Variant report

Variant	nsv1053649
Chromosome Location	chr12:82893253-83054109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1208)
CpG islands
(count:244)
Chromatin interactive
region (count:42)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1208 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:83044464-83044541	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:82917832-82918089	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:83021707-83022007	HepG2	liver:	n/a	n/a
4	ATF1	chr12:83043553-83043580	K562	blood:	n/a	n/a
5	ATF2	chr12:83044271-83044754	GM12878	blood:	n/a	n/a
6	ATF2	chr12:83044248-83044789	GM12878	blood:	n/a	n/a
7	ATF3	chr12:83045164-83045791	HCT-116	colon:	n/a	n/a
8	BACH1	chr12:83016592-83016711	K562	blood:	n/a	n/a
9	BATF	chr12:82987581-82987963	GM12878	blood:	n/a	n/a
10	BATF	chr12:82987634-82987976	GM12878	blood:	n/a	n/a
11	BATF	chr12:83044408-83044763	GM12878	blood:	n/a	chr12:83044538-83044549
12	BATF	chr12:82986910-82987255	GM12878	blood:	n/a	n/a
13	BATF	chr12:82948434-82948657	GM12878	blood:	n/a	n/a
14	BATF	chr12:82986851-82987326	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:82987585-82987949	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:82986936-82987223	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:82987643-82987969	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:82986805-82987286	GM12878	blood:	n/a	n/a
19	BCL3	chr12:83044415-83044639	GM12878	blood:	n/a	chr12:83044604-83044613 chr12:83044605-83044614
20	BCLAF1	chr12:82920894-82921334	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:82910938-82911130	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:83045133-83045147	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:82987541-82988424	GM12878	blood:	n/a	n/a
24	BRCA1	chr12:83044386-83044808	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr12:82918265-82918268	GM12878	blood:	n/a	n/a
26	BRCA1	chr12:82911060-82911109	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr12:83045217-83045776	HCT-116	colon:	n/a	n/a
28	CBX3	chr12:83044197-83044987	HCT-116	colon:	n/a	chr12:83044817-83044828
29	CBX3	chr12:83044148-83044993	HCT-116	colon:	n/a	chr12:83044817-83044828
30	CEBPB	chr12:83045105-83045838	HCT-116	colon:	n/a	n/a
31	CEBPB	chr12:82968751-82969105	Hela-S3	cervix:	n/a	chr12:82968905-82968916 chr12:82968905-82968918 chr12:82968905-82968918 chr12:82968906-82968917
32	CEBPB	chr12:83044331-83045039	A549	lung:	n/a	n/a
33	CEBPB	chr12:82993609-82993782	A549	lung:	n/a	n/a
34	CEBPB	chr12:83045358-83045688	MCF-7	breast:	n/a	n/a
35	CEBPB	chr12:82949480-82949871	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr12:83044118-83045067	HCT-116	colon:	n/a	n/a
37	CEBPB	chr12:83045261-83045751	A549	lung:	n/a	n/a
38	CEBPB	chr12:83045266-83045661	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr12:83008215-83008326	A549	lung:	n/a	chr12:83008283-83008294 chr12:83008283-83008296 chr12:83008283-83008296 chr12:83008283-83008294
40	CEBPB	chr12:82903791-82904276	MCF-7	breast:	n/a	n/a
41	CEBPB	chr12:82961669-82961955	A549	lung:	n/a	chr12:82961813-82961824
42	CEBPB	chr12:82961636-82961954	HepG2	liver:	n/a	chr12:82961813-82961824
43	CEBPB	chr12:83037699-83038002	HepG2	liver:	n/a	chr12:83037843-83037854
44	CEBPB	chr12:83044302-83045046	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr12:82925137-82925285	A549	lung:	n/a	n/a
46	CEBPB	chr12:82968759-82969085	HepG2	liver:	n/a	chr12:82968905-82968916 chr12:82968905-82968918 chr12:82968905-82968918 chr12:82968906-82968917
47	CEBPB	chr12:82972449-82973087	Hela-S3	cervix:	n/a	chr12:82972661-82972672 chr12:82972661-82972674 chr12:82972661-82972672
48	CEBPB	chr12:82979883-82980119	HepG2	liver:	n/a	chr12:82979961-82979972
49	CHD1	chr12:82987653-82988083	GM12878	blood:	n/a	n/a
50	CHD2	chr12:83044391-83045043	Hela-S3	cervix:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:83053315-83053365	HepG2	liver:	n/a
2	chr12:83053192-83053242	NT2-D1	testis:	n/a
3	chr12:83053192-83053242	HL-60	blood:	n/a
4	chr12:83053229-83053279	HEEpiC	esophagus:	n/a
5	chr12:83053315-83053365	RPTEC	kidney:	n/a
6	chr12:83053315-83053365	PANC-1	pancreas:	n/a
7	chr12:83041928-83041978	HRPEpiC	eye:	n/a
8	chr12:83053229-83053279	GM19239	blood:	n/a
9	chr12:83053192-83053242	Jurkat	blood:	n/a
10	chr12:83053192-83053242	HNPCEpiC	eye:	n/a
11	chr12:83053315-83053365	LNCaP	prostate:	n/a
