Variant report

Variant	nsv1030482
Chromosome Location	chr8:100985555-101107347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:494)
CpG islands
(count:61)
Chromatin interactive
region (count:64)
LncRNA
region (count:10)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:494 , 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	BRCA1	chr8:101037742-101037867	Hela-S3	cervix:	n/a	n/a
2	CBX3	chr8:101086685-101086975	K562	blood:	n/a	n/a
3	CEBPB	chr8:101030067-101030603	MCF-7	breast:	n/a	n/a
4	CEBPB	chr8:101098730-101099037	IMR90	lung:	n/a	chr8:101098879-101098890
5	CEBPB	chr8:101030055-101030682	HCT-116	colon:	n/a	n/a
6	CEBPB	chr8:101038628-101038753	A549	lung:	n/a	chr8:101038679-101038690 chr8:101038679-101038690
7	CEBPB	chr8:101098868-101098909	H1-hESC	embryonic stem cell:	n/a	chr8:101098879-101098890
8	CEBPB	chr8:101030153-101030570	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr8:101038561-101038788	HepG2	liver:	n/a	chr8:101038679-101038690 chr8:101038679-101038690
10	CEBPB	chr8:101048835-101049196	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:101048824-101048972	A549	lung:	n/a	n/a
12	CEBPB	chr8:101080432-101080657	H1-hESC	embryonic stem cell:	n/a	chr8:101080562-101080573
13	CEBPB	chr8:101030131-101030623	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr8:101080440-101080666	A549	lung:	n/a	chr8:101080562-101080573
15	CEBPB	chr8:101048676-101049070	MCF-7	breast:	n/a	n/a
16	CEBPB	chr8:101093730-101093803	K562	blood:	n/a	n/a
17	CEBPB	chr8:101030190-101030548	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr8:101030200-101030485	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:101030116-101030682	HCT-116	colon:	n/a	n/a
20	CEBPB	chr8:101085319-101085612	IMR90	lung:	n/a	chr8:101085458-101085471 chr8:101085458-101085469
21	CEBPB	chr8:100999847-101000079	HepG2	liver:	n/a	chr8:100999956-100999967
22	CEBPB	chr8:101029968-101030621	MCF-7	breast:	n/a	n/a
23	CEBPB	chr8:101061083-101061174	HepG2	liver:	n/a	chr8:101061130-101061141
24	CEBPB	chr8:101080478-101080716	K562	blood:	n/a	chr8:101080562-101080573
25	CEBPB	chr8:101085357-101085573	HepG2	liver:	n/a	chr8:101085458-101085471 chr8:101085458-101085469
26	CEBPB	chr8:101098734-101099023	A549	lung:	n/a	chr8:101098879-101098890
27	CEBPB	chr8:101085335-101085616	A549	lung:	n/a	chr8:101085458-101085471 chr8:101085458-101085469
28	CEBPB	chr8:101098673-101099064	MCF-7	breast:	n/a	chr8:101098879-101098890
29	CEBPB	chr8:101098800-101099034	HepG2	liver:	n/a	chr8:101098879-101098890
30	CEBPB	chr8:101080494-101080646	IMR90	lung:	n/a	chr8:101080562-101080573
31	CEBPB	chr8:101048777-101048921	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:101098799-101098938	K562	blood:	n/a	chr8:101098879-101098890
33	CEBPB	chr8:101080429-101080695	HepG2	liver:	n/a	chr8:101080562-101080573
34	CEBPB	chr8:101048792-101049017	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr8:101027940-101028090	GM06990	blood:	n/a	n/a
36	CTCF	chr8:101085780-101085930	MCF-7	breast:	n/a	chr8:101085875-101085891
37	CTCF	chr8:101085749-101085971	MCF-7	breast:	n/a	chr8:101085875-101085891
38	CTCF	chr8:100994740-100994890	NHEK	skin:	n/a	n/a
39	CTCF	chr8:101031512-101031817	IMR90	lung:	n/a	n/a
40	CTCF	chr8:100994800-100994950	GM06990	blood:	n/a	n/a
41	CTCF	chr8:101031590-101031721	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr8:101031520-101031670	GM12872	blood:	n/a	n/a
43	CTCF	chr8:100994740-100994890	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr8:101031581-101031768	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr8:101031680-101031830	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr8:101031580-101031730	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr8:101031560-101031710	GM12868	blood:	n/a	n/a
48	CTCF	chr8:101031558-101031791	LNCaP	prostate:	n/a	n/a
