Variant report

Variant	nsv519197
Chromosome Location	chr12:82831845-83056476
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1423)
CpG islands
(count:244)
Chromatin interactive
region (count:50)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1423 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:83021707-83022007	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:83044464-83044541	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:82917832-82918089	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	chr12:82832115-82832546	GM12878	blood:	n/a	n/a
7	ATF2	chr12:82832100-82832603	GM12878	blood:	n/a	n/a
8	ATF2	chr12:83044248-83044789	GM12878	blood:	n/a	n/a
9	ATF3	chr12:83045164-83045791	HCT-116	colon:	n/a	n/a
10	BACH1	chr12:83016592-83016711	K562	blood:	n/a	n/a
11	BATF	chr12:82986851-82987326	GM12878	blood:	n/a	n/a
12	BATF	chr12:82832164-82832441	GM12878	blood:	n/a	n/a
13	BATF	chr12:82875848-82876058	GM12878	blood:	n/a	chr12:82875962-82875973
14	BATF	chr12:82986910-82987255	GM12878	blood:	n/a	n/a
15	BATF	chr12:82834677-82835020	GM12878	blood:	n/a	n/a
16	BATF	chr12:83044408-83044763	GM12878	blood:	n/a	chr12:83044538-83044549
17	BATF	chr12:82987581-82987963	GM12878	blood:	n/a	n/a
18	BATF	chr12:82948434-82948657	GM12878	blood:	n/a	n/a
19	BATF	chr12:82832252-82832436	GM12878	blood:	n/a	n/a
20	BATF	chr12:82875809-82876048	GM12878	blood:	n/a	chr12:82875962-82875973
21	BATF	chr12:82987634-82987976	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:82986936-82987223	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:82832196-82832545	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:82987643-82987969	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:82986805-82987286	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:82987585-82987949	GM12878	blood:	n/a	n/a
27	BCL3	chr12:83044415-83044639	GM12878	blood:	n/a	chr12:83044604-83044613 chr12:83044605-83044614
28	BCLAF1	chr12:82920894-82921334	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:82910938-82911130	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:83045133-83045147	GM12878	blood:	n/a	n/a
31	BHLHE40	chr12:82987541-82988424	GM12878	blood:	n/a	n/a
32	BRCA1	chr12:83044386-83044808	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr12:82911060-82911109	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr12:82918265-82918268	GM12878	blood:	n/a	n/a
35	CBX3	chr12:83045217-83045776	HCT-116	colon:	n/a	n/a
36	CBX3	chr12:83044148-83044993	HCT-116	colon:	n/a	chr12:83044817-83044828
37	CBX3	chr12:83044197-83044987	HCT-116	colon:	n/a	chr12:83044817-83044828
38	CEBPB	chr12:82873334-82873694	IMR90	lung:	n/a	n/a
39	CEBPB	chr12:82979883-82980119	HepG2	liver:	n/a	chr12:82979961-82979972
40	CEBPB	chr12:82968759-82969085	HepG2	liver:	n/a	chr12:82968905-82968916 chr12:82968905-82968918 chr12:82968905-82968918 chr12:82968906-82968917
41	CEBPB	chr12:82993609-82993782	A549	lung:	n/a	n/a
42	CEBPB	chr12:82874485-82874521	K562	blood:	n/a	chr12:82874489-82874500
43	CEBPB	chr12:82961636-82961954	HepG2	liver:	n/a	chr12:82961813-82961824
44	CEBPB	chr12:83044118-83045067	HCT-116	colon:	n/a	n/a
45	CEBPB	chr12:82968751-82969105	Hela-S3	cervix:	n/a	chr12:82968905-82968916 chr12:82968905-82968918 chr12:82968905-82968918 chr12:82968906-82968917
46	CEBPB	chr12:82889679-82889933	A549	lung:	n/a	n/a
47	CEBPB	chr12:82873364-82873752	MCF-7	breast:	n/a	n/a
48	CEBPB	chr12:83045266-83045661	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr12:82889674-82889949	HepG2	liver:	n/a	n/a
50	CEBPB	chr12:82856754-82856805	K562	blood:	n/a	chr12:82856766-82856777

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:83041928-83041978	PrEC	prostate:	n/a
2	chr12:83053315-83053365	BJ	skin:	n/a
3	chr12:83053192-83053242	GM12878	blood:	n/a
4	chr12:83041928-83041978	BE2_C	brain:	n/a
5	chr12:83053229-83053279	CMK	blood:	n/a
6	chr12:83053229-83053279	SKMC	muscle:	n/a
7	chr12:83053192-83053242	Caco-2	colon:	n/a
8	chr12:83053229-83053279	Hela-S3	cervix:	n/a
9	chr12:83053229-83053279	PFSK-1	brain:	n/a
10	chr12:83053315-83053365	HMEC	breast:	n/a
11	chr12:83053229-83053279	HRE	kidney:	n/a
12	chr12:83053315-83053365	MCF-7	breast:	n/a
13	chr12:83053192-83053242	A549	lung:	n/a
14	chr12:83053192-83053242	GM12891	blood:	n/a
15	chr12:83041928-83041978	HCT-116	colon:	n/a
16	chr12:83053192-83053242	ProgFib	skin:	n/a
17	chr12:83053192-83053242	Hela-S3	cervix:	n/a
18	chr12:83053315-83053365	GM06990	blood:	n/a
19	chr12:83053229-83053279	HEK293	kidney:	embryo
20	chr12:83053229-83053279	SAEC	small airway:	n/a
21	chr12:83053315-83053365	HRPEpiC	eye:	n/a
22	chr12:83041928-83041978	SK-N-SH_RA	brain:	n/a
23	chr12:83053192-83053242	RPTEC	kidney:	n/a
