Variant report

Variant	nsv522003
Chromosome Location	chr5:74947435-74988369
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:725)
CpG islands
(count:183)
Chromatin interactive
region (count:50)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:725 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74976935-74977330	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:74964985-74965304	K562	blood:	n/a	n/a
3	ARID3A	chr5:74977101-74977345	K562	blood:	n/a	n/a
4	ARID3A	chr5:74974294-74974363	K562	blood:	n/a	n/a
5	ATF1	chr5:74964828-74965541	K562	blood:	n/a	n/a
6	ATF2	chr5:74964701-74965511	GM12878	blood:	n/a	n/a
7	ATF2	chr5:74955853-74956931	GM12878	blood:	n/a	n/a
8	ATF2	chr5:74964607-74965672	GM12878	blood:	n/a	n/a
9	ATF3	chr5:74964960-74965310	K562	blood:	n/a	n/a
10	BACH1	chr5:74965141-74965322	K562	blood:	n/a	n/a
11	BATF	chr5:74956488-74956876	GM12878	blood:	n/a	n/a
12	BATF	chr5:74964753-74965201	GM12878	blood:	n/a	n/a
13	BATF	chr5:74964664-74965323	GM12878	blood:	n/a	n/a
14	BATF	chr5:74956551-74956791	GM12878	blood:	n/a	n/a
15	BCLAF1	chr5:74964622-74965257	GM12878	blood:	n/a	chr5:74965005-74965014
16	BCLAF1	chr5:74964648-74965421	GM12878	blood:	n/a	chr5:74965005-74965014
17	BHLHE40	chr5:74964754-74965779	K562	blood:	n/a	n/a
18	BHLHE40	chr5:74962768-74962966	K562	blood:	n/a	n/a
19	BHLHE40	chr5:74964889-74965291	HepG2	liver:	n/a	n/a
20	BHLHE40	chr5:74952772-74952785	K562	blood:	n/a	n/a
21	BHLHE40	chr5:74976878-74977026	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:74964728-74965257	GM12878	blood:	n/a	n/a
23	BRCA1	chr5:74964556-74965325	GM12878	blood:	n/a	chr5:74965226-74965233
24	CBX3	chr5:74964696-74965463	K562	blood:	n/a	n/a
25	CEBPB	chr5:74966552-74966629	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:74978068-74978424	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:74955901-74956033	K562	blood:	n/a	n/a
28	CHD1	chr5:74977166-74977244	GM12878	blood:	n/a	n/a
29	CHD1	chr5:74965000-74965489	GM12878	blood:	n/a	n/a
30	CHD1	chr5:74975894-74975975	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr5:74965403-74965464	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr5:74964835-74965420	GM12878	blood:	n/a	n/a
33	CTCF	chr5:74963460-74963610	HMEC	breast:	n/a	chr5:74963587-74963605
34	CTCF	chr5:74963520-74963670	HepG2	liver:	n/a	chr5:74963587-74963605
35	CTCF	chr5:74977200-74977350	K562	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
36	CTCF	chr5:74986120-74986270	HepG2	liver:	n/a	n/a
37	CTCF	chr5:74977220-74977370	AG10803	skin:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
38	CTCF	chr5:74977200-74977350	HFF	foreskin:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
39	CTCF	chr5:74962860-74963010	A549	lung:	n/a	chr5:74962872-74962885 chr5:74962870-74962888 chr5:74962873-74962883
40	CTCF	chr5:74963520-74963670	AG09309	skin:	n/a	chr5:74963587-74963605
41	CTCF	chr5:74977164-74977398	K562	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
42	CTCF	chr5:74977125-74977358	A549	lung:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
43	CTCF	chr5:74962760-74962910	HMF	breast:	n/a	chr5:74962829-74962837 chr5:74962872-74962885 chr5:74962870-74962888 chr5:74962873-74962883
44	CTCF	chr5:74962800-74962950	HVMF	connective:	n/a	chr5:74962829-74962837 chr5:74962872-74962885 chr5:74962870-74962888 chr5:74962873-74962883
45	CTCF	chr5:74977180-74977330	HRE	kidney:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
46	CTCF	chr5:74963460-74963610	Caco-2	colon:	n/a	chr5:74963587-74963605
47	CTCF	chr5:74977074-74977413	HCT-116	colon:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
48	CTCF	chr5:74962820-74962970	HRPEpiC	eye:	n/a	chr5:74962829-74962837 chr5:74962872-74962885 chr5:74962870-74962888 chr5:74962873-74962883
49	CTCF	chr5:74977016-74977484	GM12878	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
50	CTCF	chr5:74977220-74977370	HUVEC	blood vessel:	n/a	chr5:74977265-74977281 chr5:74977259-74977280

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74965039-74965089	MCF10A-Er-Src	breast:	n/a
2	chr5:74952444-74952494	GM12891	blood:	n/a
3	chr5:74965039-74965089	SAEC	small airway:	n/a
4	chr5:74965039-74965089	SKMC	muscle:	n/a
5	chr5:74978020-74978070	NB4	blood:	n/a
6	chr5:74965039-74965089	U87	brain:	n/a
7	chr5:74978020-74978070	HCF	heart:	n/a
8	chr5:74978020-74978070	T-47D	breast:	n/a
9	chr5:74965039-74965089	SK-N-MC	brain:	n/a
10	chr5:74965039-74965089	ECC-1	luminal epithelium:	n/a
11	chr5:74952444-74952494	AG04450	lung:	fetal
12	chr5:74965039-74965089	Hela-S3	cervix:	n/a
13	chr5:74978020-74978070	Caco-2	colon:	n/a
14	chr5:74965039-74965089	HEK293	kidney:	embryo
