Variant report

Variant	nsv882565
Chromosome Location	chr5:104355383-104923878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1236)
CpG islands
(count:488)
Chromatin interactive
region (count:100)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1236 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104726542-104727019	K562	blood:	n/a	n/a
2	ARID3A	chr5:104728602-104728921	K562	blood:	n/a	n/a
3	ARID3A	chr5:104369169-104369636	K562	blood:	n/a	n/a
4	ARID3A	chr5:104574137-104574841	K562	blood:	n/a	n/a
5	ARID3A	chr5:104729126-104729280	K562	blood:	n/a	n/a
6	ARID3A	chr5:104565880-104566023	K562	blood:	n/a	n/a
7	ARID3A	chr5:104599139-104599705	K562	blood:	n/a	n/a
8	ATF1	chr5:104728486-104728895	K562	blood:	n/a	n/a
9	ATF1	chr5:104475478-104475496	K562	blood:	n/a	n/a
10	ATF1	chr5:104373680-104373755	K562	blood:	n/a	n/a
11	ATF1	chr5:104566225-104566645	K562	blood:	n/a	n/a
12	ATF1	chr5:104599299-104599581	K562	blood:	n/a	n/a
13	ATF1	chr5:104733331-104733371	K562	blood:	n/a	n/a
14	ATF1	chr5:104370024-104370214	K562	blood:	n/a	n/a
15	ATF3	chr5:104890433-104890632	K562	blood:	n/a	n/a
16	BACH1	chr5:104541248-104541265	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr5:104738330-104738373	K562	blood:	n/a	n/a
18	BACH1	chr5:104923763-104924073	K562	blood:	n/a	n/a
19	BACH1	chr5:104923724-104924138	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr5:104779909-104779930	K562	blood:	n/a	n/a
21	BCL11A	chr5:104502865-104503067	H1-hESC	embryonic stem cell:	n/a	n/a
22	BHLHE40	chr5:104728493-104728748	K562	blood:	n/a	n/a
23	BHLHE40	chr5:104369418-104369675	K562	blood:	n/a	n/a
24	BRCA1	chr5:104488401-104488414	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr5:104868861-104868905	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:104393511-104393580	GM12878	blood:	n/a	n/a
27	CBX3	chr5:104428357-104428592	K562	blood:	n/a	n/a
28	CBX3	chr5:104866542-104866887	K562	blood:	n/a	n/a
29	CBX3	chr5:104393083-104393385	K562	blood:	n/a	n/a
30	CBX3	chr5:104755037-104755389	K562	blood:	n/a	n/a
31	CBX3	chr5:104796414-104796740	K562	blood:	n/a	n/a
32	CBX3	chr5:104923689-104924055	K562	blood:	n/a	n/a
33	CBX3	chr5:104755081-104755354	K562	blood:	n/a	n/a
34	CBX3	chr5:104728363-104729015	K562	blood:	n/a	n/a
35	CBX3	chr5:104728451-104728993	K562	blood:	n/a	n/a
36	CBX3	chr5:104686453-104686733	K562	blood:	n/a	n/a
37	CBX3	chr5:104699005-104699210	K562	blood:	n/a	n/a
38	CBX3	chr5:104370642-104370939	K562	blood:	n/a	n/a
39	CBX3	chr5:104393078-104393434	K562	blood:	n/a	n/a
40	CBX3	chr5:104796463-104796676	K562	blood:	n/a	n/a
41	CBX3	chr5:104866626-104866912	K562	blood:	n/a	n/a
42	CCNT2	chr5:104599218-104599525	K562	blood:	n/a	n/a
43	CCNT2	chr5:104566220-104566624	K562	blood:	n/a	n/a
44	CCNT2	chr5:104370115-104370461	K562	blood:	n/a	n/a
45	CCNT2	chr5:104727769-104728552	K562	blood:	n/a	n/a
46	CCNT2	chr5:104890165-104890637	K562	blood:	n/a	n/a
47	CCNT2	chr5:104369421-104369754	K562	blood:	n/a	chr5:104369561-104369581
48	CEBPB	chr5:104370108-104370517	ECC-1	luminal epithelium:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
49	CEBPB	chr5:104788546-104788789	A549	lung:	n/a	chr5:104788606-104788619 chr5:104788606-104788617 chr5:104788603-104788620
50	CEBPB	chr5:104391916-104392212	A549	lung:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104728220-104728270	GM06990	blood:	n/a
2	chr5:104433849-104433899	HNPCEpiC	eye:	n/a
3	chr5:104728220-104728270	AG10803	skin:	n/a
4	chr5:104854808-104854858	MCF-7	breast:	n/a
5	chr5:104434864-104434914	Caco-2	colon:	n/a
6	chr5:104434864-104434914	SK-N-MC	brain:	n/a
7	chr5:104435062-104435112	LNCaP	prostate:	n/a
8	chr5:104433849-104433899	PrEC	prostate:	n/a
9	chr5:104728220-104728270	GM12892	blood:	n/a
10	chr5:104435062-104435112	Hela-S3	cervix:	n/a
11	chr5:104854808-104854858	PFSK-1	brain:	n/a
12	chr5:104728220-104728270	HCPEpiC	choroid plexus:	n/a
13	chr5:104728220-104728270	ProgFib	skin:	n/a
14	chr5:104434864-104434914	HRE	kidney:	n/a
15	chr5:104433849-104433899	RPTEC	kidney:	n/a
16	chr5:104728427-104728477	GM19239	blood:	n/a
17	chr5:104434827-104434877	SAEC	small airway:	n/a
18	chr5:104434864-104434914	RPTEC	kidney:	n/a
19	chr5:104435608-104435658	NHDF-neo	bronchial:	n/a
20	chr5:104728427-104728477	PFSK-1	brain:	n/a
21	chr5:104728220-104728270	Hepatocyte	liver:	n/a
22	chr5:104728427-104728477	AG04449	skin:	fetal
23	chr5:104433849-104433899	HEK293	kidney:	embryo
24	chr5:104434827-104434877	PrEC	prostate:	n/a
25	chr5:104434827-104434877	GM12892	blood:	n/a
