Variant report

Variant	nsv1017848
Chromosome Location	chr8:125432689-125489052
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2887)
CpG islands
(count:1527)
Chromatin interactive
region (count:187)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2887 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:125437620-125437841	K562	blood:	n/a	n/a
2	ARID3A	chr8:125451694-125452062	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:125488411-125488801	K562	blood:	n/a	n/a
4	ARID3A	chr8:125462417-125463181	K562	blood:	n/a	n/a
5	ARID3A	chr8:125486544-125487076	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:125437570-125437880	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:125452679-125452981	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:125452790-125453038	K562	blood:	n/a	n/a
9	ARID3A	chr8:125485691-125487043	K562	blood:	n/a	n/a
10	ARID3A	chr8:125484663-125484958	K562	blood:	n/a	n/a
11	ARID3A	chr8:125438305-125438526	HepG2	liver:	n/a	n/a
12	ARID3A	chr8:125470160-125470597	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:125488459-125488731	HepG2	liver:	n/a	n/a
14	ATF1	chr8:125462828-125463257	K562	blood:	n/a	n/a
15	ATF1	chr8:125484585-125484904	K562	blood:	n/a	n/a
16	ATF1	chr8:125488439-125488775	K562	blood:	n/a	n/a
17	ATF1	chr8:125486051-125487154	K562	blood:	n/a	n/a
18	ATF1	chr8:125462451-125462605	K562	blood:	n/a	n/a
19	ATF2	chr8:125462524-125463192	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr8:125486509-125487233	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr8:125487307-125487856	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr8:125486441-125487160	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr8:125487288-125487807	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr8:125462439-125463281	GM12878	blood:	n/a	n/a
25	ATF2	chr8:125486522-125487295	GM12878	blood:	n/a	n/a
26	ATF2	chr8:125486246-125487170	GM12878	blood:	n/a	n/a
27	ATF2	chr8:125462613-125463363	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr8:125487921-125488737	GM12878	blood:	n/a	n/a
29	ATF2	chr8:125462543-125463201	GM12878	blood:	n/a	n/a
30	ATF3	chr8:125459420-125459781	K562	blood:	n/a	n/a
31	ATF3	chr8:125486592-125487067	GM12878	blood:	n/a	n/a
32	ATF3	chr8:125486613-125487196	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF3	chr8:125486754-125487048	GM12878	blood:	n/a	n/a
34	ATF3	chr8:125486636-125487056	K562	blood:	n/a	n/a
35	ATF3	chr8:125486719-125487082	K562	blood:	n/a	n/a
36	ATF3	chr8:125486656-125487119	K562	blood:	n/a	n/a
37	ATF3	chr8:125486586-125487061	HepG2	liver:	n/a	n/a
38	ATF3	chr8:125486734-125487076	HepG2	liver:	n/a	n/a
39	ATF3	chr8:125486437-125487242	A549	lung:	n/a	n/a
40	ATF3	chr8:125486437-125487113	A549	lung:	n/a	n/a
41	ATF3	chr8:125462708-125463301	A549	lung:	n/a	n/a
42	ATF3	chr8:125486683-125487142	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr8:125485740-125485771	K562	blood:	n/a	n/a
44	BACH1	chr8:125486692-125487002	K562	blood:	n/a	n/a
45	BACH1	chr8:125463878-125463971	H1-hESC	embryonic stem cell:	n/a	n/a
46	BATF	chr8:125438311-125438642	GM12878	blood:	n/a	n/a
47	BATF	chr8:125486769-125487066	GM12878	blood:	n/a	chr8:125486892-125486905
48	BCL11A	chr8:125486682-125487036	GM12878	blood:	n/a	n/a
49	BCL3	chr8:125462438-125463291	A549	lung:	n/a	n/a
50	BCL3	chr8:125486208-125487306	A549	lung:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:125487571-125487621	SK-N-SH_RA	brain:	n/a
2	chr8:125486969-125487019	SKMC	muscle:	n/a
3	chr8:125487571-125487621	SK-N-SH_RA	brain:	n/a
4	chr8:125486969-125487019	SKMC	muscle:	n/a
5	chr8:125463310-125463360	HIPEpiC	eye:	n/a
6	chr8:125463007-125463057	HUVEC	blood vessel:	n/a
7	chr8:125463024-125463074	BE2_C	brain:	n/a
8	chr8:125463066-125463116	HL-60	blood:	n/a
9	chr8:125487055-125487105	AG09309	skin:	n/a
10	chr8:125437986-125438036	HUVEC	blood vessel:	n/a
11	chr8:125486969-125487019	HEEpiC	esophagus:	n/a
12	chr8:125487571-125487621	LNCaP	prostate:	n/a
13	chr8:125463024-125463074	NHDF-neo	bronchial:	n/a
14	chr8:125463057-125463107	Caco-2	colon:	n/a
15	chr8:125483419-125483469	SK-N-SH_RA	brain:	n/a
16	chr8:125486969-125487019	ECC-1	luminal epithelium:	n/a
