Variant report

Variant	nsv1045476
Chromosome Location	chr12:124127003-124174020
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:537)
CpG islands
(count:794)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:124165973-124166596	GM12878	blood:	n/a	n/a
2	ATF2	chr12:124165813-124166609	GM12878	blood:	n/a	n/a
3	ATF2	chr12:124144752-124145277	GM12878	blood:	n/a	n/a
4	ATF2	chr12:124172381-124172960	GM12878	blood:	n/a	n/a
5	ATF2	chr12:124172426-124172866	GM12878	blood:	n/a	n/a
6	BATF	chr12:124144875-124145201	GM12878	blood:	n/a	chr12:124145072-124145083
7	BATF	chr12:124144904-124145195	GM12878	blood:	n/a	chr12:124145072-124145083
8	BATF	chr12:124172432-124172890	GM12878	blood:	n/a	n/a
9	BATF	chr12:124166177-124166501	GM12878	blood:	n/a	n/a
10	BATF	chr12:124172484-124172812	GM12878	blood:	n/a	n/a
11	BATF	chr12:124166147-124166490	GM12878	blood:	n/a	n/a
12	BCL11A	chr12:124166091-124166461	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:124172540-124172846	GM12878	blood:	n/a	n/a
14	BCL11A	chr12:124172504-124172853	GM12878	blood:	n/a	n/a
15	BCLAF1	chr12:124139925-124140367	GM12878	blood:	n/a	n/a
16	BCLAF1	chr12:124166045-124166526	GM12878	blood:	n/a	n/a
17	BCLAF1	chr12:124172411-124172914	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:124166226-124166361	GM12878	blood:	n/a	n/a
19	BHLHE40	chr12:124146182-124146377	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:124172483-124172783	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:124139600-124140393	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:124155699-124155729	K562	blood:	n/a	n/a
23	BRCA1	chr12:124133994-124134134	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr12:124147878-124148212	K562	blood:	n/a	n/a
25	CEBPB	chr12:124172369-124173000	GM12878	blood:	n/a	n/a
26	CEBPB	chr12:124155361-124155613	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr12:124163947-124163977	HepG2	liver:	n/a	chr12:124163964-124163975
28	CEBPB	chr12:124155348-124155869	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr12:124166289-124166474	K562	blood:	n/a	chr12:124166370-124166381
30	CEBPB	chr12:124166279-124166491	IMR90	lung:	n/a	chr12:124166370-124166381
31	CEBPB	chr12:124166212-124166455	A549	lung:	n/a	chr12:124166370-124166381
32	CEBPB	chr12:124146558-124146645	K562	blood:	n/a	chr12:124146632-124146643
33	CEBPB	chr12:124146435-124146820	MCF-7	breast:	n/a	chr12:124146632-124146643
34	CEBPB	chr12:124144925-124145317	IMR90	lung:	n/a	n/a
35	CEBPB	chr12:124163883-124164027	K562	blood:	n/a	chr12:124163964-124163975
36	CEBPB	chr12:124144964-124145165	K562	blood:	n/a	n/a
37	CEBPB	chr12:124155498-124155638	K562	blood:	n/a	n/a
38	CEBPB	chr12:124144941-124145298	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr12:124146622-124146730	HepG2	liver:	n/a	chr12:124146632-124146643
40	CEBPB	chr12:124144822-124145387	A549	lung:	n/a	n/a
41	CEBPB	chr12:124144926-124145288	MCF-7	breast:	n/a	n/a
42	CEBPB	chr12:124144946-124145307	A549	lung:	n/a	n/a
43	CEBPB	chr12:124155414-124155714	HepG2	liver:	n/a	n/a
44	CEBPB	chr12:124144969-124145294	K562	blood:	n/a	n/a
45	CEBPB	chr12:124166291-124166506	HepG2	liver:	n/a	chr12:124166370-124166381
46	CHD2	chr12:124155426-124155905	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr12:124155480-124155761	K562	blood:	n/a	n/a
48	CHD2	chr12:124155466-124155802	GM12878	blood:	n/a	n/a
49	CHD2	chr12:124155500-124155791	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr12:124155556-124155802	HepG2	liver:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124155579-124155629	AG09309	skin:	n/a
2	chr12:124155579-124155629	AG09309	skin:	n/a
3	chr12:124155712-124155762	HNPCEpiC	eye:	n/a
4	chr12:124145110-124145160	PrEC	prostate:	n/a
5	chr12:124154378-124154428	BJ	skin:	n/a
6	chr12:124144432-124144482	AG04450	lung:	fetal
7	chr12:124155712-124155762	ovcar-3	ovarian:	n/a
8	chr12:124144432-124144482	PANC-1	pancreas:	n/a
9	chr12:124155594-124155644	SK-N-SH_RA	brain:	n/a
10	chr12:124155458-124155508	HCF	heart:	n/a
11	chr12:124155712-124155762	MCF10A-Er-Src	breast:	n/a
12	chr12:124155712-124155762	Jurkat	blood:	n/a
13	chr12:124155880-124155930	NT2-D1	testis:	n/a
14	chr12:124144432-124144482	HMEC	breast:	n/a
15	chr12:124144432-124144482	BJ	skin:	n/a
16	chr12:124154378-124154428	Hela-S3	cervix:	n/a
17	chr12:124155594-124155644	HL-60	blood:	n/a
18	chr12:124145110-124145160	NH-A	brain:	n/a
19	chr12:124156170-124156220	AG10803	skin:	n/a
20	chr12:124144432-124144482	HCM	heart:	n/a
21	chr12:124155620-124155670	HIPEpiC	eye:	n/a
22	chr12:124155579-124155629	NT2-D1	testis:	n/a
