Variant report

Variant	nsv830808
Chromosome Location	chr6:131521115-131735320
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1016)
CpG islands
(count:672)
Chromatin interactive
region (count:18)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1016 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:131688478-131688702	HepG2	liver:	n/a	n/a
2	ATF2	chr6:131689359-131689878	GM12878	blood:	n/a	n/a
3	ATF2	chr6:131602635-131603046	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr6:131520738-131521260	GM12878	blood:	n/a	n/a
5	BACH1	chr6:131614880-131615112	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr6:131520913-131521168	GM12878	blood:	n/a	n/a
7	BCLAF1	chr6:131520780-131521237	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:131520903-131521363	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:131638814-131638816	HepG2	liver:	n/a	n/a
10	BHLHE40	chr6:131615330-131615434	HepG2	liver:	n/a	n/a
11	BHLHE40	chr6:131658375-131658379	HepG2	liver:	n/a	n/a
12	BRCA1	chr6:131600918-131600951	GM12878	blood:	n/a	n/a
13	BRCA1	chr6:131721187-131722017	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr6:131721613-131722328	HCT-116	colon:	n/a	n/a
15	CEBPB	chr6:131552295-131552592	IMR90	lung:	n/a	n/a
16	CEBPB	chr6:131658878-131659102	K562	blood:	n/a	chr6:131659038-131659049
17	CEBPB	chr6:131658937-131659103	HepG2	liver:	n/a	chr6:131659038-131659049
18	CEBPB	chr6:131658873-131659210	HepG2	liver:	n/a	chr6:131659038-131659049
19	CEBPB	chr6:131708304-131708404	K562	blood:	n/a	n/a
20	CEBPB	chr6:131520756-131521212	MCF-7	breast:	n/a	n/a
21	CEBPB	chr6:131577172-131577461	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr6:131711535-131711716	K562	blood:	n/a	chr6:131711661-131711678
23	CEBPB	chr6:131683272-131683522	HepG2	liver:	n/a	chr6:131683349-131683360
24	CEBPB	chr6:131721441-131721949	A549	lung:	n/a	n/a
25	CEBPB	chr6:131534133-131534453	HepG2	liver:	n/a	chr6:131534279-131534290 chr6:131534277-131534294
26	CEBPB	chr6:131683177-131683666	A549	lung:	n/a	chr6:131683349-131683360
27	CEBPB	chr6:131615398-131615543	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:131533164-131533549	IMR90	lung:	n/a	chr6:131533354-131533365
29	CEBPB	chr6:131668082-131668333	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr6:131534127-131534395	A549	lung:	n/a	chr6:131534279-131534290 chr6:131534277-131534294
31	CEBPB	chr6:131582120-131582439	A549	lung:	n/a	chr6:131582286-131582297
32	CEBPB	chr6:131577153-131577476	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr6:131658998-131659060	A549	lung:	n/a	chr6:131659038-131659049
34	CEBPB	chr6:131687333-131687594	HepG2	liver:	n/a	n/a
35	CEBPB	chr6:131713735-131713978	IMR90	lung:	n/a	chr6:131713872-131713883
36	CEBPB	chr6:131689696-131690230	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr6:131582226-131582427	ECC-1	luminal epithelium:	n/a	chr6:131582286-131582297
38	CEBPB	chr6:131534108-131534455	IMR90	lung:	n/a	chr6:131534279-131534290 chr6:131534277-131534294
39	CEBPB	chr6:131641602-131641645	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr6:131683275-131683487	IMR90	lung:	n/a	chr6:131683349-131683360
41	CEBPB	chr6:131576952-131576993	A549	lung:	n/a	chr6:131576977-131576988
42	CEBPB	chr6:131713721-131714007	A549	lung:	n/a	chr6:131713872-131713883
43	CEBPB	chr6:131582217-131582400	MCF-7	breast:	n/a	chr6:131582286-131582297
44	CEBPB	chr6:131602692-131603125	H1-hESC	embryonic stem cell:	n/a	chr6:131602966-131602977 chr6:131602983-131602994
45	CEBPB	chr6:131582205-131582493	A549	lung:	n/a	chr6:131582286-131582297
46	CEBPB	chr6:131520882-131521121	K562	blood:	n/a	n/a
47	CEBPB	chr6:131552291-131552582	A549	lung:	n/a	n/a
48	CEBPB	chr6:131582186-131582336	HepG2	liver:	n/a	chr6:131582286-131582297
49	CEBPB	chr6:131721591-131721844	A549	lung:	n/a	n/a
50	CEBPB	chr6:131582217-131582460	ECC-1	luminal epithelium:	n/a	chr6:131582286-131582297

