Variant report

Variant	nsv997694
Chromosome Location	chr3:140324012-140464786
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	chr3:140418329-140419193	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:140446760-140447646	HepG2	liver:	n/a	n/a
3	ATF1	chr3:140336242-140336250	K562	blood:	n/a	n/a
4	BACH1	chr3:140367452-140367456	K562	blood:	n/a	n/a
5	BATF	chr3:140374547-140374771	GM12878	blood:	n/a	n/a
6	BATF	chr3:140435015-140435253	GM12878	blood:	n/a	n/a
7	BATF	chr3:140444290-140444583	GM12878	blood:	n/a	chr3:140444440-140444451
8	BCL11A	chr3:140435034-140435158	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:140329685-140329713	K562	blood:	n/a	n/a
10	BHLHE40	chr3:140418726-140419133	HepG2	liver:	n/a	n/a
11	BHLHE40	chr3:140444050-140444669	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:140347642-140347676	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:140444451-140444496	HepG2	liver:	n/a	n/a
14	CEBPB	chr3:140348639-140349072	MCF-7	breast:	n/a	n/a
15	CEBPB	chr3:140418669-140419087	HepG2	liver:	n/a	chr3:140418695-140418706
16	CEBPB	chr3:140396615-140396933	HepG2	liver:	n/a	chr3:140396722-140396733
17	CEBPB	chr3:140324409-140324596	HepG2	liver:	n/a	chr3:140324518-140324529
18	CEBPB	chr3:140398421-140398728	HepG2	liver:	n/a	chr3:140398565-140398578 chr3:140398567-140398576 chr3:140398566-140398577
19	CEBPB	chr3:140354064-140354201	HepG2	liver:	n/a	chr3:140354175-140354186
20	CEBPB	chr3:140418802-140419142	HepG2	liver:	n/a	n/a
21	CEBPB	chr3:140348716-140349002	HepG2	liver:	n/a	n/a
22	CEBPB	chr3:140348665-140348999	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr3:140418845-140419055	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:140446753-140447039	HepG2	liver:	n/a	n/a
25	CEBPD	chr3:140418761-140419035	HepG2	liver:	n/a	n/a
26	CEBPZ	chr3:140418629-140419199	HepG2	liver:	n/a	n/a
27	CHD2	chr3:140418743-140419066	HepG2	liver:	n/a	n/a
28	CHD2	chr3:140450636-140450892	GM12878	blood:	n/a	n/a
29	CHD2	chr3:140447203-140447475	HepG2	liver:	n/a	n/a
30	CTCF	chr3:140455925-140456206	T-47D	breast:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
31	CTCF	chr3:140456020-140456170	NB4	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
32	CTCF	chr3:140456017-140456213	A549	lung:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
33	CTCF	chr3:140456000-140456150	HEK293	kidney:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
34	CTCF	chr3:140456039-140456185	SK-N-SH_RA	brain:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
35	CTCF	chr3:140354288-140354348	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:140456020-140456170	GM12869	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
37	CTCF	chr3:140412924-140412955	GM13976	blood:	n/a	n/a
38	CTCF	chr3:140456017-140456209	GM10248	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
39	CTCF	chr3:140339469-140339560	LNCaP	prostate:	n/a	n/a
40	CTCF	chr3:140456040-140456190	HFF	foreskin:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
41	CTCF	chr3:140456020-140456170	AG09319	gingival:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
42	CTCF	chr3:140456000-140456150	HA-sp	spinal cord:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
43	CTCF	chr3:140456050-140456179	Hela-S3	cervix:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
44	CTCF	chr3:140354140-140354290	GM12875	blood:	n/a	n/a
45	CTCF	chr3:140456060-140456210	GM12864	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
46	CTCF	chr3:140464160-140464310	GM12872	blood:	n/a	n/a
47	CTCF	chr3:140456060-140456210	AoAF	blood vessel:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
48	CTCF	chr3:140405980-140406130	GM12872	blood:	n/a	n/a
49	CTCF	chr3:140456040-140456190	GM12867	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
50	CTCF	chr3:140456020-140456170	GM12871	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140396963-140397013	MCF10A-Er-Src	breast:	n/a
2	chr3:140396963-140397013	MCF10A-Er-Src	breast:	n/a
3	chr3:140395898-140395948	GM12878	blood:	n/a
4	chr3:140396963-140397013	U87	brain:	n/a
5	chr3:140395771-140395821	LNCaP	prostate:	n/a
6	chr3:140396963-140397013	HL-60	blood:	n/a
7	chr3:140402167-140402217	NHBE	bronchial:	n/a
8	chr3:140397089-140397139	ProgFib	skin:	n/a
