Variant report

Variant	nsv832037
Chromosome Location	chr1:184568194-184756597
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2191)
CpG islands
(count:1834)
Chromatin interactive
region (count:204)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:11)

(count:2191 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:184718108-184718302	K562	blood:	n/a	n/a
2	ARID3A	chr1:184723938-184725344	K562	blood:	n/a	n/a
3	ARID3A	chr1:184737630-184739782	K562	blood:	n/a	n/a
4	ARID3A	chr1:184740473-184740968	K562	blood:	n/a	n/a
5	ARID3A	chr1:184721699-184722664	K562	blood:	n/a	chr1:184721783-184721799 chr1:184721784-184721800
6	ARID3A	chr1:184721296-184721489	K562	blood:	n/a	n/a
7	ARID3A	chr1:184714297-184714467	K562	blood:	n/a	n/a
8	ARID3A	chr1:184712126-184712865	K562	blood:	n/a	n/a
9	ARID3A	chr1:184723522-184723679	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:184708580-184708874	K562	blood:	n/a	n/a
11	ARID3A	chr1:184723889-184725086	HepG2	liver:	n/a	chr1:184723910-184723918
12	ATF1	chr1:184723843-184725135	K562	blood:	n/a	n/a
13	ATF1	chr1:184737464-184737981	K562	blood:	n/a	n/a
14	ATF1	chr1:184739337-184739522	K562	blood:	n/a	n/a
15	ATF1	chr1:184742950-184743150	K562	blood:	n/a	n/a
16	ATF1	chr1:184740409-184740766	K562	blood:	n/a	n/a
17	ATF1	chr1:184580147-184580260	K562	blood:	n/a	n/a
18	ATF2	chr1:184712054-184712786	GM12878	blood:	n/a	n/a
19	ATF2	chr1:184716336-184716838	GM12878	blood:	n/a	n/a
20	ATF2	chr1:184723276-184724356	GM12878	blood:	n/a	n/a
21	ATF2	chr1:184618433-184619029	GM12878	blood:	n/a	n/a
22	ATF2	chr1:184712195-184712647	GM12878	blood:	n/a	n/a
23	BACH1	chr1:184639138-184639144	K562	blood:	n/a	n/a
24	BACH1	chr1:184723587-184723615	K562	blood:	n/a	n/a
25	BACH1	chr1:184711303-184711349	K562	blood:	n/a	n/a
26	BACH1	chr1:184723063-184723968	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr1:184741549-184741574	K562	blood:	n/a	n/a
28	BACH1	chr1:184738191-184738229	K562	blood:	n/a	n/a
29	BATF	chr1:184618613-184618874	GM12878	blood:	n/a	chr1:184618710-184618721 chr1:184618711-184618721
30	BATF	chr1:184677461-184677889	GM12878	blood:	n/a	n/a
31	BATF	chr1:184618520-184618852	GM12878	blood:	n/a	chr1:184618710-184618721 chr1:184618711-184618721
32	BATF	chr1:184712268-184712529	GM12878	blood:	n/a	chr1:184712498-184712508 chr1:184712502-184712512
33	BCL11A	chr1:184712274-184712562	GM12878	blood:	n/a	n/a
34	BCL3	chr1:184723671-184724389	GM12878	blood:	n/a	chr1:184724141-184724150
35	BCLAF1	chr1:184716228-184716855	GM12878	blood:	n/a	n/a
36	BCLAF1	chr1:184723711-184724746	GM12878	blood:	n/a	chr1:184724561-184724570 chr1:184724141-184724150
37	BCLAF1	chr1:184712079-184712626	GM12878	blood:	n/a	n/a
38	BCLAF1	chr1:184723483-184724570	GM12878	blood:	n/a	chr1:184724561-184724570 chr1:184724141-184724150
39	BHLHE40	chr1:184580067-184580381	K562	blood:	n/a	n/a
40	BHLHE40	chr1:184723187-184723518	GM12878	blood:	n/a	n/a
41	BHLHE40	chr1:184580132-184580359	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:184633186-184633331	GM12878	blood:	n/a	chr1:184633273-184633289
43	BHLHE40	chr1:184618640-184618700	GM12878	blood:	n/a	n/a
44	BHLHE40	chr1:184723223-184724627	HepG2	liver:	n/a	n/a
45	BHLHE40	chr1:184742911-184743296	K562	blood:	n/a	n/a
46	BHLHE40	chr1:184654259-184654484	GM12878	blood:	n/a	n/a
47	BHLHE40	chr1:184740351-184740561	K562	blood:	n/a	n/a
48	BHLHE40	chr1:184633138-184633382	K562	blood:	n/a	chr1:184633273-184633289
49	BHLHE40	chr1:184723112-184725155	K562	blood:	n/a	n/a
50	BHLHE40	chr1:184712199-184712666	GM12878	blood:	n/a	n/a

