Variant report

Variant	nsv1024907
Chromosome Location	chr8:95188944-95296378
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2353)
CpG islands
(count:1831)
Chromatin interactive
region (count:84)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2353 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:95254352-95254671	HepG2	liver:	n/a	n/a
2	ATF1	chr8:95218407-95218446	K562	blood:	n/a	n/a
3	ATF1	chr8:95231164-95231381	K562	blood:	n/a	n/a
4	ATF1	chr8:95274472-95274774	K562	blood:	n/a	n/a
5	ATF2	chr8:95274203-95274898	GM12878	blood:	n/a	chr8:95274607-95274618
6	ATF2	chr8:95274322-95274781	H1-hESC	embryonic stem cell:	n/a	chr8:95274607-95274618
7	ATF2	chr8:95230930-95231587	GM12878	blood:	n/a	n/a
8	ATF2	chr8:95254330-95254711	GM12878	blood:	n/a	n/a
9	ATF2	chr8:95232611-95233091	GM12878	blood:	n/a	n/a
10	ATF2	chr8:95232569-95233051	GM12878	blood:	n/a	n/a
11	ATF2	chr8:95229597-95230197	GM12878	blood:	n/a	n/a
12	ATF2	chr8:95274075-95274845	GM12878	blood:	n/a	chr8:95274607-95274618
13	ATF2	chr8:95230950-95231630	GM12878	blood:	n/a	n/a
14	ATF2	chr8:95274319-95275013	H1-hESC	embryonic stem cell:	n/a	chr8:95274607-95274618
15	ATF3	chr8:95254069-95255177	A549	lung:	n/a	n/a
16	ATF3	chr8:95274477-95274743	H1-hESC	embryonic stem cell:	n/a	chr8:95274607-95274618 chr8:95274606-95274619 chr8:95274691-95274700 chr8:95274609-95274619 chr8:95274608-95274622 chr8:95274609-95274616 chr8:95274606-95274616 chr8:95274607-95274620 chr8:95274608-95274619 chr8:95274606-95274619 chr8:95274606-95274616 chr8:95274607-95274618 chr8:95274609-95274619 chr8:95274605-95274620 chr8:95274608-95274616 chr8:95274608-95274628
17	ATF3	chr8:95254032-95255067	A549	lung:	n/a	n/a
18	BACH1	chr8:95242663-95242898	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:95284416-95284891	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr8:95231967-95232122	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr8:95274323-95274734	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr8:95250099-95250250	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr8:95246430-95246771	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr8:95254209-95254678	GM12878	blood:	n/a	chr8:95254484-95254494 chr8:95254483-95254494
25	BATF	chr8:95246603-95246925	GM12878	blood:	n/a	n/a
26	BATF	chr8:95232624-95232998	GM12878	blood:	n/a	n/a
27	BATF	chr8:95232596-95233020	GM12878	blood:	n/a	n/a
28	BATF	chr8:95231134-95231401	GM12878	blood:	n/a	n/a
29	BATF	chr8:95254321-95254662	GM12878	blood:	n/a	chr8:95254484-95254494 chr8:95254483-95254494
30	BATF	chr8:95285425-95285668	GM12878	blood:	n/a	n/a
31	BATF	chr8:95274221-95274613	GM12878	blood:	n/a	n/a
32	BATF	chr8:95229668-95229959	GM12878	blood:	n/a	n/a
33	BATF	chr8:95285349-95285742	GM12878	blood:	n/a	n/a
34	BATF	chr8:95230966-95231514	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:95231060-95231542	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:95232697-95233050	GM12878	blood:	n/a	n/a
37	BCL11A	chr8:95254262-95254659	GM12878	blood:	n/a	n/a
38	BCL11A	chr8:95246739-95247197	GM12878	blood:	n/a	chr8:95247139-95247152
39	BCL11A	chr8:95231167-95231430	GM12878	blood:	n/a	n/a
40	BCL11A	chr8:95221856-95222050	GM12878	blood:	n/a	chr8:95222039-95222048
41	BCL11A	chr8:95232740-95232973	GM12878	blood:	n/a	n/a
42	BCL3	chr8:95254109-95255295	A549	lung:	n/a	n/a
43	BCL3	chr8:95254275-95254702	GM12878	blood:	n/a	n/a
44	BCL3	chr8:95245622-95245855	GM12878	blood:	n/a	n/a
45	BCL3	chr8:95231078-95231513	GM12878	blood:	n/a	n/a
46	BCL3	chr8:95254107-95255151	A549	lung:	n/a	n/a
47	BCLAF1	chr8:95231000-95231623	GM12878	blood:	n/a	n/a
48	BCLAF1	chr8:95232585-95232979	GM12878	blood:	n/a	n/a
49	BCLAF1	chr8:95229554-95230109	GM12878	blood:	n/a	n/a
