Variant report

Variant	esv2751077
Chromosome Location	chr12:31278031-31499671
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3832)
CpG islands
(count:2505)
Chromatin interactive
region (count:137)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3832 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31476028-31476324	K562	blood:	n/a	n/a
2	ARID3A	chr12:31399086-31399282	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:31479852-31480408	K562	blood:	n/a	n/a
4	ARID3A	chr12:31424813-31425127	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:31473988-31474017	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:31391820-31391981	K562	blood:	n/a	n/a
7	ARID3A	chr12:31474374-31475158	K562	blood:	n/a	chr12:31474484-31474500
8	ARID3A	chr12:31478920-31479900	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:31477788-31477941	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:31478979-31479248	K562	blood:	n/a	n/a
11	ARID3A	chr12:31476974-31477115	K562	blood:	n/a	n/a
12	ARID3A	chr12:31490901-31491231	HepG2	liver:	n/a	n/a
13	ATF1	chr12:31476892-31477333	K562	blood:	n/a	n/a
14	ATF1	chr12:31459821-31460139	K562	blood:	n/a	n/a
15	ATF1	chr12:31424834-31425154	K562	blood:	n/a	n/a
16	ATF1	chr12:31365662-31365782	K562	blood:	n/a	n/a
17	ATF1	chr12:31478856-31479545	K562	blood:	n/a	n/a
18	ATF2	chr12:31476554-31477036	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr12:31450683-31451065	GM12878	blood:	n/a	n/a
20	ATF2	chr12:31476965-31477675	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr12:31357817-31358350	GM12878	blood:	n/a	n/a
22	ATF2	chr12:31477072-31477951	GM12878	blood:	n/a	n/a
23	ATF2	chr12:31391675-31392058	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr12:31478798-31479487	GM12878	blood:	n/a	n/a
25	ATF2	chr12:31478786-31479145	GM12878	blood:	n/a	n/a
26	ATF2	chr12:31478011-31478395	GM12878	blood:	n/a	n/a
27	ATF2	chr12:31476458-31477548	GM12878	blood:	n/a	n/a
28	ATF2	chr12:31478640-31479517	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr12:31493101-31493582	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr12:31477037-31479605	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr12:31432337-31432818	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr12:31357881-31358323	GM12878	blood:	n/a	n/a
33	ATF2	chr12:31391648-31392128	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF3	chr12:31478727-31479242	A549	lung:	n/a	chr12:31479186-31479195
35	ATF3	chr12:31476942-31477181	K562	blood:	n/a	n/a
36	ATF3	chr12:31478669-31479249	A549	lung:	n/a	chr12:31479186-31479195 chr12:31478697-31478706
37	BACH1	chr12:31476623-31477568	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr12:31477965-31479608	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr12:31464252-31464443	K562	blood:	n/a	n/a
40	BACH1	chr12:31358978-31359188	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr12:31456606-31456794	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr12:31457232-31457259	K562	blood:	n/a	n/a
43	BACH1	chr12:31478414-31479149	K562	blood:	n/a	n/a
44	BATF	chr12:31424868-31425107	GM12878	blood:	n/a	n/a
45	BATF	chr12:31453296-31453675	GM12878	blood:	n/a	n/a
46	BATF	chr12:31390681-31390963	GM12878	blood:	n/a	n/a
47	BATF	chr12:31434733-31435004	GM12878	blood:	n/a	n/a
48	BATF	chr12:31470019-31470247	GM12878	blood:	n/a	n/a
49	BATF	chr12:31434747-31435076	GM12878	blood:	n/a	n/a
50	BATF	chr12:31453298-31453548	GM12878	blood:	n/a	n/a

(count:2505 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31479148-31479198	HCPEpiC	choroid plexus:	n/a
2	chr12:31477216-31477266	HUVEC	blood vessel:	n/a
3	chr12:31402470-31402520	HCM	heart:	n/a
4	chr12:31477445-31477495	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:31479148-31479198	HCPEpiC	choroid plexus:	n/a
6	chr12:31477216-31477266	HUVEC	blood vessel:	n/a
7	chr12:31402470-31402520	HCM	heart:	n/a
8	chr12:31477445-31477495	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:31493376-31493426	Hela-S3	cervix:	n/a
10	chr12:31476565-31476615	HCT-116	colon:	n/a
