Variant report

Variant	nsv560496
Chromosome Location	chr12:124119983-124195856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:669)
CpG islands
(count:915)
Chromatin interactive
region (count:110)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:124172426-124172866	GM12878	blood:	n/a	n/a
2	ATF2	chr12:124165973-124166596	GM12878	blood:	n/a	n/a
3	ATF2	chr12:124172381-124172960	GM12878	blood:	n/a	n/a
4	ATF2	chr12:124165813-124166609	GM12878	blood:	n/a	n/a
5	ATF2	chr12:124144752-124145277	GM12878	blood:	n/a	n/a
6	ATF3	chr12:124190540-124190739	K562	blood:	n/a	n/a
7	ATF3	chr12:124190442-124190745	K562	blood:	n/a	n/a
8	BATF	chr12:124172484-124172812	GM12878	blood:	n/a	n/a
9	BATF	chr12:124166147-124166490	GM12878	blood:	n/a	n/a
10	BATF	chr12:124166177-124166501	GM12878	blood:	n/a	n/a
11	BATF	chr12:124144875-124145201	GM12878	blood:	n/a	chr12:124145072-124145083
12	BATF	chr12:124172432-124172890	GM12878	blood:	n/a	n/a
13	BATF	chr12:124144904-124145195	GM12878	blood:	n/a	chr12:124145072-124145083
14	BCL11A	chr12:124166091-124166461	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:124172540-124172846	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:124172504-124172853	GM12878	blood:	n/a	n/a
17	BCLAF1	chr12:124139925-124140367	GM12878	blood:	n/a	n/a
18	BCLAF1	chr12:124166045-124166526	GM12878	blood:	n/a	n/a
19	BCLAF1	chr12:124172411-124172914	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:124166226-124166361	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:124155699-124155729	K562	blood:	n/a	n/a
22	BHLHE40	chr12:124172483-124172783	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:124146182-124146377	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:124139600-124140393	GM12878	blood:	n/a	n/a
25	BRCA1	chr12:124133994-124134134	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr12:124147878-124148212	K562	blood:	n/a	n/a
27	CEBPB	chr12:124166289-124166474	K562	blood:	n/a	chr12:124166370-124166381
28	CEBPB	chr12:124172369-124173000	GM12878	blood:	n/a	n/a
29	CEBPB	chr12:124144964-124145165	K562	blood:	n/a	n/a
30	CEBPB	chr12:124155348-124155869	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr12:124144822-124145387	A549	lung:	n/a	n/a
32	CEBPB	chr12:124163883-124164027	K562	blood:	n/a	chr12:124163964-124163975
33	CEBPB	chr12:124144925-124145317	IMR90	lung:	n/a	n/a
34	CEBPB	chr12:124144969-124145294	K562	blood:	n/a	n/a
35	CEBPB	chr12:124144926-124145288	MCF-7	breast:	n/a	n/a
36	CEBPB	chr12:124155361-124155613	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr12:124144941-124145298	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr12:124146435-124146820	MCF-7	breast:	n/a	chr12:124146632-124146643
39	CEBPB	chr12:124146558-124146645	K562	blood:	n/a	chr12:124146632-124146643
40	CEBPB	chr12:124188889-124189157	HepG2	liver:	n/a	n/a
41	CEBPB	chr12:124163947-124163977	HepG2	liver:	n/a	chr12:124163964-124163975
42	CEBPB	chr12:124155414-124155714	HepG2	liver:	n/a	n/a
43	CEBPB	chr12:124146622-124146730	HepG2	liver:	n/a	chr12:124146632-124146643
44	CEBPB	chr12:124155498-124155638	K562	blood:	n/a	n/a
45	CEBPB	chr12:124166212-124166455	A549	lung:	n/a	chr12:124166370-124166381
46	CEBPB	chr12:124166279-124166491	IMR90	lung:	n/a	chr12:124166370-124166381
47	CEBPB	chr12:124166291-124166506	HepG2	liver:	n/a	chr12:124166370-124166381
48	CEBPB	chr12:124144946-124145307	A549	lung:	n/a	n/a
49	CEBPB	chr12:124188933-124189113	A549	lung:	n/a	n/a
50	CHD2	chr12:124140018-124140339	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124155451-124155501	Hepatocyte	liver:	n/a
2	chr12:124154378-124154428	LNCaP	prostate:	n/a
3	chr12:124144432-124144482	HL-60	blood:	n/a
4	chr12:124192819-124192869	HCM	heart:	n/a
5	chr12:124154378-124154428	H1-hESC	embryonic stem cell:	embryo
6	chr12:124156159-124156209	SK-N-MC	brain:	n/a
7	chr12:124155712-124155762	NHBE	bronchial:	n/a
8	chr12:124192819-124192869	HAEpiC	amniotic membrane:	n/a
9	chr12:124154378-124154428	HAEpiC	amniotic membrane:	n/a
10	chr12:124145110-124145160	HRCEpiC	kidney:	n/a
11	chr12:124158499-124158549	SK-N-SH_RA	brain:	n/a
12	chr12:124156159-124156209	IMR90	lung:	fetal
13	chr12:124121050-124121100	Hela-S3	cervix:	n/a
14	chr12:124156159-124156209	NH-A	brain:	n/a
15	chr12:124145110-124145160	NH-A	brain:	n/a
16	chr12:124158499-124158549	ovcar-3	ovarian:	n/a
17	chr12:124144432-124144482	NHBE	bronchial:	n/a
18	chr12:124154378-124154428	NT2-D1	testis:	n/a
19	chr12:124155880-124155930	NHBE	bronchial:	n/a
20	chr12:124144432-124144482	CMK	blood:	n/a
21	chr12:124154378-124154428	HRPEpiC	eye:	n/a
22	chr12:124155579-124155629	SK-N-SH	brain:	n/a
23	chr12:124155594-124155644	H1-hESC	embryonic stem cell:	embryo
24	chr12:124156170-124156220	MCF-7	breast:	n/a
25	chr12:124155712-124155762	CMK	blood:	n/a
26	chr12:124154378-124154428	SKMC	muscle:	n/a
27	chr12:124155579-124155629	HEK293	kidney:	embryo
