Variant report

Variant	nsv428604
Chromosome Location	chr13:67480426-67645030
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:932)
CpG islands
(count:427)
Chromatin interactive
region (count:32)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:932 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:67622610-67622815	K562	blood:	n/a	n/a
2	ARID3A	chr13:67508076-67508417	K562	blood:	n/a	n/a
3	ARID3A	chr13:67568448-67568775	K562	blood:	n/a	n/a
4	ARID3A	chr13:67623033-67623176	K562	blood:	n/a	n/a
5	ATF1	chr13:67512216-67512440	K562	blood:	n/a	n/a
6	ATF2	chr13:67568271-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr13:67508091-67508467	A549	lung:	n/a	n/a
8	ATF3	chr13:67568179-67568725	A549	lung:	n/a	n/a
9	ATF3	chr13:67514291-67514517	K562	blood:	n/a	n/a
10	ATF3	chr13:67513673-67513979	K562	blood:	n/a	n/a
11	ATF3	chr13:67508059-67508348	K562	blood:	n/a	n/a
12	BACH1	chr13:67582435-67582446	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr13:67508106-67508447	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr13:67508060-67508511	K562	blood:	n/a	n/a
15	BATF	chr13:67622442-67622857	GM12878	blood:	n/a	n/a
16	BCL3	chr13:67568092-67568724	A549	lung:	n/a	chr13:67568680-67568687
17	BCL3	chr13:67507974-67508573	A549	lung:	n/a	chr13:67508041-67508050
18	BCL3	chr13:67508048-67508565	A549	lung:	n/a	n/a
19	BHLHE40	chr13:67568386-67568547	K562	blood:	n/a	n/a
20	BHLHE40	chr13:67624901-67624918	K562	blood:	n/a	n/a
21	BHLHE40	chr13:67569138-67569828	GM12878	blood:	n/a	n/a
22	CBX3	chr13:67508097-67508421	K562	blood:	n/a	n/a
23	CCNT2	chr13:67480244-67480442	K562	blood:	n/a	n/a
24	CEBPB	chr13:67516745-67517360	Hela-S3	cervix:	n/a	chr13:67516868-67516877 chr13:67516868-67516877 chr13:67516866-67516879 chr13:67516868-67516877 chr13:67516868-67516879 chr13:67516868-67516877
25	CEBPB	chr13:67558478-67558699	HepG2	liver:	n/a	chr13:67558552-67558563
26	CEBPB	chr13:67597726-67598014	IMR90	lung:	n/a	n/a
27	CEBPB	chr13:67558401-67558722	IMR90	lung:	n/a	chr13:67558552-67558563
28	CEBPB	chr13:67484755-67485097	IMR90	lung:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
29	CEBPB	chr13:67643162-67643739	A549	lung:	n/a	n/a
30	CEBPB	chr13:67515187-67515415	HepG2	liver:	n/a	chr13:67515279-67515290
31	CEBPB	chr13:67501468-67501696	A549	lung:	n/a	n/a
32	CEBPB	chr13:67566854-67567179	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr13:67568217-67568468	HepG2	liver:	n/a	n/a
34	CEBPB	chr13:67516781-67517023	K562	blood:	n/a	chr13:67516868-67516877 chr13:67516868-67516877 chr13:67516866-67516879 chr13:67516868-67516877 chr13:67516868-67516879 chr13:67516868-67516877
35	CEBPB	chr13:67568953-67569159	A549	lung:	n/a	n/a
36	CEBPB	chr13:67484807-67485063	A549	lung:	n/a	chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
37	CEBPB	chr13:67484754-67485342	A549	lung:	n/a	chr13:67485279-67485292 chr13:67485279-67485290 chr13:67484930-67484939 chr13:67484930-67484939 chr13:67484928-67484941 chr13:67484928-67484941 chr13:67484930-67484939
38	CEBPB	chr13:67551323-67551595	IMR90	lung:	n/a	n/a
39	CEBPB	chr13:67590501-67590687	K562	blood:	n/a	n/a
40	CEBPB	chr13:67568217-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr13:67566236-67566719	A549	lung:	n/a	chr13:67566693-67566704 chr13:67566693-67566704
42	CEBPB	chr13:67643508-67643758	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr13:67566763-67567107	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr13:67568038-67568652	A549	lung:	n/a	n/a
45	CEBPB	chr13:67558407-67558682	A549	lung:	n/a	chr13:67558552-67558563
46	CEBPB	chr13:67614150-67614376	HepG2	liver:	n/a	n/a
47	CEBPB	chr13:67566342-67566648	A549	lung:	n/a	n/a
48	CEBPB	chr13:67619494-67619976	Hela-S3	cervix:	n/a	chr13:67619769-67619782
49	CEBPB	chr13:67566840-67567107	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr13:67566898-67567137	A549	lung:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67636112-67636162	SK-N-SH_RA	brain:	n/a
2	chr13:67636112-67636162	BE2_C	brain:	n/a
3	chr13:67636112-67636162	PFSK-1	brain:	n/a
4	chr13:67568473-67568523	RPTEC	kidney:	n/a
5	chr13:67548536-67548586	ECC-1	luminal epithelium:	n/a
6	chr13:67568518-67568568	SKMC	muscle:	n/a
7	chr13:67621714-67621764	HNPCEpiC	eye:	n/a
8	chr13:67621714-67621764	HEK293	kidney:	embryo
9	chr13:67611071-67611121	GM12891	blood:	n/a
10	chr13:67621714-67621764	MCF-7	breast:	n/a
11	chr13:67621714-67621764	SK-N-MC	brain:	n/a
