Variant report

Variant	nsv537767
Chromosome Location	chr5:58940594-59040762
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:58969309-58969587	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:58960994-58961180	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:58957641-58958039	HepG2	liver:	n/a	n/a
4	ATF2	chr5:59005135-59005567	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:59005081-59005496	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:59009027-59009230	K562	blood:	n/a	n/a
7	BATF	chr5:58981051-58981275	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:59005117-59005450	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr5:59005221-59005381	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr5:58948417-58948651	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:58945013-58945327	K562	blood:	n/a	n/a
12	BHLHE40	chr5:58956285-58956315	GM12878	blood:	n/a	n/a
13	BRCA1	chr5:59040298-59042224	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr5:59017406-59017428	GM12878	blood:	n/a	n/a
15	CEBPB	chr5:58948169-58948371	A549	lung:	n/a	n/a
16	CEBPB	chr5:58957167-58957569	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:59028709-59029026	Hela-S3	cervix:	n/a	chr5:59028851-59028860 chr5:59028851-59028860 chr5:59028851-59028860 chr5:59028851-59028860
18	CEBPB	chr5:59007192-59007371	H1-hESC	embryonic stem cell:	n/a	chr5:59007279-59007290 chr5:59007277-59007288
19	CEBPB	chr5:58999729-58999865	A549	lung:	n/a	n/a
20	CEBPB	chr5:59007060-59007575	A549	lung:	n/a	chr5:59007279-59007290 chr5:59007277-59007288
21	CEBPB	chr5:59007177-59007438	HepG2	liver:	n/a	chr5:59007279-59007290 chr5:59007277-59007288
22	CEBPB	chr5:58971573-58971599	A549	lung:	n/a	n/a
23	CEBPB	chr5:59040707-59042644	A549	lung:	n/a	chr5:59041353-59041366
24	CEBPB	chr5:58974742-58975231	A549	lung:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
25	CEBPB	chr5:58944191-58944463	Hela-S3	cervix:	n/a	chr5:58944238-58944247 chr5:58944238-58944249
26	CEBPB	chr5:58974840-58975030	HepG2	liver:	n/a	chr5:58974960-58974971 chr5:58974962-58974971
27	CEBPB	chr5:58974823-58975077	IMR90	lung:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
28	CEBPB	chr5:58995910-58995921	HepG2	liver:	n/a	n/a
29	CEBPB	chr5:58949378-58949483	A549	lung:	n/a	n/a
30	CEBPB	chr5:58974893-58975058	K562	blood:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
31	CEBPB	chr5:59007127-59007493	Hela-S3	cervix:	n/a	chr5:59007279-59007290 chr5:59007277-59007288
32	CEBPB	chr5:58957816-58958074	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:58969329-58969533	A549	lung:	n/a	n/a
34	CEBPB	chr5:58957188-58957502	A549	lung:	n/a	n/a
35	CEBPB	chr5:58974841-58975128	Hela-S3	cervix:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
36	CEBPB	chr5:58945122-58945447	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr5:58961386-58961585	HepG2	liver:	n/a	n/a
38	CEBPB	chr5:59040415-59042582	A549	lung:	n/a	chr5:59041353-59041366
39	CEBPB	chr5:59028745-59028968	A549	lung:	n/a	chr5:59028851-59028860 chr5:59028851-59028860 chr5:59028851-59028860 chr5:59028851-59028860
40	CEBPB	chr5:59018686-59019146	Hela-S3	cervix:	n/a	chr5:59019061-59019074
41	CEBPB	chr5:58974871-58975073	A549	lung:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
42	CEBPB	chr5:59020408-59020863	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:58961256-58961683	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:59007143-59007476	A549	lung:	n/a	chr5:59007279-59007290 chr5:59007277-59007288
45	CEBPB	chr5:58957252-58957473	HepG2	liver:	n/a	n/a
46	CEBPB	chr5:59040381-59042557	Hela-S3	cervix:	n/a	chr5:59041353-59041366
47	CHD2	chr5:59040322-59041749	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr5:59020440-59020590	HMEC	breast:	n/a	chr5:59020519-59020528 chr5:59020518-59020539 chr5:59020516-59020534
49	CTCF	chr5:58969285-58969542	A549	lung:	n/a	chr5:58969458-58969474 chr5:58969457-58969475 chr5:58969452-58969473 chr5:58969462-58969470
50	CTCF	chr5:58962680-58962830	GM12875	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:58957910-58957960	AG04449	skin:	fetal