17	chr8:125487057-125487107	PFSK-1	brain:	n/a
18	chr8:125486958-125487008	HRE	kidney:	n/a
19	chr8:125485867-125485917	HIPEpiC	eye:	n/a
20	chr8:125463024-125463074	HRE	kidney:	n/a
21	chr8:125486969-125487019	GM06990	blood:	n/a
22	chr8:125487804-125487854	AG04450	lung:	fetal
23	chr8:125483419-125483469	IMR90	lung:	fetal
24	chr8:125486752-125486802	CMK	blood:	n/a
25	chr8:125462982-125463032	HMEC	breast:	n/a
26	chr8:125483419-125483469	A549	lung:	n/a
27	chr8:125487571-125487621	GM12878	blood:	n/a
28	chr8:125463024-125463074	H1-hESC	embryonic stem cell:	embryo
29	chr8:125487804-125487854	HEK293	kidney:	embryo
30	chr8:125486969-125487019	HAEpiC	amniotic membrane:	n/a
31	chr8:125463682-125463732	Jurkat	blood:	n/a
32	chr8:125487804-125487854	Hela-S3	cervix:	n/a
33	chr8:125487804-125487854	HL-60	blood:	n/a
34	chr8:125463007-125463057	H1-hESC	embryonic stem cell:	embryo
35	chr8:125463024-125463074	HEK293	kidney:	embryo
36	chr8:125464547-125464597	RPTEC	kidney:	n/a
37	chr8:125463682-125463732	HRE	kidney:	n/a
38	chr8:125486635-125486685	HIPEpiC	eye:	n/a
39	chr8:125461772-125461822	T-47D	breast:	n/a
40	chr8:125463310-125463360	Caco-2	colon:	n/a
41	chr8:125486635-125486685	HCF	heart:	n/a
42	chr8:125486635-125486685	A549	lung:	n/a
43	chr8:125463310-125463360	AG10803	skin:	n/a
44	chr8:125463007-125463057	GM12891	blood:	n/a
45	chr8:125461772-125461822	SK-N-MC	brain:	n/a
46	chr8:125463682-125463732	HCF	heart:	n/a
47	chr8:125463024-125463074	HCF	heart:	n/a
48	chr8:125487621-125487671	PrEC	prostate:	n/a
49	chr8:125462982-125463032	Jurkat	blood:	n/a
50	chr8:125483419-125483469	AG09309	skin:	n/a

(count:187 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:125384250..125385886-chr8:125448852..125451657,2	K562	blood:
2	chr8:125484053..125491713-chr8:125548138..125554442,21	K562	blood:
3	chr3:51428671..51429493-chr8:125486419..125487202,2	HCT-116	colon:
4	chr17:59494136..59494666-chr8:125440074..125440966,2	MCF-7	breast:
5	chr8:125054722..125055473-chr8:125437734..125438246,2	MCF-7	breast:
6	chr8:125459763..125466513-chr8:125482159..125488968,22	K562	blood:
7	chr8:125484651..125486969-chr8:125535041..125537083,3	K562	blood:
8	chr3:101292430..101293477-chr8:125486635..125487650,3	Hela-S3	cervix:
9	chr8:125452770..125454591-chr8:125454611..125457488,3	K562	blood:
10	chr8:125459763..125466594-chr8:125480347..125488760,16	K562	blood:
11	chr8:125486165..125488789-chr8:125574025..125577553,3	MCF-7	breast:
12	chr1:11969658..11970500-chr8:125484907..125485513,2	NB4	blood:
13	chr8:125021959..125022557-chr8:125452409..125453053,2	MCF-7	breast:
14	chr8:125485755..125491202-chr8:125535208..125540184,8	MCF-7	breast:
15	chr14:104181470..104182117-chr8:125486026..125486841,2	Hela-S3	cervix:
16	chr8:125482257..125483957-chr8:125549259..125552139,2	K562	blood:
17	chr8:125278702..125279580-chr8:125437290..125438183,3	MCF-7	breast:
18	chr8:124778252..124779083-chr8:125452719..125453285,3	K562	blood:
19	chr8:125459763..125466594-chr8:125480347..125488760,16	K562	blood:
20	chr8:125482929..125485167-chr8:125485266..125487071,3	K562	blood:
21	chr8:125192121..125193144-chr8:125437972..125438769,3	MCF-7	breast:
22	chr8:125458816..125460797-chr8:125549847..125552574,2	MCF-7	breast:
23	chr17:76124280..76124817-chr8:125487166..125487761,2	Hela-S3	cervix:
24	chr21:9826427..9827287-chr8:125452361..125452923,2	MCF-7	breast:
25	chr8:125439253..125441012-chr8:125451870..125454314,2	K562	blood:
26	chr8:125429633..125432443-chr8:125437672..125439432,2	MCF-7	breast:
27	chr2:74698915..74699913-chr8:125486835..125487478,2	HCT-116	colon:
28	chr8:125487104..125489610-chr8:126009410..126011098,2	MCF-7	breast:
29	chr8:124780203..124782917-chr8:125454710..125456324,2	MCF-7	breast:
30	chr8:124792624..124795520-chr8:125459150..125461003,2	K562	blood:
31	chr8:124936640..124937564-chr8:125437980..125438905,3	MCF-7	breast:
32	chr8:125473161..125475978-chr8:125476087..125479372,4	K562	blood:
33	chr8:125049717..125050652-chr8:125437138..125438607,13	MCF-7	breast:
34	chr8:125383681..125384360-chr8:125437557..125438176,2	MCF-7	breast:
35	chr8:125446803..125447573-chr8:125509427..125510023,2	K562	blood:
36	chr18:12376498..12377198-chr8:125486489..125487241,2	Hela-S3	cervix:
37	chr8:125469399..125471689-chr8:125474685..125476305,2	K562	blood:
38	chr8:125438096..125438907-chr8:125451772..125452727,2	MCF-7	breast:
39	chr8:125476479..125477099-chr8:125550802..125551586,2	MCF-7	breast:
40	chr8:125456155..125458646-chr8:125470244..125472262,2	K562	blood:
41	chr10:76993820..76995624-chr8:125485040..125487047,2	MCF-7	breast:
42	chr8:125209307..125211794-chr8:125460227..125463007,2	K562	blood:
43	chr11:73471597..73472536-chr8:125486504..125487013,2	Hela-S3	cervix:
44	chr8:124835781..124838013-chr8:125487018..125488590,2	MCF-7	breast:
45	chr8:124778748..124781385-chr8:125452203..125454645,3	MCF-7	breast:
46	chr20:52521882..52524435-chr8:125467415..125469932,2	MCF-7	breast:
47	chr8:125389312..125391092-chr8:125434366..125436156,2	MCF-7	breast:
48	chr4:2964631..2965442-chr8:125486338..125486843,2	Hela-S3	cervix:
49	chr8:125465079..125467073-chr8:125471633..125474192,2	K562	blood:
50	chr8:125476504..125477354-chr8:125503331..125504125,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TATDN1-1	chr8:125484548-125487007	NONHSAT128586
2	lnc-TATDN1-1	chr8:125474738-125479899	NR_108047
3	lnc-TATDN1-1	chr8:125485051-125486817	ENSG00000245149
4	lnc-TATDN1-1	chr8:125485925-125486133	NONHSAT128584
5	lnc-TATDN1-1	chr8:125486139-125486268	NONHSAT128584
6	lnc-TATDN1-1	chr8:125486527-125486595	ENSG00000245149
7	lnc-TATDN1-1	chr8:125472840-125472996	NONHSAT128584
8	lnc-TATDN1-1	chr8:125486326-125486805	ENSG00000245149
9	lnc-TATDN1-1	chr8:125474726-125479899	ENSG00000245149
10	lnc-TATDN1-1	chr8:125477041-125477893	NONHSAT128584
11	lnc-TATDN1-1	chr8:125485049-125485228	ENSG00000245149
12	lnc-TATDN1-1	chr8:125486326-125486804	XLOC_007206
13	lnc-TATDN1-1	chr8:125474740-125479899	XLOC_007206
14	lnc-TATDN1-1	chr8:125485343-125485819	NONHSAT128584
15	lnc-TATDN1-1	chr8:125486326-125486435	ENSG00000245149
16	lnc-TATDN1-1	chr8:125479460-125479899	NONHSAT128584
17	lnc-TATDN1-1	chr8:125486326-125486804	NR_108047

No data

Variant related genes	Relation type
TRMT12	TF binding region
RNF139	TF binding region
RNF139-AS1	TF binding region
TRMT12	CpG island
RNF139	CpG island
RNF139-AS1	CpG island
ENSG00000204822	chromatin interactions
ENSG00000126215	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000110321	chromatin interactions
ENSG00000254249	chromatin interactions
ENSG00000257084	chromatin interactions
ENSG00000141524	chromatin interactions
ENSG00000147687	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000165644	chromatin interactions
ENSG00000183665	chromatin interactions
ENSG00000100908	chromatin interactions
ENSG00000133612	chromatin interactions
ENSG00000117139	chromatin interactions
ENSG00000087269	chromatin interactions
ENSG00000176853	chromatin interactions
ENSG00000198081	chromatin interactions
ENSG00000256034	chromatin interactions
ENSG00000178193	chromatin interactions
ENSG00000067066	chromatin interactions
ENSG00000245149	chromatin interactions
ENSG00000104341	chromatin interactions
ENSG00000164983	chromatin interactions
ENSG00000155287	chromatin interactions
ENSG00000081154	chromatin interactions
ENSG00000170881	chromatin interactions
ENSG00000120129	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000163399	chromatin interactions
ENSG00000246308	chromatin interactions
ENSG00000270021	chromatin interactions
ENSG00000201801	chromatin interactions
ENSG00000100711	chromatin interactions
ENSG00000179837	chromatin interactions
ENSG00000137203	chromatin interactions
ENSG00000181171	chromatin interactions
ENSG00000177352	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000141385	chromatin interactions
ENSG00000207713	chromatin interactions
ENSG00000206652	chromatin interactions
ENSG00000104549	chromatin interactions
ENSG00000125388	chromatin interactions
ENSG00000123136	chromatin interactions
ENSG00000122034	chromatin interactions
ENSG00000113648	chromatin interactions
ENSG00000175582	chromatin interactions
ENSG00000158710	chromatin interactions
ENSG00000156802	chromatin interactions
ENSG00000117054	chromatin interactions
ENSG00000147684	chromatin interactions
ENSG00000253513	chromatin interactions
ENSG00000170873	chromatin interactions
ENSG00000126749	chromatin interactions
