Variant report

Variant	nsv1012416
Chromosome Location	chr3:67546244-67615531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:416)
CpG islands
(count:123)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:67590641-67590915	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:67551099-67551461	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:67579956-67579992	HepG2	liver:	n/a	n/a
4	ATF2	chr3:67609491-67610034	GM12878	blood:	n/a	n/a
5	BHLHE40	chr3:67592929-67593210	HepG2	liver:	n/a	n/a
6	CCNT2	chr3:67584349-67584472	K562	blood:	n/a	n/a
7	CEBPB	chr3:67565375-67565628	A549	lung:	n/a	chr3:67565495-67565506
8	CEBPB	chr3:67597192-67597535	HepG2	liver:	n/a	chr3:67597351-67597362
9	CEBPB	chr3:67565345-67565646	HepG2	liver:	n/a	chr3:67565495-67565506
10	CEBPB	chr3:67565341-67565589	Hela-S3	cervix:	n/a	chr3:67565495-67565506
11	CEBPB	chr3:67565342-67565670	IMR90	lung:	n/a	chr3:67565495-67565506
12	CEBPB	chr3:67597172-67597538	IMR90	lung:	n/a	chr3:67597351-67597362
13	CEBPB	chr3:67597324-67597541	H1-hESC	embryonic stem cell:	n/a	chr3:67597351-67597362
14	CEBPB	chr3:67576450-67577006	IMR90	lung:	n/a	n/a
15	CEBPB	chr3:67566937-67567273	MCF-7	breast:	n/a	n/a
16	CEBPB	chr3:67562442-67562722	HepG2	liver:	n/a	chr3:67562585-67562596
17	CEBPB	chr3:67597204-67597527	Hela-S3	cervix:	n/a	chr3:67597351-67597362
18	CEBPB	chr3:67562483-67562669	A549	lung:	n/a	chr3:67562585-67562596
19	CEBPB	chr3:67565368-67565662	K562	blood:	n/a	chr3:67565495-67565506
20	CEBPB	chr3:67565412-67565590	H1-hESC	embryonic stem cell:	n/a	chr3:67565495-67565506
21	CEBPB	chr3:67597200-67597521	K562	blood:	n/a	chr3:67597351-67597362
22	CHD2	chr3:67566221-67566587	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr3:67566251-67566584	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr3:67579940-67580090	RPTEC	kidney:	n/a	n/a
25	CTCF	chr3:67579868-67580088	Medullo	brain:	n/a	n/a
26	CTCF	chr3:67579940-67580060	IMR90	lung:	n/a	n/a
27	CTCF	chr3:67579940-67580090	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr3:67608880-67609030	HCFaa	heart:	n/a	n/a
29	CTCF	chr3:67579840-67579990	BE2_C	brain:	n/a	n/a
30	CTCF	chr3:67579900-67580050	HMEC	breast:	n/a	n/a
31	CTCF	chr3:67591000-67591150	RPTEC	kidney:	n/a	n/a
32	CTCF	chr3:67579960-67580110	HRE	kidney:	n/a	n/a
33	CTCF	chr3:67608800-67608950	HMF	breast:	n/a	n/a
34	CTCF	chr3:67591069-67591284	HepG2	liver:	n/a	n/a
35	CTCF	chr3:67579940-67580090	GM12875	blood:	n/a	n/a
36	CTCF	chr3:67579860-67580010	GM12865	blood:	n/a	n/a
37	CTCF	chr3:67579860-67580010	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr3:67579860-67580010	A549	lung:	n/a	n/a
39	CTCF	chr3:67591080-67591230	RPTEC	kidney:	n/a	n/a
40	CTCF	chr3:67605220-67605370	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr3:67579860-67580010	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr3:67579860-67580010	HFF	foreskin:	n/a	n/a
43	CTCF	chr3:67608860-67609010	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr3:67579812-67580080	HepG2	liver:	n/a	n/a
45	CTCF	chr3:67590954-67591285	HepG2	liver:	n/a	n/a
46	CTCF	chr3:67579880-67580030	AG09309	skin:	n/a	n/a
47	CTCF	chr3:67579880-67580030	HVMF	connective:	n/a	n/a
48	CTCF	chr3:67579860-67580010	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr3:67591200-67591350	RPTEC	kidney:	n/a	n/a
50	CTCF	chr3:67579927-67580024	Hela-S3	cervix:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:67560049-67560099	NHBE	bronchial:	n/a
2	chr3:67560049-67560099	NHBE	bronchial:	n/a
3	chr3:67560049-67560099	Hepatocyte	liver:	n/a
4	chr3:67564432-67564482	AG09309	skin:	n/a
5	chr3:67564432-67564482	Jurkat	blood:	n/a
6	chr3:67560049-67560099	LNCaP	prostate:	n/a
7	chr3:67564432-67564482	HRE	kidney:	n/a
8	chr3:67564432-67564482	GM06990	blood:	n/a
9	chr3:67560049-67560099	GM12892	blood:	n/a
10	chr3:67564432-67564482	CMK	blood:	n/a
11	chr3:67564432-67564482	GM19239	blood:	n/a
12	chr3:67564432-67564482	NHBE	bronchial:	n/a
13	chr3:67564432-67564482	HIPEpiC	eye:	n/a
14	chr3:67560049-67560099	HCPEpiC	choroid plexus:	n/a
15	chr3:67560049-67560099	NH-A	brain:	n/a
16	chr3:67564432-67564482	H1-hESC	embryonic stem cell:	embryo
17	chr3:67560049-67560099	SKMC	muscle:	n/a
18	chr3:67564432-67564482	SK-N-SH	brain:	n/a
19	chr3:67560049-67560099	HRE	kidney:	n/a
20	chr3:67560049-67560099	GM12891	blood:	n/a
21	chr3:67564432-67564482	AG10803	skin:	n/a
22	chr3:67564432-67564482	HRCEpiC	kidney:	n/a
23	chr3:67564432-67564482	RPTEC	kidney:	n/a
24	chr3:67560049-67560099	HRCEpiC	kidney:	n/a
25	chr3:67564432-67564482	GM12891	blood:	n/a
26	chr3:67560049-67560099	PANC-1	pancreas:	n/a
27	chr3:67560049-67560099	HEK293	kidney:	embryo
28	chr3:67560049-67560099	AG09319	gingival:	n/a
29	chr3:67564432-67564482	U87	brain:	n/a
30	chr3:67560049-67560099	ProgFib	skin:	n/a
31	chr3:67564432-67564482	ProgFib	skin:	n/a
