Variant report

Variant	nsv890327
Chromosome Location	chr8:8065046-8123434
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1590)
CpG islands
(count:1161)
Chromatin interactive
region (count:27)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8111412-8112067	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8092931-8093297	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8102923-8103018	K562	blood:	n/a	n/a
4	ARID3A	chr8:8105348-8105599	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:8114109-8114421	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:8091892-8091896	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:8101041-8101072	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:8105314-8105669	K562	blood:	n/a	n/a
9	ARID3A	chr8:8101412-8102391	K562	blood:	n/a	n/a
10	ATF1	chr8:8101961-8102473	K562	blood:	n/a	n/a
11	ATF1	chr8:8118490-8118523	K562	blood:	n/a	n/a
12	ATF2	chr8:8096080-8096557	GM12878	blood:	n/a	n/a
13	ATF3	chr8:8101985-8102287	K562	blood:	n/a	n/a
14	ATF3	chr8:8101821-8102415	K562	blood:	n/a	n/a
15	ATF3	chr8:8096172-8096477	K562	blood:	n/a	n/a
16	BATF	chr8:8096176-8096555	GM12878	blood:	n/a	n/a
17	BATF	chr8:8095764-8096661	GM12878	blood:	n/a	n/a
18	BATF	chr8:8086606-8086880	GM12878	blood:	n/a	chr8:8086859-8086869
19	BATF	chr8:8086780-8087231	GM12878	blood:	n/a	chr8:8086859-8086869
20	BATF	chr8:8086957-8087326	GM12878	blood:	n/a	n/a
21	BATF	chr8:8091245-8091594	GM12878	blood:	n/a	n/a
22	BATF	chr8:8085189-8085406	GM12878	blood:	n/a	n/a
23	BATF	chr8:8086029-8086344	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:8096143-8096503	GM12878	blood:	n/a	chr8:8096357-8096366 chr8:8096334-8096343
25	BCL11A	chr8:8086542-8086909	GM12878	blood:	n/a	chr8:8086862-8086871
26	BCL11A	chr8:8087022-8087307	GM12878	blood:	n/a	n/a
27	BCL11A	chr8:8086100-8086324	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:8096092-8096547	GM12878	blood:	n/a	chr8:8096357-8096366 chr8:8096334-8096343
29	BCL11A	chr8:8085568-8085885	GM12878	blood:	n/a	chr8:8085759-8085772
30	BCL11A	chr8:8084587-8084739	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:8084815-8084994	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:8085159-8085355	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:8086053-8087227	GM12878	blood:	n/a	chr8:8086862-8086871
34	BCL11A	chr8:8085174-8085434	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:8070740-8071105	GM12878	blood:	n/a	n/a
36	BCL3	chr8:8085939-8086338	A549	lung:	n/a	n/a
37	BCLAF1	chr8:8096300-8096579	GM12878	blood:	n/a	chr8:8096357-8096366 chr8:8096334-8096343
38	BHLHE40	chr8:8111540-8111854	HepG2	liver:	n/a	n/a
39	BHLHE40	chr8:8096164-8096216	K562	blood:	n/a	n/a
40	BHLHE40	chr8:8091239-8091621	HepG2	liver:	n/a	n/a
41	BHLHE40	chr8:8085237-8085785	HepG2	liver:	n/a	n/a
42	BHLHE40	chr8:8092986-8093375	HepG2	liver:	n/a	n/a
43	BHLHE40	chr8:8086108-8086315	A549	lung:	n/a	n/a
44	BHLHE40	chr8:8096320-8096341	GM12878	blood:	n/a	n/a
45	BHLHE40	chr8:8101527-8101628	K562	blood:	n/a	n/a
46	BHLHE40	chr8:8086020-8086225	HepG2	liver:	n/a	n/a
47	BHLHE40	chr8:8084571-8084831	HepG2	liver:	n/a	n/a
48	BHLHE40	chr8:8101929-8102382	K562	blood:	n/a	n/a
49	BHLHE40	chr8:8086603-8086856	GM12878	blood:	n/a	n/a
50	BHLHE40	chr8:8086032-8086287	GM12878	blood:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8085973-8086023	HCPEpiC	choroid plexus:	n/a
2	chr8:8102392-8102442	AG10803	skin:	n/a
3	chr8:8085973-8086023	HCPEpiC	choroid plexus:	n/a
4	chr8:8102392-8102442	AG10803	skin:	n/a
5	chr8:8084610-8084660	BE2_C	brain:	n/a
6	chr8:8085544-8085594	Hela-S3	cervix:	n/a
7	chr8:8086146-8086196	HCF	heart:	n/a
8	chr8:8086146-8086196	LNCaP	prostate:	n/a
9	chr8:8084610-8084660	HEEpiC	esophagus:	n/a
10	chr8:8085496-8085546	HCF	heart:	n/a
11	chr8:8084126-8084176	HCF	heart:	n/a
12	chr8:8090460-8090510	ECC-1	luminal epithelium:	n/a
13	chr8:8086144-8086194	SK-N-SH	brain:	n/a
14	chr8:8102121-8102171	Hela-S3	cervix:	n/a
15	chr8:8086607-8086657	AG04449	skin:	fetal
16	chr8:8120624-8120674	U87	brain:	n/a
17	chr8:8085946-8085996	HPAEpiC	pulmonary alveolar:	n/a
18	chr8:8085532-8085582	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:8090460-8090510	GM12892	blood:	n/a
20	chr8:8084610-8084660	ECC-1	luminal epithelium:	n/a
21	chr8:8102392-8102442	LNCaP	prostate:	n/a
22	chr8:8086146-8086196	GM12878	blood:	n/a
