	chr3:67527760-67527771
22	BATF	chr3:67399874-67400310	GM12878	blood:	n/a	n/a
23	BCL3	chr3:67439639-67439945	GM12878	blood:	n/a	chr3:67439891-67439900
24	BCLAF1	chr3:67439568-67439989	GM12878	blood:	n/a	chr3:67439891-67439900
25	BCLAF1	chr3:67527533-67527894	GM12878	blood:	n/a	n/a
26	BCLAF1	chr3:67439553-67440112	GM12878	blood:	n/a	chr3:67439891-67439900
27	BHLHE40	chr3:67435360-67435422	K562	blood:	n/a	n/a
28	BHLHE40	chr3:67413114-67413409	K562	blood:	n/a	n/a
29	BRCA1	chr3:67408362-67408560	HepG2	liver:	n/a	n/a
30	CBX3	chr3:67408162-67408581	HCT-116	colon:	n/a	n/a
31	CCNT2	chr3:67584349-67584472	K562	blood:	n/a	n/a
32	CEBPB	chr3:67487490-67487859	K562	blood:	n/a	n/a
33	CEBPB	chr3:67562442-67562722	HepG2	liver:	n/a	chr3:67562585-67562596
34	CEBPB	chr3:67487586-67487779	K562	blood:	n/a	n/a
35	CEBPB	chr3:67465188-67465551	MCF-7	breast:	n/a	chr3:67465335-67465346
36	CEBPB	chr3:67465174-67465527	IMR90	lung:	n/a	chr3:67465335-67465346
37	CEBPB	chr3:67435272-67435480	MCF-7	breast:	n/a	n/a
38	CEBPB	chr3:67487464-67487972	MCF-7	breast:	n/a	n/a
39	CEBPB	chr3:67487532-67487874	IMR90	lung:	n/a	n/a
40	CEBPB	chr3:67565412-67565590	H1-hESC	embryonic stem cell:	n/a	chr3:67565495-67565506
41	CEBPB	chr3:67405542-67405785	HepG2	liver:	n/a	chr3:67405649-67405660
42	CEBPB	chr3:67487641-67487736	HepG2	liver:	n/a	n/a
43	CEBPB	chr3:67565342-67565670	IMR90	lung:	n/a	chr3:67565495-67565506
44	CEBPB	chr3:67487529-67487899	K562	blood:	n/a	n/a
45	CEBPB	chr3:67465163-67465493	K562	blood:	n/a	chr3:67465335-67465346
46	CEBPB	chr3:67520761-67520937	A549	lung:	n/a	chr3:67520830-67520841
47	CEBPB	chr3:67487526-67487842	HepG2	liver:	n/a	n/a
48	CEBPB	chr3:67576450-67577006	IMR90	lung:	n/a	n/a
49	CEBPB	chr3:67413179-67413439	K562	blood:	n/a	n/a
50	CEBPB	chr3:67487557-67487788	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:67560049-67560099	AG09319	gingival:	n/a
2	chr3:67425337-67425387	ECC-1	luminal epithelium:	n/a
3	chr3:67495517-67495567	SKMC	muscle:	n/a
4	chr3:67476282-67476332	HIPEpiC	eye:	n/a
5	chr3:67476282-67476332	PFSK-1	brain:	n/a
6	chr3:67433172-67433222	ECC-1	luminal epithelium:	n/a
7	chr3:67564432-67564482	AG10803	skin:	n/a
8	chr3:67425337-67425387	HCPEpiC	choroid plexus:	n/a
9	chr3:67495517-67495567	NHBE	bronchial:	n/a
10	chr3:67495517-67495567	AG04450	lung:	fetal
11	chr3:67564432-67564482	LNCaP	prostate:	n/a
12	chr3:67433172-67433222	GM12891	blood:	n/a
13	chr3:67511061-67511111	HCF	heart:	n/a
14	chr3:67476282-67476332	HMEC	breast:	n/a
15	chr3:67425337-67425387	AG10803	skin:	n/a
16	chr3:67495517-67495567	Hepatocyte	liver:	n/a
17	chr3:67425337-67425387	PANC-1	pancreas:	n/a
18	chr3:67433172-67433222	PANC-1	pancreas:	n/a
19	chr3:67425337-67425387	ovcar-3	ovarian:	n/a
20	chr3:67511061-67511111	GM06990	blood:	n/a
21	chr3:67511061-67511111	MCF10A-Er-Src	breast:	n/a
22	chr3:67476282-67476332	GM12892	blood:	n/a
23	chr3:67425337-67425387	HL-60	blood:	n/a
24	chr3:67495517-67495567	HepG2	liver:	n/a
25	chr3:67495517-67495567	H1-hESC	embryonic stem cell:	embryo
26	chr3:67433172-67433222	HCPEpiC	choroid plexus:	n/a
27	chr3:67476282-67476332	HAEpiC	amniotic membrane:	n/a
28	chr3:67564432-67564482	HAEpiC	amniotic membrane:	n/a
29	chr3:67476282-67476332	HRCEpiC	kidney:	n/a
30	chr3:67560049-67560099	GM06990	blood:	n/a
31	chr3:67511061-67511111	HRE	kidney:	n/a
32	chr3:67564432-67564482	AoSMC	blood vessel:	n/a
33	chr3:67511061-67511111	AG10803	skin:	n/a
34	chr3:67433172-67433222	K562	blood:	n/a
35	chr3:67511061-67511111	BJ	skin:	n/a
36	chr3:67433172-67433222	HAEpiC	amniotic membrane:	n/a
37	chr3:67425337-67425387	SK-N-SH_RA	brain:	n/a
38	chr3:67425337-67425387	GM19239	blood:	n/a
39	chr3:67564432-67564482	HCF	heart:	n/a
40	chr3:67476282-67476332	SK-N-SH_RA	brain:	n/a
41	chr3:67495517-67495567	U87	brain:	n/a
42	chr3:67433172-67433222	T-47D	breast:	n/a
43	chr3:67425337-67425387	HMEC	breast:	n/a
44	chr3:67425337-67425387	HepG2	liver:	n/a
45	chr3:67425337-67425387	SK-N-MC	brain:	n/a
46	chr3:67476282-67476332	PrEC	prostate:	n/a
47	chr3:67495517-67495567	SK-N-SH_RA	brain:	n/a
48	chr3:67476282-67476332	SK-N-SH	brain:	n/a
49	chr3:67476282-67476332	ovcar-3	ovarian:	n/a
50	chr3:67476282-67476332	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:67541283..67543981-chr3:67568913..67571810,2	K562	blood:
2	chr3:67517969..67519979-chr3:67521471..67523123,2	MCF-7	breast:
3	chr3:67159802..67160783-chr3:67408208..67408877,3	MCF-7	breast:
4	chr3:67571229..67573856-chr3:67577738..67580232,2	K562	blood:
5	chr3:67534703..67536590-chr3:67538235..67540605,2	K562	blood:
6	chr3:67498464..67501413-chr3:67503941..67505935,2	K562	blood:
7	chr3:67520630..67522600-chr3:67524252..67526349,2	MCF-7	breast:
8	chr16:85456347..85458098-chr3:67558875..67561641,2	MCF-7	breast:
9	chr3:67435199..67435789-chr3:67655564..67656111,2	MCF-7	breast:
10	chr3:67543627..67545753-chr3:67547156..67549290,2	MCF-7	breast:
11	chr3:67434937..67435840-chr3:67841382..67842248,2	MCF-7	breast:
12	chr3:67517969..67519979-chr3:67521471..67523123,2	MCF-7	breast:
13	chr3:67457865..67460434-chr3:67463200..67466004,2	K562	blood:
14	chr3:67579489..67580411-chr3:67840544..67841101,2	MCF-7	breast:
15	chr3:67431913..67433830-chr3:67434492..67436556,2	MCF-7	breast:
16	chr3:67543627..67545753-chr3:67547156..67549290,2	MCF-7	breast:
17	chr3:67457865..67460434-chr3:67463200..67466004,2	K562	blood:
18	chr3:67164313..67164922-chr3:67407940..67408860,3	MCF-7	breast:
19	chr3:67163928..67164964-chr3:67407899..67409009,8	MCF-7	breast:
20	chr3:67498464..67501413-chr3:67503941..67505935,2	K562	blood:
21	chr3:67435290..67435880-chr3:67601216..67601908,2	MCF-7	breast:
22	chr3:67435046..67435830-chr3:67840399..67841145,2	K562	blood:
23	chr3:67541283..67543981-chr3:67568913..67571810,2	K562	blood:
24	chr3:67566852..67569780-chr3:67581868..67584034,2	MCF-7	breast:
25	chr3:67431913..67433830-chr3:67434492..67436556,2	MCF-7	breast:
26	chr3:67566852..67569780-chr3:67581868..67584034,2	MCF-7	breast:
27	chr3:67534703..67536590-chr3:67538235..67540605,2	K562	blood:
28	chr3:67163998..67164779-chr3:67431870..67433240,3	MCF-7	breast:
29	chr3:67520630..67522600-chr3:67524252..67526349,2	MCF-7	breast:
30	chr3:67159948..67160863-chr3:67432225..67433233,3	MCF-7	breast:
31	chr3:67467097..67467666-chr3:67840213..67841048,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM19A1-4	chr3:67564364-67564744	NONHSAT090318

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SUCLG2	hsa-miR-124-3p	chr3:67425530-67425549
2	SUCLG2	hsa-miR-124-3p	chr3:67425535-67425529

Variant related genes	Relation type
SUCLG2	TF binding region
NDUFB4P1	TF binding region
SUCLG2	CpG island
NDUFB4P1	CpG island
ENSG00000172340	chromatin interactions

Extended variants
information (count: 8006 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:8006 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188066258	chr3:67399635-67399636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538418412	chr3:67399640-67399641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113737410	chr3:67399644-67399645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555146926	chr3:67399652-67399653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192725843	chr3:67399677-67399678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545012629	chr3:67399709-67399710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542794905	chr3:67399747-67399748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552680497	chr3:67399773-67399774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540275460	chr3:67399782-67399783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117881657	chr3:67399785-67399786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146406017	chr3:67399865-67399866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545256292	chr3:67399867-67399868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564825450	chr3:67399891-67399892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575126942	chr3:67399913-67399914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139755706	chr3:67400001-67400002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1552616	chr3:67400029-67400030	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs185039388	chr3:67400040-67400041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs199546432	chr3:67400059-67400060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562768003	chr3:67400072-67400073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186635271	chr3:67400083-67400084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144430782	chr3:67400106-67400107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1552617	chr3:67400129-67400130	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs561517249	chr3:67400170-67400171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552932018	chr3:67400180-67400181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373094952	chr3:67400207-67400208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377127480	chr3:67400217-67400218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569567404	chr3:67400257-67400258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538478777	chr3:67400311-67400312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548757532	chr3:67400320-67400321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs139590476	chr3:67400343-67400344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35131171	chr3:67400420-67400421	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs114560709	chr3:67400440-67400441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531854510	chr3:67400450-67400451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1552618	chr3:67400491-67400492	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs61317274	chr3:67400533-67400534	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs112462844	chr3:67400553-67400554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1552619	