Variant report

Variant	nsv882545
Chromosome Location	chr5:104139803-104841922
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1380)
CpG islands
(count:549)
Chromatin interactive
region (count:126)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1380 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104574137-104574841	K562	blood:	n/a	n/a
2	ARID3A	chr5:104729126-104729280	K562	blood:	n/a	n/a
3	ARID3A	chr5:104255114-104255149	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:104599139-104599705	K562	blood:	n/a	n/a
5	ARID3A	chr5:104565880-104566023	K562	blood:	n/a	n/a
6	ARID3A	chr5:104369169-104369636	K562	blood:	n/a	n/a
7	ARID3A	chr5:104726542-104727019	K562	blood:	n/a	n/a
8	ARID3A	chr5:104728602-104728921	K562	blood:	n/a	n/a
9	ATF1	chr5:104599299-104599581	K562	blood:	n/a	n/a
10	ATF1	chr5:104475478-104475496	K562	blood:	n/a	n/a
11	ATF1	chr5:104566225-104566645	K562	blood:	n/a	n/a
12	ATF1	chr5:104373680-104373755	K562	blood:	n/a	n/a
13	ATF1	chr5:104370024-104370214	K562	blood:	n/a	n/a
14	ATF1	chr5:104728486-104728895	K562	blood:	n/a	n/a
15	ATF1	chr5:104733331-104733371	K562	blood:	n/a	n/a
16	BACH1	chr5:104223199-104223207	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr5:104738330-104738373	K562	blood:	n/a	n/a
18	BACH1	chr5:104779909-104779930	K562	blood:	n/a	n/a
19	BACH1	chr5:104541248-104541265	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL11A	chr5:104502865-104503067	H1-hESC	embryonic stem cell:	n/a	n/a
21	BHLHE40	chr5:104728493-104728748	K562	blood:	n/a	n/a
22	BHLHE40	chr5:104369418-104369675	K562	blood:	n/a	n/a
23	BRCA1	chr5:104393511-104393580	GM12878	blood:	n/a	n/a
24	BRCA1	chr5:104317800-104317805	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr5:104246667-104246983	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:104325896-104325918	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr5:104488401-104488414	H1-hESC	embryonic stem cell:	n/a	n/a
28	CBX3	chr5:104686453-104686733	K562	blood:	n/a	n/a
29	CBX3	chr5:104755081-104755354	K562	blood:	n/a	n/a
30	CBX3	chr5:104428357-104428592	K562	blood:	n/a	n/a
31	CBX3	chr5:104755037-104755389	K562	blood:	n/a	n/a
32	CBX3	chr5:104393083-104393385	K562	blood:	n/a	n/a
33	CBX3	chr5:104699005-104699210	K562	blood:	n/a	n/a
34	CBX3	chr5:104393078-104393434	K562	blood:	n/a	n/a
35	CBX3	chr5:104728363-104729015	K562	blood:	n/a	n/a
36	CBX3	chr5:104728451-104728993	K562	blood:	n/a	n/a
37	CBX3	chr5:104796463-104796676	K562	blood:	n/a	n/a
38	CBX3	chr5:104370642-104370939	K562	blood:	n/a	n/a
39	CBX3	chr5:104796414-104796740	K562	blood:	n/a	n/a
40	CCNT2	chr5:104566220-104566624	K562	blood:	n/a	n/a
41	CCNT2	chr5:104599218-104599525	K562	blood:	n/a	n/a
42	CCNT2	chr5:104369421-104369754	K562	blood:	n/a	chr5:104369561-104369581
43	CCNT2	chr5:104306891-104307038	K562	blood:	n/a	n/a
44	CCNT2	chr5:104727769-104728552	K562	blood:	n/a	n/a
45	CCNT2	chr5:104370115-104370461	K562	blood:	n/a	n/a
46	CEBPB	chr5:104593448-104593544	K562	blood:	n/a	chr5:104593456-104593469 chr5:104593456-104593469 chr5:104593458-104593469 chr5:104593456-104593469 chr5:104593458-104593469
47	CEBPB	chr5:104665902-104666250	IMR90	lung:	n/a	chr5:104666084-104666093 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666082-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666083-104666094
48	CEBPB	chr5:104516185-104516507	IMR90	lung:	n/a	n/a
49	CEBPB	chr5:104195089-104195447	ECC-1	luminal epithelium:	n/a	chr5:104195252-104195263
50	CEBPB	chr5:104373830-104373968	HepG2	liver:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104265747-104265797	H1-hESC	embryonic stem cell:	embryo
2	chr5:104728220-104728270	SK-N-SH	brain:	n/a
3	chr5:104265747-104265797	SK-N-MC	brain:	n/a
4	chr5:104434827-104434877	AG10803	skin:	n/a
5	chr5:104265747-104265797	HEK293	kidney:	embryo
6	chr5:104433849-104433899	Caco-2	colon:	n/a
7	chr5:104433849-104433899	NT2-D1	testis:	n/a
8	chr5:104433849-104433899	NHBE	bronchial:	n/a
9	chr5:104434827-104434877	HRE	kidney:	n/a
10	chr5:104433849-104433899	AG09319	gingival:	n/a
11	chr5:104728220-104728270	AG09319	gingival:	n/a
12	chr5:104435062-104435112	AG09309	skin:	n/a
13	chr5:104345171-104345221	U87	brain:	n/a
14	chr5:104435608-104435658	A549	lung:	n/a
15	chr5:104728220-104728270	NHDF-neo	bronchial:	n/a
16	chr5:104434864-104434914	SKMC	muscle:	n/a
17	chr5:104433849-104433899	A549	lung:	n/a
18	chr5:104728220-104728270	Caco-2	colon:	n/a
19	chr5:104435062-104435112	NB4	blood:	n/a
20	chr5:104435608-104435658	HIPEpiC	eye:	n/a
21	chr5:104728427-104728477	MCF10A-Er-Src	breast:	n/a
22	chr5:104728220-104728270	ECC-1	luminal epithelium:	n/a
23	chr5:104435062-104435112	GM12891	blood:	n/a
