Variant report

Variant	nsv541817
Chromosome Location	chr13:67212973-68077950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5263)
CpG islands
(count:2443)
Chromatin interactive
region (count:121)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5263 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:67695093-67695440	K562	blood:	n/a	n/a
2	ARID3A	chr13:67568448-67568775	K562	blood:	n/a	n/a
3	ARID3A	chr13:67804369-67804789	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:67804263-67804856	K562	blood:	n/a	n/a
5	ARID3A	chr13:67957650-67957867	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:67798184-67798839	K562	blood:	n/a	n/a
7	ARID3A	chr13:67710420-67710641	K562	blood:	n/a	n/a
8	ARID3A	chr13:67812559-67812678	K562	blood:	n/a	n/a
9	ARID3A	chr13:67649489-67649670	K562	blood:	n/a	n/a
10	ARID3A	chr13:67623033-67623176	K562	blood:	n/a	n/a
11	ARID3A	chr13:67707700-67708119	K562	blood:	n/a	chr13:67707935-67707951
12	ARID3A	chr13:67508076-67508417	K562	blood:	n/a	n/a
13	ARID3A	chr13:67798270-67798699	HepG2	liver:	n/a	n/a
14	ARID3A	chr13:67409290-67409647	K562	blood:	n/a	n/a
15	ARID3A	chr13:67622610-67622815	K562	blood:	n/a	n/a
16	ARID3A	chr13:67857713-67858283	HepG2	liver:	n/a	n/a
17	ATF1	chr13:67710067-67710711	K562	blood:	n/a	n/a
18	ATF1	chr13:68014427-68014642	K562	blood:	n/a	n/a
19	ATF1	chr13:67704648-67704983	K562	blood:	n/a	n/a
20	ATF1	chr13:67717956-67718156	K562	blood:	n/a	n/a
21	ATF1	chr13:67512216-67512440	K562	blood:	n/a	n/a
22	ATF2	chr13:67804425-67804838	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr13:67990402-67990747	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr13:67832600-67833093	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr13:67568271-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr13:67798145-67798701	A549	lung:	n/a	n/a
27	ATF3	chr13:67513673-67513979	K562	blood:	n/a	n/a
28	ATF3	chr13:67710441-67710714	K562	blood:	n/a	n/a
29	ATF3	chr13:67693636-67694024	A549	lung:	n/a	chr13:67693821-67693834
30	ATF3	chr13:67758433-67758707	K562	blood:	n/a	n/a
31	ATF3	chr13:67704624-67704927	K562	blood:	n/a	n/a
32	ATF3	chr13:67508059-67508348	K562	blood:	n/a	n/a
33	ATF3	chr13:67231209-67231841	A549	lung:	n/a	chr13:67231614-67231627 chr13:67231613-67231624 chr13:67231616-67231624 chr13:67231614-67231625 chr13:67231613-67231626 chr13:67231614-67231625 chr13:67231612-67231627
34	ATF3	chr13:67568179-67568725	A549	lung:	n/a	n/a
35	ATF3	chr13:67695226-67695807	A549	lung:	n/a	n/a
36	ATF3	chr13:67693560-67694048	A549	lung:	n/a	chr13:67693821-67693834
37	ATF3	chr13:67508091-67508467	A549	lung:	n/a	n/a
38	ATF3	chr13:67514291-67514517	K562	blood:	n/a	n/a
39	BACH1	chr13:67508060-67508511	K562	blood:	n/a	n/a
40	BACH1	chr13:67804549-67804853	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr13:67262315-67262350	K562	blood:	n/a	n/a
42	BACH1	chr13:67582435-67582446	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr13:67508106-67508447	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr13:67847366-67847439	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr13:67805131-67805498	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr13:67798385-67798511	H1-hESC	embryonic stem cell:	n/a	n/a
47	BATF	chr13:67832570-67832820	GM12878	blood:	n/a	chr13:67832570-67832579
48	BATF	chr13:67234343-67234557	GM12878	blood:	n/a	n/a
49	BATF	chr13:67622442-67622857	GM12878	blood:	n/a	n/a
50	BATF	chr13:67234280-67234568	GM12878	blood:	n/a	n/a

(count:2443 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67804744-67804794	AG09309	skin:	n/a
2	chr13:67570127-67570177	ProgFib	skin:	n/a
3	chr13:67803911-67803961	NT2-D1	testis:	n/a
4	chr13:67804744-67804794	AG09309	skin:	n/a
5	chr13:67570127-67570177	ProgFib	skin:	n/a
6	chr13:67803911-67803961	NT2-D1	testis:	n/a
7	chr13:67548536-67548586	HRE	kidney:	n/a
8	chr13:67570127-67570177	HL-60	blood:	n/a
9	chr13:67478043-67478093	SK-N-SH	brain:	n/a
10	chr13:67311899-67311949	HRPEpiC	eye:	n/a
11	chr13:67804509-67804559	ProgFib	skin:	n/a