2	chr5:58957910-58957960	NH-A	brain:	n/a
3	chr5:58957910-58957960	PANC-1	pancreas:	n/a
4	chr5:58957910-58957960	NB4	blood:	n/a
5	chr5:58957910-58957960	BJ	skin:	n/a
6	chr5:58957910-58957960	A549	lung:	n/a
7	chr5:58957910-58957960	LNCaP	prostate:	n/a
8	chr5:58957910-58957960	CMK	blood:	n/a
9	chr5:58957910-58957960	HPAEpiC	pulmonary alveolar:	n/a
10	chr5:58957910-58957960	AG10803	skin:	n/a
11	chr5:58957910-58957960	SK-N-SH_RA	brain:	n/a
12	chr5:58957910-58957960	SKMC	muscle:	n/a
13	chr5:58957910-58957960	SK-N-SH	brain:	n/a
14	chr5:58957910-58957960	U87	brain:	n/a
15	chr5:58957910-58957960	GM12891	blood:	n/a
16	chr5:58957910-58957960	Caco-2	colon:	n/a
17	chr5:58957910-58957960	NHDF-neo	bronchial:	n/a
18	chr5:58957910-58957960	HEK293	kidney:	embryo
19	chr5:58957910-58957960	RPTEC	kidney:	n/a
20	chr5:58957910-58957960	ECC-1	luminal epithelium:	n/a
21	chr5:58957910-58957960	GM12892	blood:	n/a
22	chr5:58957910-58957960	T-47D	breast:	n/a
23	chr5:58957910-58957960	HRCEpiC	kidney:	n/a
24	chr5:58957910-58957960	SAEC	small airway:	n/a
25	chr5:58957910-58957960	HUVEC	blood vessel:	n/a
26	chr5:58957910-58957960	HIPEpiC	eye:	n/a
27	chr5:58957910-58957960	HRE	kidney:	n/a
28	chr5:58957910-58957960	NHBE	bronchial:	n/a
29	chr5:58957910-58957960	MCF10A-Er-Src	breast:	n/a
30	chr5:58957910-58957960	Jurkat	blood:	n/a
31	chr5:58957910-58957960	NT2-D1	testis:	n/a
32	chr5:58957910-58957960	HCPEpiC	choroid plexus:	n/a
33	chr5:58957910-58957960	HEEpiC	esophagus:	n/a
34	chr5:58957910-58957960	HCM	heart:	n/a
35	chr5:58957910-58957960	AG09309	skin:	n/a
36	chr5:58957910-58957960	HMEC	breast:	n/a
37	chr5:58957910-58957960	HNPCEpiC	eye:	n/a
38	chr5:58957910-58957960	ovcar-3	ovarian:	n/a
39	chr5:58957910-58957960	ProgFib	skin:	n/a
40	chr5:58957910-58957960	GM06990	blood:	n/a
41	chr5:58957910-58957960	H1-hESC	embryonic stem cell:	embryo
42	chr5:58957910-58957960	HAEpiC	amniotic membrane:	n/a
43	chr5:58957910-58957960	MCF-7	breast:	n/a
44	chr5:58957910-58957960	PrEC	prostate:	n/a
45	chr5:58957910-58957960	GM19239	blood:	n/a
46	chr5:58957910-58957960	BE2_C	brain:	n/a
47	chr5:58957910-58957960	HCF	heart:	n/a
48	chr5:58957910-58957960	HL-60	blood:	n/a
49	chr5:58957910-58957960	K562	blood:	n/a
50	chr5:58957910-58957960	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:58803367..58805536-chr5:58956722..58959458,2	MCF-7	breast:
2	chr5:58969044..58969563-chr5:59095719..59096533,2	MCF-7	breast:
3	chr5:58801867..58802786-chr5:58968976..58969858,3	MCF-7	breast:
4	chr12:17875088..17875599-chr5:58957118..58957618,2	Hela-S3	cervix:
5	chr5:58821597..58822483-chr5:58956197..58956887,3	MCF-7	breast:
6	chr5:59002219..59005898-chr5:59006477..59009673,3	K562	blood:
7	chr5:59022602..59025084-chr5:59040662..59042603,2	MCF-7	breast:
8	chr5:58685998..58686505-chr5:58956311..58957192,2	MCF-7	breast:
9	chr5:58956441..58957361-chr5:58968943..58969531,2	MCF-7	breast:
10	chr5:58802090..58802764-chr5:58956093..58957045,3	MCF-7	breast:
11	chr5:58968638..58970043-chr5:59019689..59021106,4	MCF-7	breast:
12	chr5:58801963..58802644-chr5:58962690..58963296,2	MCF-7	breast:
13	chr12:53139319..53140001-chr5:58956637..58957236,2	MCF-7	breast:
14	chr5:58801872..58802902-chr5:58956210..58957251,7	MCF-7	breast:
15	chr5:58801703..58803307-chr5:58968055..58970489,2	MCF-7	breast:
16	chr5:58956441..58957361-chr5:58968943..58969531,2	MCF-7	breast:
17	chr5:58938220..58940371-chr5:58941651..58943411,2	MCF-7	breast:
18	chr5:58921699..58924088-chr5:58961415..58963109,2	MCF-7	breast:
19	chr5:59002219..59005898-chr5:59006477..59009673,3	K562	blood:
20	chr5:58968638..58970043-chr5:59019689..59021106,4	MCF-7	breast:
21	chr5:58803075..58803840-chr5:58956390..58957074,2	MCF-7	breast:
22	chr5:59022602..59025084-chr5:59040662..59042603,2	MCF-7	breast:
23	chr5:58801995..58802802-chr5:58968998..58969985,2	MCF-7	breast:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-582-5p	chr5:58999492-58999514	MIMAT0003247
hsa-miR-582-3p	chr5:58999456-58999477	MIMAT0004797

Variant related genes	Relation type
MIR582	TF binding region
MIR582	CpG island
MCL1	Mature miRNA region