50	BCLAF1	chr8:95274173-95274789	GM12878	blood:	n/a	chr8:95274546-95274559 chr8:95274552-95274561 chr8:95274553-95274566 chr8:95274385-95274394 chr8:95274549-95274562

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:95278142-95278192	SAEC	small airway:	n/a
2	chr8:95278142-95278192	SAEC	small airway:	n/a
3	chr8:95274687-95274737	NHDF-neo	bronchial:	n/a
4	chr8:95275575-95275625	AG04449	skin:	fetal
5	chr8:95238935-95238985	HAEpiC	amniotic membrane:	n/a
6	chr8:95274342-95274392	HCPEpiC	choroid plexus:	n/a
7	chr8:95238935-95238985	AoSMC	blood vessel:	n/a
8	chr8:95246699-95246749	H1-hESC	embryonic stem cell:	embryo
9	chr8:95222020-95222070	GM06990	blood:	n/a
10	chr8:95246814-95246864	HCT-116	colon:	n/a
11	chr8:95221197-95221247	HRE	kidney:	n/a
12	chr8:95274687-95274737	BJ	skin:	n/a
13	chr8:95246814-95246864	SK-N-SH	brain:	n/a
14	chr8:95266905-95266955	HRPEpiC	eye:	n/a
15	chr8:95229872-95229922	HL-60	blood:	n/a
16	chr8:95246514-95246564	GM12878	blood:	n/a
17	chr8:95266905-95266955	GM12892	blood:	n/a
18	chr8:95274411-95274461	SKMC	muscle:	n/a
19	chr8:95278142-95278192	NB4	blood:	n/a
20	chr8:95246699-95246749	GM12891	blood:	n/a
21	chr8:95274252-95274302	LNCaP	prostate:	n/a
22	chr8:95274654-95274704	HepG2	liver:	n/a
23	chr8:95262502-95262552	HEK293	kidney:	embryo
24	chr8:95229525-95229575	CMK	blood:	n/a
25	chr8:95266905-95266955	AG04450	lung:	fetal
26	chr8:95246514-95246564	SK-N-SH_RA	brain:	n/a
27	chr8:95229872-95229922	GM12878	blood:	n/a
28	chr8:95274654-95274704	HRCEpiC	kidney:	n/a
29	chr8:95274853-95274903	HCPEpiC	choroid plexus:	n/a
30	chr8:95221197-95221247	HUVEC	blood vessel:	n/a
31	chr8:95238935-95238985	Hepatocyte	liver:	n/a
32	chr8:95286745-95286795	T-47D	breast:	n/a
33	chr8:95275575-95275625	CMK	blood:	n/a
34	chr8:95274566-95274616	BJ	skin:	n/a
35	chr8:95221197-95221247	SAEC	small airway:	n/a
36	chr8:95246814-95246864	HIPEpiC	eye:	n/a
37	chr8:95230984-95231034	ProgFib	skin:	n/a
38	chr8:95220583-95220633	GM19239	blood:	n/a
39	chr8:95262502-95262552	SKMC	muscle:	n/a
40	chr8:95222020-95222070	HepG2	liver:	n/a
41	chr8:95220779-95220829	SKMC	muscle:	n/a
42	chr8:95286745-95286795	BJ	skin:	n/a
43	chr8:95254202-95254252	AG09309	skin:	n/a
44	chr8:95230984-95231034	HUVEC	blood vessel:	n/a
45	chr8:95230984-95231034	GM19239	blood:	n/a
46	chr8:95220583-95220633	SAEC	small airway:	n/a
47	chr8:95229754-95229804	IMR90	lung:	fetal
48	chr8:95220583-95220633	NHBE	bronchial:	n/a
49	chr8:95274933-95274983	HAEpiC	amniotic membrane:	n/a
50	chr8:95229872-95229922	HMEC	breast:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:95006687..95007623-chr8:95199581..95200583,4	MCF-7	breast:
2	chr8:95240844..95244152-chr8:95245097..95248087,3	MCF-7	breast:
3	chr8:95201827..95203670-chr8:95208153..95211021,2	MCF-7	breast:
4	chr8:95199696..95200396-chr8:95284281..95284998,2	MCF-7	breast:
5	chr8:94751681..94753437-chr8:95200264..95202250,2	MCF-7	breast:
6	chr8:95252636..95255137-chr8:95271154..95272846,2	MCF-7	breast:
7	chr8:95216472..95218639-chr8:95229347..95231439,2	MCF-7	breast:
8	chr8:95091661..95092727-chr8:95199725..95200487,4	MCF-7	breast:
9	chr8:95218436..95218963-chr8:95284617..95285220,2	MCF-7	breast:
10	chr8:95224589..95225412-chr8:95369113..95370095,2	MCF-7	breast:
11	chr8:95003159..95004252-chr8:95284352..95285354,5	MCF-7	breast:
12	chr8:95228655..95231086-chr8:95245435..95247101,2	MCF-7	breast:
13	chr21:41711010..41712741-chr8:95200062..95201579,2	MCF-7	breast:
14	chr8:95091864..95092388-chr8:95200565..95201228,2	MCF-7	breast:
15	chr8:95259315..95260909-chr8:95269095..95271460,2	MCF-7	breast:
16	chr8:95206766..95209394-chr8:95210564..95212309,3	MCF-7	breast:
17	chr8:95179472..95182250-chr8:95190342..95192511,2	MCF-7	breast:
18	chr8:95200777..95202734-chr8:95202948..95204607,2	K562	blood:
19	chr8:95215544..95217656-chr8:95220305..95222366,3	MCF-7	breast:
20	chr8:95206766..95209394-chr8:95210564..95212309,3	MCF-7	breast:
21	chr8:95289048..95290782-chr8:95297301..95299654,2	MCF-7	breast:
22	chr8:95217720..95220608-chr8:95221827..95224129,2	MCF-7	breast:
23	chr8:95223330..95225554-chr8:95230383..95232655,2	MCF-7	breast:
24	chr8:95200401..95202545-chr8:95205826..95207380,2	K562	blood:
25	chr8:95218436..95218963-chr8:95284617..95285220,2	MCF-7	breast:
26	chr8:95279166..95281146-chr8:95283531..95285709,2	MCF-7	breast:
27	chr8:95256075..95257959-chr8:95283640..95285924,2	K562	blood:
28	chr8:95252312..95253964-chr8:95260272..95262421,3	MCF-7	breast:
29	chr8:95092028..95092964-chr8:95199448..95200050,4	MCF-7	breast:
30	chr8:95279166..95281146-chr8:95283531..95285709,2	MCF-7	breast:
31	chr8:95223330..95225554-chr8:95230383..95232655,2	MCF-7	breast:
32	chr8:95186993..95189427-chr8:95190911..95193460,2	MCF-7	breast:
33	chr8:95283721..95285905-chr8:95286724..95288963,2	MCF-7	breast:
34	chr8:95252911..95255194-chr8:95273270..95275304,2	MCF-7	breast:
35	chr8:95284911..95287087-chr8:95289504..95292145,3	K562	blood:
36	chr8:95093227..95094052-chr8:95283905..95284779,2	MCF-7	breast:
37	chr8:95221810..95224176-chr8:95226339..95228964,2	MCF-7	breast:
38	chr8:95003558..95004116-chr8:95284317..95285153,2	MCF-7	breast:
39	chr8:95217922..95218880-chr8:95369574..95370256,2	MCF-7	breast:
40	chr8:95256075..95257959-chr8:95283640..95285924,2	K562	blood:
41	chr8:95091740..95092613-chr8:95284287..95285362,4	MCF-7	breast:
42	chr8:95288121..95290024-chr8:95297047..95299398,2	MCF-7	breast:
43	chr8:95263857..95265470-chr8:95267384..95270034,2	MCF-7	breast:
44	chr8:95271173..95273343-chr8:95281933..95284326,2	K562	blood:
45	chr8:95264526..95268344-chr8:95270194..95275198,8	MCF-7	breast:
46	chr8:95284911..95287087-chr8:95289504..95292145,3	K562	blood:
47	chr8:95221810..95224176-chr8:95226339..95228964,2	MCF-7	breast:
48	chr8:95238887..95240526-chr8:95244307..95246160,2	MCF-7	breast:
49	chr8:95244367..95248911-chr8:95252094..95255731,6	MCF-7	breast:
50	chr8:95274119..95275817-chr8:95277862..95279971,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GEM-1	chr8:95214141-95214393	NONHSAT127766
2	lnc-GEM-1	chr8:95214701-95215280	NONHSAT127766

No data

Variant related genes	Relation type
CDH17	TF binding region
GEM	TF binding region
ENSG00000249510	TF binding region
CDH17	CpG island
GEM	CpG island
ENSG00000249510	CpG island
ENSG00000106692	chromatin interactions
ENSG00000079112	chromatin interactions
ENSG00000253848	chromatin interactions
ENSG00000183808	chromatin interactions
ENSG00000228317	chromatin interactions
ENSG00000164949	chromatin interactions
ENSG00000212998	chromatin interactions

Extended variants
information (count: 4066 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:4066 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370927561	chr8:95188962-95188963	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75480102	chr8:95189004-95189005	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576516292	chr8:95189007-95189008	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374258610	chr8:95189016-95189017	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377656912	chr8:95189030-95189031	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545388350	chr8:95189087-95189088	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs137950330	chr8:95189088-95189089	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527762023	chr8:95189095-95189096	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547706563	chr8:95189153-95189154	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561521319	