23	chr12:124154378-124154428	NHDF-neo	bronchial:	n/a
24	chr12:124154378-124154428	HCM	heart:	n/a
25	chr12:124156170-124156220	HEEpiC	esophagus:	n/a
26	chr12:124145110-124145160	RPTEC	kidney:	n/a
27	chr12:124155620-124155670	H1-hESC	embryonic stem cell:	embryo
28	chr12:124156159-124156209	MCF-7	breast:	n/a
29	chr12:124158499-124158549	HRCEpiC	kidney:	n/a
30	chr12:124155880-124155930	MCF10A-Er-Src	breast:	n/a
31	chr12:124155579-124155629	HCF	heart:	n/a
32	chr12:124155880-124155930	NB4	blood:	n/a
33	chr12:124145110-124145160	AoSMC	blood vessel:	n/a
34	chr12:124154378-124154428	HEK293	kidney:	embryo
35	chr12:124155880-124155930	HMEC	breast:	n/a
36	chr12:124155458-124155508	SKMC	muscle:	n/a
37	chr12:124155451-124155501	BE2_C	brain:	n/a
38	chr12:124156170-124156220	MCF10A-Er-Src	breast:	n/a
39	chr12:124155458-124155508	AG04450	lung:	fetal
40	chr12:124144432-124144482	SK-N-SH_RA	brain:	n/a
41	chr12:124155594-124155644	HCT-116	colon:	n/a
42	chr12:124155620-124155670	GM06990	blood:	n/a
43	chr12:124145110-124145160	HCT-116	colon:	n/a
44	chr12:124154378-124154428	SK-N-SH_RA	brain:	n/a
45	chr12:124156159-124156209	MCF10A-Er-Src	breast:	n/a
46	chr12:124156159-124156209	SAEC	small airway:	n/a
47	chr12:124144432-124144482	T-47D	breast:	n/a
48	chr12:124154378-124154428	GM06990	blood:	n/a
49	chr12:124155620-124155670	SK-N-SH_RA	brain:	n/a
50	chr12:124155712-124155762	NT2-D1	testis:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:124128608..124131370-chr12:124135245..124137740,4	K562	blood:
2	chr12:124117712..124121219-chr12:124140785..124143591,3	K562	blood:
3	chr12:124157626..124159857-chr12:124196461..124198464,2	MCF-7	breast:
4	chr12:124117633..124120865-chr12:124133499..124139438,5	K562	blood:
5	chr12:124137852..124140530-chr12:124458317..124460698,2	K562	blood:
6	chr12:124127308..124129753-chr12:124158031..124160799,2	K562	blood:
7	chr12:124154247..124158137-chr12:124158575..124163340,6	K562	blood:
8	chr12:124130618..124132144-chr12:124154341..124156246,2	MCF-7	breast:
9	chr12:124157962..124160129-chr12:124161284..124163771,2	MCF-7	breast:
10	chr12:124117774..124119426-chr12:124160532..124162075,2	K562	blood:
11	chr12:124120301..124122353-chr12:124128299..124130201,3	K562	blood:
12	chr12:124116692..124118630-chr12:124144717..124146823,2	MCF-7	breast:
13	chr12:124117612..124120056-chr12:124127858..124130457,4	K562	blood:
14	chr12:124128608..124131370-chr12:124135245..124137740,4	K562	blood:
15	chr12:124116825..124119400-chr12:124154444..124157055,3	MCF-7	breast:
16	chr12:124155436..124158746-chr12:124195101..124198299,4	MCF-7	breast:
17	chr12:124105734..124108451-chr12:124133249..124135719,2	K562	blood:
18	chr12:124134030..124137334-chr12:124197093..124199913,4	MCF-7	breast:
19	chr12:124173898..124176239-chr12:124177848..124179680,2	MCF-7	breast:
20	chr12:124154048..124155942-chr12:124162322..124165220,2	K562	blood:
21	chr12:124117633..124119272-chr12:124133499..124136176,2	K562	blood:
22	chr12:124120951..124123869-chr12:124130412..124132116,2	K562	blood:
23	chr12:124117495..124119400-chr12:124126684..124128895,2	MCF-7	breast:
24	chr12:124127308..124129753-chr12:124158031..124160799,2	K562	blood:
25	chr12:124130507..124132191-chr12:124132895..124134450,2	MCF-7	breast:
26	chr12:124117107..124120837-chr12:124123304..124127842,5	MCF-7	breast:
27	chr12:124155376..124157580-chr12:124194948..124197481,2	K562	blood:
28	chr12:124157962..124160129-chr12:124161284..124163771,2	MCF-7	breast:
29	chr12:124157620..124159905-chr12:124196914..124199226,2	K562	blood:
30	chr12:124150313..124152080-chr12:124154611..124157419,2	MCF-7	breast:
31	chr12:124171218..124172882-chr12:124173161..124174693,2	K562	blood:
32	chr12:124143980..124146532-chr12:124155769..124157495,2	MCF-7	breast:
33	chr12:124123949..124126710-chr12:124128875..124131426,2	K562	blood:
34	chr12:124137919..124140915-chr12:124140949..124142983,2	MCF-7	breast:
35	chr12:124118193..124121025-chr12:124132767..124136539,4	MCF-7	breast:
36	chr12:124125615..124128872-chr12:124133075..124135751,3	MCF-7	breast:
37	chr12:124157024..124160371-chr12:124188986..124191737,3	MCF-7	breast:
38	chr12:124117920..124120001-chr12:124129132..124130798,2	MCF-7	breast:
39	chr12:124138422..124140008-chr12:124142075..124144430,2	MCF-7	breast:
40	chr12:124171218..124172882-chr12:124173161..124174693,2	K562	blood:
41	chr12:124137919..124140915-chr12:124140949..124142983,2	MCF-7	breast:
42	chr12:124130507..124132191-chr12:124132895..124134450,2	MCF-7	breast:
43	chr12:124131124..124134135-chr12:124154416..124157411,3	K562	blood:
44	chr12:124172137..124174302-chr12:124194954..124197751,2	MCF-7	breast:
45	chr12:124131124..124134135-chr12:124154416..124157411,3	K562	blood:
46	chr12:124155020..124157089-chr12:124215035..124217819,2	MCF-7	breast:
47	chr12:124125615..124128872-chr12:124133075..124135751,3	MCF-7	breast:
48	chr12:124154972..124157295-chr12:124158575..124161176,3	K562	blood:
49	chr12:124126711..124128243-chr12:124132496..124134774,2	MCF-7	breast:
50	chr12:124141910..124144216-chr12:124195360..124197441,2	MCF-7	breast:

No data

Variant related genes	Relation type
GTF2H3	TF binding region
TCTN2	TF binding region
GTF2H3	CpG island
TCTN2	CpG island
ENSG00000185344	chromatin interactions
ENSG00000136450	chromatin interactions
ENSG00000111361	chromatin interactions
ENSG00000168778	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000111358	chromatin interactions

Extended variants
information (count: 1869 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1869 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573859342	chr12:124127039-124127040	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs565934609	chr12:124127051-124127052	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs191662392	chr12:124127069-124127070	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs553142345	chr12:124127098-124127099	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs578054997	chr12:124127112-124127113	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs545209012	chr12:124127136-124127137	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs563700123	chr12:124127138-124127139	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs184255492	chr12:124127150-124127151	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs543728229	chr12:124127272-124127273	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs571842544	chr12:124127317-124127318	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs561980384	chr12:124127402-124127403	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs562494504	chr12:124127423-124127424	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs540589494	chr12:124127437-124127438	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs529072965	chr12:124127460-124127461	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs150916971	chr12:124127485-124127486	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs559144068	chr12:124127514-124127515	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs533043493	chr12:124127614-124127615	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs139455502	chr12:124127650-124127651	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs188875394	chr12:124127671-124127672	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs370946177	chr12:124127685-124127686	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs530438108	chr12:124127716-124127717	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs149674193	chr12:124127721-124127722	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs7295064	chr12:124127725-124127726	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs567621099	chr12:124127735-124127736	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs534846309	chr12:124127768-124127769	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576356200	chr12:124127786-124127787	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs181618629	chr12:124127807-124127808	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs571797739	chr12:124127810-124127811	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs367887251	chr12:124127837-124127838	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs145472754	chr12:124127890-124127891	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs140270249	chr12:124127947-124127948	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs144048235	chr12:124127991-124127992	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs79877611	chr12:124127992-124127993	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs141061279	chr12:124128039-124128040	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs59279556	chr12:124128077-124128078	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs77452997	chr12:124128090-124128091	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559477509	chr12:124128105-124128106	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs533013698	chr12:124128124-124128125	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs545052592	chr12:124128145-124128146	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs185511471	chr12:124128148-124128149	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs143179938	