Variant report

Variant	nsv1045923
Chromosome Location	chr12:121082203-121146219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2318)
CpG islands
(count:2263)
Chromatin interactive
region (count:110)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:2318 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121130248-121130606	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:121122312-121122554	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:121125833-121126010	K562	blood:	n/a	n/a
4	ARID3A	chr12:121124299-121125000	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:121084764-121085055	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:121124549-121124863	K562	blood:	n/a	n/a
7	ATF1	chr12:121124139-121124981	K562	blood:	n/a	n/a
8	ATF2	chr12:121124176-121124899	GM12878	blood:	n/a	n/a
9	ATF2	chr12:121115440-121116426	GM12878	blood:	n/a	n/a
10	ATF2	chr12:121124399-121124833	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr12:121124294-121124781	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr12:121123807-121124929	GM12878	blood:	n/a	n/a
13	ATF2	chr12:121107142-121107682	GM12878	blood:	n/a	n/a
14	ATF2	chr12:121122225-121123187	GM12878	blood:	n/a	n/a
15	ATF2	chr12:121122116-121123234	GM12878	blood:	n/a	n/a
16	ATF3	chr12:121123809-121124375	A549	lung:	n/a	chr12:121124358-121124367
17	ATF3	chr12:121084679-121085176	A549	lung:	n/a	n/a
18	ATF3	chr12:121124378-121124882	A549	lung:	n/a	n/a
19	ATF3	chr12:121129986-121130724	A549	lung:	n/a	n/a
20	ATF3	chr12:121124358-121124914	A549	lung:	n/a	chr12:121124358-121124367
21	BACH1	chr12:121087092-121087320	K562	blood:	n/a	n/a
22	BACH1	chr12:121124459-121124765	K562	blood:	n/a	n/a
23	BACH1	chr12:121123956-121125064	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr12:121086735-121087449	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr12:121124017-121124369	GM12878	blood:	n/a	n/a
26	BATF	chr12:121115468-121115864	GM12878	blood:	n/a	chr12:121115700-121115710 chr12:121115699-121115710
27	BATF	chr12:121107301-121107579	GM12878	blood:	n/a	n/a
28	BATF	chr12:121122236-121122627	GM12878	blood:	n/a	chr12:121122418-121122429
29	BATF	chr12:121124513-121124706	GM12878	blood:	n/a	n/a
30	BATF	chr12:121108396-121108826	GM12878	blood:	n/a	chr12:121108614-121108625
31	BATF	chr12:121122786-121123104	GM12878	blood:	n/a	n/a
32	BATF	chr12:121108413-121108816	GM12878	blood:	n/a	chr12:121108614-121108625
33	BATF	chr12:121108000-121108247	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:121107310-121107555	GM12878	blood:	n/a	n/a
35	BCL11A	chr12:121118017-121118276	GM12878	blood:	n/a	n/a
36	BCL11A	chr12:121124232-121124490	GM12878	blood:	n/a	n/a
37	BCL11A	chr12:121100776-121101016	GM12878	blood:	n/a	n/a
38	BCL11A	chr12:121103277-121103510	GM12878	blood:	n/a	n/a
39	BCL11A	chr12:121122723-121123074	GM12878	blood:	n/a	n/a
40	BCL11A	chr12:121108431-121108868	GM12878	blood:	n/a	n/a
41	BCL11A	chr12:121100768-121101054	GM12878	blood:	n/a	n/a
42	BCL11A	chr12:121107270-121107537	GM12878	blood:	n/a	n/a
43	BCL11A	chr12:121124168-121124827	GM12878	blood:	n/a	chr12:121124597-121124606 chr12:121124208-121124217
44	BCL11A	chr12:121108499-121108777	GM12878	blood:	n/a	n/a
45	BCL11A	chr12:121122751-121123185	GM12878	blood:	n/a	n/a
46	BCL11A	chr12:121116060-121116263	GM12878	blood:	n/a	n/a
47	BCL3	chr12:121124162-121124523	GM12878	blood:	n/a	chr12:121124208-121124217
48	BCL3	chr12:121123941-121125037	GM12878	blood:	n/a	chr12:121124907-121124920 chr12:121124597-121124606 chr12:121124838-121124851 chr12:121124208-121124217
49	BCL3	chr12:121123759-121124840	A549	lung:	n/a	chr12:121124597-121124606 chr12:121124208-121124217
50	BCL3	chr12:121124273-121124943	A549	lung:	n/a	chr12:121124907-121124920 chr12:121124597-121124606 chr12:121124838-121124851

(count:2263 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121124877-121124927	RPTEC	kidney:	n/a
2	chr12:121124020-121124070	Caco-2	colon:	n/a
3	chr12:121124913-121124963	MCF-7	breast:	n/a
4	chr12:121088311-121088361	GM19239	blood:	n/a
5	chr12:121124877-121124927	NB4	blood:	n/a
