Variant report

Variant	nsv1045093
Chromosome Location	chr13:67517932-67693875
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1198)
CpG islands
(count:549)
Chromatin interactive
region (count:45)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1198 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:67623033-67623176	K562	blood:	n/a	n/a
2	ARID3A	chr13:67622610-67622815	K562	blood:	n/a	n/a
3	ARID3A	chr13:67568448-67568775	K562	blood:	n/a	n/a
4	ARID3A	chr13:67649489-67649670	K562	blood:	n/a	n/a
5	ATF2	chr13:67568271-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr13:67693560-67694048	A549	lung:	n/a	chr13:67693821-67693834
7	ATF3	chr13:67693636-67694024	A549	lung:	n/a	chr13:67693821-67693834
8	ATF3	chr13:67568179-67568725	A549	lung:	n/a	n/a
9	BACH1	chr13:67582435-67582446	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr13:67622442-67622857	GM12878	blood:	n/a	n/a
11	BCL3	chr13:67568092-67568724	A549	lung:	n/a	chr13:67568680-67568687
12	BCL3	chr13:67660343-67660842	A549	lung:	n/a	n/a
13	BCL3	chr13:67693457-67694274	A549	lung:	n/a	n/a
14	BCL3	chr13:67693588-67694152	A549	lung:	n/a	n/a
15	BCL3	chr13:67674834-67675319	A549	lung:	n/a	n/a
16	BCL3	chr13:67674726-67675275	A549	lung:	n/a	n/a
17	BHLHE40	chr13:67568386-67568547	K562	blood:	n/a	n/a
18	BHLHE40	chr13:67693827-67694033	A549	lung:	n/a	n/a
19	BHLHE40	chr13:67569138-67569828	GM12878	blood:	n/a	n/a
20	BHLHE40	chr13:67624901-67624918	K562	blood:	n/a	n/a
21	BRCA1	chr13:67672229-67672760	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr13:67693319-67694236	Hela-S3	cervix:	n/a	chr13:67694190-67694197
23	BRCA1	chr13:67688832-67688838	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr13:67674668-67675397	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr13:67675807-67676688	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr13:67681576-67681964	K562	blood:	n/a	n/a
27	CCNT2	chr13:67666949-67667210	K562	blood:	n/a	n/a
28	CEBPB	chr13:67677439-67677703	A549	lung:	n/a	chr13:67677586-67677599 chr13:67677583-67677600 chr13:67677588-67677599
29	CEBPB	chr13:67669791-67670120	HepG2	liver:	n/a	n/a
30	CEBPB	chr13:67643278-67643665	A549	lung:	n/a	n/a
31	CEBPB	chr13:67675889-67676239	A549	lung:	n/a	chr13:67676070-67676083
32	CEBPB	chr13:67669618-67670181	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr13:67525177-67525315	H1-hESC	embryonic stem cell:	n/a	chr13:67525201-67525214
34	CEBPB	chr13:67558401-67558722	IMR90	lung:	n/a	chr13:67558552-67558563
35	CEBPB	chr13:67622578-67623240	IMR90	lung:	n/a	n/a
36	CEBPB	chr13:67536801-67536984	HepG2	liver:	n/a	n/a
37	CEBPB	chr13:67568307-67568516	K562	blood:	n/a	n/a
38	CEBPB	chr13:67643508-67643758	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr13:67669742-67670128	A549	lung:	n/a	n/a
40	CEBPB	chr13:67675042-67675050	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr13:67596835-67597031	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr13:67558478-67558699	HepG2	liver:	n/a	chr13:67558552-67558563
43	CEBPB	chr13:67568171-67568602	A549	lung:	n/a	n/a
44	CEBPB	chr13:67566236-67566719	A549	lung:	n/a	chr13:67566693-67566704 chr13:67566693-67566704
45	CEBPB	chr13:67570660-67571082	A549	lung:	n/a	chr13:67570842-67570855
46	CEBPB	chr13:67669716-67670163	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr13:67525159-67525306	A549	lung:	n/a	chr13:67525201-67525214
48	CEBPB	chr13:67608778-67608978	HepG2	liver:	n/a	chr13:67608897-67608908
49	CEBPB	chr13:67674837-67675213	A549	lung:	n/a	n/a
50	CEBPB	chr13:67669689-67670214	A549	lung:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67621714-67621764	RPTEC	kidney:	n/a
2	chr13:67676107-67676157	NB4	blood:	n/a
3	chr13:67548536-67548586	PANC-1	pancreas:	n/a
4	chr13:67676107-67676157	AoSMC	blood vessel:	n/a
5	chr13:67568473-67568523	ProgFib	skin:	n/a
6	chr13:67636112-67636162	K562	blood:	n/a
7	chr13:67611071-67611121	HIPEpiC	eye:	n/a
8	chr13:67645170-67645220	BJ	skin:	n/a
9	chr13:67621714-67621764	AG09309	skin:	n/a
10	chr13:67621714-67621764	Hela-S3	cervix:	n/a
11	chr13:67611071-67611121	HEEpiC	esophagus:	n/a
12	chr13:67676107-67676157	NHDF-neo	bronchial:	n/a
13	chr13:67676107-67676157	SKMC	muscle:	n/a
14	chr13:67570127-67570177	U87	brain:	n/a
15	chr13:67568518-67568568	ProgFib	skin:	n/a
16	chr13:67568473-67568523	AoSMC	blood vessel:	n/a
17	chr13:67570127-67570177	HPAEpiC	pulmonary alveolar:	n/a
18	chr13:67645170-67645220	HRPEpiC	eye:	n/a
19	chr13:67636112-67636162	AG10803	skin:	n/a
20	chr13:67645170-67645220	ovcar-3	ovarian:	n/a
21	chr13:67568473-67568523	Hepatocyte	liver:	n/a