23	chr8:8085844-8085894	NT2-D1	testis:	n/a
24	chr8:8085496-8085546	HepG2	liver:	n/a
25	chr8:8086607-8086657	Jurkat	blood:	n/a
26	chr8:8086686-8086736	AG04450	lung:	fetal
27	chr8:8090460-8090510	HRCEpiC	kidney:	n/a
28	chr8:8086686-8086736	HIPEpiC	eye:	n/a
29	chr8:8085973-8086023	SK-N-MC	brain:	n/a
30	chr8:8086144-8086194	NH-A	brain:	n/a
31	chr8:8084126-8084176	HIPEpiC	eye:	n/a
32	chr8:8085946-8085996	GM19239	blood:	n/a
33	chr8:8086146-8086196	HUVEC	blood vessel:	n/a
34	chr8:8084126-8084176	AG09309	skin:	n/a
35	chr8:8085973-8086023	HNPCEpiC	eye:	n/a
36	chr8:8085973-8086023	SKMC	muscle:	n/a
37	chr8:8084126-8084176	Jurkat	blood:	n/a
38	chr8:8084974-8085024	AoSMC	blood vessel:	n/a
39	chr8:8085946-8085996	H1-hESC	embryonic stem cell:	embryo
40	chr8:8120624-8120674	GM12878	blood:	n/a
41	chr8:8084974-8085024	HRE	kidney:	n/a
42	chr8:8084610-8084660	PANC-1	pancreas:	n/a
43	chr8:8084126-8084176	NHDF-neo	bronchial:	n/a
44	chr8:8085503-8085553	NHBE	bronchial:	n/a
45	chr8:8086607-8086657	LNCaP	prostate:	n/a
46	chr8:8086144-8086194	AG09319	gingival:	n/a
47	chr8:8085544-8085594	IMR90	lung:	fetal
48	chr8:8085532-8085582	HepG2	liver:	n/a
49	chr8:8082819-8082869	GM12878	blood:	n/a
50	chr8:8084126-8084176	AoSMC	blood vessel:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8092255..8094353-chr8:8097556..8100076,2	K562	blood:
2	chr6:26031709..26032614-chr8:8085130..8085961,2	Hela-S3	cervix:
3	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
4	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
5	chr15:59062813..59063449-chr8:8085838..8086625,2	Hela-S3	cervix:
6	chr8:8086683..8088508-chr8:8193858..8196209,2	MCF-7	breast:
7	chr8:8105578..8107200-chr8:8525517..8527239,2	MCF-7	breast:
8	chr8:8094104..8094693-chr8:8146401..8147333,2	MCF-7	breast:
9	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
10	chr8:8084641..8087551-chr8:8098301..8100358,2	K562	blood:
11	chr8:8093979..8097330-chr8:8100546..8105094,4	K562	blood:
12	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
13	chr8:8092255..8094353-chr8:8097556..8100076,2	K562	blood:
14	chr8:8105365..8106008-chr8:8526894..8527465,2	K562	blood:
15	chr8:8098254..8100230-chr8:8106571..8108592,2	K562	blood:
16	chr8:8094096..8094629-chr8:8147947..8148540,2	MCF-7	breast:
17	chr8:8084641..8087551-chr8:8098301..8100358,2	K562	blood:
18	chr8:8108549..8111183-chr8:8240516..8242778,2	MCF-7	breast:
19	chr8:8093979..8097330-chr8:8100546..8105094,4	K562	blood:
20	chr8:8118434..8122893-chr8:8123384..8125953,5	MCF-7	breast:
21	chr8:8101610..8104279-chr8:8111391..8114092,2	K562	blood:
22	chr8:8101610..8104492-chr8:8112542..8114092,2	K562	blood:
23	chr11:3443497..3444149-chr8:8085706..8086350,2	HCT-116	colon:
24	chr3:129829770..129830533-chr8:8085798..8086673,3	Hela-S3	cervix:
25	chr8:8118434..8122893-chr8:8123384..8125953,5	MCF-7	breast:
26	chr8:8104258..8105835-chr8:8243426..8245376,2	MCF-7	breast:
27	chr8:8105059..8106011-chr8:8526943..8527953,6	MCF-7	breast:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRAGMIN.1-3	chr8:8084256-8084265	XLOC_006994
2	lnc-PRAGMIN.1-3	chr8:8083918-8084265	ENSG00000253893.1
3	lnc-AC068020.1-1	chr8:8097891-8099954	NONHSAT124866
4	lnc-PRAGMIN.1-7	chr8:8097017-8097128	NONHSAT124860
5	lnc-AC068020.1-1	chr8:8101621-8102385	NONHSAT124866
6	lnc-PRAGMIN.1-7	chr8:8095713-8095872	NONHSAT124858
7	lnc-PRAGMIN.1-3	chr8:8084842-8085129	XLOC_006994
8	lnc-PRAGMIN.1-3	chr8:8077566-8077704	ENSG00000253893.1
9	lnc-AC068020.1-1	chr8:8098797-8099202	NONHSAT124867
10	lnc-PRAGMIN.1-7	chr8:8097728-8097835	NONHSAT124863
11	lnc-PRAGMIN.1-3	chr8:8083918-8084136	ENSG00000253893.2
12	lnc-PRAGMIN.1-7	chr8:8095696-8095860	NONHSAT124863
13	lnc-AC068020.1-1	chr8:8094730-8094797	NONHSAT124861
14	lnc-PRAGMIN.1-7	chr8:8093525-8093885	NONHSAT124858
15	lnc-AC068020.1-1	chr8:8095815-8096448	NONHSAT124861
16	lnc-PRAGMIN.1-7	chr8:8097015-8097098	NONHSAT124863
17	lnc-PRAGMIN.1-3	chr8:8081348-8081432	XLOC_006993
18	lnc-PRAGMIN.1-3	chr8:8081348-8081409	ENSG00000253893.1
19	lnc-PRAGMIN.1-3	chr8:8081348-8081409	ENSG00000253893.2
20	lnc-PRAGMIN.1-3	chr8:8077566-8077704	ENSG00000253893.2
21	lnc-PRAGMIN.1-7	chr8:8097960-8098070	NONHSAT124863
22	lnc-AC068020.1-1	chr8:8101621-8101684	NONHSAT124868
23	lnc-PRAGMIN.1-7	chr8:8094648-8095823	NONHSAT124860
24	lnc-AC068020.1-1	chr8:8099150-8099484	NONHSAT124868