9	chr3:140405436-140405486	PANC-1	pancreas:	n/a
10	chr3:140401543-140401593	HNPCEpiC	eye:	n/a
11	chr3:140396963-140397013	CMK	blood:	n/a
12	chr3:140400911-140400961	SK-N-SH	brain:	n/a
13	chr3:140401925-140401975	GM06990	blood:	n/a
14	chr3:140401955-140402005	HCM	heart:	n/a
15	chr3:140401955-140402005	AoSMC	blood vessel:	n/a
16	chr3:140396803-140396853	GM12892	blood:	n/a
17	chr3:140401543-140401593	NH-A	brain:	n/a
18	chr3:140397089-140397139	IMR90	lung:	fetal
19	chr3:140395771-140395821	HRCEpiC	kidney:	n/a
20	chr3:140402167-140402217	ovcar-3	ovarian:	n/a
21	chr3:140396963-140397013	GM12892	blood:	n/a
22	chr3:140400911-140400961	HepG2	liver:	n/a
23	chr3:140400911-140400961	RPTEC	kidney:	n/a
24	chr3:140401955-140402005	NHBE	bronchial:	n/a
25	chr3:140401925-140401975	SK-N-SH	brain:	n/a
26	chr3:140397089-140397139	SK-N-MC	brain:	n/a
27	chr3:140401925-140401975	ovcar-3	ovarian:	n/a
28	chr3:140396803-140396853	SKMC	muscle:	n/a
29	chr3:140402167-140402217	HIPEpiC	eye:	n/a
30	chr3:140397089-140397139	BJ	skin:	n/a
31	chr3:140401925-140401975	K562	blood:	n/a
32	chr3:140397089-140397139	HEK293	kidney:	embryo
33	chr3:140395771-140395821	HepG2	liver:	n/a
34	chr3:140395771-140395821	HRPEpiC	eye:	n/a
35	chr3:140401765-140401815	HRPEpiC	eye:	n/a
36	chr3:140400911-140400961	GM12891	blood:	n/a
37	chr3:140396803-140396853	ovcar-3	ovarian:	n/a
38	chr3:140396803-140396853	SK-N-MC	brain:	n/a
39	chr3:140402167-140402217	Jurkat	blood:	n/a
40	chr3:140401765-140401815	HCT-116	colon:	n/a
41	chr3:140396803-140396853	HMEC	breast:	n/a
42	chr3:140395898-140395948	HRPEpiC	eye:	n/a
43	chr3:140397089-140397139	NB4	blood:	n/a
44	chr3:140405436-140405486	PrEC	prostate:	n/a
45	chr3:140396803-140396853	HIPEpiC	eye:	n/a
46	chr3:140405436-140405486	HL-60	blood:	n/a
47	chr3:140401765-140401815	HCM	heart:	n/a
48	chr3:140395898-140395948	MCF10A-Er-Src	breast:	n/a
49	chr3:140401765-140401815	MCF-7	breast:	n/a
50	chr3:140396963-140397013	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:140442579..140445613-chr3:140449550..140453378,3	K562	blood:
2	chr3:140354121..140354796-chr3:140455695..140456494,2	MCF-7	breast:
3	chr3:140442579..140445613-chr3:140449550..140453378,3	K562	blood:
4	chr17:41400537..41402663-chr3:140426790..140428290,2	K562	blood:
5	chr3:140398849..140401533-chr3:140405253..140408358,3	K562	blood:
6	chr3:140455659..140456657-chr3:140582285..140583107,3	MCF-7	breast:
7	chr3:140404247..140407194-chr3:140408344..140410912,4	K562	blood:
8	chr3:140328498..140333077-chr3:140333423..140336140,4	MCF-7	breast:
9	chr3:140438664..140441463-chr3:140446085..140448524,2	MCF-7	breast:
10	chr3:140418901..140421597-chr3:140424922..140429163,3	K562	blood:
11	chr3:140402179..140404321-chr3:140405178..140407110,2	K562	blood:
12	chr3:140433649..140435909-chr3:140440994..140443307,2	K562	blood:
13	chr3:140402179..140404321-chr3:140405178..140407110,2	K562	blood:
14	chr3:140435248..140437189-chr3:140439215..140440913,2	K562	blood:
15	chr3:140433649..140435909-chr3:140440994..140443307,2	K562	blood:
16	chr3:140354121..140354796-chr3:140455695..140456494,2	MCF-7	breast:
17	chr3:140438664..140441463-chr3:140446085..140448524,2	MCF-7	breast:
18	chr3:139847350..139848064-chr3:140455872..140456504,2	MCF-7	breast:
19	chr3:140398849..140401533-chr3:140405253..140408358,3	K562	blood:
20	chr3:140435248..140437189-chr3:140439215..140440913,2	K562	blood:
21	chr3:140457040..140458949-chr3:140465410..140467161,2	MCF-7	breast:
22	chr3:140328498..140333077-chr3:140333423..140336140,4	MCF-7	breast:
23	chr3:140271350..140272024-chr3:140455669..140456272,2	MCF-7	breast:
24	chr17:41462273..41463839-chr3:140426790..140428290,2	K562	blood:
25	chr3:140399760..140401307-chr3:140404568..140407227,2	MCF-7	breast:
26	chr3:140425316..140427124-chr3:140431791..140433516,2	MCF-7	breast:
27	chr3:140395530..140397595-chr3:140401305..140403330,2	K562	blood:
28	chr3:140404247..140407194-chr3:140408344..140410912,4	K562	blood:
29	chr3:140425316..140427124-chr3:140431791..140433516,2	MCF-7	breast:
30	chr3:140399760..140401307-chr3:140404568..140407227,2	MCF-7	breast:
31	chr3:140418901..140421597-chr3:140424922..140429163,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLSTN2-3	chr3:140325513-140326693	l_2484_NR_026783
