Variant report

Variant	nsv1020336
Chromosome Location	chr5:104084429-104255608
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:462)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104255114-104255149	HepG2	liver:	n/a	n/a
2	BACH1	chr5:104223199-104223207	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr5:104087746-104087944	GM12878	blood:	n/a	chr5:104087867-104087878
4	BATF	chr5:104087774-104088008	GM12878	blood:	n/a	chr5:104087867-104087878
5	BRCA1	chr5:104246667-104246983	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:104195083-104195431	A549	lung:	n/a	chr5:104195252-104195263
7	CEBPB	chr5:104102501-104102787	A549	lung:	n/a	chr5:104102656-104102667
8	CEBPB	chr5:104102566-104102783	HepG2	liver:	n/a	chr5:104102656-104102667
9	CEBPB	chr5:104136224-104136540	IMR90	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
10	CEBPB	chr5:104136117-104136616	MCF-7	breast:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
11	CEBPB	chr5:104136061-104136624	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
12	CEBPB	chr5:104136186-104136537	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
13	CEBPB	chr5:104195135-104195333	K562	blood:	n/a	chr5:104195252-104195263
14	CEBPB	chr5:104195172-104195487	MCF-7	breast:	n/a	chr5:104195252-104195263
15	CEBPB	chr5:104136255-104136426	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
16	CEBPB	chr5:104136190-104136565	H1-hESC	embryonic stem cell:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
17	CEBPB	chr5:104136136-104136548	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
18	CEBPB	chr5:104136209-104136550	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
19	CEBPB	chr5:104177422-104177540	K562	blood:	n/a	n/a
20	CEBPB	chr5:104195099-104195433	H1-hESC	embryonic stem cell:	n/a	chr5:104195252-104195263
21	CEBPB	chr5:104136032-104136689	MCF-7	breast:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
22	CEBPB	chr5:104136258-104136502	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
23	CEBPB	chr5:104136225-104136497	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
24	CEBPB	chr5:104195080-104195455	K562	blood:	n/a	chr5:104195252-104195263
25	CEBPB	chr5:104195098-104195441	HepG2	liver:	n/a	chr5:104195252-104195263
26	CEBPB	chr5:104136178-104136571	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
27	CEBPB	chr5:104136228-104136514	Hela-S3	cervix:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
28	CEBPB	chr5:104136188-104136569	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
29	CEBPB	chr5:104171648-104171720	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:104195095-104195389	MCF-7	breast:	n/a	chr5:104195252-104195263
31	CEBPB	chr5:104195073-104195449	IMR90	lung:	n/a	chr5:104195252-104195263
32	CEBPB	chr5:104195064-104195524	A549	lung:	n/a	chr5:104195252-104195263
33	CEBPB	chr5:104090393-104090670	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr5:104246629-104247018	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:104195078-104195490	Hela-S3	cervix:	n/a	chr5:104195252-104195263
36	CEBPB	chr5:104136123-104136646	HCT-116	colon:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
37	CEBPB	chr5:104195089-104195447	ECC-1	luminal epithelium:	n/a	chr5:104195252-104195263
38	CEBPB	chr5:104136181-104136567	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
39	CEBPD	chr5:104179642-104179910	K562	blood:	n/a	n/a
40	CEBPD	chr5:104136280-104136473	HepG2	liver:	n/a	n/a
41	CHD2	chr5:104246611-104246974	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr5:104136260-104136410	GM12872	blood:	n/a	n/a
43	CTCF	chr5:104136300-104136450	GM12867	blood:	n/a	n/a
44	CTCF	chr5:104136240-104136390	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:104136360-104136510	HFF	foreskin:	n/a	n/a
46	CTCF	chr5:104136300-104136450	HepG2	liver:	n/a	n/a
47	CTCF	chr5:104136200-104136350	HRE	kidney:	n/a	n/a
48	CTCF	chr5:104136300-104136450	GM12872	blood:	n/a	n/a
49	CTCF	chr5:104136260-104136410	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr5:104136243-104136423	NHEK	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104090236-104090286	ProgFib	skin:	n/a
2	chr5:104090236-104090286	HCPEpiC	choroid plexus:	n/a
3	chr5:104090236-104090286	PFSK-1	brain:	n/a
4	chr5:104090236-104090286	MCF10A-Er-Src	breast:	n/a
5	chr5:104090236-104090286	GM12892	blood:	n/a
6	chr5:104090236-104090286	ECC-1	luminal epithelium:	n/a
7	chr5:104090236-104090286	HRCEpiC	kidney:	n/a
8	chr5:104090236-104090286	HNPCEpiC	eye:	n/a