12	chr13:67804339-67804389	NHBE	bronchial:	n/a
13	chr13:67479146-67479196	ovcar-3	ovarian:	n/a
14	chr13:67721697-67721747	U87	brain:	n/a
15	chr13:67804654-67804704	SKMC	muscle:	n/a
16	chr13:67702292-67702342	HL-60	blood:	n/a
17	chr13:67804637-67804687	HNPCEpiC	eye:	n/a
18	chr13:67645170-67645220	NB4	blood:	n/a
19	chr13:67714028-67714078	HEEpiC	esophagus:	n/a
20	chr13:67702292-67702342	Hela-S3	cervix:	n/a
21	chr13:67676107-67676157	NH-A	brain:	n/a
22	chr13:67803895-67803945	HCM	heart:	n/a
23	chr13:67676107-67676157	MCF10A-Er-Src	breast:	n/a
24	chr13:67804637-67804687	SK-N-SH	brain:	n/a
25	chr13:67803251-67803301	AG04449	skin:	fetal
26	chr13:67570127-67570177	NHBE	bronchial:	n/a
27	chr13:67421996-67422046	NT2-D1	testis:	n/a
28	chr13:67805634-67805684	RPTEC	kidney:	n/a
29	chr13:67803895-67803945	HUVEC	blood vessel:	n/a
30	chr13:67805458-67805508	LNCaP	prostate:	n/a
31	chr13:67478043-67478093	CMK	blood:	n/a
32	chr13:67721697-67721747	NB4	blood:	n/a
33	chr13:67568473-67568523	AG09319	gingival:	n/a
34	chr13:67311899-67311949	HL-60	blood:	n/a
35	chr13:67872416-67872466	NT2-D1	testis:	n/a
36	chr13:67421996-67422046	T-47D	breast:	n/a
37	chr13:67621714-67621764	NHBE	bronchial:	n/a
38	chr13:67611071-67611121	HMEC	breast:	n/a
39	chr13:67805634-67805684	HepG2	liver:	n/a
40	chr13:67804339-67804389	PANC-1	pancreas:	n/a
41	chr13:67548536-67548586	SKMC	muscle:	n/a
42	chr13:67805065-67805115	HCM	heart:	n/a
43	chr13:67801551-67801601	H1-hESC	embryonic stem cell:	embryo
44	chr13:67804662-67804712	SK-N-SH	brain:	n/a
45	chr13:67872416-67872466	HIPEpiC	eye:	n/a
46	chr13:67804635-67804685	AG09309	skin:	n/a
47	chr13:67311899-67311949	GM12878	blood:	n/a
48	chr13:67804285-67804335	Hela-S3	cervix:	n/a
49	chr13:67803895-67803945	PrEC	prostate:	n/a
50	chr13:67805458-67805508	MCF10A-Er-Src	breast:	n/a

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr13:67831297..67833273-chr13:67834437..67837217,2	MCF-7	breast:
2	chr13:67686150..67689268-chr13:67693283..67697595,5	K562	blood:
3	chr13:67811680..67814191-chr13:67815076..67817886,2	K562	blood:
4	chr13:67780012..67782113-chr13:67789906..67791618,2	MCF-7	breast:
5	chr13:67644544..67646111-chr13:67718055..67719973,2	K562	blood:
6	chr13:68060280..68061789-chr13:68065167..68067699,2	K562	blood:
7	chr13:67497444..67500061-chr13:67515647..67517481,2	K562	blood:
8	chr13:67660306..67662402-chr13:67696166..67698306,2	K562	blood:
9	chr13:67066396..67067204-chr13:67263202..67263856,3	MCF-7	breast:
10	chr13:67681587..67685897-chr13:67688405..67692463,6	K562	blood:
11	chr13:67687472..67689479-chr13:67704392..67705946,2	K562	blood:
12	chr13:67273696..67276113-chr13:67277421..67279643,2	MCF-7	breast:
13	chr13:67618768..67621421-chr13:67666837..67668518,2	K562	blood:
14	chr13:67517858..67520029-chr13:67533541..67536022,2	K562	blood:
15	chr13:67659257..67661234-chr13:67663464..67666434,2	MCF-7	breast:
16	chr13:67753265..67756119-chr13:67757714..67759510,2	K562	blood:
17	chr13:67686001..67691093-chr13:67707345..67712221,5	K562	blood:
18	chr13:67624230..67626098-chr13:67628048..67629694,2	K562	blood:
19	chr13:67437418..67439470-chr13:67442003..67443610,2	MCF-7	breast:
20	chr13:67804827..67806801-chr13:67815809..67818505,2	MCF-7	breast:
21	chr13:67624230..67626098-chr13:67628048..67629694,2	K562	blood:
22	chr13:67509668..67511474-chr13:67514101..67516252,2	K562	blood:
23	chr13:67722123..67726078-chr13:67726248..67727777,3	K562	blood:
24	chr13:67675315..67677350-chr13:67683836..67685961,2	K562	blood:
25	chr13:67499121..67501052-chr13:67506413..67508246,2	K562	blood:
26	chr13:67804547..67807310-chr13:67807944..67812554,4	K562	blood:
27	chr13:67779619..67781563-chr13:67783899..67785982,2	MCF-7	breast:
28	chr13:67723500..67726078-chr13:67726248..67727751,2	K562	blood:
29	chr13:67701562..67704458-chr13:67707651..67710683,4	K562	blood:
30	chr13:67618768..67621421-chr13:67666837..67668518,2	K562	blood:
31	chr13:67065287..67067165-chr13:67261665..67264552,2	MCF-7	breast:
32	chr13:67844700..67846615-chr13:67859322..67861875,2	K562	blood:
33	chr13:67686713..67688646-chr13:67690649..67692733,2	K562	blood:
34	chr13:67767771..67770676-chr13:67771457..67773898,2	K562	blood:
35	chr13:67756177..67758762-chr13:67758795..67761086,2	K562	blood:
36	chr13:67919389..67921263-chr13:67925624..67927193,2	MCF-7	breast:
37	chr13:67673168..67676018-chr13:67680338..67682100,2	K562	blood:
38	chr13:67686001..67691093-chr13:67707345..67712221,5	K562	blood:
39	chr13:67641629..67645149-chr13:67647169..67649102,3	K562	blood:
40	chr13:67831297..67833273-chr13:67834437..67837217,2	MCF-7	breast:
41	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
42	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
43	chr13:67780012..67782113-chr13:67789906..67791618,2	MCF-7	breast:
44	chr13:67455570..67458044-chr13:67459396..67461929,2	MCF-7	breast:
45	chr13:67722123..67726078-chr13:67726248..67727777,3	K562	blood:
46	chr13:67685964..67690654-chr13:67706296..67711657,6	K562	blood:
47	chr13:67611732..67614272-chr13:67618867..67621097,2	K562	blood:
48	chr13:67767771..67770676-chr13:67771457..67773898,2	K562	blood:
49	chr13:67610771..67613638-chr13:67632502..67635346,2	K562	blood:
50	chr13:67839825..67842452-chr13:67857701..67859414,2	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL1-10	chr13:67656645-67658943	NONHSAT034217
2	lnc-AL445989.1-14	chr13:67460132-67460209	ENSG00000228842.1
3	lnc-AL445989.1-14	chr13:67489069-67489163	ENSG00000228842.2
4	lnc-AL445989.1-15	chr13:67551564-67551663	ENSG00000225263.1
5	lnc-AL445989.1-14	chr13:67460132-67460208	ENSG00000228842.2
6	lnc-AL445989.1-14	chr13:67484006-67484154	NONHSAT034214
7	lnc-AL445989.1-15	chr13:67559629-67559908	ENSG00000225263.1
8	lnc-AL445989.1-14	chr13:67433130-67433252	ENSG00000228842.1
9	lnc-AL445989.1-15	chr13:67552505-67552603	ENSG00000225263.1
10	lnc-AL445989.1-16	chr13:67565018-67565231	ENSG00000233840.1
11	lnc-AL445989.1-14	chr13:67488530-67488618	ENSG00000228842.2
12	lnc-AL445989.1-14	chr13:67489069-67489163	ENSG00000228842.1
13	lnc-AL445989.1-16	chr13:67575978-67576132	NR_046637
14	lnc-AL445989.1-14	chr13:67433120-67433252	ENSG00000228842.2
15	lnc-AL445989.1-16	chr13:67570354-67570413	NR_046637
16	lnc-AL445989.1-14	chr13:67488530-67488618	ENSG00000228842.1
17	lnc-AL445989.1-14	chr13:67488530-67488618	NONHSAT034214
18	lnc-AL445989.1-14	chr13:67450976-67451051	ENSG00000228842.1
19	lnc-KLHL1-9	chr13:67787977-67789067	NONHSAT034218
20	lnc-AL445989.1-16	chr13:67570354-67570413	ENSG00000233840.1
21	lnc-AL445989.1-14	chr13:67399301-67399368	ENSG00000228842.2
22	lnc-AL445989.1-15	chr13:67559629-67559908	NONHSAT034215
23	lnc-AL445989.1-16	chr13:67565018-67565231	NR_046637
24	lnc-AL445989.1-14	chr13:67450976-67451051	ENSG00000228842.2
25	lnc-AL445989.1-15	chr13:67552505-67552603	NONHSAT034215
26	lnc-AL445989.1-14	chr13:67517880-67518119	NONHSAT034214
27	lnc-AL445989.1-15	chr13:67551521-67551663	NONHSAT034215
28	lnc-KLHL1-9	chr13:67789094-67789866	NONHSAT034218
29	lnc-AL445989.1-16	chr13:67575978-67576139	ENSG00000233840.1

No data

Variant related genes	Relation type
PCDH9-AS4	TF binding region
PCDH9-AS2	TF binding region
PCDH9	TF binding region
LINC00364	TF binding region
RPSAP53	TF binding region
PCDH9-AS3	TF binding region
PCDH9-AS4	CpG island
PCDH9-AS2	CpG island
PCDH9	CpG island
LINC00364	CpG island
RPSAP53	CpG island
PCDH9-AS3	CpG island
ENSG00000228842	chromatin interactions
ENSG00000214263	chromatin interactions
ENSG00000233840	chromatin interactions

Extended variants
information (count: 22302 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:22302 , 50 per page) page: 1 2 3 4 5 6 7 ... 447

