Variant report

Variant	nsv592085
Chromosome Location	chr3:155827634-156012679
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1539)
CpG islands
(count:1468)
Chromatin interactive
region (count:63)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1539 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:155934687-155934994	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:155992595-155992889	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:155869622-155869940	HepG2	liver:	n/a	n/a
4	ATF1	chr3:155893519-155893659	K562	blood:	n/a	n/a
5	BACH1	chr3:155945572-155945829	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:155922991-155923003	K562	blood:	n/a	n/a
7	BATF	chr3:155914991-155915221	GM12878	blood:	n/a	chr3:155915110-155915121
8	BHLHE40	chr3:155868907-155868921	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:155934721-155934941	HepG2	liver:	n/a	n/a
10	BRCA1	chr3:155869804-155869979	HepG2	liver:	n/a	n/a
11	BRCA1	chr3:155893429-155893656	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr3:155869740-155869989	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:155936145-155936500	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:155992591-155992957	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:155992632-155992874	HepG2	liver:	n/a	n/a
16	CEBPB	chr3:155864806-155864991	K562	blood:	n/a	n/a
17	CEBPB	chr3:155879041-155879315	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:155899384-155899748	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:155866417-155866779	IMR90	lung:	n/a	chr3:155866589-155866602 chr3:155866589-155866600 chr3:155866591-155866600 chr3:155866589-155866602 chr3:155866591-155866600 chr3:155866591-155866602 chr3:155866591-155866600 chr3:155866591-155866602 chr3:155866589-155866602 chr3:155866591-155866600
20	CEBPB	chr3:155866450-155866756	A549	lung:	n/a	chr3:155866589-155866602 chr3:155866589-155866600 chr3:155866591-155866600 chr3:155866589-155866602 chr3:155866591-155866600 chr3:155866591-155866602 chr3:155866591-155866600 chr3:155866591-155866602 chr3:155866589-155866602 chr3:155866591-155866600
21	CEBPB	chr3:155992553-155992924	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:155864854-155864972	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:155866435-155866780	Hela-S3	cervix:	n/a	chr3:155866589-155866602 chr3:155866589-155866600 chr3:155866591-155866600 chr3:155866589-155866602 chr3:155866591-155866600 chr3:155866591-155866602 chr3:155866591-155866600 chr3:155866591-155866602 chr3:155866589-155866602 chr3:155866591-155866600
24	CEBPB	chr3:155992448-155992966	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:155893956-155894389	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr3:155988552-155988782	A549	lung:	n/a	chr3:155988662-155988673
27	CEBPB	chr3:155988559-155988807	IMR90	lung:	n/a	chr3:155988662-155988673
28	CEBPB	chr3:155992614-155992906	HepG2	liver:	n/a	n/a
29	CEBPB	chr3:155965247-155965260	HepG2	liver:	n/a	n/a
30	CEBPB	chr3:155904912-155905165	IMR90	lung:	n/a	n/a
31	CEBPB	chr3:155992637-155992949	MCF-7	breast:	n/a	n/a
32	CEBPB	chr3:155948088-155949063	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr3:155992601-155992840	K562	blood:	n/a	n/a
34	CEBPB	chr3:155925394-155926423	IMR90	lung:	n/a	chr3:155925548-155925557 chr3:155925548-155925559
35	CEBPB	chr3:155899380-155899738	IMR90	lung:	n/a	n/a
36	CEBPB	chr3:155866423-155866765	K562	blood:	n/a	chr3:155866589-155866602 chr3:155866589-155866600 chr3:155866591-155866600 chr3:155866589-155866602 chr3:155866591-155866600 chr3:155866591-155866602 chr3:155866591-155866600 chr3:155866591-155866602 chr3:155866589-155866602 chr3:155866591-155866600
37	CEBPB	chr3:155992546-155992927	A549	lung:	n/a	n/a
38	CEBPB	chr3:155866450-155866759	HepG2	liver:	n/a	chr3:155866589-155866602 chr3:155866589-155866600 chr3:155866591-155866600 chr3:155866589-155866602 chr3:155866591-155866600 chr3:155866591-155866602 chr3:155866591-155866600 chr3:155866591-155866602 chr3:155866589-155866602 chr3:155866591-155866600