26	chr5:104434827-104434877	H1-hESC	embryonic stem cell:	embryo
27	chr5:104728220-104728270	ovcar-3	ovarian:	n/a
28	chr5:104728427-104728477	PrEC	prostate:	n/a
29	chr5:104434827-104434877	PANC-1	pancreas:	n/a
30	chr5:104435608-104435658	SK-N-SH	brain:	n/a
31	chr5:104433849-104433899	GM19239	blood:	n/a
32	chr5:104854808-104854858	HIPEpiC	eye:	n/a
33	chr5:104728427-104728477	AG04450	lung:	fetal
34	chr5:104854808-104854858	AG04450	lung:	fetal
35	chr5:104435062-104435112	HRPEpiC	eye:	n/a
36	chr5:104433849-104433899	HAEpiC	amniotic membrane:	n/a
37	chr5:104433849-104433899	NH-A	brain:	n/a
38	chr5:104728220-104728270	AoSMC	blood vessel:	n/a
39	chr5:104434827-104434877	NB4	blood:	n/a
40	chr5:104435608-104435658	HEK293	kidney:	embryo
41	chr5:104728427-104728477	MCF-7	breast:	n/a
42	chr5:104434864-104434914	ECC-1	luminal epithelium:	n/a
43	chr5:104435062-104435112	IMR90	lung:	fetal
44	chr5:104435062-104435112	HRCEpiC	kidney:	n/a
45	chr5:104434864-104434914	SK-N-SH_RA	brain:	n/a
46	chr5:104728427-104728477	AG10803	skin:	n/a
47	chr5:104434827-104434877	IMR90	lung:	fetal
48	chr5:104434827-104434877	LNCaP	prostate:	n/a
49	chr5:104433849-104433899	HCF	heart:	n/a
50	chr5:104435062-104435112	HUVEC	blood vessel:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:104649160..104650852-chr5:104651591..104654211,3	K562	blood:
2	chr5:104645770..104648035-chr5:104661663..104663662,2	MCF-7	breast:
3	chr5:104369743..104372595-chr5:104912590..104914639,2	K562	blood:
4	chr5:104733236..104736068-chr5:104886596..104888346,2	MCF-7	breast:
5	chr19:12903711..12905991-chr5:104578289..104580216,2	MCF-7	breast:
6	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
7	chr5:104545961..104548123-chr5:104549429..104551527,2	K562	blood:
8	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
9	chr5:104710520..104712024-chr5:104741469..104744150,2	K562	blood:
10	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:
11	chr5:104645770..104648035-chr5:104661663..104663662,2	MCF-7	breast:
12	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
13	chr5:104649160..104650852-chr5:104651591..104654211,3	K562	blood:
14	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
15	chr5:104528561..104530726-chr5:104532311..104534213,2	K562	blood:
16	chr5:104716167..104718489-chr5:104728063..104729895,2	K562	blood:
17	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
18	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
19	chr5:104545961..104548123-chr5:104549429..104551527,2	K562	blood:
20	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
21	chr5:104679097..104680828-chr5:104708980..104711591,2	K562	blood:
22	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
23	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
24	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
25	chr5:104582906..104584797-chr5:104601356..104603170,2	K562	blood:
26	chr5:104805339..104808156-chr5:104810446..104813222,2	MCF-7	breast:
27	chr5:104733236..104736068-chr5:104886596..104888346,2	MCF-7	breast:
28	chr1:184434764..184435543-chr5:104792004..104792524,3	MCF-7	breast:
29	chr5:104565194..104566957-chr5:104571048..104573999,2	K562	blood:
30	chr5:104727296..104728816-chr5:104790778..104793743,2	K562	blood:
31	chr5:104711472..104715081-chr5:104725603..104729958,5	K562	blood:
32	chr5:104524711..104526370-chr5:104889242..104892104,2	K562	blood:
33	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
34	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
35	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
36	chr5:104682524..104684533-chr5:104692732..104695457,2	MCF-7	breast:
37	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
38	chr5:104712112..104715391-chr5:104727182..104729595,3	K562	blood:
39	chr5:104886320..104887974-chr5:104890366..104891898,2	MCF-7	breast:
40	chr5:104545106..104548123-chr5:104549429..104551527,3	K562	blood:
41	chr18:42792470..42793145-chr5:104821622..104822504,2	MCF-7	breast:
42	chr5:104768629..104770858-chr5:104785097..104787270,2	K562	blood:
43	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
44	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
45	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:
46	chr5:104582906..104584797-chr5:104601356..104603170,2	K562	blood:
47	chr5:104686842..104688917-chr5:104691899..104693400,2	K562	blood:
48	chr12:23105697..23106553-chr5:104539343..104540254,2	MCF-7	breast:
49	chr5:104586940..104589611-chr5:104727738..104729575,2	K562	blood:
50	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf30-8	chr5:104435175-104435799	NR_000039
2	lnc-NUDT12-7	chr5:104728462-104728989	NONHSAT103097
3	lnc-NUDT12-6	chr5:104728462-104728671	ENSG00000251574
4	lnc-NUDT12-7	chr5:104582013-104582067	NONHSAT103097
5	lnc-C5orf30-8	chr5:104435174-104435799	NONHSAT103096
6	lnc-NUDT12-7	chr5:104581998-104582065	ENSG00000253584

No data

Variant related genes	Relation type
ENSG00000253584	TF binding region
ENSG00000251574	TF binding region
RAB9BP1	TF binding region
ENSG00000253584	CpG island
ENSG00000251574	CpG island
RAB9BP1	CpG island
ENSG00000145743	chromatin interactions
ENSG00000132874	chromatin interactions
ENSG00000251574	chromatin interactions

Extended variants
information (count: 6466 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:6466 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551173771	chr5:104369411-104369412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567724461	chr5:104369424-104369425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs80213085	chr5:104369447-104369448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs13168070	chr5:104369455-104369456	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs567169618	chr5:104369459-104369460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539076977	chr5:104369475-104369476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529169327	chr5:104369491-104369492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558639915	chr5:104369503-104369504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549198741	chr5:104369506-104369507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575697070	chr5:104369514-104369515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568940603	chr5:104369547-104369548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544354833	chr5:104369582-104369583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557137686	chr5:104369592-104369593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369630905	chr5:104369605-104369606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370273956	chr5:104369717-104369718	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573791045	chr5:104369739-104369740	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs34567596	chr5:104369804-104369805	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542393671	chr5:104369836-104369837	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs7709488	chr5:104369901-104369902	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528326636	chr5:104369906-104369907	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544604571	chr5:104369921-104369922	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564695647	chr5:104369937-104369938	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs62366393	chr5:104369953-104369954	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs550436959	chr5:104369954-104369955	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs118109132	chr5:104369955-104369956	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530364091	chr5:104369956-104369957	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78189970	chr5:104369965-104369966	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs571686307	chr5:104369975-104369976	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547207899	chr5:104369990-104369991	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567181919	chr5:104369992-104369993	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs13185910	chr5:104370015-104370016	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs145869163	chr5:104370027-104370028	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs531771058	chr5:104370028-104370029	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs567997437	chr5:104370124-104370125	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs569126214	chr5:104370140-104370141	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs13168898	chr5:104370141-104370142	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552575111	chr5:104370157-104370158	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574590942	chr5:104370169-104370170	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369789657	chr5:104370184-104370185	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542422121	chr5:104370267-104370268	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552701931	chr5:104370274-104370275	