Variant report

Variant	nsv521397
Chromosome Location	chr3:120970900-121192350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:474)
CpG islands
(count:245)
Chromatin interactive
region (count:38)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:121150918-121151361	GM12878	blood:	n/a	n/a
2	ATF2	chr3:121150837-121151409	GM12878	blood:	n/a	n/a
3	BACH1	chr3:121163484-121163523	K562	blood:	n/a	n/a
4	BACH1	chr3:121182712-121182826	K562	blood:	n/a	n/a
5	BATF	chr3:121151014-121151263	GM12878	blood:	n/a	n/a
6	BCLAF1	chr3:121150752-121151398	GM12878	blood:	n/a	n/a
7	BRCA1	chr3:121014343-121015554	Hela-S3	cervix:	n/a	n/a
8	CCNT2	chr3:121132208-121132533	K562	blood:	n/a	n/a
9	CEBPB	chr3:121137052-121137334	K562	blood:	n/a	n/a
10	CEBPB	chr3:121024403-121024693	IMR90	lung:	n/a	chr3:121024540-121024551
11	CEBPB	chr3:121133855-121133981	K562	blood:	n/a	n/a
12	CEBPB	chr3:121024454-121024688	A549	lung:	n/a	chr3:121024540-121024551
13	CEBPB	chr3:121038397-121038535	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:121133819-121134072	IMR90	lung:	n/a	n/a
15	CEBPB	chr3:121137038-121137374	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr3:121137039-121137410	K562	blood:	n/a	n/a
17	CEBPB	chr3:121014181-121015355	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr3:121133848-121133998	A549	lung:	n/a	n/a
19	CEBPB	chr3:121030012-121030161	K562	blood:	n/a	chr3:121030079-121030090
20	CEBPB	chr3:121137122-121137304	HepG2	liver:	n/a	n/a
21	CEBPB	chr3:121137029-121137429	A549	lung:	n/a	n/a
22	CEBPB	chr3:121137025-121137334	MCF-7	breast:	n/a	n/a
23	CEBPB	chr3:121137097-121137339	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:121137054-121137409	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:121038287-121038620	K562	blood:	n/a	n/a
26	CEBPB	chr3:121137032-121137414	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:121137051-121137400	A549	lung:	n/a	n/a
28	CEBPB	chr3:121162488-121162582	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr3:121136957-121137462	A549	lung:	n/a	n/a
30	CEBPB	chr3:121137032-121137414	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr3:121038299-121038614	A549	lung:	n/a	n/a
32	CEBPB	chr3:121137053-121137413	IMR90	lung:	n/a	n/a
33	CEBPB	chr3:121030037-121030310	HepG2	liver:	n/a	chr3:121030079-121030090
34	CEBPB	chr3:121024385-121024688	HepG2	liver:	n/a	chr3:121024540-121024551
35	CEBPB	chr3:121024511-121024633	H1-hESC	embryonic stem cell:	n/a	chr3:121024540-121024551
36	CEBPB	chr3:121137090-121137411	MCF-7	breast:	n/a	n/a
37	CEBPB	chr3:121162351-121162667	IMR90	lung:	n/a	n/a
38	CEBPB	chr3:121137031-121137348	ECC-1	luminal epithelium:	n/a	n/a
39	CTCF	chr3:121149200-121149350	GM12866	blood:	n/a	n/a
40	CTCF	chr3:121048077-121048187	MCF-7	breast:	n/a	chr3:121048109-121048130
41	CTCF	chr3:121048060-121048210	RPTEC	kidney:	n/a	chr3:121048109-121048130
42	CTCF	chr3:120973420-120973570	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:121048013-121048318	MCF-7	breast:	n/a	chr3:121048109-121048130
44	CTCF	chr3:121150660-121150810	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr3:121152700-121152850	GM12867	blood:	n/a	n/a
46	CTCF	chr3:121048028-121048210	MCF-7	breast:	n/a	chr3:121048109-121048130
47	CTCF	chr3:121150660-121150810	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr3:121118780-121118930	GM12869	blood:	n/a	n/a
49	CTCF	chr3:121130880-121131030	HMF	breast:	n/a	chr3:121130967-121130985 chr3:121130962-121130983
50	CTCF	chr3:121008200-121008350	GM12864	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:121142525-121142575	HEEpiC	esophagus:	n/a
2	chr3:121142525-121142575	HEEpiC	esophagus:	n/a
3	chr3:121150715-121150765	CMK	blood:	n/a
4	chr3:121025407-121025457	HEEpiC	esophagus:	n/a
5	chr3:121150715-121150765	SKMC	muscle:	n/a
6	chr3:121025407-121025457	HRE	kidney:	n/a
7	chr3:121150715-121150765	HUVEC	blood vessel:	n/a
8	chr3:121150715-121150765	NHDF-neo	bronchial:	n/a
9	chr3:121142525-121142575	NHBE	bronchial:	n/a
10	chr3:121025407-121025457	BE2_C	brain:	n/a
11	chr3:121025407-121025457	AG09319	gingival:	n/a
12	chr3:121150715-121150765	AoSMC	blood vessel:	n/a
13	chr3:121150715-121150765	A549	lung:	n/a
14	chr3:121151186-121151236	AG09309	skin:	n/a
15	chr3:121150715-121150765	GM06990	blood:	n/a