chr8:95189166-95189167	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530372953	chr8:95189177-95189178	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374783321	chr8:95189182-95189183	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569972579	chr8:95189197-95189198	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185743554	chr8:95189233-95189234	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550941254	chr8:95189240-95189241	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571045949	chr8:95189307-95189308	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533877656	chr8:95189309-95189310	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190747877	chr8:95189317-95189318	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574959426	chr8:95189319-95189320	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113930355	chr8:95189337-95189338	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143083262	chr8:95189344-95189345	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116887050	chr8:95189376-95189377	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576379363	chr8:95189398-95189399	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181085460	chr8:95189413-95189414	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565260559	chr8:95189419-95189420	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10091496	chr8:95189444-95189445	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs148210361	chr8:95189450-95189451	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537546066	chr8:95189451-95189452	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561177558	chr8:95189456-95189457	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78574443	chr8:95189579-95189580	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141268750	chr8:95189655-95189656	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563668485	chr8:95189658-95189659	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150778865	chr8:95189670-95189671	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551004556	chr8:95189679-95189680	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570908571	chr8:95189688-95189689	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527247281	chr8:95189689-95189690	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547481117	chr8:95189719-95189720	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546156930	chr8:95189724-95189725	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79317393	chr8:95189780-95189781	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375938467	chr8:95189783-95189784	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201190648	chr8:95189797-95189798	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187115114	chr8:95189803-95189804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556369676	chr8:95189879-95189880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569997084	chr8:95189880-95189881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538923721	chr8:95189939-95189940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138007982	chr8:95189955-95189956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369449897	chr8:95189961-95189962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369451618	chr8:95189967-95189968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572405960	chr8:95189993-95189994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372980907	chr8:95189995-95189996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
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
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2209 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95170200-95190400	Strong transcription	Rectal Mucosa Donor 29	rectum