11	chr12:31423331-31423381	HL-60	blood:	n/a
12	chr12:31479356-31479406	Hepatocyte	liver:	n/a
13	chr12:31478643-31478693	Caco-2	colon:	n/a
14	chr12:31456880-31456930	NH-A	brain:	n/a
15	chr12:31476933-31476983	SK-N-SH_RA	brain:	n/a
16	chr12:31473577-31473627	MCF-7	breast:	n/a
17	chr12:31493376-31493426	Jurkat	blood:	n/a
18	chr12:31480184-31480234	LNCaP	prostate:	n/a
19	chr12:31405369-31405419	Hepatocyte	liver:	n/a
20	chr12:31479853-31479903	K562	blood:	n/a
21	chr12:31477737-31477787	HRCEpiC	kidney:	n/a
22	chr12:31453901-31453951	ECC-1	luminal epithelium:	n/a
23	chr12:31493376-31493426	Caco-2	colon:	n/a
24	chr12:31479318-31479368	ovcar-3	ovarian:	n/a
25	chr12:31473577-31473627	HEK293	kidney:	embryo
26	chr12:31478601-31478651	GM12878	blood:	n/a
27	chr12:31370930-31370980	PANC-1	pancreas:	n/a
28	chr12:31479148-31479198	BE2_C	brain:	n/a
29	chr12:31406441-31406491	PANC-1	pancreas:	n/a
30	chr12:31456880-31456930	SK-N-MC	brain:	n/a
31	chr12:31423331-31423381	Caco-2	colon:	n/a
32	chr12:31479853-31479903	HCF	heart:	n/a
33	chr12:31479191-31479241	SK-N-MC	brain:	n/a
34	chr12:31405359-31405409	A549	lung:	n/a
35	chr12:31479141-31479191	HCM	heart:	n/a
36	chr12:31476479-31476529	K562	blood:	n/a
37	chr12:31423331-31423381	A549	lung:	n/a
38	chr12:31479853-31479903	NHDF-neo	bronchial:	n/a
39	chr12:31479191-31479241	Jurkat	blood:	n/a
40	chr12:31475291-31475341	HEK293	kidney:	embryo
41	chr12:31479139-31479189	HepG2	liver:	n/a
42	chr12:31456880-31456930	NHBE	bronchial:	n/a
43	chr12:31473577-31473627	Jurkat	blood:	n/a
44	chr12:31479189-31479239	HNPCEpiC	eye:	n/a
45	chr12:31480300-31480350	GM19239	blood:	n/a
46	chr12:31405369-31405419	GM12891	blood:	n/a
47	chr12:31493376-31493426	HRCEpiC	kidney:	n/a
48	chr12:31478601-31478651	MCF-7	breast:	n/a
49	chr12:31479189-31479239	GM12892	blood:	n/a
50	chr12:31479318-31479368	U87	brain:	n/a

(count:137 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:31445698..31447861-chr12:31473678..31476194,2	K562	blood:
2	chr12:31354464..31355986-chr12:31358238..31360954,2	K562	blood:
3	chr12:31444404..31449296-chr12:31476824..31481020,5	K562	blood:
4	chr12:31406545..31409230-chr12:31409522..31411986,2	MCF-7	breast:
5	chr12:31478405..31480666-chr12:31485044..31487330,2	MCF-7	breast:
6	chr12:31476765..31477692-chrX:73511338..73512318,2	Hela-S3	cervix:
7	chr12:31478801..31479401-chr12:117175467..117175974,2	NB4	blood:
8	chr12:31442055..31443948-chr12:31476343..31479106,2	MCF-7	breast:
9	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
10	chr12:31452762..31457432-chr12:31476482..31479243,5	MCF-7	breast:
11	chr12:31424677..31426502-chr12:31428387..31431315,2	MCF-7	breast:
12	chr12:31442106..31444745-chr12:31447754..31449545,2	K562	blood:
13	chr12:31269943..31270748-chr12:31391487..31392373,2	K562	blood:
14	chr12:31450442..31457255-chr12:31469614..31474253,6	K562	blood:
15	chr12:31444617..31448853-chr12:31477609..31479787,4	MCF-7	breast:
16	chr12:31426550..31428867-chr8:91672656..91674769,2	MCF-7	breast:
17	chr12:31478659..31479285-chr16:30108005..30108914,2	NB4	blood:
18	chr12:31379295..31381181-chr12:31382279..31384326,2	MCF-7	breast:
19	chr11:64684299..64684850-chr12:31478277..31479265,2	Hela-S3	cervix:
20	chr12:31449879..31452217-chr12:31476391..31478263,2	MCF-7	breast:
21	chr12:31431407..31434228-chr12:31440191..31441794,2	MCF-7	breast:
22	chr12:31429753..31431642-chr12:31477161..31479179,2	MCF-7	breast:
23	chr12:31477240..31477833-chr17:62222972..62223644,2	Hela-S3	cervix:
24	chr12:31402402..31404809-chr12:31411238..31413851,2	K562	blood:
25	chr12:14956282..14956929-chr12:31478535..31479498,2	NB4	blood:
26	chr12:31477362..31478023-chr2:201729352..201729912,2	Hela-S3	cervix:
27	chr12:31473855..31475579-chr12:46775928..46777663,2	K562	blood:
28	chr12:31449879..31452217-chr12:31476391..31478263,2	MCF-7	breast:
29	chr12:31449423..31452288-chr12:31476341..31478296,3	MCF-7	breast:
30	chr12:31455579..31460655-chr12:31474962..31479501,11	K562	blood:
31	chr12:31477256..31480149-chr12:31881924..31883474,2	K562	blood:
32	chr12:31480004..31481974-chr12:31489042..31491768,2	MCF-7	breast:
33	chr12:31424984..31425698-chr12:31516137..31516810,2	MCF-7	breast:
34	chr12:31269781..31270824-chr12:31398705..31400061,4	MCF-7	breast:
35	chr12:31403415..31403922-chr12:31424976..31425527,2	MCF-7	breast:
36	chr12:31445698..31447861-chr12:31473678..31476194,2	K562	blood:
37	chr12:31478978..31479610-chr5:10353319..10353878,2	NB4	blood:
38	chr12:31477362..31479120-chr12:31489865..31491871,2	K562	blood:
39	chr12:31447880..31450711-chr12:31459405..31461625,2	K562	blood:
40	chr12:31269317..31270662-chr12:31391620..31392355,3	MCF-7	breast:
41	chr12:31379791..31381896-chr12:31385949..31387933,2	MCF-7	breast:
42	chr12:31402332..31404405-chr12:31413108..31415272,2	MCF-7	breast:
43	chr12:31402332..31404405-chr12:31413108..31415272,2	MCF-7	breast:
44	chr12:31452762..31457432-chr12:31476482..31479243,5	MCF-7	breast:
45	chr12:31458676..31462198-chr12:31475765..31478520,3	MCF-7	breast:
46	chr12:31375655..31377165-chr12:31378438..31380681,2	K562	blood:
47	chr12:31478549..31482332-chr12:31482720..31486378,4	MCF-7	breast:
48	chr12:31446277..31448012-chr12:31451966..31453945,2	K562	blood:
49	chr12:31440764..31443611-chr12:31446917..31448867,2	MCF-7	breast:
50	chr12:31477521..31479099-chr12:31743621..31745412,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-2	chr12:31412950-31413502	ucscGeneNc_uc001rkg_2
2	lnc-FAM60A-4	chr12:31367135-31367371	expReg_chr12_2391_-
3	lnc-DENND5B-3	chr12:31456429-31458057	NONHSAT027543
4	lnc-AC024940.1-2	chr12:31464551-31464763	NONHSAT027545
5	lnc-DENND5B-3	chr12:31478958-31479062	NONHSAT027543
6	lnc-FAM60A-2	chr12:31407684-31407996	ucscGeneNc_uc001rkg_2
7	lnc-AC024940.1-3	chr12:31397374-31397619	NONHSAT027541
8	lnc-AC024940.1-1	chr12:31477250-31478879	NR_026806
9	lnc-AC024940.1-2	chr12:31464861-31464963	NONHSAT027545

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FAM60A	hsa-miR-320a	chr12:31433853-31433872
2	FAM60A	hsa-miR-320a	chr12:31434102-31434124

Variant related genes	Relation type
FAM60A	TF binding region
ENSG00000243517	TF binding region
ENSG00000177359	TF binding region
ENSG00000270766	TF binding region
ENSG00000256176	TF binding region
ENSG00000238661	TF binding region
ENSG00000270395	TF binding region
ENSG00000177340	TF binding region
FAM60A	CpG island
ENSG00000243517	CpG island
ENSG00000177359	CpG island
ENSG00000270766	CpG island
ENSG00000256176	CpG island
ENSG00000238661	CpG island
ENSG00000270395	CpG island
ENSG00000177340	CpG island
ENSG00000182993	chromatin interactions
ENSG00000207783	chromatin interactions
ENSG00000133704	chromatin interactions
ENSG00000090238	chromatin interactions
ENSG00000151743	chromatin interactions
ENSG00000175215	chromatin interactions
ENSG00000081791	chromatin interactions
ENSG00000138041	chromatin interactions
ENSG00000255867	chromatin interactions
ENSG00000177340	chromatin interactions
ENSG00000111640	chromatin interactions
ENSG00000238661	chromatin interactions
ENSG00000117151	chromatin interactions
ENSG00000013441	chromatin interactions
ENSG00000257261	chromatin interactions
ENSG00000110046	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000084463	chromatin interactions
ENSG00000256232	chromatin interactions
ENSG00000139160	chromatin interactions
ENSG00000243517	chromatin interactions
ENSG00000077147	chromatin interactions
ENSG00000270395	chromatin interactions
ENSG00000139146	chromatin interactions
ENSG00000259802	chromatin interactions
ENSG00000230590	chromatin interactions
ENSG00000050426	chromatin interactions
ENSG00000169964	chromatin interactions
ENSG00000256176	chromatin interactions
ENSG00000214770	chromatin interactions
ENSG00000177359	chromatin interactions
ENSG00000270766	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000170456	chromatin interactions
ENSG00000111412	chromatin interactions
ENSG00000151849	chromatin interactions
ENSG00000145495	chromatin interactions
ENSG00000272373	chromatin interactions

Extended variants