22	chr13:67548536-67548586	SK-N-SH_RA	brain:	n/a
23	chr13:67611071-67611121	AG09319	gingival:	n/a
24	chr13:67636112-67636162	HUVEC	blood vessel:	n/a
25	chr13:67548536-67548586	Hela-S3	cervix:	n/a
26	chr13:67676107-67676157	HRPEpiC	eye:	n/a
27	chr13:67611071-67611121	AG09309	skin:	n/a
28	chr13:67611071-67611121	AG10803	skin:	n/a
29	chr13:67548536-67548586	HPAEpiC	pulmonary alveolar:	n/a
30	chr13:67568518-67568568	HRCEpiC	kidney:	n/a
31	chr13:67548536-67548586	HCPEpiC	choroid plexus:	n/a
32	chr13:67568473-67568523	HCT-116	colon:	n/a
33	chr13:67645170-67645220	A549	lung:	n/a
34	chr13:67568518-67568568	H1-hESC	embryonic stem cell:	embryo
35	chr13:67636112-67636162	Jurkat	blood:	n/a
36	chr13:67570127-67570177	SKMC	muscle:	n/a
37	chr13:67636112-67636162	NHBE	bronchial:	n/a
38	chr13:67568518-67568568	HUVEC	blood vessel:	n/a
39	chr13:67676107-67676157	HEEpiC	esophagus:	n/a
40	chr13:67570127-67570177	HNPCEpiC	eye:	n/a
41	chr13:67621714-67621764	A549	lung:	n/a
42	chr13:67611071-67611121	HCF	heart:	n/a
43	chr13:67548536-67548586	AG09309	skin:	n/a
44	chr13:67570127-67570177	HRPEpiC	eye:	n/a
45	chr13:67611071-67611121	HNPCEpiC	eye:	n/a
46	chr13:67676107-67676157	HL-60	blood:	n/a
47	chr13:67676107-67676157	ProgFib	skin:	n/a
48	chr13:67636112-67636162	SKMC	muscle:	n/a
49	chr13:67548536-67548586	K562	blood:	n/a
50	chr13:67676107-67676157	SK-N-SH	brain:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:67611732..67614272-chr13:67618867..67621097,2	K562	blood:
2	chr13:67517858..67520029-chr13:67533541..67536022,2	K562	blood:
3	chr13:67610771..67613638-chr13:67632502..67635346,2	K562	blood:
4	chr13:67618768..67621421-chr13:67666837..67668518,2	K562	blood:
5	chr13:67675315..67677350-chr13:67683836..67685961,2	K562	blood:
6	chr13:67644544..67646111-chr13:67718055..67719973,2	K562	blood:
7	chr13:67686713..67688646-chr13:67690649..67692733,2	K562	blood:
8	chr13:67618768..67621421-chr13:67666837..67668518,2	K562	blood:
9	chr13:67610771..67613638-chr13:67632502..67635346,2	K562	blood:
10	chr13:67641629..67645149-chr13:67647169..67649102,3	K562	blood:
11	chr13:67660306..67662402-chr13:67696166..67698306,2	K562	blood:
12	chr13:67562882..67565273-chr13:67566706..67568513,2	K562	blood:
13	chr13:67673168..67676018-chr13:67680338..67682100,2	K562	blood:
14	chr13:67611738..67614216-chr13:67615781..67617900,2	K562	blood:
15	chr13:67641629..67645149-chr13:67647169..67649102,3	K562	blood:
16	chr13:67611732..67614272-chr13:67618867..67621097,2	K562	blood:
17	chr13:67644343..67646660-chr13:67649224..67651999,2	K562	blood:
18	chr13:67649311..67650094-chr13:67990535..67991084,2	MCF-7	breast:
19	chr13:67659257..67661234-chr13:67663464..67666434,2	MCF-7	breast:
20	chr13:67620328..67623105-chr13:67624007..67626325,2	K562	blood:
21	chr13:67674917..67677595-chr13:67687583..67689856,3	K562	blood:
22	chr13:67542691..67545017-chr13:67591674..67594006,2	K562	blood:
23	chr13:67611738..67614216-chr13:67615781..67617900,2	K562	blood:
24	chr13:67687472..67689479-chr13:67704392..67705946,2	K562	blood:
25	chr13:67674917..67677595-chr13:67687583..67689856,3	K562	blood:
26	chr13:67681587..67685897-chr13:67688405..67692463,6	K562	blood:
27	chr13:67659257..67661234-chr13:67663464..67666434,2	MCF-7	breast:
28	chr13:67675315..67677350-chr13:67683836..67685961,2	K562	blood:
29	chr13:67681587..67685897-chr13:67688405..67692463,6	K562	blood:
30	chr13:67686150..67689268-chr13:67693283..67697595,5	K562	blood:
31	chr13:67624230..67626098-chr13:67628048..67629694,2	K562	blood:
32	chr13:67686001..67691093-chr13:67707345..67712221,5	K562	blood:
33	chr13:67517858..67520029-chr13:67533541..67536022,2	K562	blood:
34	chr13:67584111..67586911-chr13:67593760..67595933,2	K562	blood:
35	chr13:67542691..67545017-chr13:67591674..67594006,2	K562	blood:
36	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
37	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
38	chr13:67584111..67586911-chr13:67593760..67595933,2	K562	blood:
39	chr13:67624230..67626098-chr13:67628048..67629694,2	K562	blood:
40	chr13:67673168..67676018-chr13:67680338..67682100,2	K562	blood:
41	chr13:67620328..67623105-chr13:67624007..67626325,2	K562	blood:
42	chr13:67686713..67688646-chr13:67690649..67692733,2	K562	blood:
43	chr13:67644343..67646660-chr13:67649224..67651999,2	K562	blood:
44	chr13:67686150..67689268-chr13:67693283..67697595,5	K562	blood:
45	chr13:67685964..67690654-chr13:67706296..67711657,6	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-15	chr13:67559629-67559908	ENSG00000225263.1
2	lnc-AL445989.1-16	chr13:67570354-67570413	NR_046637
