Variant report

Variant	nsv1031982
Chromosome Location	chr8:47997015-48110595
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:879)
CpG islands
(count:1342)
Chromatin interactive
region (count:36)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:879 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr8:48089908-48090111	K562	blood:	n/a	n/a
2	ATF3	chr8:48079064-48079208	K562	blood:	n/a	n/a
3	BHLHE40	chr8:48089585-48090079	K562	blood:	n/a	n/a
4	BHLHE40	chr8:48091753-48092084	K562	blood:	n/a	n/a
5	BHLHE40	chr8:48079038-48079257	K562	blood:	n/a	n/a
6	CBX3	chr8:48091693-48092120	K562	blood:	n/a	n/a
7	CBX3	chr8:48091635-48092145	K562	blood:	n/a	n/a
8	CBX3	chr8:48078812-48079474	HCT-116	colon:	n/a	n/a
9	CCNT2	chr8:48100257-48100420	K562	blood:	n/a	n/a
10	CEBPB	chr8:48068594-48068897	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:48032416-48032679	IMR90	lung:	n/a	chr8:48032579-48032590
12	CEBPB	chr8:48090516-48090623	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:48002620-48002781	HepG2	liver:	n/a	chr8:48002693-48002702 chr8:48002691-48002702 chr8:48002692-48002703
14	CEBPB	chr8:48068712-48068795	K562	blood:	n/a	n/a
15	CEBPB	chr8:48095552-48095745	K562	blood:	n/a	n/a
16	CEBPB	chr8:48023940-48024087	A549	lung:	n/a	chr8:48024017-48024028
17	CEBPB	chr8:48086186-48086361	K562	blood:	n/a	chr8:48086269-48086280 chr8:48086268-48086281
18	CEBPB	chr8:48068657-48068852	A549	lung:	n/a	n/a
19	CEBPB	chr8:48023879-48024172	HepG2	liver:	n/a	chr8:48024017-48024028
20	CEBPB	chr8:48032412-48032646	HepG2	liver:	n/a	chr8:48032579-48032590
21	CEBPB	chr8:48096843-48096859	K562	blood:	n/a	n/a
22	CEBPB	chr8:48086158-48086415	HepG2	liver:	n/a	chr8:48086269-48086280 chr8:48086268-48086281
23	CEBPB	chr8:48068628-48068812	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:47996999-47997259	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:48032411-48032645	Hela-S3	cervix:	n/a	chr8:48032579-48032590
26	CEBPB	chr8:48101848-48102044	K562	blood:	n/a	n/a
27	CEBPB	chr8:48032398-48032699	A549	lung:	n/a	chr8:48032579-48032590
28	CEBPB	chr8:48055365-48055518	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:48086214-48086414	A549	lung:	n/a	chr8:48086269-48086280 chr8:48086268-48086281
30	CEBPB	chr8:48021946-48022103	HepG2	liver:	n/a	chr8:48021953-48021964 chr8:48022013-48022026 chr8:48022013-48022024
31	CHD2	chr8:48079186-48079217	HepG2	liver:	n/a	n/a
32	CHD2	chr8:48110225-48110343	GM12878	blood:	n/a	n/a
33	CTCF	chr8:48053580-48053730	GM12873	blood:	n/a	n/a
34	CTCF	chr8:48100380-48100530	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr8:48079039-48079295	HepG2	liver:	n/a	chr8:48079185-48079203 chr8:48079155-48079164 chr8:48079100-48079108
36	CTCF	chr8:48105760-48105910	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr8:48105498-48106158	HCT-116	colon:	n/a	n/a
38	CTCF	chr8:48078929-48079378	K562	blood:	n/a	chr8:48079185-48079203 chr8:48079155-48079164 chr8:48079100-48079108
39	CTCF	chr8:48100420-48100570	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:48079016-48079287	H1-hESC	embryonic stem cell:	n/a	chr8:48079185-48079203 chr8:48079155-48079164 chr8:48079100-48079108
41	CTCF	chr8:48078970-48079311	MCF-7	breast:	n/a	chr8:48079185-48079203 chr8:48079155-48079164 chr8:48079100-48079108
42	CTCF	chr8:48079020-48079294	LNCaP	prostate:	n/a	chr8:48079185-48079203 chr8:48079155-48079164 chr8:48079100-48079108
43	CTCF	chr8:48100220-48100370	BJ	skin:	n/a	n/a
44	CTCF	chr8:48105740-48105890	NB4	blood:	n/a	n/a
45	CTCF	chr8:48105760-48105910	AG04450	lung:	n/a	n/a
46	CTCF	chr8:48078952-48079305	GM12891	blood:	n/a	chr8:48079185-48079203 chr8:48079155-48079164 chr8:48079100-48079108
47	CTCF	chr8:48105680-48105830	K562	blood:	n/a	n/a
48	CTCF	chr8:48079046-48079277	Medullo	brain:	n/a	chr8:48079185-48079203 chr8:48079155-48079164 chr8:48079100-48079108
49	CTCF	chr8:48091880-48092030	GM12873	blood:	n/a	n/a
50	CTCF	chr8:48078580-48078730	GM12872	blood:	n/a	n/a

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48100186-48100236	HCF	heart:	n/a
2	chr8:48100410-48100460	SK-N-MC	brain:	n/a
3	chr8:48100081-48100131	ProgFib	skin:	n/a
4	chr8:48100868-48100918	SKMC	muscle:	n/a
5	chr8:48099615-48099665	HCT-116	colon:	n/a
6	chr8:48100179-48100229	IMR90	lung:	fetal
7	chr8:48091864-48091914	HCT-116	colon:	n/a
8	chr8:48038289-48038339	BE2_C	brain:	n/a
9	chr8:48100179-48100229	Caco-2	colon:	n/a
10	chr8:48091424-48091474	HL-60	blood:	n/a
11	chr8:48091864-48091914	HRE	kidney:	n/a
12	chr8:48100429-48100479	AG09319	gingival:	n/a
13	chr8:48100410-48100460	HMEC	breast:	n/a
14	chr8:48105707-48105757	NB4	blood:	n/a
15	chr8:48091487-48091537	ProgFib	skin:	n/a