39	CEBPB	chr3:155992629-155992894	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr3:155992459-155992928	IMR90	lung:	n/a	n/a
41	CEBPB	chr3:155988602-155988727	HepG2	liver:	n/a	chr3:155988662-155988673
42	CEBPB	chr3:155878999-155879341	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr3:155948137-155948375	A549	lung:	n/a	n/a
44	CEBPD	chr3:155992604-155992850	HepG2	liver:	n/a	n/a
45	CHD1	chr3:156009613-156009643	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr3:155908039-155908161	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr3:155879084-155879232	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr3:155883936-155883944	GM12878	blood:	n/a	n/a
49	CTBP2	chr3:156008784-156009698	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr3:155853860-155854010	HMEC	breast:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:155838317-155838367	T-47D	breast:	n/a
2	chr3:156009151-156009201	AG09309	skin:	n/a
3	chr3:156008127-156008177	CMK	blood:	n/a
4	chr3:156009151-156009201	SKMC	muscle:	n/a
5	chr3:155838317-155838367	T-47D	breast:	n/a
6	chr3:156009151-156009201	AG09309	skin:	n/a
7	chr3:156008127-156008177	CMK	blood:	n/a
8	chr3:156009151-156009201	SKMC	muscle:	n/a
9	chr3:155838317-155838367	PANC-1	pancreas:	n/a
10	chr3:155837322-155837372	GM12892	blood:	n/a
11	chr3:155838399-155838449	HIPEpiC	eye:	n/a
12	chr3:155838109-155838159	GM06990	blood:	n/a
13	chr3:156012496-156012546	ovcar-3	ovarian:	n/a
14	chr3:155867120-155867170	GM19239	blood:	n/a
15	chr3:155859344-155859394	HIPEpiC	eye:	n/a
16	chr3:156009465-156009515	GM19239	blood:	n/a
17	chr3:155925405-155925455	NT2-D1	testis:	n/a
18	chr3:155838109-155838159	HCT-116	colon:	n/a
19	chr3:156008770-156008820	AG10803	skin:	n/a
20	chr3:155860792-155860842	GM06990	blood:	n/a
21	chr3:156002617-156002667	HL-60	blood:	n/a
22	chr3:155838625-155838675	SK-N-SH	brain:	n/a
23	chr3:155837322-155837372	ovcar-3	ovarian:	n/a
24	chr3:156008770-156008820	HepG2	liver:	n/a
25	chr3:155925405-155925455	HCT-116	colon:	n/a
26	chr3:155838399-155838449	HRPEpiC	eye:	n/a
27	chr3:156009398-156009448	MCF-7	breast:	n/a
28	chr3:155860792-155860842	HMEC	breast:	n/a
29	chr3:156012496-156012546	HNPCEpiC	eye:	n/a
30	chr3:156009151-156009201	A549	lung:	n/a
31	chr3:156009398-156009448	HRCEpiC	kidney:	n/a
32	chr3:156009465-156009515	SK-N-SH	brain:	n/a
33	chr3:155859344-155859394	H1-hESC	embryonic stem cell:	embryo
34	chr3:156005296-156005346	H1-hESC	embryonic stem cell:	embryo
35	chr3:156009398-156009448	HEK293	kidney:	embryo
36	chr3:156002617-156002667	HAEpiC	amniotic membrane:	n/a
37	chr3:155838399-155838449	NH-A	brain:	n/a
38	chr3:155838625-155838675	HIPEpiC	eye:	n/a
39	chr3:155859344-155859394	AG10803	skin:	n/a
40	chr3:156009465-156009515	GM06990	blood:	n/a
41	chr3:155867120-155867170	NHBE	bronchial:	n/a
42	chr3:155838625-155838675	GM12891	blood:	n/a
43	chr3:156002617-156002667	RPTEC	kidney:	n/a
44	chr3:155925405-155925455	AG09319	gingival:	n/a
45	chr3:156009319-156009369	HUVEC	blood vessel:	n/a
46	chr3:155860278-155860328	A549	lung:	n/a
47	chr3:155860278-155860328	NHBE	bronchial:	n/a
48	chr3:155860792-155860842	GM19239	blood:	n/a
49	chr3:155860932-155860982	HCM	heart:	n/a
50	chr3:156009680-156009730	HCF	heart:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:155891752..155892645-chr3:156192096..156193523,3	MCF-7	breast:
2	chr3:155864395..155866159-chr3:155866850..155868427,2	K562	blood:
3	chr3:155965049..155968394-chr3:155968737..155971623,3	MCF-7	breast:
4	chr3:155869205..155870233-chr3:156227404..156228192,3	K562	blood:
5	chr3:155869736..155870260-chr3:156192819..156193450,2	MCF-7	breast:
6	chr3:155838351..155841179-chr3:155842335..155844140,2	MCF-7	breast:
7	chr3:155869037..155871183-chr3:156875218..156876767,2	K562	blood:
8	chr3:155867882..155869031-chr3:156227090..156228302,7	MCF-7	breast:
9	chr3:155869353..155870217-chr3:156391481..156391983,2	K562	blood:
10	chr3:155867932..155869023-chr3:156099965..156100884,3	K562	blood:
11	chr3:156006145..156008311-chr3:156010060..156013059,2	K562	blood:
12	chr3:155874004..155875829-chr3:155876476..155878948,2	K562	blood:
13	chr3:155882700..155884920-chr3:155887109..155888631,2	K562	blood:
14	chr3:155934377..155935248-chr3:155944547..155945136,2	MCF-7	breast:
15	chr3:155867950..155869167-chr3:156391442..156392069,3	MCF-7	breast:
16	chr3:155891080..155892817-chr3:156167708..156168458,4	MCF-7	breast:
17	chr20:49378121..49380816-chr3:156003979..156005904,2	MCF-7	breast:
18	chr3:155871054..155871626-chr3:156799263..156799804,2	K562	blood:
19	chr3:155869256..155870827-chr3:156099723..156101077,13	MCF-7	breast:
20	chr3:155842632..155844479-chr3:155847006..155849045,2	K562	blood:
21	chr3:155869288..155870259-chr3:156227206..156228043,3	MCF-7	breast:
22	chr3:155868156..155868774-chr3:156192493..156193283,2	MCF-7	breast:
23	chr3:155869753..155870360-chr3:156258546..156259049,2	K562	blood:
24	chr3:155882700..155884920-chr3:155887109..155888631,2	K562	blood:
25	chr3:156006145..156008311-chr3:156010060..156013059,2	K562	blood:
26	chr3:155965049..155968394-chr3:155968737..155971623,3	MCF-7	breast:
27	chr3:155869742..155871357-chr3:155874306..155876247,2	K562	blood:
28	chr3:155728335..155729330-chr3:155867949..155869190,6	MCF-7	breast:
29	chr3:155872011..155872725-chr3:156100054..156100965,2	K562	blood:
30	chr3:155841678..155843255-chr3:155859656..155862270,2	K562	blood:
31	chr3:155875929..155878267-chr3:155880209..155881864,2	K562	blood:
32	chr3:155874004..155875829-chr3:155876476..155878948,2	K562	blood:
33	chr3:155862023..155863592-chr3:155867276..155869925,2	K562	blood:
34	chr3:155868407..155868954-chr3:156226580..156227527,2	MCF-7	breast:
35	chr3:155842632..155844479-chr3:155847006..155849045,2	K562	blood:
36	chr3:155868368..155868971-chr3:156258538..156259204,2	K562	blood:
37	chr3:155869333..155870149-chr3:156919186..156919689,2	K562	blood:
38	chr3:155934377..155935248-chr3:155944547..155945136,2	MCF-7	breast:
39	chr3:155867627..155868538-chr3:156225916..156226586,2	K562	blood:
40	chr3:155867887..155868494-chr3:156167558..156168383,2	MCF-7	breast:
41	chr3:155891772..155892464-chr3:156227676..156228429,2	K562	blood:
42	chr3:155868132..155868862-chr3:156919595..156920136,2	MCF-7	breast:
43	chr3:155925817..155926573-chr5:116060845..116061700,2	MCF-7	breast:
44	chr3:155869321..155870239-chr3:156099929..156100470,4	K562	blood:
45	chr3:155870131..155872683-chr3:155876390..155878620,2	K562	blood:
46	chr3:155903039..155905679-chr3:156268018..156270226,2	K562	blood:
47	chr3:155848600..155850678-chr3:155862966..155865880,2	MCF-7	breast:
48	chr3:155870131..155872683-chr3:155876390..155878620,2	K562	blood:
49	chr3:155848600..155850678-chr3:155862966..155865880,2	MCF-7	breast:
50	chr3:155969617..155971976-chr3:155974281..155977618,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SSR3-4	chr3:155934725-155934828	ENSG00000240596.1
2	lnc-SSR3-4	chr3:155945478-155945672	ENSG00000240596.1
3	lnc-SSR3-4	chr3:155933349-155933527	ENSG00000240596.1
4	lnc-SSR3-4	chr3:155935766-155935825	ENSG00000240596.1
5	lnc-KCNAB1-1	chr3:155836000-155836128	NONHSAT092851

No data

Variant related genes	Relation type
ENSG00000242537	TF binding region
ENSG00000227709	TF binding region
KCNAB1-AS2	TF binding region
KCNAB1	TF binding region
ENSG00000242537	CpG island
ENSG00000227709	CpG island
KCNAB1-AS2	CpG island
KCNAB1	CpG island
ENSG00000243926	chromatin interactions
ENSG00000169282	chromatin interactions
ENSG00000241544	chromatin interactions
ENSG00000114850	chromatin interactions
ENSG00000163660	chromatin interactions

Extended variants