15	chr5:74952444-74952494	GM06990	blood:	n/a
16	chr5:74965039-74965089	HCM	heart:	n/a
17	chr5:74952444-74952494	NHDF-neo	bronchial:	n/a
18	chr5:74965039-74965089	NB4	blood:	n/a
19	chr5:74952444-74952494	SK-N-SH	brain:	n/a
20	chr5:74978020-74978070	Hela-S3	cervix:	n/a
21	chr5:74978020-74978070	BE2_C	brain:	n/a
22	chr5:74965039-74965089	HEEpiC	esophagus:	n/a
23	chr5:74952444-74952494	GM19239	blood:	n/a
24	chr5:74965039-74965089	NHDF-neo	bronchial:	n/a
25	chr5:74978020-74978070	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:74965039-74965089	NHBE	bronchial:	n/a
27	chr5:74952444-74952494	ovcar-3	ovarian:	n/a
28	chr5:74952444-74952494	Caco-2	colon:	n/a
29	chr5:74952444-74952494	HMEC	breast:	n/a
30	chr5:74978020-74978070	NHDF-neo	bronchial:	n/a
31	chr5:74952444-74952494	Jurkat	blood:	n/a
32	chr5:74965039-74965089	AG10803	skin:	n/a
33	chr5:74965039-74965089	HMEC	breast:	n/a
34	chr5:74965039-74965089	HCPEpiC	choroid plexus:	n/a
35	chr5:74952444-74952494	K562	blood:	n/a
36	chr5:74978020-74978070	HRPEpiC	eye:	n/a
37	chr5:74952444-74952494	HIPEpiC	eye:	n/a
38	chr5:74978020-74978070	GM12891	blood:	n/a
39	chr5:74978020-74978070	K562	blood:	n/a
40	chr5:74978020-74978070	BJ	skin:	n/a
41	chr5:74952444-74952494	HCPEpiC	choroid plexus:	n/a
42	chr5:74978020-74978070	H1-hESC	embryonic stem cell:	embryo
43	chr5:74965039-74965089	IMR90	lung:	fetal
44	chr5:74952444-74952494	ProgFib	skin:	n/a
45	chr5:74978020-74978070	HCPEpiC	choroid plexus:	n/a
46	chr5:74952444-74952494	PANC-1	pancreas:	n/a
47	chr5:74952444-74952494	GM12878	blood:	n/a
48	chr5:74952444-74952494	NHBE	bronchial:	n/a
49	chr5:74978020-74978070	PFSK-1	brain:	n/a
50	chr5:74978020-74978070	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:74950997..74952941-chr5:74954987..74957253,2	K562	blood:
2	chr5:74952495..74955459-chr5:74961686..74963716,2	K562	blood:
3	chr5:74804046..74805995-chr5:74976601..74978123,2	K562	blood:
4	chr5:74880080..74881244-chr5:74962362..74964218,14	MCF-7	breast:
5	chr5:74956949..74958847-chr5:74961293..74964249,2	K562	blood:
6	chr5:74986233..74988640-chr5:74991256..74992996,3	K562	blood:
7	chr5:74956949..74958847-chr5:74961293..74964249,2	K562	blood:
8	chr5:74969854..74971391-chr5:74974162..74975941,2	K562	blood:
9	chr5:74951852..74953716-chr5:74968580..74970630,2	K562	blood:
10	chr5:74804574..74807080-chr5:74963425..74964973,2	K562	blood:
11	chr5:74965127..74967340-chr5:75010605..75013451,3	K562	blood:
12	chr5:74955921..74958847-chr5:74961478..74964262,3	K562	blood:
13	chr5:74952495..74954524-chr5:74962216..74966504,3	K562	blood:
14	chr5:74735308..74738290-chr5:74961776..74964047,2	K562	blood:
15	chr5:74880200..74881111-chr5:74976869..74977697,3	MCF-7	breast:
16	chr5:74950997..74952941-chr5:74954987..74957253,2	K562	blood:
17	chr5:74986312..74988640-chr5:74991101..74992756,2	K562	blood:
18	chr5:74959970..74961673-chr5:74963157..74964976,2	K562	blood:
19	chr5:74633002..74635499-chr5:74966644..74968332,2	K562	blood:
20	chr5:74969854..74971391-chr5:74974162..74975941,2	K562	blood:
21	chr5:74632028..74633564-chr5:74970269..74971790,2	MCF-7	breast:
22	chr5:74967624..74970426-chr5:74970966..74973992,3	K562	blood:
23	chr5:74980503..74982901-chr5:74987691..74991437,3	K562	blood:
24	chr5:74959210..74961845-chr5:74965195..74967227,2	K562	blood:
25	chr5:74983383..74985816-chr5:74986584..74989106,2	MCF-7	breast:
26	chr5:74880212..74881196-chr5:74962425..74963375,4	MCF-7	breast:
27	chr5:74532317..74532921-chr5:74976842..74977712,2	K562	blood:
28	chr5:74915137..74917681-chr5:74948612..74950531,2	K562	blood:
29	chr5:74959210..74961845-chr5:74965195..74967227,2	K562	blood:
30	chr5:74983383..74985816-chr5:74986584..74989106,2	MCF-7	breast:
31	chr5:74786766..74788653-chr5:74965428..74967574,2	K562	blood:
32	chr5:74961965..74963917-chr5:74970216..74971914,2	K562	blood:
33	chr5:74967624..74970426-chr5:74970966..74973992,3	K562	blood:
34	chr5:74955921..74958847-chr5:74961478..74964262,3	K562	blood:
35	chr5:74880501..74881472-chr5:74976763..74977639,2	MCF-7	breast:
36	chr5:74986971..74989471-chr5:74989787..74992402,2	MCF-7	breast:
37	chr5:74987714..74990328-chr5:75012640..75014673,2	MCF-7	breast:
38	chr5:74532263..74533179-chr5:74962383..74963086,2	K562	blood:
39	chr5:74953873..74956590-chr5:75014538..75016068,2	K562	blood:
40	chr5:74980613..74983267-chr5:74984574..74986964,2	K562	blood:
41	chr5:74961965..74963917-chr5:74970216..74971914,2	K562	blood:
42	chr5:74933475..74935667-chr5:74961312..74963106,2	K562	blood:
43	chr5:74981038..74984120-chr5:75011699..75013859,3	K562	blood:
44	chr5:74915137..74918881-chr5:74947780..74950531,3	K562	blood:
45	chr5:74952495..74954524-chr5:74962216..74966504,3	K562	blood:
46	chr5:74951852..74953716-chr5:74968580..74970630,2	K562	blood:
47	chr5:74952495..74955459-chr5:74961686..74963716,2	K562	blood:
48	chr5:74959970..74961673-chr5:74963157..74964976,2	K562	blood:
49	chr5:74972829..74974939-chr5:74988828..74991642,2	K562	blood:
50	chr5:74944742..74946556-chr5:74948688..74950561,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLK-1	chr5:74948967-74949065	NONHSAT102215
2	lnc-POLK-2	chr5:74966804-74967175	NONHSAT102216
3	lnc-ANKDD1B-4	chr5:74984723-74984821	ucscGeneNc_uc010izt_1
4	lnc-POLK-1	chr5:74955108-74955129	NONHSAT102215
5	lnc-POLK-2	chr5:74965019-74965208	NONHSAT102216
6	lnc-POLK-1	chr5:74951854-74951952	NONHSAT102215
7	lnc-ANKDD1B-4	chr5:74987610-74987708	ucscGeneNc_uc010izt_1

No data

Variant related genes	Relation type
POC5	TF binding region
POC5	CpG island
ENSG00000152359	chromatin interactions
ENSG00000247372	chromatin interactions
ENSG00000145700	chromatin interactions
ENSG00000113161	chromatin interactions

Extended variants
information (count: 1467 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386689137	chr5:74947435-74947436	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs190868730	chr5:74947454-74947455	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs555771449	chr5:74947482-74947483	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs116345515	chr5:74947494-74947495	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs560702098	chr5:74947495-74947496	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs140334495	chr5:74947520-74947521	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs142707868	chr5:74947521-74947522	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs578125491	chr5:74947522-74947523	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs373821713	chr5:74947554-74947555	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs557244639	chr5:74947672-74947673	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs60609097	chr5:74947687-74947688	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs142697903	chr5:74947722-74947723	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs374821933	chr5:74947723-74947724	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs183137564	chr5:74947729-74947730	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs147344486	chr5:74947747-74947748	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs186299521	chr5:74947750-74947751	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs541121220	chr5:74947809-74947810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563980895	chr5:74947818-74947819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533163925	chr5:74947872-74947873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191542117	chr5:74947934-74947935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563597794	chr5:74947958-74947959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs16872701	chr5:74947983-74947984	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs549435129	chr5:74948088-74948089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566060440	chr5:74948102-74948103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534662000	chr5:74948125-74948126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551862907	chr5:74948158-74948159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372668461	chr5:74948193-74948194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542347298	chr5:74948204-74948205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7734430	chr5:74948245-74948246	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs557107675	chr5:74948260-74948261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553329257	chr5:74948262-74948263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574026371	chr5:74948295-74948296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557892970	chr5:74948299-74948300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs368769980	chr5:74948333-74948334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572012052	chr5:74948426-74948427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540632272	chr5:74948427-74948428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183036082	chr5:74948463-74948464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115053612	chr5:74948475-74948476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543670237	chr5:74948513-74948514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11953883	chr5:74948538-74948539	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs529245766	