3	lnc-AL445989.1-15	chr13:67551521-67551663	NONHSAT034215
4	lnc-KLHL1-10	chr13:67656645-67658943	NONHSAT034217
5	lnc-AL445989.1-16	chr13:67565018-67565231	NR_046637
6	lnc-AL445989.1-14	chr13:67517880-67518119	NONHSAT034214
7	lnc-AL445989.1-15	chr13:67552505-67552603	NONHSAT034215
8	lnc-AL445989.1-15	chr13:67559629-67559908	NONHSAT034215
9	lnc-AL445989.1-16	chr13:67565018-67565231	ENSG00000233840.1
10	lnc-AL445989.1-16	chr13:67575978-67576132	NR_046637
11	lnc-AL445989.1-15	chr13:67551564-67551663	ENSG00000225263.1
12	lnc-AL445989.1-15	chr13:67552505-67552603	ENSG00000225263.1
13	lnc-AL445989.1-16	chr13:67575978-67576139	ENSG00000233840.1
14	lnc-AL445989.1-16	chr13:67570354-67570413	ENSG00000233840.1

No data

Variant related genes	Relation type
PCDH9-AS4	TF binding region
PCDH9-AS3	TF binding region
PCDH9-AS4	CpG island
PCDH9-AS3	CpG island
ENSG00000233840	chromatin interactions

Extended variants
information (count: 5919 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5919 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191768625	chr13:67517951-67517952	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs183120580	chr13:67518001-67518002	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs143741165	chr13:67518013-67518014	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs560907793	chr13:67518023-67518024	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs35644427	chr13:67518028-67518029	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs187135342	chr13:67518039-67518040	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs7995710	chr13:67518071-67518072	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs190092686	chr13:67518079-67518080	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs182698144	chr13:67518080-67518081	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs370577968	chr13:67518207-67518208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544150055	chr13:67518209-67518210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374283037	chr13:67518227-67518228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73505314	chr13:67518236-67518237	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs550786616	chr13:67518265-67518266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186682361	chr13:67518275-67518276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34863785	chr13:67518377-67518378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs66571672	chr13:67518380-67518381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529975575	chr13:67518418-67518419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs114436046	chr13:67518521-67518522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560206366	chr13:67518548-67518549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192390236	chr13:67518604-67518605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552279083	chr13:67518631-67518632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563121984	chr13:67518681-67518682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185628696	chr13:67518689-67518690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145170968	chr13:67518781-67518782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568614951	chr13:67518791-67518792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114878710	chr13:67518807-67518808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547441728	chr13:67518831-67518832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116068411	chr13:67518856-67518857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553411433	chr13:67518930-67518931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377641456	chr13:67518949-67518950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs67182136	chr13:67518950-67518951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375415873	chr13:67518975-67518976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs398023180	chr13:67518988-67518989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139693818	chr13:67518989-67518990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539575622	chr13:67519078-67519079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556238342	chr13:67519079-67519080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9564364	chr13:67519121-67519122	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs566382129	chr13:67519158-67519159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537600341	chr13:67519187-67519188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372244991	chr13:67519196-67519197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376645772	