16	chr8:48091487-48091537	NHDF-neo	bronchial:	n/a
17	chr8:48091487-48091537	A549	lung:	n/a
18	chr8:48049326-48049376	PrEC	prostate:	n/a
19	chr8:48091801-48091851	NHDF-neo	bronchial:	n/a
20	chr8:48099615-48099665	ProgFib	skin:	n/a
21	chr8:48049326-48049376	NB4	blood:	n/a
22	chr8:48097610-48097660	PFSK-1	brain:	n/a
23	chr8:48100957-48101007	NB4	blood:	n/a
24	chr8:48044856-48044906	SK-N-MC	brain:	n/a
25	chr8:48100429-48100479	ECC-1	luminal epithelium:	n/a
26	chr8:48105707-48105757	SK-N-SH	brain:	n/a
27	chr8:48044616-48044666	HEK293	kidney:	embryo
28	chr8:48044616-48044666	GM06990	blood:	n/a
29	chr8:48100868-48100918	Hepatocyte	liver:	n/a
30	chr8:48091801-48091851	LNCaP	prostate:	n/a
31	chr8:48100957-48101007	T-47D	breast:	n/a
32	chr8:48100081-48100131	HCF	heart:	n/a
33	chr8:48091424-48091474	MCF10A-Er-Src	breast:	n/a
34	chr8:48091801-48091851	HEEpiC	esophagus:	n/a
35	chr8:48100957-48101007	GM06990	blood:	n/a
36	chr8:48100898-48100948	GM12878	blood:	n/a
37	chr8:48100898-48100948	MCF-7	breast:	n/a
38	chr8:48100179-48100229	GM12892	blood:	n/a
39	chr8:48100179-48100229	ovcar-3	ovarian:	n/a
40	chr8:48100868-48100918	H1-hESC	embryonic stem cell:	embryo
41	chr8:48099615-48099665	GM19239	blood:	n/a
42	chr8:48100898-48100948	PrEC	prostate:	n/a
43	chr8:48045001-48045051	HNPCEpiC	eye:	n/a
44	chr8:48091864-48091914	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:48105707-48105757	SKMC	muscle:	n/a
46	chr8:48044616-48044666	HCF	heart:	n/a
47	chr8:48091864-48091914	HAEpiC	amniotic membrane:	n/a
48	chr8:48100898-48100948	HCF	heart:	n/a
49	chr8:48100908-48100958	Caco-2	colon:	n/a
50	chr8:48038289-48038339	NB4	blood:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:48089038..48091327-chr8:48097909..48100771,2	MCF-7	breast:
2	chr8:48106145..48109361-chr8:48113197..48116087,3	K562	blood:
3	chr8:48102394..48104985-chr8:48106310..48110221,3	MCF-7	breast:
4	chr8:48090559..48092887-chr8:48171914..48174846,2	MCF-7	breast:
5	chr8:48081046..48083214-chr8:48086488..48088139,2	K562	blood:
6	chr8:48015941..48018518-chr8:48020123..48022156,2	K562	blood:
7	chr17:41464809..41468263-chr8:48018253..48019773,7	K562	blood:
8	chr8:47868480..47869132-chr8:48100099..48100692,2	MCF-7	breast:
9	chr8:48102394..48104985-chr8:48106310..48110221,3	MCF-7	breast:
10	chr8:47868390..47869335-chr8:48103589..48104192,2	MCF-7	breast:
11	chr8:48089038..48091327-chr8:48097909..48100771,2	MCF-7	breast:
12	chr8:48015941..48018518-chr8:48020123..48022156,2	K562	blood:
13	chr8:48099672..48101533-chr8:48102749..48105335,2	MCF-7	breast:
14	chr8:48011750..48014188-chr8:48015386..48017652,2	MCF-7	breast:
15	chr8:47868355..47869368-chr8:48078653..48079520,3	MCF-7	breast:
16	chr8:48090533..48093121-chr8:48649815..48651920,2	MCF-7	breast:
17	chr8:48078768..48081017-chr8:48097820..48099416,2	MCF-7	breast:
18	chr8:48078768..48081017-chr8:48097820..48099416,2	MCF-7	breast:
19	chr8:47868712..47869324-chr8:48091494..48092220,2	K562	blood:
20	chr8:48078537..48080562-chr8:48085847..48088452,2	MCF-7	breast:
21	chr8:48013635..48015583-chr8:48017920..48019595,2	MCF-7	breast:
22	chr17:41382019..41383699-chr8:48018253..48019773,2	K562	blood:
23	chr8:48077834..48080111-chr8:48648682..48651633,2	MCF-7	breast:
24	chr8:48091200..48093897-chr8:48104866..48107848,2	K562	blood:
25	chr8:48013635..48015583-chr8:48017920..48019595,2	MCF-7	breast:
26	chr8:48105045..48107718-chr8:48171845..48174415,2	MCF-7	breast:
27	chr8:48078161..48080655-chr8:48649461..48651455,2	MCF-7	breast:
28	chr8:48011750..48014188-chr8:48015386..48017652,2	MCF-7	breast:
29	chr8:48081046..48083214-chr8:48086488..48088139,2	K562	blood:
30	chr8:48105532..48109361-chr8:48112947..48117010,3	K562	blood:
31	chr8:48109425..48112056-chr8:48171977..48173853,2	MCF-7	breast:
32	chr6:151936576..151938783-chr8:48037858..48040574,2	MCF-7	breast:
33	chr8:48078537..48080562-chr8:48085847..48088452,2	MCF-7	breast:
34	chr14:71789873..71790710-chr8:48051511..48052153,2	MCF-7	breast:
35	chr8:48094665..48096718-chr8:48111922..48113998,2	MCF-7	breast:
36	chr8:48079045..48079614-chr8:48100462..48100993,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-350F16.2.1-8	chr8:48109655-48109946	NONHSAT126439
2	lnc-RP11-1134I14.8.1-1	chr8:48100928-48101183	NONHSAT126434
3	lnc-RP11-1134I14.8.1-1	chr8:48102596-48104139	NONHSAT126436
4	lnc-RP11-1134I14.8.1-1	chr8:48102395-48104885	ENSG00000255366.1
5	lnc-RP11-1134I14.8.1-4	chr8:48077043-48077147	NONHSAT126433
6	lnc-RP11-1134I14.8.1-4	chr8:48076493-48076730	NONHSAT126433
7	lnc-RP11-1134I14.8.1-1	chr8:48101531-48101575	NONHSAT126436
8	lnc-RP11-1134I14.8.1-2	chr8:47999009-47999207	XLOC_006786