(count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:184662234-184662284	HEEpiC	esophagus:	n/a
2	chr1:184721222-184721272	ProgFib	skin:	n/a
3	chr1:184724631-184724681	HEK293	kidney:	embryo
4	chr1:184723906-184723956	Jurkat	blood:	n/a
5	chr1:184662234-184662284	HEEpiC	esophagus:	n/a
6	chr1:184721222-184721272	ProgFib	skin:	n/a
7	chr1:184724631-184724681	HEK293	kidney:	embryo
8	chr1:184723906-184723956	Jurkat	blood:	n/a
9	chr1:184721222-184721272	NH-A	brain:	n/a
10	chr1:184723906-184723956	Hela-S3	cervix:	n/a
11	chr1:184724195-184724245	T-47D	breast:	n/a
12	chr1:184723951-184724001	HCPEpiC	choroid plexus:	n/a
13	chr1:184634036-184634086	GM06990	blood:	n/a
14	chr1:184724775-184724825	Caco-2	colon:	n/a
15	chr1:184715203-184715253	HAEpiC	amniotic membrane:	n/a
16	chr1:184633847-184633897	GM12891	blood:	n/a
17	chr1:184724775-184724825	K562	blood:	n/a
18	chr1:184662234-184662284	SK-N-SH	brain:	n/a
19	chr1:184724631-184724681	HepG2	liver:	n/a
20	chr1:184723951-184724001	AoSMC	blood vessel:	n/a
21	chr1:184633523-184633573	GM12892	blood:	n/a
22	chr1:184654165-184654215	BE2_C	brain:	n/a
23	chr1:184662234-184662284	Caco-2	colon:	n/a
24	chr1:184616329-184616379	A549	lung:	n/a
25	chr1:184633572-184633622	HCM	heart:	n/a
26	chr1:184633039-184633089	SK-N-SH	brain:	n/a
27	chr1:184723906-184723956	LNCaP	prostate:	n/a
28	chr1:184723524-184723574	HEEpiC	esophagus:	n/a
29	chr1:184724736-184724786	HMEC	breast:	n/a
30	chr1:184598594-184598644	NHDF-neo	bronchial:	n/a
31	chr1:184633039-184633089	HRE	kidney:	n/a
32	chr1:184616329-184616379	HepG2	liver:	n/a
33	chr1:184633847-184633897	AG04449	skin:	fetal
34	chr1:184723524-184723574	ECC-1	luminal epithelium:	n/a
35	chr1:184724631-184724681	NH-A	brain:	n/a
36	chr1:184633572-184633622	HUVEC	blood vessel:	n/a
37	chr1:184724800-184724850	HCF	heart:	n/a
38	chr1:184633523-184633573	MCF-7	breast:	n/a
39	chr1:184633273-184633323	PrEC	prostate:	n/a
40	chr1:184654165-184654215	HIPEpiC	eye:	n/a
41	chr1:184724800-184724850	K562	blood:	n/a
42	chr1:184723906-184723956	HL-60	blood:	n/a
43	chr1:184724631-184724681	HIPEpiC	eye:	n/a
44	chr1:184633273-184633323	Jurkat	blood:	n/a
45	chr1:184722970-184723020	HAEpiC	amniotic membrane:	n/a
46	chr1:184724388-184724438	U87	brain:	n/a
47	chr1:184641175-184641225	GM19239	blood:	n/a
48	chr1:184715203-184715253	HL-60	blood:	n/a
49	chr1:184723253-184723303	PFSK-1	brain:	n/a
50	chr1:184723524-184723574	PrEC	prostate:	n/a