9	chr5:104090236-104090286	ovcar-3	ovarian:	n/a
10	chr5:104090236-104090286	SK-N-SH_RA	brain:	n/a
11	chr5:104090236-104090286	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:104090236-104090286	Hepatocyte	liver:	n/a
13	chr5:104090236-104090286	Jurkat	blood:	n/a
14	chr5:104090236-104090286	HCT-116	colon:	n/a
15	chr5:104090236-104090286	HEEpiC	esophagus:	n/a
16	chr5:104090236-104090286	T-47D	breast:	n/a
17	chr5:104090236-104090286	SK-N-MC	brain:	n/a
18	chr5:104090236-104090286	U87	brain:	n/a
19	chr5:104090236-104090286	NH-A	brain:	n/a
20	chr5:104090236-104090286	CMK	blood:	n/a
21	chr5:104090236-104090286	K562	blood:	n/a
22	chr5:104090236-104090286	AG04449	skin:	fetal
23	chr5:104090236-104090286	HEK293	kidney:	embryo
24	chr5:104090236-104090286	NB4	blood:	n/a
25	chr5:104090236-104090286	SK-N-SH	brain:	n/a
26	chr5:104090236-104090286	HRE	kidney:	n/a
27	chr5:104090236-104090286	IMR90	lung:	fetal
28	chr5:104090236-104090286	LNCaP	prostate:	n/a
29	chr5:104090236-104090286	PrEC	prostate:	n/a
30	chr5:104090236-104090286	AG09309	skin:	n/a
31	chr5:104090236-104090286	BJ	skin:	n/a
32	chr5:104090236-104090286	RPTEC	kidney:	n/a
33	chr5:104090236-104090286	GM12878	blood:	n/a
34	chr5:104090236-104090286	SAEC	small airway:	n/a
35	chr5:104090236-104090286	AoSMC	blood vessel:	n/a
36	chr5:104090236-104090286	Caco-2	colon:	n/a
37	chr5:104090236-104090286	HUVEC	blood vessel:	n/a
38	chr5:104090236-104090286	AG10803	skin:	n/a
39	chr5:104090236-104090286	PANC-1	pancreas:	n/a
40	chr5:104090236-104090286	GM19239	blood:	n/a
41	chr5:104090236-104090286	A549	lung:	n/a
42	chr5:104090236-104090286	SKMC	muscle:	n/a
43	chr5:104090236-104090286	NHDF-neo	bronchial:	n/a
44	chr5:104090236-104090286	Hela-S3	cervix:	n/a
45	chr5:104090236-104090286	HepG2	liver:	n/a
46	chr5:104090236-104090286	GM12891	blood:	n/a
47	chr5:104090236-104090286	HL-60	blood:	n/a
48	chr5:104090236-104090286	HRPEpiC	eye:	n/a
49	chr5:104090236-104090286	H1-hESC	embryonic stem cell:	embryo
50	chr5:104090236-104090286	NHBE	bronchial:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:
2	chr5:104227529..104229773-chr5:104240979..104242491,2	MCF-7	breast:
3	chr5:104086946..104088891-chr5:104090048..104092847,2	MCF-7	breast:
4	chr5:104223049..104225474-chr5:104235768..104238593,2	MCF-7	breast:
5	chr5:104239889..104241844-chr5:104241951..104244541,2	MCF-7	breast:
6	chr5:104091669..104093962-chr5:104097846..104099466,2	MCF-7	breast:
7	chr5:104234931..104236476-chr5:104238248..104241105,2	MCF-7	breast:
8	chr5:104234931..104236476-chr5:104238248..104241105,2	MCF-7	breast:
9	chr5:104248370..104250240-chr5:104261197..104262793,2	MCF-7	breast:
10	chr5:104227529..104229773-chr5:104240979..104242491,2	MCF-7	breast:
11	chr17:57939158..57941470-chr5:104246724..104248724,2	MCF-7	breast:
12	chr5:104226367..104227906-chr5:104228376..104230821,2	MCF-7	breast:
13	chr5:104223049..104225474-chr5:104235768..104238593,2	MCF-7	breast:
14	chr5:104091669..104093962-chr5:104097846..104099466,2	MCF-7	breast:
15	chr5:104080992..104082950-chr5:104084605..104086219,2	K562	blood:
16	chr5:104239889..104241844-chr5:104241951..104244541,2	MCF-7	breast:
17	chr5:104086946..104088891-chr5:104090048..104092847,2	MCF-7	breast:
18	chr5:104226367..104227906-chr5:104228376..104230821,2	MCF-7	breast:
19	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
2	lnc-NUDT12-7	chr5:104253193-104253599	ENSG00000253584
3	lnc-NUDT12-5	chr5:104109314-104109492	ENSG00000251574
4	lnc-NUDT12-5	chr5:104109314-104109485	ENSG00000251574
5	lnc-NUDT12-13	chr5:104103132-104103235	l_2988_chr5:104103131-104137422_testes
6	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
7	lnc-NUDT12-13	chr5:104137254-104137422	l_2988_chr5:104103131-104137422_testes
8	lnc-NUDT12-6	chr5:104222559-104222676	ENSG00000251574
9	lnc-NUDT12-13	chr5:104118423-104118445	l_2988_chr5:104103131-104137422_testes
10	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
11	lnc-NUDT12-5	chr5:104109314-104109524	NONHSAT103088
12	lnc-NUDT12-5	chr5:104098932-104099084	ENSG00000251574
13	lnc-C5orf30-3	chr5:104109342-104109441	ENSG00000253776
14	lnc-NUDT12-5	chr5:104109314-104109524	NONHSAT103082
15	lnc-NUDT12-5	chr5:104109314-104109397	ENSG00000251574
16	lnc-NUDT12-5	chr5:104109434-104109524	NONHSAT103081
17	lnc-NUDT12-5	chr5:104098981-104099084	NONHSAT103082
18	lnc-NUDT12-6	chr5:104222559-104222676	ENSG00000251574
19	lnc-C5orf30-3	chr5:104135007-104135473	ENSG00000253776
20	lnc-NUDT12-5	chr5:104109434-104109523	ENSG00000251574