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574779136	chr13:67213078-67213079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564657899	chr13:67213119-67213120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183168707	chr13:67213284-67213285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553730782	chr13:67213295-67213296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576815263	chr13:67213305-67213306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186783862	chr13:67213320-67213321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189958637	chr13:67213427-67213428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562816155	chr13:67213431-67213432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553226213	chr13:67213472-67213473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183311072	chr13:67213556-67213557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544382917	chr13:67213615-67213616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561107557	chr13:67213672-67213673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530014522	chr13:67213680-67213681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546950228	chr13:67213718-67213719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554809999	chr13:67213774-67213775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560343122	chr13:67213798-67213799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187739898	chr13:67213800-67213801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531982293	chr13:67213830-67213831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552153603	chr13:67213870-67213871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs193119628	chr13:67213892-67213893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542132257	chr13:67213945-67213946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537588055	chr13:67213953-67213954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554737766	chr13:67214011-67214012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560456225	chr13:67214037-67214038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568346843	chr13:67214086-67214087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534208641	chr13:67214134-67214135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371540639	chr13:67214178-67214179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183468984	chr13:67214205-67214206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577490618	chr13:67214233-67214234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188546488	chr13:67214312-67214313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572994125	chr13:67214331-67214332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113941039	chr13:67214341-67214342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192910693	chr13:67214352-67214353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556531667	chr13:67214364-67214365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2224741	chr13:67214390-67214391	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs542389292	chr13:67214403-67214404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184102689	chr13:67214467-67214468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552558885	chr13:67214495-67214496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188093685	chr13:67214580-67214581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560140716	chr13:67214620-67214621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532443997	chr13:67214638-67214639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs369467111	chr13:67214648-67214649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568879241	chr13:67214661-67214662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138247532	chr13:67214663-67214664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs55758444	chr13:67214688-67214689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10579281	chr13:67214692-67214693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531282522	chr13:67214723-67214724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs547918285	chr13:67214743-67214744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369479118	chr13:67214752-67214753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570934274	chr13:67214753-67214754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Myelofibrosis	22110671	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4716 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67210000-67213000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:67210000-67213200	Weak transcription	Brain Anterior Caudate	brain