32	chr3:67560049-67560099	GM19239	blood:	n/a
33	chr3:67560049-67560099	GM06990	blood:	n/a
34	chr3:67560049-67560099	AG10803	skin:	n/a
35	chr3:67564432-67564482	Hela-S3	cervix:	n/a
36	chr3:67564432-67564482	NHDF-neo	bronchial:	n/a
37	chr3:67564432-67564482	Hepatocyte	liver:	n/a
38	chr3:67564432-67564482	K562	blood:	n/a
39	chr3:67564432-67564482	HRPEpiC	eye:	n/a
40	chr3:67564432-67564482	Caco-2	colon:	n/a
41	chr3:67560049-67560099	NT2-D1	testis:	n/a
42	chr3:67564432-67564482	HEK293	kidney:	embryo
43	chr3:67564432-67564482	HCPEpiC	choroid plexus:	n/a
44	chr3:67560049-67560099	Hela-S3	cervix:	n/a
45	chr3:67560049-67560099	ovcar-3	ovarian:	n/a
46	chr3:67560049-67560099	SK-N-MC	brain:	n/a
47	chr3:67560049-67560099	AG09309	skin:	n/a
48	chr3:67564432-67564482	HCF	heart:	n/a
49	chr3:67560049-67560099	HUVEC	blood vessel:	n/a
50	chr3:67560049-67560099	HCM	heart:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:67435290..67435880-chr3:67601216..67601908,2	MCF-7	breast:
2	chr3:67571229..67573856-chr3:67577738..67580232,2	K562	blood:
3	chr3:67603334..67606300-chr3:67607954..67610100,2	K562	blood:
4	chr3:67603334..67606300-chr3:67607954..67610100,2	K562	blood:
5	chr3:67543627..67545753-chr3:67547156..67549290,2	MCF-7	breast:
6	chr3:67541283..67543981-chr3:67568913..67571810,2	K562	blood:
7	chr3:67566852..67569780-chr3:67581868..67584034,2	MCF-7	breast:
8	chr3:67579489..67580411-chr3:67840544..67841101,2	MCF-7	breast:
9	chr16:85456347..85458098-chr3:67558875..67561641,2	MCF-7	breast:
10	chr3:67566852..67569780-chr3:67581868..67584034,2	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

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: 2847 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2847 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9843840	chr3:67546244-67546245	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375087627	chr3:67546270-67546271	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200728731	chr3:67546314-67546315	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368002457	chr3:67546327-67546328	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575833641	chr3:67546338-67546339	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370894892	chr3:67546370-67546371	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375720485	chr3:67546382-67546383	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376636098	chr3:67546402-67546403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187221449	chr3:67546416-67546417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555057156	chr3:67546426-67546427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572089311	chr3:67546440-67546441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540719147	chr3:67546472-67546473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564101748	chr3:67546477-67546478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570807597	chr3:67546519-67546520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141745292	chr3:67546551-67546552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562789275	chr3:67546611-67546612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563945533	chr3:67546615-67546616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145897441	chr3:67546627-67546628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9840334	chr3:67546645-67546646	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs559619147	chr3:67546656-67546657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551137481	chr3:67546657-67546658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556678931	chr3:67546664-67546665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369873240	chr3:67546680-67546681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576578848	chr3:67546739-67546740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73088934	chr3:67546764-67546765	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs571623960	chr3:67546772-67546773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192200555	chr3:67546852-67546853	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200163831	chr3:67546871-67546872	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs5849759	chr3:67546874-67546875	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs397938831	chr3:67546875-67546876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200357023	chr3:67546876-67546877	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574623819	chr3:67546982-67546983	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544047347	chr3:67547010-67547011	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535297718	chr3:67547018-67547019	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555513621	chr3:67547028-67547029	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572089072	chr3:67547036-67547037	