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:131657922-131657972	HCM	heart:	n/a
2	chr6:131657922-131657972	HCM	heart:	n/a
3	chr6:131650733-131650783	MCF-7	breast:	n/a
4	chr6:131690266-131690316	IMR90	lung:	fetal
5	chr6:131613706-131613756	AG09309	skin:	n/a
6	chr6:131705123-131705173	AG04450	lung:	fetal
7	chr6:131642853-131642903	PANC-1	pancreas:	n/a
8	chr6:131657922-131657972	AG04449	skin:	fetal
9	chr6:131571435-131571485	AG10803	skin:	n/a
10	chr6:131613706-131613756	HEK293	kidney:	embryo
11	chr6:131690266-131690316	ProgFib	skin:	n/a
12	chr6:131613706-131613756	IMR90	lung:	fetal
13	chr6:131642853-131642903	GM06990	blood:	n/a
14	chr6:131613706-131613756	GM12878	blood:	n/a
15	chr6:131613706-131613756	HMEC	breast:	n/a
16	chr6:131571669-131571719	ECC-1	luminal epithelium:	n/a
17	chr6:131650733-131650783	Hepatocyte	liver:	n/a
18	chr6:131548063-131548113	HIPEpiC	eye:	n/a
19	chr6:131571435-131571485	HIPEpiC	eye:	n/a
20	chr6:131657922-131657972	AG09309	skin:	n/a
21	chr6:131705123-131705173	Hela-S3	cervix:	n/a
22	chr6:131571435-131571485	Hela-S3	cervix:	n/a
23	chr6:131705123-131705173	BE2_C	brain:	n/a
24	chr6:131642853-131642903	SKMC	muscle:	n/a
25	chr6:131602870-131602920	HEK293	kidney:	embryo
26	chr6:131690266-131690316	HMEC	breast:	n/a
27	chr6:131642853-131642903	GM19239	blood:	n/a
28	chr6:131722497-131722547	HRE	kidney:	n/a
29	chr6:131657922-131657972	HIPEpiC	eye:	n/a
30	chr6:131571669-131571719	HL-60	blood:	n/a
31	chr6:131650733-131650783	ovcar-3	ovarian:	n/a
32	chr6:131548063-131548113	NB4	blood:	n/a
33	chr6:131571669-131571719	AoSMC	blood vessel:	n/a
34	chr6:131690266-131690316	HCF	heart:	n/a
35	chr6:131642853-131642903	AG04450	lung:	fetal
36	chr6:131602870-131602920	HCF	heart:	n/a
37	chr6:131650733-131650783	HEK293	kidney:	embryo
38	chr6:131548063-131548113	HNPCEpiC	eye:	n/a
39	chr6:131571435-131571485	SAEC	small airway:	n/a
40	chr6:131690266-131690316	HEEpiC	esophagus:	n/a
41	chr6:131705123-131705173	A549	lung:	n/a
42	chr6:131642853-131642903	AoSMC	blood vessel:	n/a
43	chr6:131722497-131722547	SK-N-SH_RA	brain:	n/a
44	chr6:131722497-131722547	LNCaP	prostate:	n/a
45	chr6:131722497-131722547	BJ	skin:	n/a
46	chr6:131657922-131657972	HNPCEpiC	eye:	n/a
47	chr6:131642853-131642903	HRPEpiC	eye:	n/a
48	chr6:131571669-131571719	GM06990	blood:	n/a
49	chr6:131602870-131602920	HRE	kidney:	n/a
50	chr6:131657922-131657972	HCPEpiC	choroid plexus:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:131591823..131594173-chr6:131613820..131615536,2	K562	blood:
2	chr6:131562493..131564861-chr6:131566716..131568915,2	MCF-7	breast:
3	chr6:131709683..131711909-chr6:131717715..131719994,2	MCF-7	breast:
4	chr6:131614360..131616508-chr6:131705803..131707677,2	K562	blood:
5	chr6:131698297..131700688-chr6:131701676..131704606,3	K562	blood:
6	chr6:131731836..131734655-chr6:131749824..131752389,2	K562	blood:
7	chr6:131520473..131521448-chr6:131582980..131583832,4	MCF-7	breast:
8	chr6:131562493..131564861-chr6:131566716..131568915,2	MCF-7	breast:
9	chr6:131574679..131577194-chr6:131577773..131580608,2	MCF-7	breast:
10	chr6:131591823..131594173-chr6:131613820..131615536,2	K562	blood:
11	chr6:131526933..131527448-chr6:131918295..131918857,2	MCF-7	breast:
12	chr6:131715833..131718825-chr6:131734370..131736424,2	K562	blood:
13	chr6:131698297..131700688-chr6:131701676..131704606,3	K562	blood:
14	chr6:131709683..131711909-chr6:131717715..131719994,2	MCF-7	breast:
15	chr6:131526816..131527805-chr6:131855115..131855774,2	MCF-7	breast:
16	chr6:131614360..131616508-chr6:131705803..131707677,2	K562	blood:
17	chr6:131715833..131718825-chr6:131734370..131736424,2	K562	blood:
18	chr6:131574679..131577194-chr6:131577773..131580608,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MED23-1	chr6:131652426-131652634	NONHSAT114916
2	lnc-AKAP7-1	chr6:131619214-131619459	NONHSAT114915
3	lnc-AKAP7-1	chr6:131630402-131630414	NONHSAT114915
4	lnc-MED23-1	chr6:131649280-131649342	NONHSAT114916