25	lnc-PRAGMIN.1-3	chr8:8084720-8085385	ENSG00000253893.1
26	lnc-PRAGMIN.1-3	chr8:8077586-8077704	XLOC_006993
27	lnc-AC068020.1-1	chr8:8101621-8101707	NONHSAT124867
28	lnc-PRAGMIN.1-7	chr8:8098818-8098933	NONHSAT124863

No data

Variant related genes	Relation type
FAM86B3P	TF binding region
FAM85B	TF binding region
ALG1L13P	TF binding region
FAM86B3P	CpG island
FAM85B	CpG island
ALG1L13P	CpG island
ENSG00000124693	chromatin interactions
ENSG00000245975	chromatin interactions
ENSG00000253981	chromatin interactions
ENSG00000166492	chromatin interactions
ENSG00000128923	chromatin interactions
ENSG00000173295	chromatin interactions
ENSG00000253540	chromatin interactions
ENSG00000182319	chromatin interactions
UBQLN1	miRNA target sites

Extended variants
information (count: 3393 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:3393 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576543068	chr8:8067443-8067444	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs545740805	chr8:8067470-8067471	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs199843761	chr8:8067507-8067508	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs185260371	chr8:8067521-8067522	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs576035316	chr8:8067525-8067526	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs190485644	chr8:8067526-8067527	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs182315492	chr8:8067533-8067534	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs542149358	chr8:8067576-8067577	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs562401810	chr8:8067577-8067578	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs527864785	chr8:8067647-8067648	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs548034452	chr8:8067674-8067675	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs564539255	chr8:8067683-8067684	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs74605650	chr8:8067684-8067685	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs374265789	chr8:8067695-8067696	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs187036761	chr8:8067700-8067701	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs188378934	chr8:8067710-8067711	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs180688272	chr8:8067712-8067713	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs76792382	chr8:8067727-8067728	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs185751004	chr8:8067731-8067732	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs185634291	chr8:8067768-8067769	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs61386661	chr8:8067773-8067774	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs149830540	chr8:8067778-8067779	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs28405114	chr8:8067803-8067804	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs28464701	chr8:8067805-8067806	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs186880470	chr8:8067821-8067822	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs528355108	chr8:8067826-8067827	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs553558373	chr8:8067827-8067828	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs57857358	chr8:8067832-8067833	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs28393046	chr8:8067840-8067841	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs561730067	chr8:8067885-8067886	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs28561892	chr8:8067920-8067921	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs541837052	chr8:8067923-8067924	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs192079021	chr8:8067933-8067934	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs369182289	chr8:8067989-8067990	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs541598169	chr8:8068004-8068005	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs201401687	chr8:8068029-8068030	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs533624118	chr8:8068067-8068068	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs200690814	chr8:8068096-8068097	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs543545461	chr8:8068119-8068120	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs75680163	chr8:8068128-8068129	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs187545878	