24	chr5:104433849-104433899	Jurkat	blood:	n/a
25	chr5:104434864-104434914	HCF	heart:	n/a
26	chr5:104345171-104345221	HPAEpiC	pulmonary alveolar:	n/a
27	chr5:104728427-104728477	CMK	blood:	n/a
28	chr5:104728220-104728270	NT2-D1	testis:	n/a
29	chr5:104434864-104434914	SK-N-MC	brain:	n/a
30	chr5:104435608-104435658	AG04449	skin:	fetal
31	chr5:104435608-104435658	BJ	skin:	n/a
32	chr5:104345171-104345221	GM06990	blood:	n/a
33	chr5:104434864-104434914	HMEC	breast:	n/a
34	chr5:104434827-104434877	HUVEC	blood vessel:	n/a
35	chr5:104728220-104728270	GM12891	blood:	n/a
36	chr5:104265747-104265797	HCF	heart:	n/a
37	chr5:104728220-104728270	HNPCEpiC	eye:	n/a
38	chr5:104435062-104435112	Jurkat	blood:	n/a
39	chr5:104433849-104433899	BJ	skin:	n/a
40	chr5:104345171-104345221	SK-N-SH_RA	brain:	n/a
41	chr5:104435062-104435112	BJ	skin:	n/a
42	chr5:104728220-104728270	HRPEpiC	eye:	n/a
43	chr5:104345171-104345221	MCF-7	breast:	n/a
44	chr5:104435062-104435112	HEEpiC	esophagus:	n/a
45	chr5:104434827-104434877	ECC-1	luminal epithelium:	n/a
46	chr5:104434827-104434877	Hela-S3	cervix:	n/a
47	chr5:104434864-104434914	MCF10A-Er-Src	breast:	n/a
48	chr5:104433849-104433899	GM12891	blood:	n/a
49	chr5:104435062-104435112	A549	lung:	n/a
50	chr5:104434827-104434877	HAEpiC	amniotic membrane:	n/a

(count:126 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
2	chr5:104604624..104606834-chr5:104613480..104615859,2	K562	blood:
3	chr5:104810915..104813579-chr5:104817384..104819206,2	MCF-7	breast:
4	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:
5	chr19:12903711..12905991-chr5:104578289..104580216,2	MCF-7	breast:
6	chr5:104248370..104250240-chr5:104261197..104262793,2	MCF-7	breast:
7	chr5:104582906..104584797-chr5:104601356..104603170,2	K562	blood:
8	chr5:104682989..104685447-chr5:104726579..104728705,2	K562	blood:
9	chr5:104726359..104728666-chr5:105131284..105132821,2	K562	blood:
10	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
11	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
12	chr5:104256936..104259316-chr5:104275958..104278631,2	K562	blood:
13	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
14	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
15	chr5:104733236..104736068-chr5:104886596..104888346,2	MCF-7	breast:
16	chr5:104545106..104548123-chr5:104549429..104551527,3	K562	blood:
17	chr5:104277822..104279427-chr5:104300449..104302157,2	MCF-7	breast:
18	chr5:104270441..104272983-chr5:104273696..104275223,2	K562	blood:
19	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:
20	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
21	chr18:42792470..42793145-chr5:104821622..104822504,2	MCF-7	breast:
22	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
23	chr5:104545106..104548123-chr5:104549429..104551527,3	K562	blood:
24	chr5:104271936..104274851-chr5:104276428..104278480,3	MCF-7	breast:
25	chr5:104649160..104650852-chr5:104651591..104654211,3	K562	blood:
26	chr1:184434764..184435543-chr5:104792004..104792524,3	MCF-7	breast:
27	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
28	chr5:104716167..104718489-chr5:104728063..104729895,2	K562	blood:
29	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
30	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
31	chr5:104540117..104542340-chr5:104543485..104546477,2	MCF-7	breast:
32	chr5:104234931..104236476-chr5:104238248..104241105,2	MCF-7	breast:
33	chr5:104727742..104729434-chr5:104763198..104765492,2	K562	blood:
34	chr5:104649160..104650852-chr5:104651591..104654211,3	K562	blood:
35	chr5:104308244..104309781-chr5:104310392..104313289,2	K562	blood:
36	chr5:104567163..104569932-chr5:104572220..104574679,2	MCF-7	breast:
37	chr5:104524711..104526370-chr5:104889242..104892104,2	K562	blood:
38	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
39	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
40	chr5:104369743..104372595-chr5:104912590..104914639,2	K562	blood:
41	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:
42	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
43	chr5:104302225..104304920-chr5:104306783..104309637,2	MCF-7	breast:
44	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
45	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
46	chr5:104565194..104566957-chr5:104571048..104573999,2	K562	blood:
47	chr5:104768629..104770858-chr5:104785097..104787270,2	K562	blood:
48	chr5:104645770..104648035-chr5:104661663..104663662,2	MCF-7	breast:
49	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
50	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:

(count:15 , 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	chr5:104311375-104311586	ENSG00000253584