49	CTCF	chr8:101031580-101031730	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr8:100994829-100994890	Medullo	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:101017845-101017895	HIPEpiC	eye:	n/a
2	chr8:101017845-101017895	MCF10A-Er-Src	breast:	n/a
3	chr8:101017845-101017895	K562	blood:	n/a
4	chr8:101017845-101017895	AG04450	lung:	fetal
5	chr8:101017845-101017895	GM12892	blood:	n/a
6	chr8:101017845-101017895	HCPEpiC	choroid plexus:	n/a
7	chr8:101017845-101017895	GM12891	blood:	n/a
8	chr8:101017845-101017895	GM12878	blood:	n/a
9	chr8:101017845-101017895	ECC-1	luminal epithelium:	n/a
10	chr8:101017845-101017895	GM19239	blood:	n/a
11	chr8:101017845-101017895	GM06990	blood:	n/a
12	chr8:101017845-101017895	HRE	kidney:	n/a
13	chr8:101017845-101017895	H1-hESC	embryonic stem cell:	embryo
14	chr8:101017845-101017895	PANC-1	pancreas:	n/a
15	chr8:101017845-101017895	Hepatocyte	liver:	n/a
16	chr8:101017845-101017895	HRCEpiC	kidney:	n/a
17	chr8:101017845-101017895	MCF-7	breast:	n/a
18	chr8:101017845-101017895	HNPCEpiC	eye:	n/a
19	chr8:101017845-101017895	SK-N-SH	brain:	n/a
20	chr8:101017845-101017895	Hela-S3	cervix:	n/a
21	chr8:101017845-101017895	LNCaP	prostate:	n/a
22	chr8:101017845-101017895	A549	lung:	n/a
23	chr8:101017845-101017895	ProgFib	skin:	n/a
24	chr8:101017845-101017895	BJ	skin:	n/a
25	chr8:101017845-101017895	SAEC	small airway:	n/a
26	chr8:101017845-101017895	HepG2	liver:	n/a
27	chr8:101017845-101017895	NHBE	bronchial:	n/a
28	chr8:101017845-101017895	IMR90	lung:	fetal
29	chr8:101017845-101017895	PFSK-1	brain:	n/a
30	chr8:101017845-101017895	RPTEC	kidney:	n/a
31	chr8:101017845-101017895	Caco-2	colon:	n/a
32	chr8:101017845-101017895	Jurkat	blood:	n/a
33	chr8:101017845-101017895	HL-60	blood:	n/a
34	chr8:101017845-101017895	HUVEC	blood vessel:	n/a
35	chr8:101017845-101017895	HEEpiC	esophagus:	n/a
36	chr8:101017845-101017895	SK-N-MC	brain:	n/a
37	chr8:101017845-101017895	T-47D	breast:	n/a
38	chr8:101017845-101017895	PrEC	prostate:	n/a
39	chr8:101017845-101017895	HAEpiC	amniotic membrane:	n/a
40	chr8:101017845-101017895	U87	brain:	n/a
41	chr8:101017845-101017895	AG09309	skin:	n/a
42	chr8:101017845-101017895	HRPEpiC	eye:	n/a
43	chr8:101017845-101017895	SKMC	muscle:	n/a
44	chr8:101017845-101017895	AG10803	skin:	n/a
45	chr8:101017845-101017895	AoSMC	blood vessel:	n/a
46	chr8:101017845-101017895	HEK293	kidney:	embryo
47	chr8:101017845-101017895	HCM	heart:	n/a
48	chr8:101017845-101017895	AG09319	gingival:	n/a
49	chr8:101017845-101017895	NH-A	brain:	n/a
50	chr8:101017845-101017895	ovcar-3	ovarian:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:100994434..100995012-chr8:101137934..101138482,2	MCF-7	breast:
2	chr8:101066176..101067823-chr8:101069547..101072216,2	MCF-7	breast:
3	chr8:101099517..101101112-chr8:101110697..101112905,2	MCF-7	breast:
4	chr8:101040805..101043624-chr8:101048468..101051410,2	MCF-7	breast:
5	chr8:100877780..100878549-chr8:100994242..100995413,5	MCF-7	breast:
6	chr8:101031079..101032807-chr8:101038166..101039739,2	MCF-7	breast:
7	chr8:101078348..101080182-chr8:101083582..101086480,2	K562	blood:
8	chr8:101060088..101062497-chr8:101076282..101079858,3	K562	blood:
9	chr8:101031079..101032807-chr8:101038166..101039739,2	MCF-7	breast:
10	chr8:100903710..100906363-chr8:101026281..101028844,3	MCF-7	breast:
11	chr8:101028026..101030107-chr8:101031177..101033593,3	K562	blood:
12	chr8:101104526..101107349-chr8:101108093..101110938,3	K562	blood:
13	chr8:101080214..101083035-chr8:101089948..101092142,2	MCF-7	breast:
14	chr8:100904036..100906374-chr8:101015983..101018100,2	MCF-7	breast:
15	chr8:100559744..100561257-chr8:101041447..101043428,2	K562	blood:
16	chr8:101009084..101010967-chr8:101016254..101019583,3	MCF-7	breast:
17	chr8:101016235..101017966-chr8:101029514..101031159,2	MCF-7	breast:
18	chr8:101029716..101032245-chr8:101033800..101036282,3	MCF-7	breast:
19	chr8:101078348..101080182-chr8:101083582..101086480,2	K562	blood:
20	chr8:100877771..100878763-chr8:101031217..101031760,2	MCF-7	breast:
21	chr8:101033525..101035604-chr8:101035658..101037862,2	MCF-7	breast:
22	chr8:100403842..100404899-chr8:100994134..100995356,3	MCF-7	breast:
23	chr8:101028063..101030791-chr8:101034516..101036174,2	MCF-7	breast:
24	chr8:100877575..100878417-chr8:100994390..100995379,2	MCF-7	breast:
25	chr8:101010661..101013099-chr8:144464725..144467000,2	MCF-7	breast:
26	chr8:100241348..100243532-chr8:101014262..101016207,2	MCF-7	breast:
27	chr8:101018644..101020624-chr8:101028570..101030711,2	MCF-7	breast:
28	chr8:101060088..101062497-chr8:101076282..101079858,3	K562	blood:
29	chr8:100904566..100906132-chr8:101040405..101043105,2	MCF-7	breast:
30	chr8:101055343..101057696-chr8:101061415..101063128,2	MCF-7	breast:
31	chr8:100903932..100909623-chr8:100990935..100995846,4	MCF-7	breast:
32	chr8:101092534..101094190-chr8:101095302..101097339,2	MCF-7	breast:
33	chr8:100844190..100847017-chr8:101086686..101088410,2	MCF-7	breast:
34	chr8:101018663..101021565-chr8:101028027..101031176,4	MCF-7	breast:
35	chr6:27829699..27832078-chr8:101028376..101031173,2	MCF-7	breast:
36	chr8:101028026..101030107-chr8:101031177..101033593,3	K562	blood:
37	chr8:101048954..101051126-chr8:101052860..101055208,2	K562	blood:
38	chr8:101018644..101020624-chr8:101028570..101030711,2	MCF-7	breast:
39	chr8:101025901..101028872-chr8:101030199..101032276,2	MCF-7	breast:
40	chr8:101018071..101020210-chr8:101320912..101323682,2	MCF-7	breast:
41	chr8:101036588..101038502-chr8:101052692..101054764,2	K562	blood:
42	chr8:101030828..101032763-chr8:101064981..101066943,2	K562	blood:
43	chr8:101029058..101031952-chr8:101032145..101034268,2	MCF-7	breast:
44	chr8:101092534..101094190-chr8:101095302..101097339,2	MCF-7	breast:
45	chr8:100877868..100878775-chr8:101031265..101032087,5	MCF-7	breast:
46	chr8:101040805..101043624-chr8:101048468..101051410,2	MCF-7	breast:
47	chr8:101028063..101030791-chr8:101034516..101036174,2	MCF-7	breast:
48	chr8:100903755..100906341-chr8:101029205..101031997,3	MCF-7	breast:
49	chr8:101036278..101038638-chr8:101040139..101042442,2	K562	blood:
50	chr8:101025901..101028872-chr8:101030199..101032276,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO43-3	chr8:101105390-101105737	NONHSAT127971
2	lnc-FBXO43-4	chr8:101059691-101059824	NONHSAT127968
3	lnc-FBXO43-3	chr8:101104106-101104215	NONHSAT127970
4	lnc-FBXO43-3	chr8:101092523-101092583	NONHSAT127969
5	lnc-FBXO43-3	chr8:101092922-101093076	NONHSAT127970
6	lnc-FBXO43-3	chr8:101092883-101093076	NONHSAT127969
7	lnc-FBXO43-3	chr8:101105675-101105737	NONHSAT127970
8	lnc-FBXO43-4	chr8:101058461-101058706	NONHSAT127968
9	lnc-FBXO43-4	chr8:101063079-101063124	NONHSAT127968
10	lnc-FBXO43-3	chr8:101105675-101105737	NONHSAT127969

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1273a	chr8:101036213-101036237	MIMAT0005926

No data

Variant related genes	Relation type
RGS22	TF binding region
MIR1273A	TF binding region
ENSG00000212414	TF binding region
RGS22	CpG island
MIR1273A	CpG island
ENSG00000212414	CpG island
ENSG00000132554	chromatin interactions
ENSG00000034677	chromatin interactions
ENSG00000164919	chromatin interactions
ENSG00000212414	chromatin interactions
ENSG00000221753	chromatin interactions
ENSG00000132549	chromatin interactions

Extended variants