2	lnc-NMNAT3-10	chr3:140434525-140435054	refGeneNc_2651_NR_027070

Variant related genes	Relation type
TRIM42	TF binding region
ENSG00000249305	TF binding region
TRIM42	CpG island
ENSG00000249305	CpG island
ENSG00000155890	chromatin interactions

Extended variants
information (count: 3485 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3485 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1466847	chr3:140324012-140324013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534136223	chr3:140324019-140324020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558677559	chr3:140324020-140324021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370529820	chr3:140324087-140324088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570852616	chr3:140324103-140324104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76996324	chr3:140324111-140324112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73870125	chr3:140324177-140324178	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs575154794	chr3:140324212-140324213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77400812	chr3:140324251-140324252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554720966	chr3:140324257-140324258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371715064	chr3:140324282-140324283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572933755	chr3:140324390-140324391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74455745	chr3:140324413-140324414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565064339	chr3:140324428-140324429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532484462	chr3:140324434-140324435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544474523	chr3:140324437-140324438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77352153	chr3:140324438-140324439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557558470	chr3:140324500-140324501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9865529	chr3:140324518-140324519	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs537146290	chr3:140324519-140324520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548252126	chr3:140324533-140324534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560218875	chr3:140324541-140324542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527774866	chr3:140324547-140324548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9865940	chr3:140324574-140324575	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs13080458	chr3:140324587-140324588	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs570376472	chr3:140324599-140324600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141242932	chr3:140324610-140324611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72979246	chr3:140324611-140324612	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs568625470	chr3:140324626-140324627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34514921	chr3:140324632-140324633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs397877302	chr3:140324634-140324635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201681769	chr3:140324635-140324636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536253098	chr3:140324638-140324639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372010044	chr3:140324654-140324655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150749162	chr3:140324684-140324685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533858508	chr3:140324691-140324692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558816336	chr3:140324707-140324708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368486230	chr3:140324708-140324709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139084347	chr3:140324765-140324766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376824545	chr3:140324773-140324774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72979248	chr3:140324836-140324837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs562813759	chr3:140324837-140324838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116341077	chr3:140324844-140324845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538990164	