16	chr3:121142525-121142575	RPTEC	kidney:	n/a
17	chr3:121142525-121142575	MCF-7	breast:	n/a
18	chr3:121150715-121150765	AG04449	skin:	fetal
19	chr3:121151186-121151236	ProgFib	skin:	n/a
20	chr3:121151186-121151236	GM12892	blood:	n/a
21	chr3:121142525-121142575	LNCaP	prostate:	n/a
22	chr3:121025407-121025457	CMK	blood:	n/a
23	chr3:121151186-121151236	AG09319	gingival:	n/a
24	chr3:121150715-121150765	SAEC	small airway:	n/a
25	chr3:121151186-121151236	Jurkat	blood:	n/a
26	chr3:121025407-121025457	HepG2	liver:	n/a
27	chr3:121025407-121025457	IMR90	lung:	fetal
28	chr3:121151186-121151236	HRE	kidney:	n/a
29	chr3:121025407-121025457	NH-A	brain:	n/a
30	chr3:121150715-121150765	ovcar-3	ovarian:	n/a
31	chr3:121142525-121142575	Hepatocyte	liver:	n/a
32	chr3:121151186-121151236	H1-hESC	embryonic stem cell:	embryo
33	chr3:121150715-121150765	AG04450	lung:	fetal
34	chr3:121151186-121151236	GM19239	blood:	n/a
35	chr3:121142525-121142575	HCPEpiC	choroid plexus:	n/a
36	chr3:121025407-121025457	HEK293	kidney:	embryo
37	chr3:121150715-121150765	PFSK-1	brain:	n/a
38	chr3:121150715-121150765	HEEpiC	esophagus:	n/a
39	chr3:121025407-121025457	Jurkat	blood:	n/a
40	chr3:121150715-121150765	HCM	heart:	n/a
41	chr3:121150715-121150765	SK-N-SH	brain:	n/a
42	chr3:121150715-121150765	HEK293	kidney:	embryo
43	chr3:121142525-121142575	ovcar-3	ovarian:	n/a
44	chr3:121025407-121025457	RPTEC	kidney:	n/a
45	chr3:121151186-121151236	Caco-2	colon:	n/a
46	chr3:121151186-121151236	HL-60	blood:	n/a
47	chr3:121151186-121151236	GM12891	blood:	n/a
48	chr3:121025407-121025457	Caco-2	colon:	n/a
49	chr3:121150715-121150765	NH-A	brain:	n/a
50	chr3:121142525-121142575	Jurkat	blood:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:121183395..121185152-chr3:121186567..121189009,2	MCF-7	breast:
2	chr3:121152541..121155166-chr3:121158856..121160501,2	K562	blood:
3	chr3:121125400..121127225-chr3:121128769..121131952,3	K562	blood:
4	chr3:121138259..121140292-chr3:121185745..121188174,2	K562	blood:
5	chr3:121129952..121132930-chr3:121134868..121138546,3	K562	blood:
6	chr3:121181463..121184397-chr3:121190122..121192546,2	K562	blood:
7	chr3:121152758..121154352-chr3:121155971..121158501,2	MCF-7	breast:
8	chr3:121129952..121132930-chr3:121134868..121138546,3	K562	blood:
9	chr3:121181463..121184397-chr3:121190122..121192546,2	K562	blood:
10	chr3:121121830..121124199-chr3:121125934..121129748,5	K562	blood:
11	chr3:121185562..121187444-chr3:121190250..121193182,2	K562	blood:
12	chr3:121190019..121192256-chr3:121194520..121196847,2	K562	blood:
13	chr3:121183395..121185152-chr3:121186567..121189009,2	MCF-7	breast:
14	chr3:121135285..121138210-chr3:121139443..121141521,3	K562	blood:
15	chr3:121134688..121138349-chr3:121139086..121141700,5	K562	blood:
16	chr3:121190756..121192749-chr3:121194520..121196467,2	K562	blood:
17	chr3:121122561..121125182-chr3:121127949..121129748,3	K562	blood:
18	chr3:121122561..121125182-chr3:121127949..121129748,3	K562	blood:
19	chr20:17868453..17869206-chr3:121103732..121104423,2	MCF-7	breast:
20	chr3:121143314..121145833-chr3:121149976..121152815,2	MCF-7	breast:
21	chr3:121152541..121155166-chr3:121158856..121160501,2	K562	blood:
22	chr3:121158690..121160312-chr3:121166384..121168910,2	K562	blood:
23	chr3:121125400..121127225-chr3:121128769..121131952,3	K562	blood:
24	chr3:121047561..121048621-chr3:121247919..121248785,3	MCF-7	breast:
25	chr3:121138259..121140292-chr3:121185745..121188174,2	K562	blood:
26	chr3:121152758..121154352-chr3:121155971..121158501,2	MCF-7	breast:
27	chr3:121134688..121138349-chr3:121139086..121141700,5	K562	blood:
28	chr3:121158690..121160312-chr3:121166384..121168910,2	K562	blood:
29	chr3:121185944..121189270-chr3:121190973..121193182,3	K562	blood:
30	chr3:121135285..121138210-chr3:121139443..121141521,3	K562	blood:
31	chr3:121121830..121124199-chr3:121125934..121129748,5	K562	blood:
32	chr3:121004364..121006948-chr3:121012227..121014018,2	MCF-7	breast:
33	chr3:121004364..121006948-chr3:121012227..121014018,2	MCF-7	breast:
34	chr3:120133952..120135964-chr3:121186805..121189623,2	MCF-7	breast:
35	chr3:121143314..121145833-chr3:121149976..121152815,2	MCF-7	breast:
36	chr3:121185944..121189270-chr3:121190973..121193182,3	K562	blood:
37	chr3:121185562..121187444-chr3:121190250..121193182,2	K562	blood:
38	chr3:121150437..121151324-chr3:121212003..121212905,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARGFX-1	chr3:121075838-121076787	NONHSAT091471

No data

Variant related genes	Relation type
ENSG00000242103	TF binding region
ENSG00000242103	CpG island
ENSG00000233625	chromatin interactions

Extended variants
information (count: 6241 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:6241 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs338999	chr3:120970900-120970901	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373693099	chr3:120970980-120970981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs193105745	chr3:120971084-120971085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566769957	chr3:120971140-120971141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184171582	chr3:120971177-120971178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373574332	chr3:120971228-120971229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369035489	chr3:120971229-120971230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs386397759	chr3:120971236-120971237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35454737	chr3:120971251-120971252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552373008	chr3:120971252-120971253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188916648	chr3:120971282-120971283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538026585	chr3:120971393-120971394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370416706	chr3:120971436-120971437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555126318	chr3:120971472-120971473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181660888	chr3:120971483-120971484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534236354	chr3:120971519-120971520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553838643	chr3:120971558-120971559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546946806	chr3:120971617-120971618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138433578	chr3:120971636-120971637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546150739	chr3:120971638-120971639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148834479	chr3:120971642-120971643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185422421	chr3:120971656-120971657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143442716	chr3:120971700-120971701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189715941	chr3:120971710-120971711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529715824	chr3:120971794-120971795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546579866	chr3:120971857-120971858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559867112	chr3:120971859-120971860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532454360	chr3:120971918-120971919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552542526	chr3:120972009-120972010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569153888	chr3:120972017-120972018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538082002	chr3:120972027-120972028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148388400	chr3:120972101-120972102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74508775	chr3:120972103-120972104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548393323	chr3:120972115-120972116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75405916	chr3:120972200-120972201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115732915	chr3:120972247-120972248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72968036	chr3:120972288-120972289	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs554157982	chr3:120972304-120972305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143070299	chr3:120972325-120972326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373861850	chr3:120972343-120972344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146142731	chr3:120972383-120972384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551223216	chr3:120972428-120972429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548469728	