Extended variants
information (count: 3504 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3504 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190661979	chr5:58940630-58940631	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553686616	chr5:58940716-58940717	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572084216	chr5:58940737-58940738	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74777447	chr5:58940782-58940783	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560971159	chr5:58940787-58940788	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115784553	chr5:58940791-58940792	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543496189	chr5:58940793-58940794	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142409821	chr5:58940798-58940799	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570091750	chr5:58940805-58940806	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs180901009	chr5:58940818-58940819	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552088175	chr5:58940859-58940860	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74383912	chr5:58940879-58940880	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528490215	chr5:58940890-58940891	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369481292	chr5:58940895-58940896	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568433145	chr5:58940920-58940921	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537194671	chr5:58940959-58940960	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186296540	chr5:58940984-58940985	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191194910	chr5:58941000-58941001	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555832033	chr5:58941047-58941048	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540002009	chr5:58941053-58941054	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183028828	chr5:58941064-58941065	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186197152	chr5:58941083-58941084	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534612947	chr5:58941118-58941119	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554649345	chr5:58941123-58941124	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34434958	chr5:58941128-58941129	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377195665	chr5:58941137-58941138	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574373122	chr5:58941138-58941139	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs151262342	chr5:58941143-58941144	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs298026	chr5:58941211-58941212	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs535252049	chr5:58941224-58941225	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs298025	chr5:58941239-58941240	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs141694390	chr5:58941326-58941327	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545565956	chr5:58941353-58941354	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559226531	chr5:58941355-58941356	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147033432	chr5:58941372-58941373	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572215529	chr5:58941460-58941461	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541716391	chr5:58941476-58941477	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371298667	chr5:58941489-58941490	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147676351	chr5:58941494-58941495	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564640584	chr5:58941500-58941501	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111241665	chr5:58941545-58941546	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570893305	chr5:58941553-58941554	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73101105	chr5:58941619-58941620	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs550277699	chr5:58941642-58941643	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs298024	chr5:58941676-58941677	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs567064680	chr5:58941696-58941697	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs56007967	chr5:58941697-58941698	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs556005492	chr5:58941714-58941715	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567998678	chr5:58941731-58941732	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56666128	chr5:58941755-58941756	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Hepatocellular carcinoma	16750200	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD

Chromatin state (count:990 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58923600-58957200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr5:58923800-58945000	Weak transcription	Aorta	Aorta
3	chr5:58934800-58943800	Weak transcription	HUVEC	blood vessel
4	chr5:58936600-58949200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:58937400-58940800	Weak transcription	A549	lung
6	chr5:58938800-58940800	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr5:58939600-58940600	Enhancers	Primary hematopoietic stem cells	blood
8	chr5:58939600-58941000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:58939800-58941600	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr5:58940000-58940600	Enhancers	Stomach Mucosa	stomach
11	chr5:58940000-58941000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:58940200-58940600	Enhancers	Hela-S3	cervix
13	chr5:58940400-58941600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:58940600-58940800	Flanking Active TSS	Primary hematopoietic stem cells	blood
15	chr5:58940600-58941000	Weak transcription	Stomach Mucosa	stomach
16	chr5:58940600-58941000	Weak transcription	Hela-S3	cervix
17	chr5:58940800-58941000	Enhancers	Primary hematopoietic stem cells	blood
18	chr5:58940800-58941600	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr5:58940800-58941600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
20	chr5:58940800-58941800	Genic enhancers	A549	lung
21	chr5:58941000-58941200	Strong transcription	Hela-S3	cervix
22	chr5:58941000-58941400	Flanking Active TSS	Primary hematopoietic stem cells	blood
23	chr5:58941000-58941400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr5:58941000-58941400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:58941000-58941400	Enhancers	Fetal Thymus	thymus
26	chr5:58941000-58941600	Enhancers	Primary B cells from peripheral blood	blood
27	chr5:58941000-58941600	Enhancers	Stomach Mucosa	stomach
28	chr5:58941200-58941400	Genic enhancers	Hela-S3	cervix
29	chr5:58941400-58941600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr5:58941400-58941800	Enhancers	Primary hematopoietic stem cells	blood
31	chr5:58941400-58942600	Strong transcription	Hela-S3	cervix
32	chr5:58941400-58944800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:58941600-58941800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr5:58941600-58943800	Weak transcription	Stomach Mucosa	stomach
35	chr5:58941600-58944400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr5:58941600-58944400	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr5:58941600-58946400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr5:58941600-58951600	Weak transcription	Primary B cells from peripheral blood	blood
39	chr5:58941800-58943800	Weak transcription	A549	lung
40	chr5:58941800-58944000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:58941800-58944400	Weak transcription	Primary hematopoietic stem cells	blood
42	chr5:58942600-58944400	Weak transcription	Hela-S3	cervix
43	chr5:58943600-58945000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:58943800-58944000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr5:58943800-58945600	Enhancers	Stomach Mucosa	stomach
46	chr5:58943800-58946400	Enhancers	A549	lung
47	chr5:58943800-58946600	Enhancers	HUVEC	blood vessel
48	chr5:58944000-58944400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr5:58944000-58944600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr5:58944200-58945200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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