Variant report

Variant	nsv882625
Chromosome Location	chr5:104717739-105081035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1079)
CpG islands
(count:184)
Chromatin interactive
region (count:57)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104729126-104729280	K562	blood:	n/a	n/a
2	ARID3A	chr5:104726542-104727019	K562	blood:	n/a	n/a
3	ARID3A	chr5:104728602-104728921	K562	blood:	n/a	n/a
4	ATF1	chr5:104728486-104728895	K562	blood:	n/a	n/a
5	ATF1	chr5:104733331-104733371	K562	blood:	n/a	n/a
6	ATF3	chr5:104890433-104890632	K562	blood:	n/a	n/a
7	BACH1	chr5:104923724-104924138	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:104738330-104738373	K562	blood:	n/a	n/a
9	BACH1	chr5:104923763-104924073	K562	blood:	n/a	n/a
10	BACH1	chr5:104779909-104779930	K562	blood:	n/a	n/a
11	BHLHE40	chr5:104728493-104728748	K562	blood:	n/a	n/a
12	BHLHE40	chr5:104928859-104929002	K562	blood:	n/a	n/a
13	BRCA1	chr5:104868861-104868905	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr5:105023264-105023360	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr5:104796463-104796676	K562	blood:	n/a	n/a
16	CBX3	chr5:104728363-104729015	K562	blood:	n/a	n/a
17	CBX3	chr5:104866542-104866887	K562	blood:	n/a	n/a
18	CBX3	chr5:104928778-104929345	K562	blood:	n/a	n/a
19	CBX3	chr5:104796414-104796740	K562	blood:	n/a	n/a
20	CBX3	chr5:104923689-104924055	K562	blood:	n/a	n/a
21	CBX3	chr5:105037977-105038410	HCT-116	colon:	n/a	n/a
22	CBX3	chr5:104728451-104728993	K562	blood:	n/a	n/a
23	CBX3	chr5:104755081-104755354	K562	blood:	n/a	n/a
24	CBX3	chr5:104866626-104866912	K562	blood:	n/a	n/a
25	CBX3	chr5:104939067-104939376	K562	blood:	n/a	n/a
26	CBX3	chr5:104755037-104755389	K562	blood:	n/a	n/a
27	CCNT2	chr5:104890165-104890637	K562	blood:	n/a	n/a
28	CCNT2	chr5:104727769-104728552	K562	blood:	n/a	n/a
29	CCNT2	chr5:104928811-104929257	K562	blood:	n/a	n/a
30	CEBPB	chr5:104845452-104845652	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr5:104876322-104876498	K562	blood:	n/a	n/a
32	CEBPB	chr5:104928385-104928674	K562	blood:	n/a	chr5:104928408-104928420 chr5:104928519-104928532
33	CEBPB	chr5:104859617-104859857	A549	lung:	n/a	chr5:104859773-104859784
34	CEBPB	chr5:104965103-104965346	HepG2	liver:	n/a	chr5:104965201-104965212
35	CEBPB	chr5:104968601-104968824	HepG2	liver:	n/a	chr5:104968706-104968717
36	CEBPB	chr5:104923760-104923972	K562	blood:	n/a	n/a
37	CEBPB	chr5:104875263-104875486	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr5:104965121-104965319	K562	blood:	n/a	chr5:104965201-104965212
39	CEBPB	chr5:104859757-104859805	K562	blood:	n/a	chr5:104859773-104859784
40	CEBPB	chr5:105049278-105049363	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr5:104952330-104952720	MCF-7	breast:	n/a	n/a
42	CEBPB	chr5:104890358-104890650	K562	blood:	n/a	n/a
43	CEBPB	chr5:104872393-104872674	HepG2	liver:	n/a	n/a
44	CEBPB	chr5:104953385-104953682	K562	blood:	n/a	n/a
45	CEBPB	chr5:105049174-105049388	A549	lung:	n/a	n/a
46	CEBPB	chr5:104979408-104979673	HepG2	liver:	n/a	chr5:104979522-104979533
47	CEBPB	chr5:104901458-104901701	HepG2	liver:	n/a	chr5:104901515-104901526 chr5:104901515-104901528 chr5:104901517-104901528 chr5:104901515-104901528 chr5:104901517-104901526
48	CEBPB	chr5:105013023-105013519	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr5:104847008-104847283	K562	blood:	n/a	chr5:104847143-104847156
50	CEBPB	chr5:104788546-104788789	A549	lung:	n/a	chr5:104788606-104788619 chr5:104788606-104788617 chr5:104788603-104788620

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104728427-104728477	SAEC	small airway:	n/a
2	chr5:104728427-104728477	SAEC	small airway:	n/a
3	chr5:104728427-104728477	Caco-2	colon:	n/a
4	chr5:104728220-104728270	PFSK-1	brain:	n/a
5	chr5:104728220-104728270	Caco-2	colon:	n/a
6	chr5:104854808-104854858	AoSMC	blood vessel:	n/a
7	chr5:104728220-104728270	GM06990	blood:	n/a
8	chr5:104728427-104728477	K562	blood:	n/a
9	chr5:104728220-104728270	HMEC	breast:	n/a
10	chr5:104854808-104854858	HIPEpiC	eye:	n/a
11	chr5:104728220-104728270	K562	blood:	n/a
12	chr5:104854808-104854858	GM06990	blood:	n/a
13	chr5:104728220-104728270	HRCEpiC	kidney:	n/a
14	chr5:104728220-104728270	ECC-1	luminal epithelium:	n/a
15	chr5:104854808-104854858	HEK293	kidney:	embryo
16	chr5:104728220-104728270	GM12892	blood:	n/a
17	chr5:104728427-104728477	HEK293	kidney:	embryo
18	chr5:104854808-104854858	T-47D	breast:	n/a
19	chr5:104728220-104728270	CMK	blood:	n/a
20	chr5:104728220-104728270	HRPEpiC	eye:	n/a