chr3:120972450-120972451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs338998	chr3:120972618-120972619	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs373767147	chr3:120972645-120972646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74434277	chr3:120972656-120972657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7429411	chr3:120972657-120972658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7431446	chr3:120972658-120972659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34678687	chr3:120972673-120972674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs168118	chr3:120972675-120972676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	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
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	22241247	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	17953491	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:120962000-120993000	Weak transcription	Ovary	ovary
2	chr3:120980400-120982800	Weak transcription	Brain Germinal Matrix	brain
3	chr3:120993000-120993600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
4	chr3:120993000-120993800	ZNF genes & repeats	Ovary	ovary
5	chr3:120993200-120993600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:120993200-120993800	ZNF genes & repeats	Pancreas	Pancrea
7	chr3:120993400-120993800	ZNF genes & repeats	Gastric	stomach
8	chr3:120993800-120996600	Weak transcription	Ovary	ovary
9	chr3:120996600-120997200	Strong transcription	Ovary	ovary
10	chr3:120997200-121015600	Weak transcription	Ovary	ovary
11	chr3:121011800-121015600	Enhancers	HUVEC	blood vessel
12	chr3:121013000-121015800	Enhancers	Hela-S3	cervix
13	chr3:121014000-121015600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr3:121023600-121024400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr3:121023800-121024200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr3:121023800-121024400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr3:121033600-121052200	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr3:121043000-121043200	Enhancers	Ovary	ovary
19	chr3:121043200-121049000	Weak transcription	Ovary	ovary
20	chr3:121048400-121049400	Enhancers	Fetal Heart	heart
21	chr3:121049000-121050000	Strong transcription	Ovary	ovary
22	chr3:121049000-121050000	Enhancers	HSMMtube	muscle
23	chr3:121049400-121049600	Flanking Active TSS	Fetal Heart	heart
24	chr3:121049600-121049800	Enhancers	Fetal Heart	heart
25	chr3:121049600-121050000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr3:121049800-121050000	Flanking Active TSS	Fetal Heart	heart
27	chr3:121050000-121050600	Enhancers	Fetal Heart	heart
28	chr3:121050000-121051600	Weak transcription	Ovary	ovary
29	chr3:121051600-121052000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:121075800-121076200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
31	chr3:121081200-121081800	Enhancers	Hela-S3	cervix
32	chr3:121087600-121087800	Weak transcription	Ovary	ovary
33	chr3:121087600-121087800	Bivalent/Poised TSS	Right Atrium	heart
34	chr3:121087800-121088000	ZNF genes & repeats	Ovary	ovary
35	chr3:121088000-121092200	Weak transcription	Ovary	ovary
36	chr3:121088200-121099000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr3:121089400-121091600	Weak transcription	Brain Cingulate Gyrus	brain
38	chr3:121090200-121090800	ZNF genes & repeats	Brain Hippocampus Middle	brain
39	chr3:121090200-121090800	ZNF genes & repeats	Pancreas	Pancrea
40	chr3:121090200-121091000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr3:121090800-121094200	Weak transcription	Brain Hippocampus Middle	brain
42	chr3:121091400-121092800	Weak transcription	Brain Anterior Caudate	brain
43	chr3:121092200-121093000	Strong transcription	Ovary	ovary
44	chr3:121092600-121093000	ZNF genes & repeats	Gastric	stomach
45	chr3:121093000-121117000	Weak transcription	Ovary	ovary
46	chr3:121099200-121099400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:121099400-121099800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr3:121099400-121102800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:121099800-121101800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr3:121102800-121103000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links