chr3:140324913-140324914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9879403	chr3:140324979-140324980	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs9879413	chr3:140324987-140324988	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs184762078	chr3:140325010-140325011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144003159	chr3:140325021-140325022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564213009	chr3:140325093-140325094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189536425	chr3:140325147-140325148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	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
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Schizophrenia	17989066	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	23621864	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140310600-140325400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:140322200-140324400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:140324400-140324800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:140327600-140328400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:140329200-140330000	Enhancers	NH-A	brain
6	chr3:140329200-140331000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr3:140329400-140329800	Enhancers	Osteobl	bone
8	chr3:140329400-140330000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr3:140329600-140329800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:140331600-140332200	Weak transcription	Psoas Muscle	Psoas
11	chr3:140332400-140332600	Enhancers	Psoas Muscle	Psoas
12	chr3:140336000-140346800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr3:140344400-140348200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:140345600-140346200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr3:140346200-140346400	Enhancers	Placenta	Placenta
16	chr3:140346200-140349000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr3:140346200-140349600	Enhancers	HSMM	muscle
18	chr3:140346200-140352800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr3:140346400-140346600	Enhancers	HSMMtube	muscle
20	chr3:140346400-140348200	Enhancers	Muscle Satellite Cultured Cells	--
21	chr3:140346400-140350000	Enhancers	Osteobl	bone
22	chr3:140346400-140350200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr3:140346400-140350200	Enhancers	NHDF-Ad	bronchial
24	chr3:140346400-140350200	Enhancers	NHEK	skin
25	chr3:140346600-140347600	Weak transcription	HSMMtube	muscle
26	chr3:140346600-140350000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:140346600-140350200	Enhancers	HMEC	breast
28	chr3:140346600-140352000	Enhancers	Placenta Amnion	Placenta Amnion
29	chr3:140346800-140350000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr3:140346800-140350000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr3:140346800-140350200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr3:140346800-140350200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr3:140346800-140350400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr3:140347000-140348400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr3:140347400-140349400	Enhancers	NHLF	lung
36	chr3:140347400-140350200	Enhancers	NH-A	brain
37	chr3:140347600-140349800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:140347600-140350000	Enhancers	HSMMtube	muscle
39	chr3:140348200-140348600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
40	chr3:140348200-140349200	Enhancers	Adipose Nuclei	Adipose
41	chr3:140348200-140349400	Enhancers	HUVEC	blood vessel
42	chr3:140348200-140350400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr3:140348200-140352000	Enhancers	Placenta	Placenta
44	chr3:140348400-140348600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr3:140348400-140348800	Enhancers	Pancreas	Pancrea
46	chr3:140348400-140349000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr3:140348400-140349000	Enhancers	Brain Substantia Nigra	brain
48	chr3:140348400-140349400	Enhancers	Brain Hippocampus Middle	brain
49	chr3:140348600-140349000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr3:140348600-140349000	Enhancers	Brain Cingulate Gyrus	brain

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