6	chr12:121087689-121087739	HL-60	blood:	n/a
7	chr12:121124877-121124927	RPTEC	kidney:	n/a
8	chr12:121124020-121124070	Caco-2	colon:	n/a
9	chr12:121124913-121124963	MCF-7	breast:	n/a
10	chr12:121088311-121088361	GM19239	blood:	n/a
11	chr12:121124877-121124927	NB4	blood:	n/a
12	chr12:121087689-121087739	HL-60	blood:	n/a
13	chr12:121106640-121106690	SK-N-MC	brain:	n/a
14	chr12:121087382-121087432	Hela-S3	cervix:	n/a
15	chr12:121128268-121128318	AG09319	gingival:	n/a
16	chr12:121093709-121093759	SKMC	muscle:	n/a
17	chr12:121088311-121088361	A549	lung:	n/a
18	chr12:121125837-121125887	PFSK-1	brain:	n/a
19	chr12:121087689-121087739	NB4	blood:	n/a
20	chr12:121125137-121125187	PFSK-1	brain:	n/a
21	chr12:121106640-121106690	A549	lung:	n/a
22	chr12:121124611-121124661	K562	blood:	n/a
23	chr12:121093625-121093675	NT2-D1	testis:	n/a
24	chr12:121124407-121124457	BJ	skin:	n/a
25	chr12:121130567-121130617	HEK293	kidney:	embryo
26	chr12:121092968-121093018	GM12878	blood:	n/a
27	chr12:121093709-121093759	AG09309	skin:	n/a
28	chr12:121088368-121088418	ECC-1	luminal epithelium:	n/a
29	chr12:121107042-121107092	SKMC	muscle:	n/a
30	chr12:121104839-121104889	HCT-116	colon:	n/a
31	chr12:121128268-121128318	ECC-1	luminal epithelium:	n/a
32	chr12:121124687-121124737	Caco-2	colon:	n/a
33	chr12:121093625-121093675	HCT-116	colon:	n/a
34	chr12:121107042-121107092	PrEC	prostate:	n/a
35	chr12:121124611-121124661	AG09309	skin:	n/a
36	chr12:121139042-121139092	U87	brain:	n/a
37	chr12:121124951-121125001	HPAEpiC	pulmonary alveolar:	n/a
38	chr12:121087689-121087739	GM12892	blood:	n/a
39	chr12:121130567-121130617	HCT-116	colon:	n/a
40	chr12:121088311-121088361	AoSMC	blood vessel:	n/a
41	chr12:121145536-121145586	PANC-1	pancreas:	n/a
42	chr12:121092968-121093018	SK-N-SH_RA	brain:	n/a
43	chr12:121121641-121121691	AoSMC	blood vessel:	n/a
44	chr12:121087382-121087432	NHBE	bronchial:	n/a
45	chr12:121093629-121093679	MCF-7	breast:	n/a
46	chr12:121124913-121124963	AG04450	lung:	fetal
47	chr12:121124893-121124943	H1-hESC	embryonic stem cell:	embryo
48	chr12:121104809-121104859	U87	brain:	n/a
49	chr12:121104839-121104889	SKMC	muscle:	n/a
50	chr12:121104809-121104859	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:120882880..120885596-chr12:121086494..121088113,2	K562	blood:
2	chr12:121140803..121142860-chr12:121453147..121455600,2	K562	blood:
3	chr12:121122674..121127779-chr12:121131254..121137297,11	MCF-7	breast:
4	chr12:120728399..120731246-chr12:121124112..121127371,3	MCF-7	breast:
5	chr12:121126786..121129760-chr12:121147311..121149770,4	MCF-7	breast:
6	chr12:121088300..121090817-chr12:121098579..121100889,2	MCF-7	breast:
7	chr12:121142047..121145691-chr12:121146142..121149647,3	MCF-7	breast:
8	chr12:121020078..121022631-chr12:121125640..121127142,2	K562	blood:
9	chr12:121128710..121131143-chr12:121131360..121132906,2	MCF-7	breast:
10	chr12:120630041..120632673-chr12:121124063..121125965,2	MCF-7	breast:
11	chr12:121122170..121123860-chr12:121162845..121164992,2	K562	blood:
12	chr12:121145921..121147941-chr12:121149529..121151514,2	MCF-7	breast:
13	chr12:121122969..121126872-chr12:121145365..121151601,10	K562	blood:
14	chr12:121093575..121096637-chr12:121103077..121105014,3	MCF-7	breast:
15	chr12:121086713..121087372-chr12:121107159..121108129,2	MCF-7	breast:
16	chr12:121018631..121021385-chr12:121124185..121125689,2	MCF-7	breast:
17	chr12:121079111..121082636-chr12:121084242..121087390,3	K562	blood:
18	chr12:121128598..121131378-chr12:121142040..121143642,2	K562	blood:
19	chr12:121106092..121108586-chr12:121122971..121126312,3	MCF-7	breast:
20	chr12:121017632..121023235-chr12:121123750..121127979,5	K562	blood:
21	chr12:121136675..121138856-chr12:121162469..121164078,2	K562	blood:
22	chr12:121122969..121126872-chr12:121145365..121151601,10	K562	blood:
23	chr12:121125276..121128582-chr12:121139011..121141679,3	MCF-7	breast:
24	chr12:121082536..121084918-chr12:121088940..121091677,2	K562	blood:
25	chr12:121093575..121096637-chr12:121103077..121105014,3	MCF-7	breast:
26	chr12:121126318..121128176-chr12:121135786..121137880,3	MCF-7	breast:
27	chr12:121077855..121079516-chr12:121124357..121126482,2	MCF-7	breast:
28	chr12:121092373..121094051-chr12:121128187..121130355,2	MCF-7	breast:
29	chr12:121123033..121125000-chr12:121205934..121208435,2	K562	blood:
30	chr12:121123292..121126341-chr12:121146632..121149740,5	MCF-7	breast:
31	chr12:121128598..121131378-chr12:121142040..121143642,2	K562	blood:
32	chr12:121125134..121127601-chr20:52821438..52823168,2	MCF-7	breast:
33	chr12:121085923..121088804-chr12:121121977..121126483,5	MCF-7	breast:
34	chr12:121084859..121087400-chr12:121088955..121093657,4	MCF-7	breast:
35	chr12:121090915..121093239-chr12:121142651..121145027,2	K562	blood:
36	chr12:121086713..121087372-chr12:121107159..121108129,2	MCF-7	breast:
37	chr12:121008513..121011933-chr12:121126000..121127892,3	MCF-7	breast:
38	chr12:120875946..120878903-chr12:121123173..121125911,2	K562	blood:
39	chr12:121084960..121086596-chr12:121087744..121089271,2	K562	blood:
40	chr12:121095512..121100910-chr12:121122531..121126551,5	MCF-7	breast:
41	chr12:121121435..121124259-chr12:121418231..121420548,2	MCF-7	breast:
42	chr12:120762972..120763850-chr12:121086347..121087643,3	K562	blood:
43	chr12:121021209..121021867-chr12:121087027..121087660,3	MCF-7	breast:
44	chr12:121084620..121085655-chr12:121151382..121152024,4	K562	blood:
45	chr12:121114453..121120002-chr12:121123011..121126758,6	MCF-7	breast:
46	chr12:121133471..121136112-chr12:121146959..121149468,2	MCF-7	breast:
47	chr12:121122617..121126013-chr12:121146742..121149972,4	MCF-7	breast:
48	chr12:121083368..121085683-chr12:121126949..121129432,2	MCF-7	breast:
49	chr12:121123987..121128994-chr12:121141779..121145101,4	MCF-7	breast:
50	chr12:121121278..121123096-chr12:121123406..121125757,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPPL3.1-3	chr12:121136067-121136154	ENSG00000256364.1
2	lnc-SPPL3.1-4	chr12:121120697-121120808	NONHSAT031190
3	lnc-SPPL3.1-4	chr12:121124950-121126702	NONHSAT031190
4	lnc-SPPL3.1-3	chr12:121134927-121135250	ENSG00000256364.1
5	lnc-SPPL3.1-3	chr12:121137054-121137304	ENSG00000256364.1
6	lnc-SPPL3.1-3	chr12:121136850-121137344	ENSG00000256364.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	MLEC	hsa-miR-24-3p	chr12:121135283-121135290
2	MLEC	hsa-miR-124-3p	chr12:121137983-121137989
3	MLEC	hsa-miR-24-3p	chr12:121138003-121138010

Variant related genes	Relation type
MLEC	TF binding region
CABP1	TF binding region
UNC119B	TF binding region
ENSG00000256364	TF binding region
ENSG00000256008	TF binding region
MLEC	CpG island
CABP1	CpG island
UNC119B	CpG island
ENSG00000256364	CpG island
ENSG00000256008	CpG island
ENSG00000184260	chromatin interactions
ENSG00000157895	chromatin interactions
ENSG00000175970	chromatin interactions
ENSG00000225850	chromatin interactions
ENSG00000257218	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000111780	chromatin interactions
ENSG00000089154	chromatin interactions
ENSG00000110917	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000256008	chromatin interactions
ENSG00000157837	chromatin interactions
ENSG00000181274	chromatin interactions
ENSG00000241388	chromatin interactions
ENSG00000256364	chromatin interactions
ENSG00000122971	chromatin interactions
ENSG00000022840	chromatin interactions
ENSG00000167272	chromatin interactions
ENSG00000157782	chromatin interactions
ENSG00000170855	chromatin interactions
ENSG00000111775	chromatin interactions