information (count: 6156 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:6156 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370775371	chr12:31280412-31280413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572118401	chr12:31280423-31280424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541116795	chr12:31280497-31280498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554685181	chr12:31280526-31280527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574526775	chr12:31280574-31280575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371128354	chr12:31280586-31280587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375427500	chr12:31280605-31280606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs368426461	chr12:31280626-31280627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188007942	chr12:31280630-31280631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563403299	chr12:31280689-31280690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112073491	chr12:31280692-31280693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112325033	chr12:31280695-31280696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371294864	chr12:31280697-31280698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139000169	chr12:31280811-31280812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192240745	chr12:31280825-31280826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142259793	chr12:31280834-31280835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2536827	chr12:31280904-31280905	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs150491838	chr12:31280916-31280917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548369801	chr12:31280918-31280919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568560161	chr12:31280919-31280920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530975718	chr12:31280941-31280942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551160992	chr12:31280951-31280952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571110696	chr12:31280966-31280967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540134032	chr12:31281016-31281017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553742003	chr12:31281044-31281045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138131414	chr12:31281098-31281099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565663106	chr12:31281117-31281118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183451124	chr12:31281126-31281127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115596083	chr12:31298250-31298251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557016183	chr12:31298282-31298283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553382464	chr12:31298315-31298316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140043334	chr12:31298362-31298363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375606935	chr12:31298383-31298384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562246304	chr12:31298391-31298392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376737212	chr12:31298394-31298395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140219382	chr12:31298430-31298431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150331088	chr12:31298444-31298445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372747972	chr12:31298448-31298449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377036543	chr12:31298457-31298458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2639039	chr12:31298463-31298464	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs370232830	chr12:31298469-31298470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367883880	chr12:31298476-31298477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139087089	chr12:31298506-31298507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs80112226	chr12:31298691-31298692	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