12	chr13:67621714-67621764	HMEC	breast:	n/a
13	chr13:67568518-67568568	ProgFib	skin:	n/a
14	chr13:67621714-67621764	T-47D	breast:	n/a
15	chr13:67636112-67636162	MCF-7	breast:	n/a
16	chr13:67568518-67568568	BE2_C	brain:	n/a
17	chr13:67568518-67568568	NH-A	brain:	n/a
18	chr13:67636112-67636162	HEEpiC	esophagus:	n/a
19	chr13:67636112-67636162	GM12891	blood:	n/a
20	chr13:67611071-67611121	GM19239	blood:	n/a
21	chr13:67636112-67636162	AG09309	skin:	n/a
22	chr13:67568473-67568523	SK-N-SH	brain:	n/a
23	chr13:67568473-67568523	ECC-1	luminal epithelium:	n/a
24	chr13:67621714-67621764	SK-N-SH	brain:	n/a
25	chr13:67611071-67611121	HL-60	blood:	n/a
26	chr13:67636112-67636162	BJ	skin:	n/a
27	chr13:67568473-67568523	HEEpiC	esophagus:	n/a
28	chr13:67548536-67548586	NB4	blood:	n/a
29	chr13:67636112-67636162	AoSMC	blood vessel:	n/a
30	chr13:67570127-67570177	Hela-S3	cervix:	n/a
31	chr13:67636112-67636162	ProgFib	skin:	n/a
32	chr13:67621714-67621764	HEEpiC	esophagus:	n/a
33	chr13:67621714-67621764	LNCaP	prostate:	n/a
34	chr13:67611071-67611121	ProgFib	skin:	n/a
35	chr13:67548536-67548586	Hela-S3	cervix:	n/a
36	chr13:67621714-67621764	K562	blood:	n/a
37	chr13:67568518-67568568	ECC-1	luminal epithelium:	n/a
38	chr13:67548536-67548586	Hepatocyte	liver:	n/a
39	chr13:67548536-67548586	CMK	blood:	n/a
40	chr13:67636112-67636162	NHBE	bronchial:	n/a
41	chr13:67568473-67568523	NHBE	bronchial:	n/a
42	chr13:67611071-67611121	SK-N-SH_RA	brain:	n/a
43	chr13:67568473-67568523	IMR90	lung:	fetal
44	chr13:67621714-67621764	IMR90	lung:	fetal
45	chr13:67636112-67636162	HCT-116	colon:	n/a
46	chr13:67568518-67568568	NHBE	bronchial:	n/a
47	chr13:67570127-67570177	HIPEpiC	eye:	n/a
48	chr13:67568518-67568568	HMEC	breast:	n/a
49	chr13:67636112-67636162	U87	brain:	n/a
50	chr13:67636112-67636162	AG09319	gingival:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:67499121..67501052-chr13:67506413..67508246,2	K562	blood:
2	chr13:67644544..67646111-chr13:67718055..67719973,2	K562	blood:
3	chr13:67641629..67645149-chr13:67647169..67649102,3	K562	blood:
4	chr13:67517858..67520029-chr13:67533541..67536022,2	K562	blood:
5	chr13:67644343..67646660-chr13:67649224..67651999,2	K562	blood:
6	chr13:67611738..67614216-chr13:67615781..67617900,2	K562	blood:
7	chr13:67611738..67614216-chr13:67615781..67617900,2	K562	blood:
8	chr13:67483833..67485636-chr13:67488451..67490558,2	MCF-7	breast:
9	chr13:67517858..67520029-chr13:67533541..67536022,2	K562	blood:
10	chr13:67620328..67623105-chr13:67624007..67626325,2	K562	blood:
11	chr13:67503858..67504708-chr5:34924011..34924781,2	Hela-S3	cervix:
12	chr13:67624230..67626098-chr13:67628048..67629694,2	K562	blood:
13	chr13:67483833..67485636-chr13:67488451..67490558,2	MCF-7	breast:
14	chr13:67618768..67621421-chr13:67666837..67668518,2	K562	blood:
15	chr13:67584111..67586911-chr13:67593760..67595933,2	K562	blood:
16	chr13:67610771..67613638-chr13:67632502..67635346,2	K562	blood:
17	chr13:67542691..67545017-chr13:67591674..67594006,2	K562	blood:
18	chr13:67620328..67623105-chr13:67624007..67626325,2	K562	blood:
19	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
20	chr13:67497444..67500061-chr13:67515647..67517481,2	K562	blood:
21	chr13:67499121..67501052-chr13:67506413..67508246,2	K562	blood:
22	chr13:67624230..67626098-chr13:67628048..67629694,2	K562	blood:
23	chr13:67611732..67614272-chr13:67618867..67621097,2	K562	blood:
24	chr13:67497444..67500061-chr13:67515647..67517481,2	K562	blood:
25	chr13:67584111..67586911-chr13:67593760..67595933,2	K562	blood:
26	chr13:67542691..67545017-chr13:67591674..67594006,2	K562	blood:
27	chr13:67611732..67614272-chr13:67618867..67621097,2	K562	blood:
28	chr13:67509668..67511474-chr13:67514101..67516252,2	K562	blood:
29	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
30	chr13:67562882..67565273-chr13:67566706..67568513,2	K562	blood:
31	chr13:67509668..67511474-chr13:67514101..67516252,2	K562	blood:
32	chr13:67610771..67613638-chr13:67632502..67635346,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-14	chr13:67488530-67488618	NONHSAT034214
2	lnc-AL445989.1-14	chr13:67484006-67484154	NONHSAT034214
3	lnc-AL445989.1-15	chr13:67552505-67552603	ENSG00000225263.1
4	lnc-AL445989.1-15	chr13:67551564-67551663	ENSG00000225263.1
5	lnc-AL445989.1-15	chr13:67559629-67559908	ENSG00000225263.1
6	lnc-AL445989.1-14	chr13:67489069-67489163	ENSG00000228842.2