21	lnc-NUDT12-5	chr5:104109314-104109361	ENSG00000251574
22	lnc-NUDT12-6	chr5:104246363-104246434	ENSG00000251574
23	lnc-C5orf30-2	chr5:104098977-104099084	XLOC_004497
24	lnc-NUDT12-5	chr5:104098981-104099084	NONHSAT103081
25	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574

No data

Variant related genes	Relation type
ENSG00000253776	TF binding region
RNU6-334P	TF binding region
ENSG00000251574	TF binding region
ENSG00000253776	CpG island
RNU6-334P	CpG island
ENSG00000251574	CpG island
ENSG00000251574	chromatin interactions
CREB3L2	miRNA target sites

Extended variants
information (count: 2426 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2426 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140157953	chr5:104084605-104084606	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs193269803	chr5:104084608-104084609	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547630207	chr5:104084644-104084645	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538162848	chr5:104084646-104084647	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs143912558	chr5:104084653-104084654	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs555783111	chr5:104084658-104084659	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs569399135	chr5:104084673-104084674	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs62361867	chr5:104084693-104084694	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs62361868	chr5:104084698-104084699	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs145885938	chr5:104084704-104084705	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs113080754	chr5:104084738-104084739	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs558421819	chr5:104084800-104084801	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182393299	chr5:104084834-104084835	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145143571	chr5:104084836-104084837	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs58583594	chr5:104084843-104084844	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs146326780	chr5:104084846-104084847	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541880334	chr5:104084882-104084883	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs71588366	chr5:104084883-104084884	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs529325578	chr5:104084903-104084904	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543109130	chr5:104084915-104084916	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs559603558	chr5:104084930-104084931	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527435412	chr5:104084937-104084938	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs187879291	chr5:104084962-104084963	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs570716093	chr5:104084968-104084969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs533093729	chr5:104084979-104084980	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs77958317	chr5:104085001-104085002	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs569283338	chr5:104085002-104085003	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs531837050	chr5:104085006-104085007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs151058377	chr5:104085030-104085031	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs192510815	chr5:104085033-104085034	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs10043901	chr5:104085034-104085035	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs373148963	chr5:104085063-104085064	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs183950595	chr5:104085097-104085098	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs578244459	chr5:104085101-104085102	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188680342	chr5:104085107-104085108	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564352066	chr5:104085113-104085114	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573382761	chr5:104085212-104085213	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142450065	chr5:104085213-104085214	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574044326	chr5:104085246-104085247	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs561890225	chr5:104085259-104085260	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs191994977	chr5:104085319-104085320	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs184408990	chr5:104085321-104085322	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs190240358	