information (count: 4417 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:4417 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201493519	chr8:100985600-100985601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs199591767	chr8:100985639-100985640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200987215	chr8:100985677-100985678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542238308	chr8:100985711-100985712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553805463	chr8:100985723-100985724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555618913	chr8:100985729-100985730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112842961	chr8:100985765-100985766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542347727	chr8:100985771-100985772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562639015	chr8:100985785-100985786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111899164	chr8:100985791-100985792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533576644	chr8:100985814-100985815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540331237	chr8:100985827-100985828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560653405	chr8:100985836-100985837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545605935	chr8:100985940-100985941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368139990	chr8:100985965-100985966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113565484	chr8:100985966-100985967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527990242	chr8:100985969-100985970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182569196	chr8:100985984-100985985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531682274	chr8:100986039-100986040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563552845	chr8:100986096-100986097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551654719	chr8:100986118-100986119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571312484	chr8:100986120-100986121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534006625	chr8:100986175-100986176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547147816	chr8:100986181-100986182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563602490	chr8:100986196-100986197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200069894	chr8:100986203-100986204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142819781	chr8:100986224-100986225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs151044438	chr8:100986241-100986242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185129560	chr8:100986247-100986248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189889217	chr8:100986251-100986252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558438341	chr8:100986341-100986342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs578086853	chr8:100986382-100986383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372198709	chr8:100986427-100986428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540845669	chr8:100986432-100986433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140927470	chr8:100986544-100986545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574223968	chr8:100986582-100986583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182553899	chr8:100986626-100986627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562823415	chr8:100986650-100986651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531746119	chr8:100986721-100986722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74731986	chr8:100986727-100986728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565206474	chr8:100986750-100986751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563214274	chr8:100986754-100986755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527473554	chr8:100986762-100986763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547605315	chr8:100986771-100986772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201591127	chr8:100986789-100986790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373782611	chr8:100986803-100986804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145185159	chr8:100986823-100986824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549470984	chr8:100986844-100986845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569272125	chr8:100986850-100986851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530068771	chr8:100986857-100986858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