ENSG00000092010	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 2435 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2435 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73222778	chr12:121082224-121082225	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570300897	chr12:121082225-121082226	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs10849774	chr12:121082228-121082229	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs558019299	chr12:121082300-121082301	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553274380	chr12:121082334-121082335	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552106296	chr12:121082338-121082339	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs184878192	chr12:121082356-121082357	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs540002392	chr12:121082459-121082460	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs1168067	chr12:121082469-121082470	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs140837908	chr12:121082517-121082518	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs144593389	chr12:121082528-121082529	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189289395	chr12:121082579-121082580	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373881859	chr12:121082580-121082581	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113498779	chr12:121082659-121082660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs146649867	chr12:121082712-121082713	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs141420830	chr12:121082718-121082719	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs556999745	chr12:121082727-121082728	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs564384524	chr12:121082739-121082740	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs533574417	chr12:121082762-121082763	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs573754163	chr12:121082765-121082766	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs546735452	chr12:121082771-121082772	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs566971364	chr12:121082806-121082807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs542761889	chr12:121082809-121082810	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs529242765	chr12:121082854-121082855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs549426760	chr12:121082871-121082872	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs181651554	chr12:121082884-121082885	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538185064	chr12:121082903-121082904	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs11613823	chr12:121082943-121082944	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs115592995	chr12:121083000-121083001	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571310146	chr12:121083029-121083030	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs186671020	chr12:121083089-121083090	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371523032	chr12:121083148-121083149	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553555440	chr12:121083167-121083168	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs573706632	chr12:121083188-121083189	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs143341930	chr12:121083223-121083224	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs1109480	chr12:121083279-121083280	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs148342943	chr12:121083308-121083309	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs572974010	chr12:121083466-121083467	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs368413332	chr12:121083513-121083514	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs564810100	chr12:121083594-121083595	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs535608212	chr12:121083692-121083693	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs540843327	chr12:121083707-121083708	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs560362543	chr12:121083731-121083732	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs556988385	chr12:121083776-121083777	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150437826	chr12:121083863-121083864	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs569321522	chr12:121083881-121083882	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs531743793	chr12:121083882-121083883	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs138371963	chr12:121083885-121083886	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs571537423	chr12:121083984-121083985	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs147242989	chr12:121083986-121083987	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Autism	22495311	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