24	chr12:83041928-83041978	Caco-2	colon:	n/a
25	chr12:83053192-83053242	HMEC	breast:	n/a
26	chr12:83053315-83053365	A549	lung:	n/a
27	chr12:83041928-83041978	NB4	blood:	n/a
28	chr12:83053192-83053242	NT2-D1	testis:	n/a
29	chr12:83053192-83053242	T-47D	breast:	n/a
30	chr12:83053229-83053279	HL-60	blood:	n/a
31	chr12:83053229-83053279	HMEC	breast:	n/a
32	chr12:83053229-83053279	HepG2	liver:	n/a
33	chr12:83053315-83053365	HCT-116	colon:	n/a
34	chr12:83053229-83053279	PANC-1	pancreas:	n/a
35	chr12:83041928-83041978	AG10803	skin:	n/a
36	chr12:83053315-83053365	Jurkat	blood:	n/a
37	chr12:83053315-83053365	U87	brain:	n/a
38	chr12:83053192-83053242	SKMC	muscle:	n/a
39	chr12:83053315-83053365	HPAEpiC	pulmonary alveolar:	n/a
40	chr12:83053192-83053242	SK-N-SH_RA	brain:	n/a
41	chr12:83053229-83053279	HRPEpiC	eye:	n/a
42	chr12:83053315-83053365	Hepatocyte	liver:	n/a
43	chr12:83053315-83053365	SKMC	muscle:	n/a
44	chr12:83053315-83053365	SK-N-MC	brain:	n/a
45	chr12:83053229-83053279	NHDF-neo	bronchial:	n/a
46	chr12:83053229-83053279	Hepatocyte	liver:	n/a
47	chr12:83053229-83053279	AoSMC	blood vessel:	n/a
48	chr12:83053229-83053279	NH-A	brain:	n/a
49	chr12:83053229-83053279	T-47D	breast:	n/a
50	chr12:83041928-83041978	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:82920672..82921613-chr12:83021112..83021885,4	MCF-7	breast:
2	chr12:82920677..82921535-chr12:83019931..83020685,2	MCF-7	breast:
3	chr12:82920677..82921535-chr12:83019931..83020685,2	MCF-7	breast:
4	chr12:82819815..82822098-chr12:82840091..82842622,2	MCF-7	breast:
5	chr12:83042183..83044298-chr12:83079732..83081351,2	MCF-7	breast:
6	chr12:82910494..82911273-chr12:84217531..84218136,2	MCF-7	breast:
7	chr12:82920722..82921355-chr12:84217213..84217834,2	MCF-7	breast:
8	chr12:83054169..83057951-chr12:83058253..83061323,3	MCF-7	breast:
9	chr12:82752165..82753058-chr12:83021424..83022313,3	MCF-7	breast:
10	chr12:82920686..82921567-chr12:83021333..83022314,4	MCF-7	breast:
11	chr12:82853805..82855324-chr12:82862383..82864290,2	MCF-7	breast:
12	chr12:82971566..82972433-chr13:51277425..51278166,2	MCF-7	breast:
13	chr12:83038079..83039947-chr12:83043283..83045373,2	MCF-7	breast:
14	chr12:82777410..82778076-chr12:83021381..83021922,3	MCF-7	breast:
15	chr12:83027721..83031479-chr12:83077251..83081760,5	MCF-7	breast:
16	chr12:82911302..82912194-chr12:84896846..84897638,2	MCF-7	breast:
17	chr12:82936658..82939200-chr2:183214684..183217154,2	MCF-7	breast:
18	chr12:83042670..83045643-chr12:83080310..83082308,2	MCF-7	breast:
19	chr12:82920672..82921613-chr12:83021112..83021885,4	MCF-7	breast:
20	chr12:82897683..82899798-chr12:82902108..82905656,3	K562	blood:
21	chr12:83045168..83046859-chr12:83077129..83078918,2	MCF-7	breast:
22	chr12:82925575..82927084-chr12:82928129..82930719,2	K562	blood:
23	chr12:82805259..82807721-chr12:82854362..82856467,2	MCF-7	breast:
24	chr12:82910516..82911793-chr12:83021377..83022217,4	MCF-7	breast:
25	chr12:83038079..83039947-chr12:83043283..83045373,2	MCF-7	breast:
26	chr12:82777578..82778449-chr12:82911138..82912044,4	MCF-7	breast:
27	chr12:82920697..82921255-chr12:83783256..83783780,2	MCF-7	breast:
28	chr12:82923391..82925939-chr12:82931956..82934379,2	MCF-7	breast:
29	chr12:82914569..82916151-chr12:82919148..82921113,2	MCF-7	breast:
30	chr12:82864287..82866811-chr3:130394292..130397010,2	MCF-7	breast:
31	chr12:82908001..82909681-chr12:82912211..82915012,2	MCF-7	breast:
32	chr12:83053691..83056419-chr12:83078760..83082343,3	MCF-7	breast:
33	chr12:83030541..83031126-chr2:73772566..73773410,2	MCF-7	breast:
34	chr12:82906271..82907794-chr12:82911019..82912547,2	MCF-7	breast:
35	chr12:83053486..83055016-chr12:83080125..83081869,2	MCF-7	breast:
36	chr12:82923391..82925939-chr12:82931956..82934379,2	MCF-7	breast:
37	chr12:82855086..82857984-chr12:82863232..82865138,2	MCF-7	breast:
38	chr12:82897683..82899798-chr12:82902108..82905656,3	K562	blood:
39	chr12:82908001..82909681-chr12:82912211..82915012,2	MCF-7	breast:
40	chr12:82914569..82916151-chr12:82919148..82921113,2	MCF-7	breast:
41	chr12:83052210..83053962-chr12:83070728..83072436,2	MCF-7	breast:
42	chr12:82920686..82921567-chr12:83021333..83022314,4	MCF-7	breast:
43	chr12:83041018..83042538-chr12:83044192..83045758,2	MCF-7	breast:
44	chr12:83041018..83042538-chr12:83044192..83045758,2	MCF-7	breast:
45	chr12:82750650..82752724-chr12:82920411..82922639,2	MCF-7	breast:
46	chr12:82910516..82911793-chr12:83021377..83022217,4	MCF-7	breast:
47	chr12:82853805..82855324-chr12:82862383..82864290,2	MCF-7	breast:
48	chr12:82925575..82927084-chr12:82928129..82930719,2	K562	blood:
49	chr12:82753521..82754075-chr12:83021392..83022207,3	MCF-7	breast:
50	chr12:82855086..82857984-chr12:82863232..82865138,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMTC2-4	chr12:82862235-82862727	NONHSAT029720
2	lnc-CCDC59-4	chr12:82954894-82954933	XLOC_010141
3	lnc-C12orf26-1	chr12:82906456-82909596	ENSG00000257431
4	lnc-CCDC59-3	chr12:82898990-82899178	ENSG00000257837
5	lnc-CCDC59-2	chr12:82891313-82891339	ENSG00000258170.1
6	lnc-CCDC59-4	chr12:82950644-82950876	XLOC_010141
7	lnc-CCDC59-2	chr12:82875739-82875807	ENSG00000258170.1
8	lnc-CCDC59-3	chr12:82899880-82899967	ENSG00000257837
9	lnc-CCDC59-2	chr12:82874897-82875259	ENSG00000258170.1

No data

Variant related genes	Relation type
ENSG00000257837	TF binding region
ENSG00000257875	TF binding region
METTL25	TF binding region
ENSG00000258170	TF binding region
ENSG00000257431	TF binding region
ENSG00000257837	CpG island
ENSG00000257875	CpG island
METTL25	CpG island
ENSG00000258170	CpG island
ENSG00000257431	CpG island
ENSG00000257431	chromatin interactions
ENSG00000133773	chromatin interactions
ENSG00000127720	chromatin interactions
ENSG00000179104	chromatin interactions
NAA15	miRNA target sites
N4BP1	miRNA target sites

Extended variants
information (count: 5234 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:5234 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17719063	chr12:82831845-82831846	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs61929493	chr12:82831887-82831888	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs371584712	chr12:82831913-82831914	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563266818	chr12:82831967-82831968	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs530622466	chr12:82832024-82832025	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs34077051	chr12:82832042-82832043	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs186704277	chr12:82832055-82832056	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs552260812	chr12:82832075-82832076	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs189487539	chr12:82832086-82832087	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs528649446	chr12:82832089-82832090	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs117128815	chr12:82832132-82832133	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs139998011	chr12:82832159-82832160	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs535744655	chr12:82832219-82832220	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs181181552	chr12:82832232-82832233	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs376268570	chr12:82832260-82832261	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs568872997	chr12:82832286-82832287	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs201478510	chr12:82832291-82832292	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs536041422	chr12:82832292-82832293	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs58370071	chr12:82832306-82832307	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376276005	chr12:82832309-82832310	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539563152	chr12:82832400-82832401	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77870060	chr12:82832407-82832408	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149449024	chr12:82832411-82832412	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2717448	chr12:82832418-82832419	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs199570487	chr12:82832452-82832453	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs372571599	chr12:82832468-82832469	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376346738	chr12:82832475-82832476	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148345125	chr12:82832519-82832520	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371509833	chr12:82832548-82832549	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186814835	chr12:82832564-82832565	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200336143	chr12:82832592-82832593	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557077694	chr12:82832600-82832601	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574830565	chr12:82832609-82832610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373543468	chr12:82832612-82832613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376218644	chr12:82832617-82832618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536261739	chr12:82832624-82832625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563282195	chr12:82832648-82832649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541472485	chr12:82832668-82832669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555001252	chr12:82832691-82832692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575277390	