Variant report

Variant	nsv1016050
Chromosome Location	chr8:87167790-87335197
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:820)
CpG islands
(count:305)
Chromatin interactive
region (count:152)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:820 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:87332587-87333433	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:87317607-87317927	HepG2	liver:	n/a	chr8:87317682-87317698
3	ARID3A	chr8:87302190-87302818	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:87179989-87180133	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:87267265-87268652	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:87333701-87333702	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:87237988-87238154	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:87269106-87269601	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:87251126-87251828	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:87249992-87250780	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:87332260-87332381	HepG2	liver:	n/a	n/a
12	ARID3A	chr8:87269806-87269918	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:87249730-87249762	HepG2	liver:	n/a	n/a
14	ARID3A	chr8:87222381-87222600	HepG2	liver:	n/a	n/a
15	ARID3A	chr8:87307822-87308253	HepG2	liver:	n/a	n/a
16	ARID3A	chr8:87313199-87313488	HepG2	liver:	n/a	n/a
17	ATF1	chr8:87274360-87274458	K562	blood:	n/a	n/a
18	ATF3	chr8:87302234-87302791	A549	lung:	n/a	n/a
19	BHLHE40	chr8:87324016-87324235	K562	blood:	n/a	n/a
20	BHLHE40	chr8:87250154-87250425	HepG2	liver:	n/a	n/a
21	BHLHE40	chr8:87267833-87268266	HepG2	liver:	n/a	n/a
22	CBX3	chr8:87292590-87293043	HCT-116	colon:	n/a	n/a
23	CBX3	chr8:87292707-87292924	K562	blood:	n/a	n/a
24	CEBPB	chr8:87302376-87302751	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:87282297-87282482	K562	blood:	n/a	chr8:87282437-87282448
26	CEBPB	chr8:87302309-87302793	A549	lung:	n/a	n/a
27	CEBPB	chr8:87215442-87215754	A549	lung:	n/a	n/a
28	CEBPB	chr8:87274075-87274343	A549	lung:	n/a	n/a
29	CEBPB	chr8:87282270-87282612	HepG2	liver:	n/a	chr8:87282437-87282448
30	CEBPB	chr8:87269300-87269537	A549	lung:	n/a	n/a
31	CEBPB	chr8:87178969-87179150	HepG2	liver:	n/a	chr8:87179079-87179092 chr8:87179079-87179092 chr8:87179079-87179090 chr8:87179081-87179090 chr8:87179080-87179091
32	CEBPB	chr8:87301802-87301962	HepG2	liver:	n/a	chr8:87301893-87301904
33	CEBPB	chr8:87317612-87318002	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr8:87331224-87331422	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:87301764-87302059	A549	lung:	n/a	chr8:87301893-87301904
36	CEBPB	chr8:87209560-87209808	HepG2	liver:	n/a	chr8:87209668-87209679
37	CEBPB	chr8:87274635-87274945	HepG2	liver:	n/a	chr8:87274760-87274771
38	CEBPB	chr8:87209639-87209709	IMR90	lung:	n/a	chr8:87209668-87209679
39	CEBPB	chr8:87302364-87302751	HepG2	liver:	n/a	n/a
40	CEBPB	chr8:87256017-87256246	K562	blood:	n/a	n/a
41	CEBPB	chr8:87302363-87302733	A549	lung:	n/a	n/a
42	CEBPB	chr8:87179916-87180199	HepG2	liver:	n/a	n/a
43	CEBPB	chr8:87269304-87269571	K562	blood:	n/a	n/a
44	CEBPB	chr8:87314186-87314434	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:87224775-87224930	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:87302196-87302935	A549	lung:	n/a	n/a
47	CEBPB	chr8:87195401-87195660	K562	blood:	n/a	n/a
48	CEBPB	chr8:87274645-87274931	Hela-S3	cervix:	n/a	chr8:87274760-87274771
49	CEBPB	chr8:87302198-87302848	MCF-7	breast:	n/a	n/a
50	CEBPB	chr8:87269244-87269623	HepG2	liver:	n/a	chr8:87269246-87269263 chr8:87269247-87269260