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
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
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
Multiple myeloma	16461302	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
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
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	22341455	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Esophageal adenocarcinoma	18519675	CNVD

Chromatin state (count:198 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100980400-101001800	Weak transcription	Ovary	ovary
2	chr8:101001800-101002000	Genic enhancers	Ovary	ovary
3	chr8:101002000-101003000	Strong transcription	Ovary	ovary
4	chr8:101003000-101004200	Weak transcription	Ovary	ovary
5	chr8:101004200-101004400	Strong transcription	Ovary	ovary
6	chr8:101004400-101004600	ZNF genes & repeats	Ovary	ovary
7	chr8:101004600-101009200	Weak transcription	Ovary	ovary
8	chr8:101009200-101009600	Enhancers	Ovary	ovary
9	chr8:101009600-101010600	Weak transcription	Ovary	ovary
10	chr8:101010600-101011400	Genic enhancers	Ovary	ovary
11	chr8:101011000-101011200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:101011400-101012600	Weak transcription	Ovary	ovary
13	chr8:101012600-101013200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr8:101012600-101013200	Enhancers	Ovary	ovary
15	chr8:101013200-101015000	Weak transcription	Ovary	ovary
16	chr8:101014600-101014800	Enhancers	NHDF-Ad	bronchial
17	chr8:101014800-101018000	Weak transcription	NHDF-Ad	bronchial
18	chr8:101015000-101015200	Flanking Active TSS	Ovary	ovary
19	chr8:101015200-101016600	Active TSS	Ovary	ovary
20	chr8:101016200-101016400	Enhancers	Fetal Lung	lung
21	chr8:101016400-101017400	Weak transcription	Fetal Lung	lung
22	chr8:101016600-101017800	Weak transcription	Ovary	ovary
23	chr8:101017400-101017600	Enhancers	Fetal Lung	lung
24	chr8:101017600-101018000	Active TSS	Fetal Lung	lung
25	chr8:101017600-101018600	Enhancers	Fetal Kidney	kidney
26	chr8:101017800-101018200	Enhancers	Fetal Stomach	stomach
27	chr8:101017800-101018400	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr8:101017800-101019000	Active TSS	Ovary	ovary
29	chr8:101018000-101018400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr8:101018000-101018400	Enhancers	Colon Smooth Muscle	Colon
31	chr8:101018000-101018400	Enhancers	Hela-S3	cervix
32	chr8:101018000-101018600	Flanking Active TSS	Fetal Lung	lung
33	chr8:101018000-101019800	Enhancers	NHDF-Ad	bronchial
34	chr8:101018200-101018600	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr8:101018600-101018800	Enhancers	Fetal Lung	lung
36	chr8:101019000-101032400	Weak transcription	Ovary	ovary
37	chr8:101027600-101027800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:101028000-101028200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr8:101028000-101029200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr8:101028400-101029400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr8:101029200-101029400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
42	chr8:101029200-101029400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
43	chr8:101029200-101029600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr8:101029400-101030200	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr8:101029400-101031000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr8:101029400-101031400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr8:101029600-101030400	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr8:101029600-101035600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr8:101029800-101030400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr8:101030000-101030400	Enhancers	HUES48 Cell Line	embryonic stem cell

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