chr12:124128168-124128169	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs190813902	chr12:124128198-124128199	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs566962005	chr12:124128219-124128220	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs563482811	chr12:124128255-124128256	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs528776920	chr12:124128256-124128257	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs180811438	chr12:124128281-124128282	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs571799244	chr12:124128282-124128283	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs11572942	chr12:124128323-124128324	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs371054564	chr12:124128399-124128400	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs139385801	chr12:124128409-124128410	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1812 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124119200-124129800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:124119200-124129800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:124119200-124130000	Weak transcription	Pancreas	Pancrea
4	chr12:124119200-124130200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:124119200-124130200	Weak transcription	Right Ventricle	heart
6	chr12:124119200-124141000	Weak transcription	Aorta	Aorta
7	chr12:124119200-124155200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr12:124119400-124127200	Weak transcription	Placenta	Placenta
9	chr12:124119400-124129600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr12:124119400-124129600	Weak transcription	HSMMtube	muscle
11	chr12:124119400-124129800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr12:124119400-124129800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr12:124119400-124129800	Weak transcription	Lung	lung
14	chr12:124119400-124129800	Weak transcription	Ovary	ovary
15	chr12:124119400-124130200	Weak transcription	Fetal Kidney	kidney
16	chr12:124119400-124130200	Weak transcription	Gastric	stomach
17	chr12:124119400-124131200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr12:124119400-124132000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr12:124119600-124127200	Weak transcription	Colon Smooth Muscle	Colon
20	chr12:124119600-124127800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr12:124119600-124128800	Weak transcription	Fetal Brain Female	brain
22	chr12:124119600-124129200	Weak transcription	Colonic Mucosa	Colon
23	chr12:124119600-124129200	Weak transcription	HSMM	muscle
24	chr12:124119600-124129600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:124119600-124129600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr12:124119600-124129800	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr12:124119600-124130000	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr12:124119600-124139000	Weak transcription	Fetal Heart	heart
29	chr12:124119600-124140600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr12:124119600-124143000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr12:124119800-124127200	Weak transcription	GM12878-XiMat	blood
32	chr12:124119800-124127200	Weak transcription	NHDF-Ad	bronchial
33	chr12:124119800-124127800	Weak transcription	Primary B cells from cord blood	blood
34	chr12:124119800-124127800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr12:124119800-124127800	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr12:124119800-124127800	Weak transcription	NHEK	skin
37	chr12:124119800-124129600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr12:124119800-124129600	Weak transcription	Brain Hippocampus Middle	brain
39	chr12:124119800-124129800	Weak transcription	Fetal Lung	lung
40	chr12:124119800-124130000	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr12:124119800-124130200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr12:124119800-124130200	Weak transcription	Spleen	Spleen
43	chr12:124119800-124134000	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr12:124119800-124134800	Weak transcription	Brain Germinal Matrix	brain
45	chr12:124119800-124146200	Weak transcription	Psoas Muscle	Psoas
46	chr12:124119800-124155200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr12:124120400-124127800	Weak transcription	HepG2	liver
48	chr12:124120400-124129800	Weak transcription	Brain Cingulate Gyrus	brain
49	chr12:124120600-124129600	Weak transcription	HUVEC	blood vessel
50	chr12:124121400-124128000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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