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs62366394	chr5:104370306-104370307	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs73777388	chr5:104370319-104370320	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs565170705	chr5:104370322-104370323	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12518114	chr5:104370486-104370487	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs115934720	chr5:104370516-104370517	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs12518136	chr5:104370570-104370571	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs560862111	chr5:104370605-104370606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529774703	chr5:104370607-104370608	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547219910	chr5:104370638-104370639	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Myelofibrosis	22110671	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
Obesity	20622171	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104369400-104369800	Enhancers	K562	blood
2	chr5:104369400-104370000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr5:104369400-104370200	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr5:104369800-104370200	Flanking Active TSS	K562	blood
5	chr5:104370200-104370400	Enhancers	K562	blood
6	chr5:104370200-104370600	Enhancers	Hela-S3	cervix
7	chr5:104370400-104371600	Weak transcription	K562	blood
8	chr5:104376200-104376600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:104380200-104380600	Enhancers	Fetal Brain Male	brain
10	chr5:104388000-104392400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:104389600-104390600	Enhancers	Fetal Lung	lung
12	chr5:104390200-104390800	Active TSS	Fetal Brain Male	brain
13	chr5:104392400-104393200	ZNF genes & repeats	Esophagus	oesophagus
14	chr5:104392400-104394000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr5:104392400-104394000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:104392400-104394000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr5:104398800-104402000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr5:104421400-104421600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:104421600-104422200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:104422400-104422600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:104422600-104423600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:104423600-104425000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr5:104424000-104424400	Enhancers	Primary hematopoietic stem cells	blood
24	chr5:104425000-104428000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:104428000-104428200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:104437400-104438000	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr5:104446800-104447200	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr5:104451200-104451400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:104453600-104455000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr5:104459600-104460200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr5:104468200-104468800	Enhancers	Brain Germinal Matrix	brain
32	chr5:104469400-104470600	Enhancers	Liver	Liver
33	chr5:104472600-104473200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:104473200-104474200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:104474200-104474400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:104485600-104486600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:104486000-104486600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:104488800-104489000	Enhancers	Fetal Lung	lung
39	chr5:104489000-104490800	Weak transcription	Fetal Lung	lung
40	chr5:104490800-104491200	ZNF genes & repeats	Fetal Lung	lung
41	chr5:104492600-104492800	ZNF genes & repeats	Aorta	Aorta
42	chr5:104492800-104494200	Weak transcription	Aorta	Aorta
43	chr5:104494000-104495600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr5:104503600-104504400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr5:104503800-104504400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr5:104503800-104504600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr5:104503800-104504600	Enhancers	Hela-S3	cervix
48	chr5:104504400-104505400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr5:104505800-104506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:104512000-104512400	Active TSS	Breast Myoepithelial Primary Cells	Breast

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