ENSG00000196923	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000237190	chromatin interactions
ENSG00000207708	chromatin interactions
ENSG00000185950	chromatin interactions

Extended variants
information (count: 1916 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:1916 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575787528	chr8:125432694-125432695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs544516840	chr8:125432695-125432696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567412042	chr8:125432705-125432706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79097409	chr8:125432751-125432752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539809187	chr8:125432769-125432770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10956182	chr8:125432794-125432795	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs72710885	chr8:125432806-125432807	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs77907435	chr8:125432832-125432833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs151303773	chr8:125432835-125432836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78206651	chr8:125432838-125432839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183518906	chr8:125432865-125432866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs67450518	chr8:125432886-125432887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116554371	chr8:125432887-125432888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546973036	chr8:125432895-125432896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12543081	chr8:125432900-125432901	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs188165412	chr8:125432939-125432940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555885443	chr8:125432961-125432962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544941841	chr8:125433011-125433012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201643278	chr8:125433117-125433118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150312920	chr8:125433130-125433131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11396136	chr8:125433134-125433135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536158713	chr8:125433135-125433136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199926633	chr8:125433136-125433137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538406932	chr8:125433184-125433185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558085395	chr8:125433199-125433200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs578167493	chr8:125433206-125433207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181748883	chr8:125433235-125433236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554089937	chr8:125433241-125433242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113008112	chr8:125433242-125433243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200378491	chr8:125433295-125433296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564743047	chr8:125433319-125433320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542248768	chr8:125433320-125433321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189326729	chr8:125433323-125433324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531809104	chr8:125433341-125433342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564734208	chr8:125433355-125433356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs60121570	chr8:125433372-125433373	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs545152123	chr8:125433393-125433394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564939192	chr8:125433396-125433397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527535310	chr8:125433411-125433412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547707007	chr8:125433418-125433419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187634334	chr8:125433474-125433475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529286157	chr8:125433477-125433478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs578115992	chr8:125433485-125433486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569300460	chr8:125433530-125433531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6982205	