chr8:8068134-8068135	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs191312495	chr8:8068165-8068166	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs61688686	chr8:8068181-8068182	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs527580617	chr8:8068208-8068209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182173231	chr8:8068215-8068216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570544387	chr8:8068218-8068219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187182576	chr8:8068229-8068230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191580688	chr8:8068240-8068241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185296211	chr8:8068256-8068257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190292862	chr8:8068260-8068261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:141)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:686 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8067400-8068200	Active TSS	Stomach Smooth Muscle	stomach
2	chr8:8067600-8068000	Enhancers	Left Ventricle	heart
3	chr8:8067600-8068000	Enhancers	Right Ventricle	heart
4	chr8:8067600-8068000	Enhancers	Hela-S3	cervix
5	chr8:8067600-8068200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:8068000-8068400	Enhancers	H1 Cell Line	embryonic stem cell
7	chr8:8068000-8068400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr8:8068200-8076200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:8068400-8069400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr8:8069400-8069600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr8:8076200-8076800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:8080400-8080600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr8:8080600-8080800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr8:8080800-8081600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr8:8081600-8081800	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr8:8081600-8082000	Enhancers	NHLF	lung
17	chr8:8081600-8082400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:8081600-8082400	Enhancers	Muscle Satellite Cultured Cells	--
19	chr8:8081800-8084600	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr8:8082000-8082400	Enhancers	Hela-S3	cervix
21	chr8:8082000-8082400	Weak transcription	NHLF	lung
22	chr8:8082000-8084800	Weak transcription	Stomach Mucosa	stomach
23	chr8:8082200-8084000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr8:8082400-8082600	Enhancers	NHLF	lung
25	chr8:8082400-8084000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr8:8082400-8084000	Weak transcription	Hela-S3	cervix
27	chr8:8082400-8084800	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr8:8082600-8084800	Weak transcription	NHLF	lung
29	chr8:8084000-8084200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr8:8084000-8084200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr8:8084000-8084200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr8:8084000-8084200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:8084000-8084200	Enhancers	Hela-S3	cervix
34	chr8:8084000-8084600	Enhancers	Fetal Intestine Large	intestine
35	chr8:8084000-8084800	Enhancers	Liver	Liver
36	chr8:8084200-8084400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr8:8084200-8084400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr8:8084200-8084400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr8:8084200-8084600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr8:8084200-8084600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:8084200-8084600	Weak transcription	Hela-S3	cervix
42	chr8:8084200-8085200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
43	chr8:8084200-8086800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:8084200-8087200	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr8:8084400-8084600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr8:8084400-8086800	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr8:8084400-8086800	Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr8:8084400-8087000	Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr8:8084400-8087000	Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr8:8084600-8084800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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