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:87242630-87242680	SK-N-SH	brain:	n/a
2	chr8:87243677-87243727	A549	lung:	n/a
3	chr8:87243983-87244033	NB4	blood:	n/a
4	chr8:87226434-87226484	IMR90	lung:	fetal
5	chr8:87243979-87244029	HRCEpiC	kidney:	n/a
6	chr8:87226434-87226484	HL-60	blood:	n/a
7	chr8:87226434-87226484	SK-N-MC	brain:	n/a
8	chr8:87243983-87244033	AG04450	lung:	fetal
9	chr8:87242630-87242680	K562	blood:	n/a
10	chr8:87243677-87243727	SAEC	small airway:	n/a
11	chr8:87243979-87244029	U87	brain:	n/a
12	chr8:87243983-87244033	AG10803	skin:	n/a
13	chr8:87226434-87226484	MCF10A-Er-Src	breast:	n/a
14	chr8:87226434-87226484	HCF	heart:	n/a
15	chr8:87243677-87243727	HNPCEpiC	eye:	n/a
16	chr8:87243979-87244029	ProgFib	skin:	n/a
17	chr8:87226434-87226484	HCPEpiC	choroid plexus:	n/a
18	chr8:87226434-87226484	PFSK-1	brain:	n/a
19	chr8:87226434-87226484	A549	lung:	n/a
20	chr8:87242630-87242680	ECC-1	luminal epithelium:	n/a
21	chr8:87243983-87244033	AG09309	skin:	n/a
22	chr8:87243983-87244033	IMR90	lung:	fetal
23	chr8:87243983-87244033	PANC-1	pancreas:	n/a
24	chr8:87243983-87244033	HRCEpiC	kidney:	n/a
25	chr8:87243983-87244033	HRE	kidney:	n/a
26	chr8:87243979-87244029	SK-N-SH_RA	brain:	n/a
27	chr8:87242630-87242680	HL-60	blood:	n/a
28	chr8:87242630-87242680	H1-hESC	embryonic stem cell:	embryo
29	chr8:87243677-87243727	NB4	blood:	n/a
30	chr8:87243983-87244033	BJ	skin:	n/a
31	chr8:87242630-87242680	AoSMC	blood vessel:	n/a
32	chr8:87243979-87244029	AG04450	lung:	fetal
33	chr8:87226434-87226484	HCM	heart:	n/a
34	chr8:87243979-87244029	NHDF-neo	bronchial:	n/a
35	chr8:87243983-87244033	AG09319	gingival:	n/a
36	chr8:87226434-87226484	GM12891	blood:	n/a
37	chr8:87243983-87244033	ECC-1	luminal epithelium:	n/a
38	chr8:87242630-87242680	BE2_C	brain:	n/a
39	chr8:87243677-87243727	NHBE	bronchial:	n/a
40	chr8:87243979-87244029	A549	lung:	n/a
41	chr8:87243979-87244029	HepG2	liver:	n/a
42	chr8:87243979-87244029	SAEC	small airway:	n/a
43	chr8:87243983-87244033	HEEpiC	esophagus:	n/a
44	chr8:87243979-87244029	GM06990	blood:	n/a
45	chr8:87243983-87244033	Hela-S3	cervix:	n/a
46	chr8:87242630-87242680	HEEpiC	esophagus:	n/a
47	chr8:87242630-87242680	RPTEC	kidney:	n/a
48	chr8:87243677-87243727	HepG2	liver:	n/a
49	chr8:87242630-87242680	A549	lung:	n/a
50	chr8:87243979-87244029	HCF	heart:	n/a