information (count: 6069 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:6069 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7622968	chr3:155827634-155827635	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553195457	chr3:155827675-155827676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375514400	chr3:155827683-155827684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187878590	chr3:155827728-155827729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574848314	chr3:155827766-155827767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558857689	chr3:155827793-155827794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561123486	chr3:155827840-155827841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571540151	chr3:155827879-155827880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543311585	chr3:155827880-155827881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs16825744	chr3:155827895-155827896	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs531981865	chr3:155827910-155827911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7613000	chr3:155827911-155827912	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs79381064	chr3:155827932-155827933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144066317	chr3:155827945-155827946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548526862	chr3:155828088-155828089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73026652	chr3:155828089-155828090	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs7645641	chr3:155828147-155828148	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs552915566	chr3:155828177-155828178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146457154	chr3:155828192-155828193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192948781	chr3:155828248-155828249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554729825	chr3:155828254-155828255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140751867	chr3:155828331-155828332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568497850	chr3:155828340-155828341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183494358	chr3:155828347-155828348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554516659	chr3:155828348-155828349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575825351	chr3:155828378-155828379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556543306	chr3:155828481-155828482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188169023	chr3:155828594-155828595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541434220	chr3:155828598-155828599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576689494	chr3:155828606-155828607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576654314	chr3:155828690-155828691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181865126	chr3:155828715-155828716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35732695	chr3:155828730-155828731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529797609	chr3:155828758-155828759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541898530	chr3:155828798-155828799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573131418	chr3:155828814-155828815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531131864	chr3:155828826-155828827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552776964	chr3:155828830-155828831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571176498	chr3:155828833-155828834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528767015	chr3:155828859-155828860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149831061	chr3:155828864-155828865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568441587	chr3:155828867-155828868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184847924	chr3:155828894-155828895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35941131	chr3:155828906-155828907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557036043	chr3:155828955-155828956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145796715	chr3:155828957-155828958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116330185	chr3:155828964-155828965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149016701	chr3:155828994-155828995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112954535	chr3:155829038-155829039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs199757506	chr3:155829056-155829057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Cancer	17440070	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Sudden cardiac death	19188705	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1051 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155823000-155827800	Weak transcription	Pancreas	Pancrea