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	AKAP7	hsa-miR-375	chr6:131604029-131604050
2	AKAP7	hsa-miR-375	chr6:131604183-131604206

Variant related genes	Relation type
AKAP7	TF binding region
AKAP7	CpG island
ENSG00000118507	chromatin interactions

Extended variants
information (count: 8218 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:8218 , 50 per page) page: 1 2 3 4 5 6 7 ... 165

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558678058	chr6:131521129-131521130	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs188530460	chr6:131521190-131521191	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs117449205	chr6:131521209-131521210	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs193162484	chr6:131521210-131521211	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs528707892	chr6:131521242-131521243	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs184991565	chr6:131521358-131521359	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs541974723	chr6:131521365-131521366	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs560288714	chr6:131521373-131521374	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs3777469	chr6:131521374-131521375	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs546890077	chr6:131521379-131521380	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs142407257	chr6:131521382-131521383	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs563947624	chr6:131521402-131521403	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs532707932	chr6:131521453-131521454	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs190732322	chr6:131521470-131521471	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs79599095	chr6:131521484-131521485	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs536239439	chr6:131521535-131521536	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs3777470	chr6:131521554-131521555	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs192369366	chr6:131521555-131521556	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370222599	chr6:131521558-131521559	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559844800	chr6:131521585-131521586	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs534250885	chr6:131521627-131521628	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs558494909	chr6:131521676-131521677	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs183743601	chr6:131521703-131521704	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs1190813	chr6:131521704-131521705	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs556400923	chr6:131521736-131521737	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs574534304	chr6:131521742-131521743	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs541839752	chr6:131521789-131521790	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs77194493	chr6:131521799-131521800	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs3777471	chr6:131521828-131521829	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs1190812	chr6:131521830-131521831	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs545847173	chr6:131521875-131521876	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs146487155	chr6:131521947-131521948	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs532715405	chr6:131521961-131521962	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs147906146	chr6:131521993-131521994	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs562833110	chr6:131522010-131522011	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs188079151	chr6:131522021-131522022	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs116709306	chr6:131522049-131522050	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs566499737	chr6:131522062-131522063	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs534050216	chr6:131522075-131522076	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs551033570	chr6:131522109-131522110	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs558413102	chr6:131522136-131522137	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs570582913	chr6:131522148-131522149	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs538042089	chr6:131522211-131522212	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs556540788	