45	rs199837462	chr12:31298696-31298697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200890804	chr12:31298699-31298700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201574646	chr12:31298717-31298718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577963097	chr12:31298731-31298732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528169685	chr12:31298747-31298748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547908067	chr12:31298753-31298754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Ovarian cancer	21720365	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3116 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31280400-31281200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr12:31298200-31298400	Enhancers	Duodenum Mucosa	Duodenum
3	chr12:31298400-31299400	Weak transcription	Duodenum Mucosa	Duodenum
4	chr12:31299400-31300200	Enhancers	Duodenum Mucosa	Duodenum
5	chr12:31300200-31301400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr12:31300800-31301200	Enhancers	Fetal Intestine Small	intestine
7	chr12:31301400-31301600	Enhancers	Duodenum Mucosa	Duodenum
8	chr12:31315600-31316200	Active TSS	A549	lung
9	chr12:31316000-31316400	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr12:31316000-31316400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
11	chr12:31316000-31316400	Active TSS	H1 Cell Line	embryonic stem cell
12	chr12:31316000-31316400	Active TSS	H9 Cell Line	embryonic stem cell
13	chr12:31316000-31316400	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr12:31316000-31316400	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr12:31316000-31316400	Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr12:31316000-31316400	Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr12:31316000-31316400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr12:31316000-31316400	Active TSS	Placenta	Placenta
19	chr12:31316000-31316400	Active TSS	K562	blood
20	chr12:31327200-31328000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr12:31327200-31328400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr12:31327400-31328400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr12:31327800-31328200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr12:31327800-31328400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr12:31327800-31328400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr12:31327800-31328400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr12:31327800-31328400	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr12:31327800-31328400	Enhancers	Brain Germinal Matrix	brain
29	chr12:31331600-31332800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr12:31331800-31333000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:31331800-31333000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:31331800-31333200	Enhancers	Primary B cells from peripheral blood	blood
33	chr12:31332000-31332400	Enhancers	Primary hematopoietic stem cells	blood
34	chr12:31332200-31333000	Enhancers	Primary B cells from cord blood	blood
35	chr12:31332400-31333200	Enhancers	GM12878-XiMat	blood
36	chr12:31332600-31333000	Enhancers	Primary T cells from cord blood	blood
37	chr12:31351800-31352000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:31353400-31354800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr12:31353600-31354600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:31353800-31355000	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr12:31355200-31362600	Enhancers	HMEC	breast
42	chr12:31355800-31356400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr12:31356000-31356400	Enhancers	Primary B cells from peripheral blood	blood
44	chr12:31356000-31356400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr12:31356000-31356600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr12:31356000-31356600	Enhancers	Primary T cells from cord blood	blood
47	chr12:31356000-31357000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr12:31356200-31356400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr12:31356200-31356800	Enhancers	NHEK	skin
50	chr12:31356400-31356800	Enhancers	Sigmoid Colon	Sigmoid Colon

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