3	lnc-NUDT12-6	chr5:104728462-104728671	ENSG00000251574
4	lnc-NUDT12-6	chr5:104222559-104222676	ENSG00000251574
5	lnc-NUDT12-7	chr5:104582013-104582067	NONHSAT103097
6	lnc-NUDT12-7	chr5:104728462-104728989	NONHSAT103097
7	lnc-NUDT12-7	chr5:104315392-104315477	ENSG00000253584
8	lnc-NUDT12-7	chr5:104344562-104344618	ENSG00000253584
9	lnc-NUDT12-7	chr5:104344562-104344612	ENSG00000253584
10	lnc-NUDT12-6	chr5:104222559-104222676	ENSG00000251574
11	lnc-NUDT12-7	chr5:104308988-104309359	ENSG00000253584
12	lnc-C5orf30-8	chr5:104435174-104435799	NONHSAT103096
13	lnc-NUDT12-7	chr5:104581998-104582065	ENSG00000253584
14	lnc-NUDT12-6	chr5:104246363-104246434	ENSG00000251574
15	lnc-NUDT12-7	chr5:104253193-104253599	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
ENSG00000251574	chromatin interactions
ENSG00000132874	chromatin interactions
ENSG00000145743	chromatin interactions

Extended variants
information (count: 7642 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:7642 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371198418	chr5:104150891-104150892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188012894	chr5:104150929-104150930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566974982	chr5:104150946-104150947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201884112	chr5:104150947-104150948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371906733	chr5:104150962-104150963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374751927	chr5:104150988-104150989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191306470	chr5:104150998-104150999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147948832	chr5:104151004-104151005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536973500	chr5:104151006-104151007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556533962	chr5:104151013-104151014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200510575	chr5:104151027-104151028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566961896	chr5:104151031-104151032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535853236	chr5:104151040-104151041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552601356	chr5:104151049-104151050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572870075	chr5:104151109-104151110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369130916	chr5:104151119-104151120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571147393	chr5:104151123-104151124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534961045	chr5:104151156-104151157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553541609	chr5:104151166-104151167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149007274	chr5:104151218-104151219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375246845	chr5:104151223-104151224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575894257	chr5:104151302-104151303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143740543	chr5:104151311-104151312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561577261	chr5:104151336-104151337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574840551	chr5:104151367-104151368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183845810	chr5:104151380-104151381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560599982	chr5:104151411-104151412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532530682	chr5:104151427-104151428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551531868	chr5:104151432-104151433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116158954	chr5:104151483-104151484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148136893	chr5:104151497-104151498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141071232	chr5:104151524-104151525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552479797	chr5:104151665-104151666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546215864	chr5:104151673-104151674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs386690736	chr5:104151674-104151675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567224432	chr5:104151675-104151676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189400062	chr5:104151678-104151679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369393926	chr5:104151682-104151683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs17157157	chr5:104151733-104151734	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs145044355	chr5:104151744-104151745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116741938	chr5:104151756-104151757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35846204	