28	chr12:124121050-124121100	GM12891	blood:	n/a
29	chr12:124121050-124121100	Caco-2	colon:	n/a
30	chr12:124158499-124158549	AoSMC	blood vessel:	n/a
31	chr12:124121050-124121100	BJ	skin:	n/a
32	chr12:124155594-124155644	HCPEpiC	choroid plexus:	n/a
33	chr12:124145110-124145160	NT2-D1	testis:	n/a
34	chr12:124155712-124155762	K562	blood:	n/a
35	chr12:124192819-124192869	NT2-D1	testis:	n/a
36	chr12:124121050-124121100	H1-hESC	embryonic stem cell:	embryo
37	chr12:124158499-124158549	U87	brain:	n/a
38	chr12:124156170-124156220	HNPCEpiC	eye:	n/a
39	chr12:124155620-124155670	Jurkat	blood:	n/a
40	chr12:124155579-124155629	Caco-2	colon:	n/a
41	chr12:124154378-124154428	AG09319	gingival:	n/a
42	chr12:124145110-124145160	AoSMC	blood vessel:	n/a
43	chr12:124154378-124154428	SK-N-SH_RA	brain:	n/a
44	chr12:124156170-124156220	HIPEpiC	eye:	n/a
45	chr12:124121050-124121100	AG09309	skin:	n/a
46	chr12:124155620-124155670	IMR90	lung:	fetal
47	chr12:124154378-124154428	SAEC	small airway:	n/a
48	chr12:124155458-124155508	HAEpiC	amniotic membrane:	n/a
49	chr12:124155594-124155644	HUVEC	blood vessel:	n/a
50	chr12:124155712-124155762	HMEC	breast:	n/a

(count:110 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:124188235..124191139-chr12:124193941..124195953,3	MCF-7	breast:
2	chr12:124130507..124132191-chr12:124132895..124134450,2	MCF-7	breast:
3	chr12:123716636..123719388-chr12:124194108..124196844,2	K562	blood:
4	chr12:124189784..124191716-chr12:124194882..124197193,2	K562	blood:
5	chr12:124195458..124197705-chr12:124223204..124225071,2	MCF-7	breast:
6	chr12:124138422..124140008-chr12:124142075..124144430,2	MCF-7	breast:
7	chr12:124177268..124179844-chr12:124184486..124185994,2	K562	blood:
8	chr12:124185897..124191093-chr12:124195290..124198994,7	MCF-7	breast:
9	chr12:124194853..124196399-chr12:124201524..124203920,2	K562	blood:
10	chr12:124117712..124121219-chr12:124140785..124143591,3	K562	blood:
11	chr12:124117612..124120056-chr12:124127858..124130457,4	K562	blood:
12	chr12:124190696..124192494-chr12:124194252..124196865,2	K562	blood:
13	chr12:123847301..123849584-chr12:124117443..124120110,3	K562	blood:
14	chr12:124190696..124192494-chr12:124194252..124196865,2	K562	blood:
15	chr12:124143980..124146532-chr12:124155769..124157495,2	MCF-7	breast:
16	chr12:124117633..124119272-chr12:124133499..124136176,2	K562	blood:
17	chr12:124157962..124160129-chr12:124161284..124163771,2	MCF-7	breast:
18	chr12:124191295..124193347-chr12:124194777..124198625,4	MCF-7	breast:
19	chr12:124118119..124120182-chr12:124196891..124198426,2	K562	blood:
20	chr12:124185982..124187602-chr12:124193943..124196577,2	K562	blood:
21	chr12:123847805..123850449-chr12:124195534..124198038,2	K562	blood:
22	chr12:124117107..124120837-chr12:124123304..124127842,5	MCF-7	breast:
23	chr12:124068831..124072178-chr12:124116882..124120107,5	K562	blood:
24	chr12:124117107..124120837-chr12:124123304..124127842,5	MCF-7	breast:
25	chr12:124154048..124155942-chr12:124162322..124165220,2	K562	blood:
26	chr12:124157626..124159857-chr12:124196461..124198464,2	MCF-7	breast:
27	chr12:124157024..124160371-chr12:124188986..124191737,3	MCF-7	breast:
28	chr12:124172137..124174302-chr12:124194954..124197751,2	MCF-7	breast:
29	chr12:124187896..124189887-chr12:124195478..124197199,2	K562	blood:
30	chr12:123753793..123756876-chr12:124117523..124121813,4	K562	blood:
31	chr12:124118193..124121025-chr12:124132767..124136539,4	MCF-7	breast:
32	chr12:124123949..124126710-chr12:124128875..124131426,2	K562	blood:
33	chr12:124086664..124088557-chr12:124117448..124120033,4	K562	blood:
34	chr12:124180128..124181646-chr12:124198369..124200192,2	MCF-7	breast:
35	chr12:124150219..124152252-chr12:124155815..124157987,2	MCF-7	breast:
36	chr12:124095180..124096998-chr12:124140972..124143607,2	MCF-7	breast:
37	chr12:124117920..124120001-chr12:124129132..124130798,2	MCF-7	breast:
38	chr12:124120301..124122353-chr12:124128299..124130201,3	K562	blood:
39	chr12:124119318..124121767-chr12:124194183..124197056,2	MCF-7	breast:
40	chr12:124116825..124119400-chr12:124154444..124157055,3	MCF-7	breast:
41	chr12:124155436..124158746-chr12:124195101..124198299,4	MCF-7	breast:
42	chr12:124128608..124131370-chr12:124135245..124137740,4	K562	blood:
43	chr12:124123949..124126710-chr12:124128875..124131426,2	K562	blood:
44	chr12:123716636..123719469-chr12:124192807..124195608,2	K562	blood:
45	chr12:124084988..124092992-chr12:124114351..124121638,14	K562	blood:
46	chr12:124185982..124187602-chr12:124193943..124196577,2	K562	blood:
47	chr12:124125615..124128872-chr12:124133075..124135751,3	MCF-7	breast:
48	chr12:124195456..124198460-chr12:124455550..124458339,3	MCF-7	breast:
49	chr12:124141910..124144216-chr12:124195360..124197441,2	MCF-7	breast:
50	chr12:124084914..124087862-chr12:124122413..124125179,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2B1-3	chr12:124192149-124192324	ENSG00000255839
2	lnc-EIF2B1-3	chr12:124192789-124192933	ENSG00000255839

No data

Variant related genes	Relation type
EIF2B1	TF binding region
GTF2H3	TF binding region
ENSG00000255839	TF binding region
ATP6V0A2	TF binding region
TCTN2	TF binding region
EIF2B1	CpG island
GTF2H3	CpG island
ENSG00000255839	CpG island
ATP6V0A2	CpG island
TCTN2	CpG island
ENSG00000111328	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000051825	chromatin interactions
ENSG00000255839	chromatin interactions
ENSG00000183955	chromatin interactions
ENSG00000270095	chromatin interactions
ENSG00000086598	chromatin interactions
ENSG00000179195	chromatin interactions
ENSG00000119242	chromatin interactions
ENSG00000247373	chromatin interactions
ENSG00000168778	chromatin interactions
ENSG00000136450	chromatin interactions
ENSG00000139697	chromatin interactions
ENSG00000185344	chromatin interactions
ENSG00000256092	chromatin interactions
ENSG00000111361	chromatin interactions
ENSG00000178882	chromatin interactions
ENSG00000111358	chromatin interactions
ENSG00000111364	chromatin interactions

Extended variants
information (count: 3003 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3003 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11572920	chr12:124119983-124119984	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575539318	chr12:124120014-124120015	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
3	rs557880611	chr12:124120026-124120027	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
4	rs569535840	chr12:124120085-124120086	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
5	rs544640310	chr12:124120098-124120099	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
6	rs555757949	chr12:124120115-124120116	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs573999387	chr12:124120117-124120118	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
8	rs370227888	chr12:124120120-124120121	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs541189677	chr12:124120145-124120146	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs553143605	chr12:124120147-124120148	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs577866724	chr12:124120159-124120160	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs545153461	chr12:124120165-124120166	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
13	rs6488886	chr12:124120205-124120206	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs11572921	chr12:124120212-124120213	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs543028190	chr12:124120227-124120228	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
16	rs561916456	chr12:124120239-124120240	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
17	rs201211573	chr12:124120240-124120241	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
18	rs141104697	chr12:124120351-124120352	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs547754168	chr12:124120507-124120508	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
20	rs116368893	chr12:124120527-124120528	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs533196501	chr12:124120681-124120682	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs556073524	chr12:124120697-124120698	Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs374299593	chr12:124120713-124120714	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs60567004	chr12:124120906-124120907	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs184786928	chr12:124120960-124120961	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs12830927	chr12:124120991-124120992	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs146937547	chr12:124121025-124121026	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs200502273	chr12:124121046-124121047	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs11572922	chr12:124121051-124121052	Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs566966111	chr12:124121058-124121059	Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs534986147	chr12:124121061-124121062	Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs553282531	chr12:124121113-124121114	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs187443398	chr12:124121120-124121121	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs539234248	chr12:124121208-124121209	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs532204887	chr12:124121235-124121236	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs147568071	chr12:124121236-124121237	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs542614111	chr12:124121247-124121248	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs561256614	chr12:124121254-124121255	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs7298048	chr12:124121263-124121264	