21	chr5:104728220-104728270	MCF-7	breast:	n/a
22	chr5:104728220-104728270	HIPEpiC	eye:	n/a
23	chr5:104728427-104728477	AG10803	skin:	n/a
24	chr5:104728427-104728477	AoSMC	blood vessel:	n/a
25	chr5:104728427-104728477	NH-A	brain:	n/a
26	chr5:104728220-104728270	Hela-S3	cervix:	n/a
27	chr5:104728427-104728477	HMEC	breast:	n/a
28	chr5:104728220-104728270	AG10803	skin:	n/a
29	chr5:104728427-104728477	PrEC	prostate:	n/a
30	chr5:104728427-104728477	ECC-1	luminal epithelium:	n/a
31	chr5:104854808-104854858	HL-60	blood:	n/a
32	chr5:104854808-104854858	NH-A	brain:	n/a
33	chr5:104854808-104854858	SK-N-SH	brain:	n/a
34	chr5:104728427-104728477	SK-N-MC	brain:	n/a
35	chr5:104854808-104854858	HCF	heart:	n/a
36	chr5:104728220-104728270	NB4	blood:	n/a
37	chr5:104728427-104728477	HL-60	blood:	n/a
38	chr5:104728220-104728270	U87	brain:	n/a
39	chr5:104854808-104854858	HRCEpiC	kidney:	n/a
40	chr5:104854808-104854858	CMK	blood:	n/a
41	chr5:104728220-104728270	PrEC	prostate:	n/a
42	chr5:104854808-104854858	A549	lung:	n/a
43	chr5:104728427-104728477	HCM	heart:	n/a
44	chr5:104728427-104728477	AG04450	lung:	fetal
45	chr5:104728220-104728270	Jurkat	blood:	n/a
46	chr5:104728220-104728270	SK-N-SH_RA	brain:	n/a
47	chr5:104854808-104854858	SK-N-SH_RA	brain:	n/a
48	chr5:104854808-104854858	BE2_C	brain:	n/a
49	chr5:104854808-104854858	HPAEpiC	pulmonary alveolar:	n/a
50	chr5:104728427-104728477	Jurkat	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:104886320..104887974-chr5:104890366..104891898,2	MCF-7	breast:
2	chr5:104716167..104718489-chr5:104728063..104729895,2	K562	blood:
3	chr5:104726534..104729492-chr5:107716153..107718681,2	K562	blood:
4	chr5:104927470..104929144-chr5:104929220..104932182,2	K562	blood:
5	chr5:104733236..104736068-chr5:104886596..104888346,2	MCF-7	breast:
6	chr5:104952005..104953083-chr5:105576858..105577888,8	MCF-7	breast:
7	chr5:104727742..104729434-chr5:104763198..104765492,2	K562	blood:
8	chr5:104929507..104932104-chr5:104932394..104934135,2	MCF-7	breast:
9	chr5:104810915..104813579-chr5:104817384..104819206,2	MCF-7	breast:
10	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
11	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
12	chr5:104710520..104712024-chr5:104741469..104744150,2	K562	blood:
13	chr5:105020604..105022819-chr5:105026023..105028609,2	K562	blood:
14	chr5:104928031..104930264-chr5:104952247..104955234,2	MCF-7	breast:
15	chr5:104950620..104953196-chr5:104960454..104963137,2	K562	blood:
16	chr5:104805339..104808156-chr5:104810446..104813222,2	MCF-7	breast:
17	chr5:104726359..104728666-chr5:105131284..105132821,2	K562	blood:
18	chr5:104955524..104956144-chr5:105577134..105577974,2	MCF-7	breast:
19	chr5:104727296..104728816-chr5:104790778..104793743,2	K562	blood:
20	chr5:104995980..104998958-chr5:105000581..105003176,3	MCF-7	breast:
21	chr4:114611671..114612572-chr5:104870661..104871343,2	MCF-7	breast:
22	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
23	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
24	chr5:104369743..104372595-chr5:104912590..104914639,2	K562	blood:
25	chr5:104950620..104953196-chr5:104960454..104963137,2	K562	blood:
26	chr5:104733236..104736068-chr5:104886596..104888346,2	MCF-7	breast:
27	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
28	chr5:104952005..104953083-chr5:105576858..105577888,9	MCF-7	breast:
29	chr18:42792470..42793145-chr5:104821622..104822504,2	MCF-7	breast:
30	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
31	chr5:104929507..104932104-chr5:104932394..104934135,2	MCF-7	breast:
32	chr5:104810915..104813579-chr5:104817384..104819206,2	MCF-7	breast:
33	chr5:104768629..104770858-chr5:104785097..104787270,2	K562	blood:
34	chr5:104952039..104952571-chr5:105577029..105577838,2	MCF-7	breast:
35	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
36	chr1:184434764..184435543-chr5:104792004..104792524,3	MCF-7	breast:
37	chr5:104886320..104887974-chr5:104890366..104891898,2	MCF-7	breast:
38	chr5:104926004..104928970-chr5:104930124..104932222,3	K562	blood:
39	chr5:104943469..104946264-chr5:104959458..104962320,2	K562	blood:
40	chr5:105069835..105071621-chr5:105082502..105084277,2	K562	blood:
41	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
42	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
43	chr5:104524711..104526370-chr5:104889242..104892104,2	K562	blood:
44	chr5:104955261..104956180-chr5:105577014..105577827,4	MCF-7	breast:
45	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
46	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
47	chr5:105020604..105022819-chr5:105026023..105028609,2	K562	blood:
48	chr5:104928031..104930264-chr5:104952247..104955234,2	MCF-7	breast:
49	chr5:104995980..104998958-chr5:105000581..105003176,3	MCF-7	breast:
50	chr5:104927470..104929144-chr5:104929220..104932182,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104728462-104728989	NONHSAT103097
2	lnc-NUDT12-6	chr5:104728462-104728671	ENSG00000251574

No data

Variant related genes	Relation type
ENSG00000251574	TF binding region
ENSG00000251574	CpG island
ENSG00000132874	chromatin interactions
ENSG00000251574	chromatin interactions
ENSG00000145743	chromatin interactions

Extended variants
information (count: 4615 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:4615 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1423208	chr5:104717739-104717740	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566461538	chr5:104717744-104717745	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs576940562	chr5:104717746-104717747	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550164360	chr5:104717750-104717751	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571607225	chr5:104717764-104717765	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs538296745	chr5:104717770-104717771	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372055159	chr5:104717778-104717779	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558785224	chr5:104717821-104717822	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs575535931	chr5:104717824-104717825	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538747739	chr5:104717883-104717884	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547531126	chr5:104717907-104717908	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541964979	chr5:104717923-104717924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554758289	chr5:104717968-104717969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs6860623	chr5:104717974-104717975	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs540699321	chr5:104718011-104718012	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs560426030	chr5:104718026-104718027	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566319236	chr5:104718039-104718040	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs201720300	chr5:104718045-104718046	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545884352	chr5:104718049-104718050	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs565126826	chr5:104718054-104718055	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs530844659	chr5:104718202-104718203	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs550931465	chr5:104718259-104718260	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567448906	chr5:104718341-104718342	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs141164184	chr5:104718371-104718372	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs369139216	chr5:104718376-104718377	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs555353734	chr5:104718379-104718380	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145653068	chr5:104718383-104718384	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538582259	chr5:104718416-104718417	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs73196665	chr5:104718441-104718442	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182718122	chr5:104718471-104718472	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs11951892	chr5:104718477-104718478	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs556087121	chr5:104722002-104722003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs193213303	chr5:104722034-104722035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11955463	chr5:104722062-104722063	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs72786079	chr5:104722072-104722073	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs572127539	chr5:104722079-104722080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375413183	chr5:104722110-104722111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541050877	chr5:104722131-104722132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185562880	chr5:104722136-104722137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564056253	chr5:104722161-104722162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75001211	