chr5:104085367-104085368	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs528619649	chr5:104085521-104085522	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs146318215	chr5:104085526-104085527	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564157189	chr5:104085531-104085532	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547962990	chr5:104085578-104085579	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs150404605	chr5:104085642-104085643	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532983689	chr5:104085649-104085650	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs572303992	chr5:104085656-104085657	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104089600-104090800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr5:104089800-104090000	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr5:104089800-104090200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr5:104089800-104091200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr5:104089800-104091200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:104089800-104091200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr5:104089800-104091200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr5:104089800-104091400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr5:104090000-104090600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr5:104090000-104090600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr5:104090200-104090400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr5:104090200-104090600	Enhancers	Brain Germinal Matrix	brain
13	chr5:104090200-104091000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:104090400-104090800	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr5:104090600-104090800	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr5:104090800-104091000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr5:104091200-104092600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr5:104091400-104095000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr5:104095000-104095800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr5:104112400-104113000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr5:104112600-104113000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:104124800-104125400	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr5:104124800-104125400	Enhancers	Rectal Smooth Muscle	rectum
24	chr5:104124800-104125600	Enhancers	Fetal Lung	lung
25	chr5:104124800-104126400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:104126400-104130000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr5:104127800-104129000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr5:104128400-104129800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:104128600-104129000	Enhancers	Fetal Intestine Small	intestine
30	chr5:104128600-104129000	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr5:104128600-104129200	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr5:104128600-104129400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:104128600-104129400	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr5:104128600-104130000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
35	chr5:104128600-104130200	Enhancers	Fetal Intestine Large	intestine
36	chr5:104128800-104129200	Enhancers	NH-A	brain
37	chr5:104129000-104129400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
38	chr5:104129000-104129400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr5:104129200-104129400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
40	chr5:104129200-104130000	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr5:104130000-104130200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
42	chr5:104130000-104130200	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr5:104130000-104132000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr5:104136200-104136400	ZNF genes & repeats	Aorta	Aorta
45	chr5:104137600-104138400	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr5:104150800-104151200	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr5:104151200-104154800	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr5:104157200-104157800	Enhancers	Fetal Intestine Large	intestine
49	chr5:104157200-104159600	Enhancers	Fetal Intestine Small	intestine
50	chr5:104173200-104173400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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