12	chr12:83053192-83053242	H1-hESC	embryonic stem cell:	embryo
13	chr12:83053229-83053279	NHBE	bronchial:	n/a
14	chr12:83053192-83053242	CMK	blood:	n/a
15	chr12:83053229-83053279	HIPEpiC	eye:	n/a
16	chr12:83053229-83053279	IMR90	lung:	fetal
17	chr12:83053229-83053279	Jurkat	blood:	n/a
18	chr12:83053315-83053365	GM12891	blood:	n/a
19	chr12:83053229-83053279	PFSK-1	brain:	n/a
20	chr12:83041928-83041978	SKMC	muscle:	n/a
21	chr12:83053192-83053242	HRPEpiC	eye:	n/a
22	chr12:83041928-83041978	AG09319	gingival:	n/a
23	chr12:83053192-83053242	HIPEpiC	eye:	n/a
24	chr12:83053192-83053242	Caco-2	colon:	n/a
25	chr12:83053192-83053242	SK-N-SH_RA	brain:	n/a
26	chr12:83041928-83041978	RPTEC	kidney:	n/a
27	chr12:83053229-83053279	GM12891	blood:	n/a
28	chr12:83053315-83053365	AG04450	lung:	fetal
29	chr12:83053315-83053365	SK-N-SH	brain:	n/a
30	chr12:83041928-83041978	Hepatocyte	liver:	n/a
31	chr12:83053192-83053242	SK-N-SH	brain:	n/a
32	chr12:83053229-83053279	HepG2	liver:	n/a
33	chr12:83041928-83041978	GM19239	blood:	n/a
34	chr12:83053315-83053365	AG09319	gingival:	n/a
35	chr12:83053192-83053242	SKMC	muscle:	n/a
36	chr12:83053192-83053242	U87	brain:	n/a
37	chr12:83053229-83053279	ovcar-3	ovarian:	n/a
38	chr12:83053192-83053242	AG04450	lung:	fetal
39	chr12:83053229-83053279	Hela-S3	cervix:	n/a
40	chr12:83041928-83041978	SK-N-SH	brain:	n/a
41	chr12:83053315-83053365	HCM	heart:	n/a
42	chr12:83053192-83053242	SAEC	small airway:	n/a
43	chr12:83053229-83053279	MCF-7	breast:	n/a
44	chr12:83053315-83053365	HCT-116	colon:	n/a
45	chr12:83053315-83053365	GM12878	blood:	n/a
46	chr12:83053229-83053279	SK-N-MC	brain:	n/a
47	chr12:83053315-83053365	U87	brain:	n/a
48	chr12:83053192-83053242	GM12892	blood:	n/a
49	chr12:83053192-83053242	HCT-116	colon:	n/a
50	chr12:83053229-83053279	AG09319	gingival:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:82752165..82753058-chr12:83021424..83022313,3	MCF-7	breast:
2	chr12:82925575..82927084-chr12:82928129..82930719,2	K562	blood:
3	chr12:82777410..82778076-chr12:83021381..83021922,3	MCF-7	breast:
4	chr12:83053486..83055016-chr12:83080125..83081869,2	MCF-7	breast:
5	chr12:83027721..83031479-chr12:83077251..83081760,5	MCF-7	breast:
6	chr12:82908001..82909681-chr12:82912211..82915012,2	MCF-7	breast:
7	chr12:83052210..83053962-chr12:83070728..83072436,2	MCF-7	breast:
8	chr12:82911302..82912194-chr12:84896846..84897638,2	MCF-7	breast:
9	chr12:83053691..83056419-chr12:83078760..83082343,3	MCF-7	breast:
10	chr12:82923391..82925939-chr12:82931956..82934379,2	MCF-7	breast:
11	chr12:82914569..82916151-chr12:82919148..82921113,2	MCF-7	breast:
12	chr12:82925575..82927084-chr12:82928129..82930719,2	K562	blood:
13	chr12:82920686..82921567-chr12:83021333..83022314,4	MCF-7	breast:
14	chr12:82753521..82754075-chr12:83021392..83022207,3	MCF-7	breast:
15	chr12:82906271..82907794-chr12:82911019..82912547,2	MCF-7	breast:
16	chr12:82920722..82921355-chr12:84217213..84217834,2	MCF-7	breast:
17	chr12:82910494..82911273-chr12:84217531..84218136,2	MCF-7	breast:
18	chr12:82920672..82921613-chr12:83021112..83021885,4	MCF-7	breast:
19	chr12:82897683..82899798-chr12:82902108..82905656,3	K562	blood:
20	chr12:82920697..82921255-chr12:83783256..83783780,2	MCF-7	breast:
21	chr12:83038079..83039947-chr12:83043283..83045373,2	MCF-7	breast:
22	chr12:83030541..83031126-chr2:73772566..73773410,2	MCF-7	breast:
23	chr12:83038079..83039947-chr12:83043283..83045373,2	MCF-7	breast:
24	chr12:82750650..82752724-chr12:82920411..82922639,2	MCF-7	breast:
25	chr12:82908001..82909681-chr12:82912211..82915012,2	MCF-7	breast:
26	chr12:82777578..82778449-chr12:82911138..82912044,4	MCF-7	breast:
27	chr12:82920672..82921613-chr12:83021112..83021885,4	MCF-7	breast:
28	chr12:82923391..82925939-chr12:82931956..82934379,2	MCF-7	breast:
29	chr12:83042670..83045643-chr12:83080310..83082308,2	MCF-7	breast:
30	chr12:82897683..82899798-chr12:82902108..82905656,3	K562	blood:
31	chr12:83042183..83044298-chr12:83079732..83081351,2	MCF-7	breast:
32	chr12:82914569..82916151-chr12:82919148..82921113,2	MCF-7	breast:
33	chr12:83041018..83042538-chr12:83044192..83045758,2	MCF-7	breast:
34	chr12:82971566..82972433-chr13:51277425..51278166,2	MCF-7	breast:
35	chr12:82910516..82911793-chr12:83021377..83022217,4	MCF-7	breast:
36	chr12:82920677..82921535-chr12:83019931..83020685,2	MCF-7	breast:
37	chr12:82920677..82921535-chr12:83019931..83020685,2	MCF-7	breast:
38	chr12:82910516..82911793-chr12:83021377..83022217,4	MCF-7	breast:
39	chr12:83045168..83046859-chr12:83077129..83078918,2	MCF-7	breast:
40	chr12:82936658..82939200-chr2:183214684..183217154,2	MCF-7	breast:
41	chr12:82920686..82921567-chr12:83021333..83022314,4	MCF-7	breast:
42	chr12:83041018..83042538-chr12:83044192..83045758,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC59-4	chr12:82954894-82954933	XLOC_010141
2	lnc-CCDC59-4	chr12:82950644-82950876	XLOC_010141
3	lnc-CCDC59-3	chr12:82899880-82899967	ENSG00000257837
4	lnc-C12orf26-1	chr12:82906456-82909596	ENSG00000257431
5	lnc-CCDC59-3	chr12:82898990-82899178	ENSG00000257837

No data

Variant related genes	Relation type
ENSG00000257837	TF binding region
ENSG00000258170	TF binding region
ENSG00000257431	TF binding region
ENSG00000257837	CpG island
ENSG00000258170	CpG island
ENSG00000257431	CpG island
ENSG00000133773	chromatin interactions
ENSG00000257431	chromatin interactions
ENSG00000127720	chromatin interactions
ENSG00000179104	chromatin interactions
N4BP1	miRNA target sites
NAA15	miRNA target sites

Extended variants
information (count: 3308 )
Associated
traits (count: 68 )

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	rs554668629	chr12:82893459-82893460	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs576147550	chr12:82893501-82893502	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs543515121	chr12:82893504-82893505	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs12304203	chr12:82893518-82893519	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs562710745	chr12:82893529-82893530	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs112820563	chr12:82893533-82893534	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs75864902	chr12:82893544-82893545	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs13377737	chr12:82893572-82893573	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs13377738	chr12:82893575-82893576	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs78529607	chr12:82893632-82893633	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs75842690	chr12:82893669-82893670	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs567238874	chr12:82893696-82893697	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs543427889	chr12:82893703-82893704	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs185123081	chr12:82897651-82897652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551538362	chr12:82897673-82897674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190750059	chr12:82897678-82897679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141461809	chr12:82897760-82897761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530509896	chr12:82897780-82897781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs80244414	chr12:82897877-82897878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567718423	chr12:82897898-82897899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538576441	chr12:82897907-82897908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115143946	chr12:82897911-82897912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376712529	chr12:82897912-82897913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs57375394	chr12:82897925-82897926	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs150440963	chr12:82897974-82897975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183458122	chr12:82898141-82898142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572220501	chr12:82898165-82898166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138372187	chr12:82898182-82898183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35040515	chr12:82898189-82898190	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs77884563	chr12:82898226-82898227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146142327	chr12:82898256-82898257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76976926	chr12:82898259-82898260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532986695	chr12:82898468-82898469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551420329	chr12:82898502-82898503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76668203	chr12:82898531-82898532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114402116	chr12:82898541-82898542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548800412	chr12:82898577-82898578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73155441	