2	chr3:155826200-155828200	Enhancers	Fetal Lung	lung
3	chr3:155827200-155828000	Enhancers	Aorta	Aorta
4	chr3:155827400-155828000	Weak transcription	Adipose Nuclei	Adipose
5	chr3:155827400-155828400	Enhancers	Fetal Muscle Leg	muscle
6	chr3:155827600-155827800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr3:155827600-155828000	Enhancers	Duodenum Smooth Muscle	Duodenum
8	chr3:155827600-155828200	Enhancers	Fetal Muscle Trunk	muscle
9	chr3:155827600-155828200	Enhancers	Ovary	ovary
10	chr3:155827600-155828200	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr3:155827800-155828000	Enhancers	Pancreas	Pancrea
12	chr3:155827800-155828000	Enhancers	Rectal Smooth Muscle	rectum
13	chr3:155827800-155828200	Enhancers	Right Atrium	heart
14	chr3:155827800-155828400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr3:155828000-155828200	Enhancers	Adipose Nuclei	Adipose
16	chr3:155828000-155829200	Weak transcription	Pancreas	Pancrea
17	chr3:155829200-155829800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:155829400-155829800	Enhancers	Muscle Satellite Cultured Cells	--
19	chr3:155835200-155836600	Weak transcription	Pancreas	Pancrea
20	chr3:155836600-155836800	Enhancers	Pancreas	Pancrea
21	chr3:155836800-155838400	Weak transcription	Pancreas	Pancrea
22	chr3:155838200-155838800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
23	chr3:155838200-155838800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr3:155838200-155839000	Enhancers	H9 Cell Line	embryonic stem cell
25	chr3:155838400-155838600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
26	chr3:155838400-155838600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr3:155838400-155838600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr3:155838400-155838600	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
29	chr3:155838400-155838600	Active TSS	Left Ventricle	heart
30	chr3:155838400-155838600	Bivalent Enhancer	HSMMtube	muscle
31	chr3:155838400-155838800	Enhancers	H1 Cell Line	embryonic stem cell
32	chr3:155838400-155838800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr3:155838400-155838800	Enhancers	Pancreas	Pancrea
34	chr3:155838400-155839000	Active TSS	Fetal Muscle Leg	muscle
35	chr3:155838400-155839200	Active TSS	Adipose Nuclei	Adipose
36	chr3:155838600-155838800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
37	chr3:155838600-155838800	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr3:155838600-155838800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:155838600-155838800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr3:155838600-155838800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
41	chr3:155838600-155838800	Flanking Active TSS	Left Ventricle	heart
42	chr3:155838600-155839000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
43	chr3:155838600-155839000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr3:155838800-155850200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr3:155839000-155839200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
46	chr3:155839200-155840400	Weak transcription	Adipose Nuclei	Adipose
47	chr3:155840400-155840800	Active TSS	Adipose Nuclei	Adipose
48	chr3:155843400-155844600	Enhancers	Brain Hippocampus Middle	brain
49	chr3:155844600-155845000	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr3:155844600-155849200	Weak transcription	Brain Hippocampus Middle	brain

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