chr8:125433536-125433537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551905972	chr8:125433538-125433539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7002164	chr8:125433558-125433559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs534162951	chr8:125433559-125433560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6982217	chr8:125433565-125433566	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs574022106	chr8:125433582-125433583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:2120 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125427200-125433800	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr8:125430600-125437800	Weak transcription	Left Ventricle	heart
3	chr8:125431000-125434400	Weak transcription	Fetal Heart	heart
4	chr8:125433800-125435400	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr8:125434200-125435400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr8:125434400-125435000	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr8:125434400-125435000	Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr8:125434400-125435200	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr8:125434400-125435200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr8:125434400-125435200	Enhancers	Fetal Heart	heart
11	chr8:125434400-125438000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:125434600-125434800	Enhancers	Brain Germinal Matrix	brain
13	chr8:125434600-125435000	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr8:125434600-125435000	Enhancers	Placenta	Placenta
15	chr8:125434600-125435000	Enhancers	Spleen	Spleen
16	chr8:125434600-125435000	Enhancers	HUVEC	blood vessel
17	chr8:125434600-125435000	Enhancers	K562	blood
18	chr8:125434600-125435000	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr8:125434600-125435200	Enhancers	Primary hematopoietic stem cells	blood
20	chr8:125434800-125435000	Enhancers	Fetal Intestine Small	intestine
21	chr8:125434800-125435000	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr8:125434800-125435200	Enhancers	Fetal Brain Female	brain
23	chr8:125434800-125435400	Enhancers	Fetal Brain Male	brain
24	chr8:125434800-125437600	Weak transcription	Brain Germinal Matrix	brain
25	chr8:125434800-125437800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:125435000-125437600	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr8:125435000-125437600	Weak transcription	Placenta	Placenta
28	chr8:125435000-125437600	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr8:125435000-125437600	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr8:125435000-125437800	Weak transcription	Fetal Intestine Small	intestine
31	chr8:125435000-125437800	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr8:125435000-125437800	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr8:125435000-125437800	Weak transcription	Spleen	Spleen
34	chr8:125435000-125437800	Weak transcription	HUVEC	blood vessel
35	chr8:125435000-125437800	Weak transcription	K562	blood
36	chr8:125435200-125437600	Weak transcription	Primary hematopoietic stem cells	blood
37	chr8:125435200-125437600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr8:125435200-125437600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr8:125435200-125437600	Weak transcription	Fetal Brain Female	brain
40	chr8:125435200-125437800	Weak transcription	Fetal Heart	heart
41	chr8:125435400-125436400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr8:125435400-125437400	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr8:125435400-125437600	Weak transcription	Fetal Brain Male	brain
44	chr8:125436400-125437600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr8:125436600-125436800	Enhancers	HSMM	muscle
46	chr8:125437400-125437600	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr8:125437400-125437600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr8:125437400-125437600	Enhancers	Brain Anterior Caudate	brain
49	chr8:125437400-125437600	Enhancers	Brain Hippocampus Middle	brain
50	chr8:125437400-125437600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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