chr5:74948546-74948547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557458948	chr5:74948553-74948554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549301244	chr5:74948573-74948574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs36013455	chr5:74948585-74948586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74664877	chr5:74948607-74948608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs75349293	chr5:74948634-74948635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187663177	chr5:74948665-74948666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529850537	chr5:74948732-74948733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142646821	chr5:74948734-74948735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537130931	chr5:74948748-74948749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	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
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
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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74921800-74964400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:74944800-74952200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr5:74945000-74962800	Weak transcription	Fetal Intestine Large	intestine
4	chr5:74945800-74950800	Weak transcription	Right Atrium	heart
5	chr5:74946600-74952200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:74946600-74952400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr5:74947000-74947600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr5:74947000-74947600	Enhancers	Fetal Intestine Small	intestine
9	chr5:74947200-74948000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr5:74947200-74948000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr5:74947200-74952200	Enhancers	Fetal Heart	heart
12	chr5:74947400-74947800	Active TSS	Rectal Mucosa Donor 31	rectum
13	chr5:74947400-74948000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr5:74947400-74948000	Enhancers	NHEK	skin
15	chr5:74947400-74948800	Weak transcription	Brain Substantia Nigra	brain
16	chr5:74947600-74949800	Weak transcription	Fetal Intestine Small	intestine
17	chr5:74947600-74952000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr5:74947800-74948000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr5:74947800-74948200	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr5:74948000-74950400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr5:74948000-74950400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr5:74948000-74950600	Weak transcription	NHEK	skin
23	chr5:74948000-74951800	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr5:74948000-74959200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr5:74948200-74949200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr5:74948200-74952000	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr5:74948400-74952400	Weak transcription	Fetal Brain Male	brain
28	chr5:74948600-74950600	Enhancers	Fetal Kidney	kidney
29	chr5:74948800-74949600	Enhancers	Brain Hippocampus Middle	brain
30	chr5:74948800-74950000	Enhancers	Brain Substantia Nigra	brain
31	chr5:74949000-74949200	Enhancers	Left Ventricle	heart
32	chr5:74949000-74949400	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr5:74949000-74949400	Enhancers	Fetal Stomach	stomach
34	chr5:74949000-74949800	Enhancers	Brain Cingulate Gyrus	brain
35	chr5:74949200-74950000	Weak transcription	Left Ventricle	heart
36	chr5:74949200-74952000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr5:74949400-74951600	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr5:74949600-74949800	Bivalent Enhancer	Fetal Stomach	stomach
39	chr5:74949600-74950200	Enhancers	Fetal Muscle Trunk	muscle
40	chr5:74949600-74951600	Weak transcription	Brain Hippocampus Middle	brain
41	chr5:74949800-74950000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr5:74949800-74950000	Enhancers	Fetal Muscle Leg	muscle
43	chr5:74949800-74951200	Strong transcription	Fetal Intestine Small	intestine
44	chr5:74949800-74951600	Weak transcription	Brain Cingulate Gyrus	brain
45	chr5:74950000-74951000	Enhancers	Right Ventricle	heart
46	chr5:74950000-74951200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr5:74950000-74951200	Enhancers	Left Ventricle	heart
48	chr5:74950000-74951600	Weak transcription	Brain Substantia Nigra	brain
49	chr5:74950200-74952200	Weak transcription	Fetal Muscle Trunk	muscle
50	chr5:74950400-74950600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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