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs113273857	chr12:124121280-124121281	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs11572923	chr12:124121346-124121347	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs559701184	chr12:124121348-124121349	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs532954723	chr12:124121350-124121351	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs551557965	chr12:124121378-124121379	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs563196713	chr12:124121405-124121406	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs530622029	chr12:124121415-124121416	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs548716546	chr12:124121420-124121421	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs11057311	chr12:124121429-124121430	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs11572924	chr12:124121432-124121433	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs546853610	chr12:124121459-124121460	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 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:2428 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124119200-124124400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr12:124119200-124129800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:124119200-124129800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:124119200-124130000	Weak transcription	Pancreas	Pancrea
5	chr12:124119200-124130200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:124119200-124130200	Weak transcription	Right Ventricle	heart
7	chr12:124119200-124141000	Weak transcription	Aorta	Aorta
8	chr12:124119200-124155200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr12:124119400-124123000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:124119400-124123800	Weak transcription	Fetal Muscle Trunk	muscle
11	chr12:124119400-124124000	Weak transcription	Esophagus	oesophagus
12	chr12:124119400-124124400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr12:124119400-124124400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr12:124119400-124124600	Weak transcription	Fetal Intestine Large	intestine
15	chr12:124119400-124124600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr12:124119400-124127200	Weak transcription	Placenta	Placenta
17	chr12:124119400-124129600	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr12:124119400-124129600	Weak transcription	HSMMtube	muscle
19	chr12:124119400-124129800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr12:124119400-124129800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr12:124119400-124129800	Weak transcription	Lung	lung
22	chr12:124119400-124129800	Weak transcription	Ovary	ovary
23	chr12:124119400-124130200	Weak transcription	Fetal Kidney	kidney
24	chr12:124119400-124130200	Weak transcription	Gastric	stomach
25	chr12:124119400-124131200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr12:124119400-124132000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr12:124119600-124120000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr12:124119600-124120000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:124119600-124120000	Enhancers	HUVEC	blood vessel
30	chr12:124119600-124120400	Enhancers	Brain Cingulate Gyrus	brain
31	chr12:124119600-124120400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr12:124119600-124121600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr12:124119600-124121800	Weak transcription	Fetal Stomach	stomach
34	chr12:124119600-124123000	Weak transcription	Fetal Intestine Small	intestine
35	chr12:124119600-124123200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:124119600-124123600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr12:124119600-124123800	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr12:124119600-124124000	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr12:124119600-124124000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr12:124119600-124124000	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr12:124119600-124124000	Weak transcription	Duodenum Mucosa	Duodenum
42	chr12:124119600-124124000	Weak transcription	Fetal Thymus	thymus
43	chr12:124119600-124124200	Weak transcription	Primary B cells from peripheral blood	blood
44	chr12:124119600-124124200	Weak transcription	Fetal Brain Male	brain
45	chr12:124119600-124124400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr12:124119600-124124400	Weak transcription	Brain Substantia Nigra	brain
47	chr12:124119600-124124400	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr12:124119600-124124400	Weak transcription	Stomach Smooth Muscle	stomach
49	chr12:124119600-124124400	Weak transcription	Thymus	Thymus
50	chr12:124119600-124124600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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