chr5:104722164-104722165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544123140	chr5:104722172-104722173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187751653	chr5:104722239-104722240	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375479981	chr5:104722252-104722253	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72786080	chr5:104722261-104722262	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559558535	chr5:104722275-104722276	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548857574	chr5:104722285-104722286	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562537092	chr5:104722292-104722293	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528599609	chr5:104722372-104722373	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112591478	chr5:104722426-104722427	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Obesity	20622171	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104722000-104722200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr5:104722200-104722600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr5:104722200-104722800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr5:104722200-104723200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:104722400-104723400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr5:104722400-104723600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:104722600-104723000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:104724800-104725800	Enhancers	K562	blood
9	chr5:104725800-104726400	Weak transcription	K562	blood
10	chr5:104726400-104729200	Active TSS	K562	blood
11	chr5:104727400-104727600	Enhancers	Placenta	Placenta
12	chr5:104727600-104727800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr5:104727600-104728000	Flanking Active TSS	Placenta	Placenta
14	chr5:104727600-104729000	Active TSS	HepG2	liver
15	chr5:104727800-104728000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:104727800-104728600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:104728000-104728400	Active TSS	Placenta	Placenta
18	chr5:104728400-104728800	ZNF genes & repeats	Placenta	Placenta
19	chr5:104742400-104743400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:104742400-104743600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr5:104742400-104743600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr5:104742600-104743400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr5:104742800-104743200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr5:104742800-104743400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr5:104748600-104749200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:104748800-104749200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr5:104749200-104749600	Bivalent Enhancer	Placenta	Placenta
28	chr5:104749200-104749800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:104757800-104758600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:104763400-104764400	Enhancers	Fetal Intestine Large	intestine
31	chr5:104766000-104767600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr5:104767600-104768600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:104768600-104769000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr5:104768600-104769200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr5:104796000-104801800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr5:104811600-104811800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:104817600-104817800	Enhancers	Liver	Liver
38	chr5:104817800-104818200	Active TSS	Liver	Liver
39	chr5:104820000-104820600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:104828000-104828600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:104829400-104829600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:104833800-104834200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:104833800-104834400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:104833800-104834400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr5:104833800-104834400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr5:104834000-104834400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr5:104834000-104834400	Active TSS	Spleen	Spleen
48	chr5:104834400-104836200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr5:104836200-104837000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr5:104836200-104837200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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