chr13:67519205-67519206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140491938	chr13:67519225-67519226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188892552	chr13:67519244-67519245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs193146484	chr13:67519279-67519280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34503264	chr13:67519337-67519338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs71207613	chr13:67519338-67519339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200754799	chr13:67519343-67519344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540503951	chr13:67519376-67519377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139034161	chr13:67519465-67519466	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Schizophrenia	23813976	CNVD
Prostate cancer	22341455	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:1300 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67518200-67519200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr13:67518600-67519600	Enhancers	Primary B cells from peripheral blood	blood
3	chr13:67518600-67519600	Enhancers	Dnd41	blood
4	chr13:67518800-67519400	Enhancers	Primary B cells from cord blood	blood
5	chr13:67519400-67520000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr13:67521600-67523400	Enhancers	A549	lung
7	chr13:67521800-67526400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr13:67522000-67522200	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr13:67522400-67525400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr13:67522400-67526800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr13:67522600-67523000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr13:67522600-67526400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr13:67522800-67523000	Enhancers	Brain Anterior Caudate	brain
14	chr13:67522800-67523200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr13:67522800-67526400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr13:67522800-67526600	Enhancers	Brain Hippocampus Middle	brain
17	chr13:67523000-67523400	Flanking Active TSS	Brain Anterior Caudate	brain
18	chr13:67523000-67523400	Active TSS	Brain Inferior Temporal Lobe	brain
19	chr13:67523000-67524600	Enhancers	Brain Cingulate Gyrus	brain
20	chr13:67523000-67525800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr13:67523000-67526400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr13:67523200-67523600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr13:67523200-67523800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr13:67523200-67523800	Enhancers	H1 Cell Line	embryonic stem cell
25	chr13:67523200-67524600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr13:67523400-67523600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr13:67523400-67523600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
28	chr13:67523400-67523800	Enhancers	H9 Cell Line	embryonic stem cell
29	chr13:67523400-67523800	Enhancers	Brain Angular Gyrus	brain
30	chr13:67523400-67523800	Enhancers	Fetal Brain Male	brain
31	chr13:67523400-67526400	Enhancers	Brain Anterior Caudate	brain
32	chr13:67523400-67531200	Weak transcription	A549	lung
33	chr13:67523600-67523800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr13:67523600-67524400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr13:67523600-67525400	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr13:67523800-67524200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr13:67523800-67524800	Weak transcription	Brain Angular Gyrus	brain
38	chr13:67523800-67525200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr13:67523800-67525200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr13:67523800-67526600	Enhancers	Brain Substantia Nigra	brain
41	chr13:67524200-67524400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr13:67524400-67524800	Enhancers	Brain Germinal Matrix	brain
43	chr13:67524400-67525200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr13:67524400-67526400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr13:67524400-67526400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr13:67524600-67525000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr13:67524600-67525200	Weak transcription	Brain Cingulate Gyrus	brain
48	chr13:67524800-67525600	Enhancers	Brain Angular Gyrus	brain
49	chr13:67525000-67526400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr13:67525200-67525400	Enhancers	Brain Cingulate Gyrus	brain

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