9	lnc-RP11-350F16.2.1-7	chr8:48105625-48105970	NONHSAT126438
10	lnc-RP11-1134I14.8.1-1	chr8:48100930-48104439	NONHSAT126435

No data

Variant related genes	Relation type
ATP6V1G1P2	TF binding region
NDUFA5P12	TF binding region
RPL10AP2	TF binding region
ENSG00000253817	TF binding region
ENSG00000248347	TF binding region
ENSG00000254348	TF binding region
RNU6-819P	TF binding region
ENSG00000255366	TF binding region
ATP6V1G1P2	CpG island
NDUFA5P12	CpG island
RPL10AP2	CpG island
ENSG00000253817	CpG island
ENSG00000248347	CpG island
ENSG00000254348	CpG island
RNU6-819P	CpG island
ENSG00000255366	CpG island
ENSG00000164808	chromatin interactions
ENSG00000221869	chromatin interactions
ENSG00000255366	chromatin interactions
ENSG00000254348	chromatin interactions
ENSG00000253502	chromatin interactions
ENSG00000253817	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000215177	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000207422	chromatin interactions
EFNB2	miRNA target sites

Extended variants
information (count: 2750 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2750 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76957143	chr8:47997027-47997028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs138956425	chr8:47997043-47997044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142191449	chr8:47997059-47997060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1846506	chr8:47997066-47997067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184646076	chr8:47997081-47997082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573619363	chr8:47997100-47997101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539385500	chr8:47997101-47997102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534492668	chr8:47997113-47997114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146386378	chr8:47997127-47997128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577550170	chr8:47997138-47997139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10092312	chr8:47997140-47997141	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs188969488	chr8:47997190-47997191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575100391	chr8:47997225-47997226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181333575	chr8:47997229-47997230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568052632	chr8:47997356-47997357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189823674	chr8:47997383-47997384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181027081	chr8:47997384-47997385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546559049	chr8:47997396-47997397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs71548422	chr8:47997398-47997399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34091351	chr8:47997399-47997400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs397753296	chr8:47997406-47997407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs397892291	chr8:47997407-47997408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565293421	chr8:47997481-47997482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532372489	chr8:47997521-47997522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551054658	chr8:47997543-47997544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373272639	chr8:47997584-47997585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569331554	chr8:47997611-47997612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536733036	chr8:47997612-47997613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4392906	chr8:47997636-47997637	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs567048453	chr8:47997650-47997651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534532340	chr8:47997702-47997703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558951388	chr8:47997716-47997717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371507925	chr8:47997723-47997724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553442995	chr8:47997738-47997739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs80139818	chr8:47997748-47997749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539311451	chr8:47997757-47997758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186014464	chr8:47997774-47997775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75303505	chr8:47997791-47997792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557030654	chr8:47997800-47997801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6995008	chr8:47997810-47997811	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs139777243	