3	chr13:67210000-67214600	Weak transcription	Brain Substantia Nigra	brain
4	chr13:67211200-67213400	Weak transcription	Brain Hippocampus Middle	brain
5	chr13:67212400-67213000	Enhancers	Brain Germinal Matrix	brain
6	chr13:67212400-67215000	Enhancers	Fetal Kidney	kidney
7	chr13:67212800-67213200	Enhancers	Fetal Brain Female	brain
8	chr13:67212800-67213400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr13:67212800-67213400	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr13:67212800-67213600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr13:67212800-67213600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr13:67213000-67213400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr13:67213000-67213600	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr13:67213200-67213600	Enhancers	Brain Anterior Caudate	brain
15	chr13:67213200-67214200	Enhancers	Primary B cells from peripheral blood	blood
16	chr13:67213400-67213600	Enhancers	Brain Hippocampus Middle	brain
17	chr13:67213400-67214200	Enhancers	Primary B cells from cord blood	blood
18	chr13:67213600-67218600	Weak transcription	Brain Hippocampus Middle	brain
19	chr13:67214200-67217600	Weak transcription	Primary B cells from cord blood	blood
20	chr13:67214200-67219000	Weak transcription	Primary B cells from peripheral blood	blood
21	chr13:67214600-67214800	Enhancers	Brain Substantia Nigra	brain
22	chr13:67214800-67215200	Weak transcription	Brain Substantia Nigra	brain
23	chr13:67215200-67215800	Enhancers	Brain Substantia Nigra	brain
24	chr13:67215800-67221200	Weak transcription	Brain Substantia Nigra	brain
25	chr13:67217600-67218400	Enhancers	Primary B cells from cord blood	blood
26	chr13:67218000-67218800	Enhancers	Primary hematopoietic stem cells	blood
27	chr13:67218400-67218800	Flanking Active TSS	Primary B cells from cord blood	blood
28	chr13:67218400-67218800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr13:67218400-67218800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr13:67218600-67218800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr13:67218600-67218800	Enhancers	Brain Hippocampus Middle	brain
32	chr13:67218800-67219000	Active TSS	Primary B cells from cord blood	blood
33	chr13:67218800-67219200	Weak transcription	Brain Hippocampus Middle	brain
34	chr13:67219000-67219200	Flanking Active TSS	Primary B cells from cord blood	blood
35	chr13:67219000-67220200	Enhancers	Primary B cells from peripheral blood	blood
36	chr13:67219200-67219400	Active TSS	Primary B cells from cord blood	blood
37	chr13:67219200-67219400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr13:67219200-67219400	Enhancers	Brain Hippocampus Middle	brain
39	chr13:67219400-67219600	Flanking Active TSS	Primary B cells from cord blood	blood
40	chr13:67219400-67221000	Weak transcription	Brain Hippocampus Middle	brain
41	chr13:67219600-67221400	Enhancers	Primary B cells from cord blood	blood
42	chr13:67220200-67221000	Weak transcription	Primary B cells from peripheral blood	blood
43	chr13:67221000-67221200	Enhancers	Brain Hippocampus Middle	brain
44	chr13:67221000-67221200	Enhancers	Left Ventricle	heart
45	chr13:67221000-67221400	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr13:67221000-67221600	Enhancers	Primary B cells from peripheral blood	blood
47	chr13:67221200-67222600	Weak transcription	Brain Hippocampus Middle	brain
48	chr13:67221200-67222600	Enhancers	Brain Substantia Nigra	brain
49	chr13:67221200-67222600	Weak transcription	Left Ventricle	heart
50	chr13:67222600-67222800	Enhancers	Brain Hippocampus Middle	brain

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