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540228332	chr3:67547056-67547057	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534726895	chr3:67547066-67547067	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557523465	chr3:67547079-67547080	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183857932	chr3:67547108-67547109	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141159975	chr3:67547116-67547117	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566263842	chr3:67547136-67547137	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs13099732	chr3:67547204-67547205	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374610592	chr3:67547224-67547225	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577167704	chr3:67547255-67547256	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189510668	chr3:67547411-67547412	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559887792	chr3:67547455-67547456	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs62256397	chr3:67547457-67547458	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115344589	chr3:67547476-67547477	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565204797	chr3:67547515-67547516	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1172 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67488400-67566400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr3:67500800-67567000	Weak transcription	Pancreas	Pancrea
3	chr3:67504000-67559800	Weak transcription	Esophagus	oesophagus
4	chr3:67508200-67577600	Weak transcription	Spleen	Spleen
5	chr3:67511600-67560000	Weak transcription	Lung	lung
6	chr3:67511800-67565000	Weak transcription	Stomach Smooth Muscle	stomach
7	chr3:67512800-67554800	Weak transcription	Fetal Muscle Leg	muscle
8	chr3:67513200-67564800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr3:67513400-67567800	Weak transcription	NHLF	lung
10	chr3:67513600-67559800	Weak transcription	NHDF-Ad	bronchial
11	chr3:67514600-67559800	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr3:67519800-67557400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr3:67520800-67559800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr3:67521600-67580400	Weak transcription	Stomach Mucosa	stomach
15	chr3:67524200-67567000	Weak transcription	Placenta	Placenta
16	chr3:67526800-67583200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr3:67528200-67564400	Weak transcription	Fetal Lung	lung
18	chr3:67528200-67564800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr3:67529000-67559200	Weak transcription	GM12878-XiMat	blood
20	chr3:67530200-67560200	Weak transcription	NHEK	skin
21	chr3:67530800-67548200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr3:67531400-67576200	Weak transcription	HMEC	breast
23	chr3:67533200-67577000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr3:67533400-67577600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr3:67534400-67576400	Weak transcription	Aorta	Aorta
26	chr3:67534600-67560000	Weak transcription	Right Ventricle	heart
27	chr3:67534600-67566200	Weak transcription	Gastric	stomach
28	chr3:67534800-67554200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr3:67534800-67554800	Weak transcription	Left Ventricle	heart
30	chr3:67534800-67560200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr3:67534800-67566200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr3:67535000-67578800	Weak transcription	Brain Hippocampus Middle	brain
33	chr3:67537400-67559800	Weak transcription	Ovary	ovary
34	chr3:67537400-67579600	Weak transcription	Small Intestine	intestine
35	chr3:67537600-67560200	Weak transcription	HSMMtube	muscle
36	chr3:67537600-67566800	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr3:67539200-67549800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr3:67540400-67547200	Strong transcription	Primary B cells from cord blood	blood
39	chr3:67540800-67564400	Weak transcription	Fetal Kidney	kidney
40	chr3:67541000-67546400	Weak transcription	HUVEC	blood vessel
41	chr3:67541000-67546800	Weak transcription	Colon Smooth Muscle	Colon
42	chr3:67541200-67547000	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr3:67541400-67550000	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr3:67541400-67582000	Weak transcription	Rectal Smooth Muscle	rectum
45	chr3:67542200-67548400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr3:67542200-67559000	Strong transcription	Primary T cells from cord blood	blood
47	chr3:67542400-67548600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr3:67542400-67564800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr3:67542400-67566400	Weak transcription	NH-A	brain
50	chr3:67542600-67549400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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