chr5:104151782-104151783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535989597	chr5:104151793-104151794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372765240	chr5:104151805-104151806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575709029	chr5:104151859-104151860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192918087	chr5:104151885-104151886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549145662	chr5:104151923-104151924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184962050	chr5:104151931-104151932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575225486	chr5:104151934-104151935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569193219	chr5:104151953-104151954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	21346763	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD

Chromatin state (count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104150800-104151200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr5:104151200-104154800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr5:104157200-104157800	Enhancers	Fetal Intestine Large	intestine
4	chr5:104157200-104159600	Enhancers	Fetal Intestine Small	intestine
5	chr5:104173200-104173400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr5:104173200-104173400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr5:104173200-104173400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr5:104173200-104173400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr5:104173200-104173400	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr5:104173200-104173400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr5:104173400-104179600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr5:104174800-104176200	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr5:104175000-104175800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:104175000-104176200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr5:104175000-104177000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr5:104175000-104180000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr5:104175200-104175600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr5:104175200-104175600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:104175200-104175800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr5:104175200-104176200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr5:104175400-104176200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr5:104175600-104178600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr5:104175800-104181200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:104176200-104178200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr5:104176200-104178400	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr5:104176200-104179600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr5:104177000-104178200	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr5:104178200-104178800	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr5:104178200-104179000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr5:104178400-104178800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr5:104178600-104179000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:104178800-104181200	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr5:104179000-104181400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr5:104179000-104181800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr5:104179400-104180200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr5:104179600-104180200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr5:104179600-104180200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr5:104179600-104180200	Enhancers	Gastric	stomach
39	chr5:104180000-104182800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr5:104180200-104181400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr5:104180200-104181600	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr5:104181200-104181800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:104181200-104182000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr5:104181400-104181600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr5:104181400-104182000	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr5:104181600-104181800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr5:104181800-104182000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr5:104181800-104183000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:104182800-104183600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr5:104183000-104183200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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