chr3:67400567-67400568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139099689	chr3:67400582-67400583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11329737	chr3:67403001-67403002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564382040	chr3:67403002-67403003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs397877286	chr3:67403003-67403004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs377469099	chr3:67403004-67403005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533216607	chr3:67403038-67403039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188331776	chr3:67403085-67403086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77382581	chr3:67403089-67403090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535624516	chr3:67403113-67403114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542560146	chr3:67403116-67403117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs199996148	chr3:67403128-67403129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369053209	chr3:67403129-67403130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77056373	chr3:67403156-67403157	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	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
Oral squamous cell carcinoma	17134496	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Breast cancer	17142309	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2142 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67399600-67400400	Enhancers	GM12878-XiMat	blood
2	chr3:67399800-67400400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr3:67399800-67400400	Enhancers	NH-A	brain
4	chr3:67399800-67400600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr3:67403000-67403800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr3:67403400-67403800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr3:67403400-67404000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr3:67403400-67404000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr3:67403600-67403800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr3:67403600-67403800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr3:67403600-67404000	Enhancers	H9 Cell Line	embryonic stem cell
12	chr3:67403600-67404000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr3:67403600-67404200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr3:67403800-67408400	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr3:67403800-67408400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr3:67403800-67412600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr3:67404000-67405600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr3:67405600-67405800	Enhancers	H9 Cell Line	embryonic stem cell
19	chr3:67406600-67408800	Weak transcription	A549	lung
20	chr3:67408200-67408400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:67408200-67408600	Enhancers	Placenta	Placenta
22	chr3:67408400-67408800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr3:67408400-67408800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr3:67408400-67408800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr3:67408400-67408800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr3:67408400-67411800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr3:67408800-67412800	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr3:67408800-67412800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr3:67411200-67415000	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr3:67411200-67415000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr3:67411200-67415200	Enhancers	Primary hematopoietic stem cells	blood
32	chr3:67411600-67414200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr3:67411800-67412400	Enhancers	GM12878-XiMat	blood
34	chr3:67411800-67413200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:67412200-67413200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr3:67412200-67413400	Weak transcription	Primary T cells from cord blood	blood
37	chr3:67412400-67453000	Weak transcription	Rectal Smooth Muscle	rectum
38	chr3:67412600-67413400	Enhancers	K562	blood
39	chr3:67412600-67414000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr3:67412600-67414000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr3:67412600-67414800	Enhancers	Dnd41	blood
42	chr3:67412600-67417000	Weak transcription	Aorta	Aorta
43	chr3:67412800-67413200	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr3:67412800-67413400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr3:67412800-67413400	Enhancers	NHEK	skin
46	chr3:67413000-67413200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr3:67413000-67413400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr3:67413000-67413400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr3:67413000-67413600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:67413000-67414200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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