7	lnc-AL445989.1-15	chr13:67552505-67552603	NONHSAT034215
8	lnc-AL445989.1-14	chr13:67517880-67518119	NONHSAT034214
9	lnc-AL445989.1-16	chr13:67565018-67565231	ENSG00000233840.1
10	lnc-AL445989.1-15	chr13:67559629-67559908	NONHSAT034215
11	lnc-AL445989.1-16	chr13:67570354-67570413	NR_046637
12	lnc-AL445989.1-14	chr13:67488530-67488618	ENSG00000228842.2
13	lnc-AL445989.1-14	chr13:67488530-67488618	ENSG00000228842.1
14	lnc-AL445989.1-16	chr13:67575978-67576132	NR_046637
15	lnc-AL445989.1-15	chr13:67551521-67551663	NONHSAT034215
16	lnc-AL445989.1-16	chr13:67570354-67570413	ENSG00000233840.1
17	lnc-AL445989.1-14	chr13:67489069-67489163	ENSG00000228842.1
18	lnc-AL445989.1-16	chr13:67575978-67576139	ENSG00000233840.1
19	lnc-AL445989.1-16	chr13:67565018-67565231	NR_046637

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: 5450 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5450 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114080359	chr13:67480450-67480451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs17081998	chr13:67480561-67480562	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs575232646	chr13:67480620-67480621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543787540	chr13:67480642-67480643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554115453	chr13:67480656-67480657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553854191	chr13:67480723-67480724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9571689	chr13:67480776-67480777	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs540433765	chr13:67480781-67480782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183190862	chr13:67480845-67480846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560269847	chr13:67480917-67480918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532713751	chr13:67480940-67480941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74802107	chr13:67480952-67480953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541247729	chr13:67480988-67480989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552800060	chr13:67480991-67480992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569433847	chr13:67480995-67480996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531760619	chr13:67481001-67481002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548597457	chr13:67481009-67481010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568607946	chr13:67481039-67481040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534238842	chr13:67481045-67481046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147761757	chr13:67481064-67481065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187076796	chr13:67481076-67481077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538440218	chr13:67481103-67481104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558843818	chr13:67481113-67481114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575448477	chr13:67481126-67481127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141104591	chr13:67481129-67481130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554106190	chr13:67481140-67481141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574195030	chr13:67481165-67481166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191888631	chr13:67481166-67481167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560533607	chr13:67481173-67481174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148589620	chr13:67481204-67481205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369348965	chr13:67481208-67481209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532772720	chr13:67481218-67481219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559552353	chr13:67481227-67481228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs578022835	chr13:67481243-67481244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183062599	chr13:67481314-67481315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563242597	chr13:67481323-67481324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146938310	chr13:67481372-67481373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545298459	chr13:67481388-67481389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563752819	chr13:67481422-67481423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7990449	chr13:67481549-67481550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548607323	