chr6:131522212-131522213	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs569356628	chr6:131522232-131522233	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs141702629	chr6:131522254-131522255	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs539574965	chr6:131522281-131522282	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs553827684	chr6:131522362-131522363	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs181360515	chr6:131522386-131522387	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs545606496	chr6:131522391-131522392	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2698 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131488200-131534800	Weak transcription	Gastric	stomach
2	chr6:131505000-131521800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:131505200-131522600	Weak transcription	HSMMtube	muscle
4	chr6:131505800-131534600	Weak transcription	Brain Substantia Nigra	brain
5	chr6:131505800-131534800	Weak transcription	Pancreas	Pancrea
6	chr6:131506600-131523800	Weak transcription	HepG2	liver
7	chr6:131506600-131524000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr6:131506600-131529800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr6:131506600-131532000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:131506800-131551800	Weak transcription	Ovary	ovary
11	chr6:131510400-131534800	Weak transcription	Small Intestine	intestine
12	chr6:131513000-131522600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr6:131513000-131523000	Weak transcription	Placenta	Placenta
14	chr6:131513200-131526400	Weak transcription	Fetal Intestine Small	intestine
15	chr6:131513200-131536400	Weak transcription	Esophagus	oesophagus
16	chr6:131514400-131529800	Weak transcription	Brain Germinal Matrix	brain
17	chr6:131514400-131541400	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr6:131514600-131521200	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr6:131516600-131521200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr6:131518200-131521200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr6:131518200-131525600	Weak transcription	Fetal Brain Male	brain
22	chr6:131518200-131531800	Weak transcription	Colon Smooth Muscle	Colon
23	chr6:131518400-131522600	Enhancers	Primary hematopoietic stem cells	blood
24	chr6:131518800-131534600	Weak transcription	Brain Cingulate Gyrus	brain
25	chr6:131519200-131521200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:131519200-131522600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr6:131519600-131521200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:131519800-131521200	Strong transcription	Stomach Smooth Muscle	stomach
29	chr6:131520000-131522400	Strong transcription	Brain Anterior Caudate	brain
30	chr6:131520200-131521200	Enhancers	Dnd41	blood
31	chr6:131520200-131521600	Strong transcription	Adipose Nuclei	Adipose
32	chr6:131520400-131521800	Strong transcription	Liver	Liver
33	chr6:131520600-131521200	Strong transcription	Fetal Lung	lung
34	chr6:131520600-131521200	Enhancers	GM12878-XiMat	blood
35	chr6:131520600-131521400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr6:131520600-131521400	Strong transcription	Left Ventricle	heart
37	chr6:131520600-131521400	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr6:131520600-131521600	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr6:131520600-131521600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
40	chr6:131520600-131521600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:131520600-131521600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr6:131520600-131521600	Strong transcription	Fetal Muscle Leg	muscle
43	chr6:131520600-131522400	Strong transcription	Brain Hippocampus Middle	brain
44	chr6:131520600-131522600	Strong transcription	Fetal Stomach	stomach
45	chr6:131520800-131521200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr6:131520800-131521200	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr6:131520800-131521200	ZNF genes & repeats	Lung	lung
48	chr6:131520800-131521400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr6:131520800-131521600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr6:131520800-131521600	Strong transcription	Aorta	Aorta

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