(count:204 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr1:184580848..184583559-chr1:184594169..184597015,2	MCF-7	breast:
2	chr1:184673163..184675215-chr1:184695509..184697119,2	K562	blood:
3	chr1:184703854..184706366-chr1:184709752..184714206,4	K562	blood:
4	chr1:184707417..184709159-chr1:184712217..184714987,3	MCF-7	breast:
5	chr1:184613842..184615528-chr1:184617217..184618948,2	MCF-7	breast:
6	chr1:184573829..184575413-chr1:184578962..184580470,2	MCF-7	breast:
7	chr1:184605092..184607430-chr1:184608808..184610449,2	MCF-7	breast:
8	chr1:28831842..28832710-chr1:184723609..184724521,2	HCT-116	colon:
9	chr1:184681652..184683327-chr1:184949938..184952588,2	K562	blood:
10	chr1:184602139..184603898-chr17:57922496..57924162,2	MCF-7	breast:
11	chr1:184721401..184724315-chr1:184750771..184753282,3	K562	blood:
12	chr1:184700886..184703045-chr1:184708042..184709740,3	K562	blood:
13	chr1:184707417..184709159-chr1:184712217..184714987,3	MCF-7	breast:
14	chr1:184595855..184598931-chr1:184605508..184607778,3	K562	blood:
15	chr1:184675990..184678598-chr1:184680103..184682341,2	K562	blood:
16	chr1:184722694..184725691-chr1:184732009..184735000,2	MCF-7	breast:
17	chr1:184725745..184728657-chr1:184756568..184759148,2	MCF-7	breast:
18	chr1:184706332..184708758-chr1:184714030..184715698,2	K562	blood:
19	chr1:184595979..184598591-chr1:184630812..184634151,3	MCF-7	breast:
20	chr1:184591640..184593631-chr1:184596636..184598528,2	K562	blood:
21	chr1:184700886..184703045-chr1:184708042..184709740,3	K562	blood:
22	chr1:184581306..184582992-chr1:184601033..184602907,2	MCF-7	breast:
23	chr1:184684929..184687575-chr1:184691047..184693770,2	K562	blood:
24	chr1:183955480..183958472-chr1:184655445..184658160,2	K562	blood:
25	chr1:184709738..184712321-chr1:184713250..184716697,3	K562	blood:
26	chr1:184570974..184573914-chr1:184574295..184577206,3	MCF-7	breast:
27	chr1:184355848..184357753-chr1:184661585..184663546,2	MCF-7	breast:
28	chr1:184738281..184740809-chr1:184942127..184944338,2	K562	blood:
29	chr1:184641175..184643659-chr1:184651481..184653037,2	MCF-7	breast:
30	chr1:184691316..184693435-chr1:184696792..184698671,2	K562	blood:
31	chr1:184702362..184703932-chr1:184704085..184706758,2	K562	blood:
32	chr1:184688642..184690448-chr1:184695282..184698252,2	K562	blood:
33	chr1:184725745..184728657-chr1:184756568..184759148,2	MCF-7	breast:
34	chr1:184692034..184695028-chr1:184695067..184697135,2	K562	blood:
35	chr1:184722046..184724182-chr1:184741436..184743327,3	K562	blood:
36	chr1:184687987..184690948-chr1:184692371..184695173,3	K562	blood:
37	chr1:184731513..184734205-chr1:184752298..184754564,2	MCF-7	breast:
38	chr1:184670636..184673038-chr1:184723688..184726485,2	MCF-7	breast:
39	chr1:184754385..184756569-chr1:184766259..184767996,2	K562	blood:
40	chr1:184595699..184596315-chr1:184604140..184605096,2	MCF-7	breast:
41	chr1:184742694..184744938-chr1:184747222..184748918,2	MCF-7	breast:
42	chr1:184610419..184613412-chr1:184629459..184632397,2	MCF-7	breast:
43	chr1:184637359..184638932-chr1:184640228..184642032,2	K562	blood:
44	chr1:184595300..184598106-chr1:184610588..184612513,2	K562	blood:
45	chr1:184722946..184726170-chr1:184728619..184730766,3	MCF-7	breast:
46	chr1:184683246..184684894-chr1:185126908..185129341,2	K562	blood:
47	chr1:184595300..184598106-chr1:184610588..184612513,2	K562	blood:
48	chr1:184744382..184746292-chr1:184746582..184749303,2	K562	blood:
49	chr1:184708496..184710858-chr1:184733789..184736072,2	K562	blood:
50	chr1:184591640..184593631-chr1:184596636..184598528,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EDEM3-2	chr1:184618284-184618516	XLOC_001124
2	lnc-C1orf21-3	chr1:184746600-184746633	XLOC_000493
3	lnc-EDEM3-3	chr1:184632551-184633736	NONHSAT008391
4	lnc-C1orf21-3	chr1:184748361-184748797	XLOC_000493
5	lnc-EDEM3-1	chr1:184638176-184638544	XLOC_001125
6	lnc-C1orf21-1	chr1:184633030-184633562	NONHSAT008394
7	lnc-C1orf21-1	chr1:184634403-184634810	XLOC_000492
8	lnc-EDEM3-3	chr1:184614119-184614158	NONHSAT008391
9	lnc-C1orf21-6	chr1:184726198-184726468	NONHSAT008398
10	lnc-C1orf21-7	chr1:184727266-184730133	NONHSAT008399
11	lnc-C1orf21-5	chr1:184659060-184659280	NONHSAT008397
12	lnc-C1orf21-1	chr1:184642494-184642635	NONHSAT008394
13	lnc-C1orf21-1	chr1:184632075-184633562	XLOC_000492
14	lnc-EDEM3-1	chr1:184641163-184641354	XLOC_001125
15	lnc-EDEM3-2	chr1:184622320-184622348	XLOC_001124