Urothelial carcinoma	21177765	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2226 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121079600-121086800	Weak transcription	Right Atrium	heart
2	chr12:121081800-121082400	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
3	chr12:121083000-121083200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
4	chr12:121083200-121084600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr12:121083800-121085200	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr12:121084000-121084800	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr12:121084000-121084800	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr12:121084600-121084800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
9	chr12:121084600-121084800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr12:121084600-121084800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr12:121084600-121084800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
12	chr12:121084600-121085000	Flanking Active TSS	Brain Anterior Caudate	brain
13	chr12:121084600-121085000	Enhancers	Brain Cingulate Gyrus	brain
14	chr12:121084600-121085000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
15	chr12:121084600-121085200	Enhancers	Primary B cells from peripheral blood	blood
16	chr12:121084600-121085200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
17	chr12:121084600-121085200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr12:121084600-121085400	Enhancers	Brain Angular Gyrus	brain
19	chr12:121084600-121085400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr12:121084800-121085000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr12:121084800-121085000	Enhancers	Brain Substantia Nigra	brain
22	chr12:121084800-121085000	Enhancers	Esophagus	oesophagus
23	chr12:121084800-121085000	Bivalent Enhancer	HepG2	liver
24	chr12:121084800-121085000	Bivalent Enhancer	NH-A	brain
25	chr12:121084800-121085200	Enhancers	Primary B cells from cord blood	blood
26	chr12:121084800-121085200	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
27	chr12:121084800-121085400	Enhancers	GM12878-XiMat	blood
28	chr12:121084800-121086600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr12:121084800-121086600	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr12:121085000-121085200	Enhancers	A549	lung
31	chr12:121085000-121086000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr12:121085000-121086000	Weak transcription	Brain Cingulate Gyrus	brain
33	chr12:121085000-121086800	Weak transcription	Brain Anterior Caudate	brain
34	chr12:121085000-121086800	Weak transcription	Esophagus	oesophagus
35	chr12:121085200-121086600	Weak transcription	Primary B cells from cord blood	blood
36	chr12:121085200-121086800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr12:121085200-121086800	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr12:121085400-121085800	Weak transcription	GM12878-XiMat	blood
39	chr12:121085400-121086200	Weak transcription	Brain Angular Gyrus	brain
40	chr12:121085400-121086600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr12:121085800-121086800	Enhancers	GM12878-XiMat	blood
42	chr12:121086000-121086400	Enhancers	Fetal Kidney	kidney
43	chr12:121086000-121086600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr12:121086000-121086600	Enhancers	Brain Germinal Matrix	brain
45	chr12:121086000-121086800	Enhancers	Brain Cingulate Gyrus	brain
46	chr12:121086000-121086800	Enhancers	Fetal Stomach	stomach
47	chr12:121086200-121086400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
48	chr12:121086200-121086600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr12:121086200-121086600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:121086200-121086600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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