(count:152 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:87192734..87196437-chr8:87354857..87357737,4	MCF-7	breast:
2	chr8:87227505..87230392-chr8:87231801..87233486,2	MCF-7	breast:
3	chr8:87175555..87177638-chr8:87179061..87180687,2	K562	blood:
4	chr8:87207725..87209616-chr8:87210524..87212253,2	MCF-7	breast:
5	chr8:87267716..87270046-chr8:87281008..87283289,2	MCF-7	breast:
6	chr8:87214685..87217092-chr8:87228293..87229889,2	MCF-7	breast:
7	chr8:87320900..87322835-chr8:87353695..87355851,2	MCF-7	breast:
8	chr8:87268486..87272936-chr8:87352776..87356432,5	MCF-7	breast:
9	chr8:87212467..87215365-chr8:87302266..87303837,2	MCF-7	breast:
10	chr4:103729408..103730314-chr8:87178649..87179164,2	MCF-7	breast:
11	chr8:87149425..87151033-chr8:87215624..87217848,2	MCF-7	breast:
12	chr8:87232831..87235143-chr8:87256917..87258574,2	MCF-7	breast:
13	chr8:87274626..87278061-chr8:87304076..87307581,3	MCF-7	breast:
14	chr8:87163948..87165822-chr8:87168496..87170737,2	MCF-7	breast:
15	chr8:87187218..87190589-chr8:87353304..87356196,4	MCF-7	breast:
16	chr8:87334379..87336674-chr8:87338339..87340717,2	MCF-7	breast:
17	chr8:87228877..87232522-chr8:87233381..87236697,3	MCF-7	breast:
18	chr8:87315946..87318767-chr8:87320826..87322918,2	MCF-7	breast:
19	chr8:87227505..87230392-chr8:87231801..87233486,2	MCF-7	breast:
20	chr8:87210841..87213760-chr8:87426169..87428047,2	MCF-7	breast:
21	chr8:87225336..87228071-chr8:87228709..87231733,3	MCF-7	breast:
22	chr12:132380546..132381123-chr8:87287679..87288623,2	MCF-7	breast:
23	chr8:87185465..87188007-chr8:87211775..87213428,2	MCF-7	breast:
24	chr8:87148020..87150641-chr8:87251875..87254676,2	MCF-7	breast:
25	chr8:87212192..87213055-chr8:87354638..87355564,2	MCF-7	breast:
26	chr8:87188610..87190453-chr8:87196607..87198359,2	MCF-7	breast:
27	chr8:87189537..87192109-chr8:87199086..87201093,2	MCF-7	breast:
28	chr8:87175555..87177638-chr8:87179061..87180687,2	K562	blood:
29	chr8:87234703..87239197-chr8:87353081..87358100,5	MCF-7	breast:
30	chr8:87315946..87318767-chr8:87320826..87322918,2	MCF-7	breast:
31	chr8:87186847..87188623-chr8:87190111..87192908,2	MCF-7	breast:
32	chr8:87329069..87335338-chr8:87352769..87359177,10	MCF-7	breast:
33	chr8:87180089..87182207-chr8:87303826..87306523,2	MCF-7	breast:
34	chr8:87301270..87304931-chr8:87353185..87356602,8	MCF-7	breast:
35	chr8:87144904..87147607-chr8:87176565..87179307,2	MCF-7	breast:
36	chr8:87140754..87142619-chr8:87176258..87179083,2	MCF-7	breast:
37	chr8:87187644..87190858-chr8:87193352..87196070,3	MCF-7	breast:
38	chr8:87212235..87212767-chr8:87269592..87270289,2	MCF-7	breast:
39	chr8:87202647..87205379-chr8:87353769..87356042,2	MCF-7	breast:
40	chr8:87232831..87235143-chr8:87256917..87258574,2	MCF-7	breast:
41	chr8:87212467..87215365-chr8:87302266..87303837,2	MCF-7	breast:
42	chr8:87137737..87138511-chr8:87318980..87319543,2	MCF-7	breast:
43	chr8:87272517..87276008-chr8:87285333..87287881,3	MCF-7	breast:
44	chr8:87180089..87182207-chr8:87303826..87306523,2	MCF-7	breast:
45	chr8:87185465..87188007-chr8:87211775..87213428,2	MCF-7	breast:
46	chr8:87213959..87216666-chr8:87241758..87244737,2	MCF-7	breast:
47	chr8:87312932..87319525-chr8:87352143..87356441,7	MCF-7	breast:
48	chr8:87232045..87233654-chr8:87330272..87332535,2	MCF-7	breast:
49	chr8:87294678..87297186-chr8:87297891..87299648,2	K562	blood:
50	chr8:87329552..87331858-chr8:87353480..87355927,3	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V0D2-1	chr8:87198876-87198935	ENSG00000253699.1
2	lnc-ATP6V0D2-1	chr8:87208116-87208230	ENSG00000253699.1
3	lnc-ATP6V0D2-1	chr8:87224424-87224465	ENSG00000253699.1
4	lnc-ATP6V0D2-1	chr8:87212370-87212451	ENSG00000253699.1
5	lnc-ATP6V0D2-1	chr8:87192647-87192848	ENSG00000253699.1

No data

Variant related genes	Relation type
ENSG00000253675	TF binding region
ENSG00000253699	TF binding region
SLC7A13	TF binding region
ENSG00000253675	CpG island
ENSG00000253699	CpG island
SLC7A13	CpG island
ENSG00000254231	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000164893	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000123124	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000187735	chromatin interactions
ENSG00000253699	chromatin interactions