2	chr8:95177800-95190000	Strong transcription	Fetal Intestine Large	intestine
3	chr8:95179200-95190000	Strong transcription	Duodenum Mucosa	Duodenum
4	chr8:95184400-95190000	Strong transcription	Rectal Mucosa Donor 31	rectum
5	chr8:95187600-95189600	Strong transcription	Fetal Intestine Small	intestine
6	chr8:95188000-95189600	Strong transcription	Colonic Mucosa	Colon
7	chr8:95188200-95189800	Strong transcription	Sigmoid Colon	Sigmoid Colon
8	chr8:95188400-95189800	Strong transcription	Rectal Smooth Muscle	rectum
9	chr8:95189400-95189800	Enhancers	Adipose Nuclei	Adipose
10	chr8:95189600-95191400	Weak transcription	Fetal Intestine Small	intestine
11	chr8:95189600-95200600	Weak transcription	Colonic Mucosa	Colon
12	chr8:95189800-95191800	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr8:95189800-95205800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr8:95190000-95191600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:95190000-95191800	Weak transcription	Fetal Intestine Large	intestine
16	chr8:95190000-95195400	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr8:95190000-95195800	Weak transcription	Duodenum Mucosa	Duodenum
18	chr8:95190400-95191200	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr8:95191200-95192000	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr8:95191400-95191800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr8:95191400-95192000	ZNF genes & repeats	Fetal Intestine Small	intestine
22	chr8:95191600-95192000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:95191600-95192000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:95191600-95192000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr8:95191800-95192000	ZNF genes & repeats	Fetal Intestine Large	intestine
26	chr8:95191800-95192000	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr8:95192000-95192800	Weak transcription	Fetal Intestine Large	intestine
28	chr8:95192000-95192800	Weak transcription	Fetal Intestine Small	intestine
29	chr8:95192000-95195600	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr8:95192000-95198600	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr8:95192800-95193200	ZNF genes & repeats	Fetal Intestine Large	intestine
32	chr8:95192800-95193200	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr8:95193200-95197200	Weak transcription	Fetal Intestine Small	intestine
34	chr8:95194400-95196800	Weak transcription	Fetal Intestine Large	intestine
35	chr8:95195400-95196600	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr8:95195600-95195800	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr8:95195800-95196200	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr8:95195800-95196400	Enhancers	Duodenum Mucosa	Duodenum
39	chr8:95196200-95196400	Weak transcription	Small Intestine	intestine
40	chr8:95196200-95196800	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr8:95196400-95196600	Enhancers	Small Intestine	intestine
42	chr8:95196400-95197200	Weak transcription	Duodenum Mucosa	Duodenum
43	chr8:95196600-95197000	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr8:95196600-95202600	Weak transcription	Small Intestine	intestine
45	chr8:95196800-95197600	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr8:95196800-95200600	Strong transcription	Fetal Intestine Large	intestine
47	chr8:95197000-95200200	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr8:95197200-95197400	Strong transcription	Fetal Intestine Small	intestine
49	chr8:95197200-95197600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr8:95197200-95197800	Enhancers	NHDF-Ad	bronchial

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