chr8:47997843-47997844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146980207	chr8:47997894-47997895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192047284	chr8:47997896-47997897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181789086	chr8:47997914-47997915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35931929	chr8:47997924-47997925	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs564984368	chr8:47997931-47997932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532546047	chr8:47997993-47997994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572475045	chr8:47999006-47999007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546273280	chr8:47999015-47999016	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs188164875	chr8:47999057-47999058	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	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
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	20409316	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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD

Chromatin state (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:47996600-47998000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr8:47996800-47997800	Enhancers	Adipose Nuclei	Adipose
3	chr8:47999000-47999200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:47999200-48012200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:48012000-48012800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr8:48012200-48012400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:48012200-48012600	Active TSS	K562	blood
8	chr8:48012200-48013000	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr8:48013000-48013200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr8:48021800-48022000	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr8:48040600-48061200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr8:48041400-48041600	Enhancers	Gastric	stomach
13	chr8:48041600-48044600	Weak transcription	Gastric	stomach
14	chr8:48044400-48045000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:48044600-48044800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:48044600-48045000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:48044600-48045200	ZNF genes & repeats	Gastric	stomach
18	chr8:48044800-48045000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:48045000-48045200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:48045000-48045200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:48045200-48046600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:48056600-48057000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr8:48064400-48064800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
24	chr8:48076200-48076600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
25	chr8:48076600-48078800	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr8:48078800-48079000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr8:48078800-48079200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
28	chr8:48078800-48079200	Enhancers	Primary B cells from peripheral blood	blood
29	chr8:48078800-48079200	Enhancers	Liver	Liver
30	chr8:48078800-48079200	Active TSS	Colonic Mucosa	Colon
31	chr8:48078800-48079200	Active TSS	Duodenum Mucosa	Duodenum
32	chr8:48078800-48079200	Active TSS	Fetal Intestine Large	intestine
33	chr8:48078800-48079200	Enhancers	Gastric	stomach
34	chr8:48078800-48079200	Active TSS	Rectal Mucosa Donor 29	rectum
35	chr8:48078800-48079200	Active TSS	Rectal Mucosa Donor 31	rectum
36	chr8:48078800-48079200	Active TSS	A549	lung
37	chr8:48078800-48079200	Active TSS	Hela-S3	cervix
38	chr8:48085200-48085600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr8:48085200-48085600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr8:48085600-48086400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr8:48085600-48087000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr8:48086400-48087600	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr8:48086600-48087600	Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr8:48087000-48087400	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr8:48087000-48087800	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr8:48087200-48087600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr8:48087400-48087600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr8:48087600-48089000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr8:48087600-48089400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr8:48087600-48089600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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