Extended variants
information (count: 5904 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:5904 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7820770	chr8:87167790-87167791	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561648238	chr8:87167822-87167823	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs571965717	chr8:87167840-87167841	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs540940436	chr8:87167849-87167850	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs563907953	chr8:87167857-87167858	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs533006120	chr8:87167858-87167859	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs12680278	chr8:87167872-87167873	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs190484460	chr8:87168022-87168023	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs181794609	chr8:87168023-87168024	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs563278738	chr8:87168060-87168061	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs112727729	chr8:87168074-87168075	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs562033174	chr8:87168085-87168086	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs185990582	chr8:87168112-87168113	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs188992941	chr8:87168160-87168161	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs78555668	chr8:87168161-87168162	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs10090032	chr8:87168210-87168211	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs375278799	chr8:87168216-87168217	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs115986597	chr8:87168229-87168230	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs145410468	chr8:87168243-87168244	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs7834662	chr8:87168263-87168264	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs539177642	chr8:87168274-87168275	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs181386510	chr8:87168282-87168283	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs535950988	chr8:87168293-87168294	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs147695064	chr8:87168337-87168338	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs140674841	chr8:87168362-87168363	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs73263107	chr8:87168381-87168382	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs7813986	chr8:87168413-87168414	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs566504260	chr8:87168427-87168428	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs533755946	chr8:87168439-87168440	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs577757645	chr8:87168450-87168451	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs543298536	chr8:87168459-87168460	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs185670226	chr8:87168516-87168517	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs555740641	chr8:87168523-87168524	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs373188566	chr8:87168532-87168533	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs190967122	chr8:87168538-87168539	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs549115495	chr8:87168550-87168551	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs145623820	chr8:87168558-87168559	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs573981693	chr8:87168562-87168563	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs375222096	chr8:87168575-87168576	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs77596212	chr8:87168619-87168620	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs571100606	chr8:87168661-87168662	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs533570491	chr8:87168713-87168714	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556094609	chr8:87168729-87168730	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570244061	chr8:87168760-87168761	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs535548238	chr8:87168763-87168764	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs555467079	chr8:87168803-87168804	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs565719462	chr8:87168840-87168841	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs534736010	chr8:87168871-87168872	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557626662	chr8:87168872-87168873	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs9693993	chr8:87168882-87168883	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Rett syndrome	21593744	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21990379	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	19805367	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87165000-87168600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr8:87177200-87180000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr8:87178400-87179000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:87178800-87180000	Enhancers	HepG2	liver
5	chr8:87179800-87180000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:87180000-87185400	Weak transcription	HepG2	liver
7	chr8:87180000-87187400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:87185400-87186000	Enhancers	HepG2	liver
9	chr8:87185800-87186200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr8:87186000-87186200	Flanking Active TSS	HepG2	liver
11	chr8:87186000-87186400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:87186000-87186400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr8:87186000-87186400	Enhancers	Gastric	stomach
14	chr8:87186000-87186600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr8:87186000-87186800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr8:87186200-87186400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
17	chr8:87186200-87188400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr8:87186200-87189200	Enhancers	HepG2	liver
19	chr8:87186400-87186600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:87186400-87187400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:87186600-87186800	Enhancers	A549	lung
22	chr8:87186600-87187200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:87186600-87188400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr8:87186800-87187800	Weak transcription	A549	lung
25	chr8:87186800-87188400	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr8:87187000-87189800	Enhancers	Hela-S3	cervix
27	chr8:87187200-87188200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr8:87187400-87187600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr8:87187400-87188000	Enhancers	HUVEC	blood vessel
30	chr8:87187400-87188200	Enhancers	HMEC	breast
31	chr8:87187400-87188400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr8:87187600-87188200	Enhancers	Muscle Satellite Cultured Cells	--
33	chr8:87187600-87188200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr8:87187600-87188200	Enhancers	NHEK	skin
35	chr8:87187600-87189000	Enhancers	Fetal Lung	lung
36	chr8:87187600-87189800	Enhancers	Placenta Amnion	Placenta Amnion
37	chr8:87187800-87188000	Enhancers	A549	lung
38	chr8:87187800-87188000	Enhancers	HSMMtube	muscle
39	chr8:87187800-87188000	Enhancers	NH-A	brain
40	chr8:87187800-87188200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr8:87187800-87188400	Enhancers	HSMM	muscle
42	chr8:87187800-87189400	Enhancers	Osteobl	bone
43	chr8:87187800-87190000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr8:87188000-87188200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:87188000-87188400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:87188000-87188400	Flanking Active TSS	HSMMtube	muscle
47	chr8:87188000-87188600	Enhancers	Fetal Brain Female	brain
48	chr8:87188000-87189000	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr8:87188000-87189200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:87188000-87189200	Flanking Active TSS	A549	lung

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