chr13:67481559-67481560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568437869	chr13:67481632-67481633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373490686	chr13:67481678-67481679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527803085	chr13:67481910-67481911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530804838	chr13:67481992-67481993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376758632	chr13:67482023-67482024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138009003	chr13:67482136-67482137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112498056	chr13:67482149-67482150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570837726	chr13:67482159-67482160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187757483	chr13:67482166-67482167	Weak transcription	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:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67474400-67485000	Weak transcription	Brain Hippocampus Middle	brain
2	chr13:67474600-67484000	Weak transcription	Brain Angular Gyrus	brain
3	chr13:67475200-67485200	Weak transcription	Brain Substantia Nigra	brain
4	chr13:67479000-67480600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr13:67479600-67482200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr13:67482200-67482400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr13:67483800-67484000	Enhancers	Liver	Liver
8	chr13:67484000-67484400	Flanking Active TSS	Liver	Liver
9	chr13:67484000-67484400	Enhancers	A549	lung
10	chr13:67484000-67486400	Enhancers	Brain Angular Gyrus	brain
11	chr13:67484200-67484400	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr13:67484400-67485200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr13:67484400-67486600	Active TSS	Liver	Liver
14	chr13:67484400-67488200	Weak transcription	A549	lung
15	chr13:67485000-67486600	Enhancers	Brain Hippocampus Middle	brain
16	chr13:67485200-67485800	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr13:67485200-67488400	Enhancers	Brain Substantia Nigra	brain
18	chr13:67485400-67485600	Enhancers	Brain Anterior Caudate	brain
19	chr13:67485400-67486600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr13:67485600-67485800	Enhancers	Brain Cingulate Gyrus	brain
21	chr13:67485600-67489600	Weak transcription	Brain Anterior Caudate	brain
22	chr13:67485800-67486400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr13:67485800-67488000	Weak transcription	Brain Cingulate Gyrus	brain
24	chr13:67486400-67486600	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr13:67486400-67486800	Weak transcription	Brain Angular Gyrus	brain
26	chr13:67486600-67487400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr13:67486600-67489800	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr13:67486600-67490000	Weak transcription	Brain Hippocampus Middle	brain
29	chr13:67486800-67487600	Enhancers	Brain Angular Gyrus	brain
30	chr13:67487200-67489000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr13:67487200-67489400	Enhancers	Primary T cells from cord blood	blood
32	chr13:67487400-67488000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr13:67487600-67489000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr13:67487600-67490800	Weak transcription	Brain Angular Gyrus	brain
35	chr13:67488000-67488200	Enhancers	Brain Cingulate Gyrus	brain
36	chr13:67488000-67489600	Enhancers	Dnd41	blood
37	chr13:67488000-67490000	Enhancers	Primary B cells from cord blood	blood
38	chr13:67488200-67488400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr13:67488200-67488600	Weak transcription	Brain Cingulate Gyrus	brain
40	chr13:67488200-67489000	Enhancers	A549	lung
41	chr13:67488400-67488600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr13:67488400-67489600	Weak transcription	Brain Substantia Nigra	brain
43	chr13:67488600-67489800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr13:67488600-67490000	Enhancers	Brain Cingulate Gyrus	brain
45	chr13:67488800-67489800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr13:67489000-67489400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr13:67489000-67489400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr13:67489000-67489400	Weak transcription	A549	lung
49	chr13:67489000-67490400	Enhancers	HUVEC	blood vessel
50	chr13:67489400-67489600	Enhancers	A549	lung

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