chr12:82832698-82832699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190342032	chr12:82832707-82832708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564054412	chr12:82832714-82832715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183264415	chr12:82832754-82832755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546924817	chr12:82832779-82832780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562263205	chr12:82832817-82832818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530692258	chr12:82832819-82832820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555950283	chr12:82832833-82832834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573397200	chr12:82832837-82832838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529552933	chr12:82832861-82832862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550830731	chr12:82832867-82832868	Weak transcription Strong transcription	n/a	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	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:82758400-82835600	Weak transcription	Psoas Muscle	Psoas
2	chr12:82783000-82838000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr12:82789200-82833800	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr12:82791200-82852000	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr12:82793400-82834400	Weak transcription	Liver	Liver
6	chr12:82793600-82833000	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr12:82793600-82833200	Weak transcription	Primary B cells from cord blood	blood
8	chr12:82802200-82834400	Weak transcription	Aorta	Aorta
9	chr12:82802200-82834400	Weak transcription	Ovary	ovary
10	chr12:82803600-82852000	Weak transcription	Left Ventricle	heart
11	chr12:82804600-82869400	Weak transcription	Colon Smooth Muscle	Colon
12	chr12:82809600-82832000	Weak transcription	Adipose Nuclei	Adipose
13	chr12:82809600-82834400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr12:82819600-82833400	Weak transcription	Primary T cells from cord blood	blood
15	chr12:82819600-82835600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr12:82821000-82836200	Weak transcription	Fetal Heart	heart
17	chr12:82821200-82836800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr12:82822400-82862000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr12:82822800-82835600	Weak transcription	Primary hematopoietic stem cells	blood
20	chr12:82823000-82852400	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr12:82823000-82862200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr12:82823200-82834400	Weak transcription	Fetal Intestine Large	intestine
23	chr12:82823200-82868000	Weak transcription	Brain Angular Gyrus	brain
24	chr12:82824200-82850000	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr12:82824200-82868200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr12:82825000-82833600	Weak transcription	Primary B cells from peripheral blood	blood
27	chr12:82825200-82851400	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr12:82825400-82833000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr12:82825600-82833400	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr12:82826000-82835600	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr12:82826400-82843000	Weak transcription	Brain Substantia Nigra	brain
32	chr12:82826400-82844400	Weak transcription	Fetal Kidney	kidney
33	chr12:82827000-82834000	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr12:82827200-82862200	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr12:82827400-82837600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr12:82828400-82835800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr12:82828600-82835800	Weak transcription	Duodenum Mucosa	Duodenum
38	chr12:82828600-82852200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr12:82828800-82834400	Weak transcription	Brain Anterior Caudate	brain
40	chr12:82829000-82835600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr12:82829600-82836200	Weak transcription	HSMMtube	muscle
42	chr12:82830000-82836200	Weak transcription	Fetal Lung	lung
43	chr12:82830000-82836800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr12:82830200-82836800	Weak transcription	HSMM	muscle
45	chr12:82831400-82862200	Weak transcription	Pancreas	Pancrea
46	chr12:82831800-82841200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:82832000-82832600	Enhancers	NHEK	skin
48	chr12:82832000-82834400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:82832000-82837000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr12:82832000-82840000	Strong transcription	Adipose Nuclei	Adipose

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