chr12:82898625-82898626	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs538038524	chr12:82898661-82898662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558765569	chr12:82898690-82898691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143311954	chr12:82898826-82898827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577203560	chr12:82898842-82898843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544481017	chr12:82898866-82898867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550476930	chr12:82898867-82898868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187897180	chr12:82898896-82898897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562772186	chr12:82898921-82898922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541619979	chr12:82898922-82898923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553757217	chr12:82898961-82898962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530086767	chr12:82899000-82899001	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs139027012	chr12:82899002-82899003	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:82897600-82899400	Enhancers	HUVEC	blood vessel
2	chr12:82898200-82899000	Enhancers	Fetal Kidney	kidney
3	chr12:82898400-82899600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:82899400-82899800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr12:82903000-82903200	Enhancers	Fetal Stomach	stomach
6	chr12:82903400-82904600	Weak transcription	Fetal Stomach	stomach
7	chr12:82904600-82905200	Enhancers	Fetal Stomach	stomach
8	chr12:82907600-82908400	Enhancers	Fetal Heart	heart
9	chr12:82908400-82909000	Flanking Active TSS	Fetal Heart	heart
10	chr12:82909000-82909800	Enhancers	Fetal Heart	heart
11	chr12:82916400-82916600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:82916400-82916800	Enhancers	Pancreas	Pancrea
13	chr12:82916400-82917000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr12:82916400-82917600	Enhancers	Fetal Intestine Large	intestine
15	chr12:82916600-82917000	Enhancers	Fetal Muscle Leg	muscle
16	chr12:82916800-82919000	Enhancers	Fetal Stomach	stomach
17	chr12:82917000-82917600	Enhancers	A549	lung
18	chr12:82917000-82918000	Weak transcription	Fetal Muscle Leg	muscle
19	chr12:82917200-82917600	Enhancers	Liver	Liver
20	chr12:82917200-82917600	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr12:82917200-82918000	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr12:82917200-82918200	Enhancers	Brain Hippocampus Middle	brain
23	chr12:82917400-82917600	Enhancers	HepG2	liver
24	chr12:82917600-82917800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr12:82917600-82917800	Flanking Active TSS	HepG2	liver
26	chr12:82917600-82918000	Active TSS	Fetal Intestine Large	intestine
27	chr12:82917600-82918000	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr12:82917600-82918200	Flanking Active TSS	Liver	Liver
29	chr12:82917600-82918200	Enhancers	Brain Cingulate Gyrus	brain
30	chr12:82917600-82918400	Enhancers	Fetal Kidney	kidney
31	chr12:82917600-82918600	Flanking Active TSS	A549	lung
32	chr12:82917600-82919000	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr12:82917600-82919000	Enhancers	Brain Angular Gyrus	brain
34	chr12:82917600-82919000	Enhancers	Brain Anterior Caudate	brain
35	chr12:82917600-82919000	Enhancers	Fetal Heart	heart
36	chr12:82917600-82919200	Enhancers	Brain Substantia Nigra	brain
37	chr12:82917600-82920000	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr12:82917800-82918000	Enhancers	HepG2	liver
39	chr12:82917800-82918600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:82917800-82918800	Enhancers	Fetal Lung	lung
41	chr12:82917800-82919200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr12:82918000-82918200	Enhancers	Fetal Muscle Leg	muscle
43	chr12:82918000-82918400	Flanking Active TSS	HepG2	liver
44	chr12:82918000-82918600	Enhancers	Fetal Intestine Small	intestine
45	chr12:82918000-82919000	Enhancers	Fetal Intestine Large	intestine
46	chr12:82918200-82918600	Active TSS	Brain Cingulate Gyrus	brain
47	chr12:82918200-82918800	Flanking Active TSS	Brain Hippocampus Middle	brain
48	chr12:82918200-82919000	Enhancers	Liver	Liver
49	chr12:82918400-82918600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr12:82918400-82918800	Enhancers	HepG2	liver

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