No data

(count:11 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	EDEM3	hsa-miR-142-3p	chr1:184659808-184659802
2	C1orf21	hsa-miR-186-5p	chr1:184597918-184597924
3	C1orf21	hsa-miR-7-5p	chr1:184590774-184590780
4	EDEM3	hsa-miR-155-5p	chr1:184662356-184662381
5	EDEM3	hsa-let-7b-5p	chr1:184660659-184660652
6	C1orf21	hsa-miR-16-5p	chr1:184588897-184588917
7	EDEM3	hsa-miR-142-3p	chr1:184661971-184661994
8	EDEM3	hsa-miR-142-3p	chr1:184659802-184659825
9	C1orf21	hsa-miR-7-5p	chr1:184590735-184590742
10	C1orf21	hsa-miR-16-5p	chr1:184588910-184588917
11	EDEM3	hsa-let-7b-5p	chr1:184660653-184660675

Variant related genes	Relation type
ENSG00000252790	TF binding region
EDEM3	TF binding region
ENSG00000252790	CpG island
EDEM3	CpG island
ENSG00000271387	chromatin interactions
ENSG00000198860	chromatin interactions
ENSG00000156976	chromatin interactions
ENSG00000121481	chromatin interactions
ENSG00000252790	chromatin interactions
ENSG00000242125	chromatin interactions
ENSG00000135842	chromatin interactions
ENSG00000116668	chromatin interactions
ENSG00000116406	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000116667	chromatin interactions
ENSG00000121486	chromatin interactions
ENSG00000158286	chromatin interactions
BCL2L11	miRNA target sites

Extended variants
information (count: 6732 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:6732 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549544758	chr1:184568270-184568271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190686939	chr1:184568288-184568289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376481138	chr1:184568314-184568315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535375172	chr1:184568319-184568320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139944637	chr1:184568326-184568327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192819712	chr1:184568421-184568422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566704013	chr1:184568434-184568435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557108766	chr1:184568453-184568454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541511631	chr1:184568466-184568467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs207460760	chr1:184568498-184568499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552979512	chr1:184568502-184568503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534322321	chr1:184568535-184568536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559060792	chr1:184568556-184568557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577399403	chr1:184568580-184568581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538467450	chr1:184568594-184568595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185290139	chr1:184568595-184568596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575086727	chr1:184568655-184568656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569259222	chr1:184568668-184568669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12119118	chr1:184568671-184568672	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs147508895	chr1:184568695-184568696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571915630	chr1:184568710-184568711	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545769614	chr1:184568732-184568733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563868638	chr1:184568838-184568839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188661106	chr1:184568875-184568876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543252606	chr1:184568911-184568912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114609153	chr1:184568917-184568918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529188138	chr1:184568951-184568952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563404421	chr1:184568957-184568958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566874112	chr1:184568969-184568970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112698036	chr1:184568988-184568989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140426973	chr1:184569023-184569024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185251470	chr1:184569059-184569060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538303528	chr1:184569086-184569087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530587929	chr1:184569099-184569100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568534305	chr1:184569105-184569106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372385503	chr1:184569124-184569125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34418556	chr1:184569132-184569133	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs188393022	chr1:184569158-184569159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs180990974	chr1:184569159-184569160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545442261	chr1:184569268-184569269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187049265	chr1:184569269-184569270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192336200	chr1:184569272-184569273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573987191	chr1:184569301-184569302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543064615	chr1:184569311-184569312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376452282	chr1:184569315-184569316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183245590	chr1:184569352-184569353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12081808	chr1:184569420-184569421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544413089	chr1:184569517-184569518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190079547	chr1:184569546-184569547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12072648	chr1:184569548-184569549	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Barrett''s syndrome	19417022	CNVD

Chromatin state (count:3727 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:184547800-184580000	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:184557200-184574000	Weak transcription	Fetal Muscle Trunk	muscle
3	chr1:184557200-184591600	Weak transcription	Aorta	Aorta
4	chr1:184558600-184572600	Weak transcription	Lung	lung
5	chr1:184559000-184588400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr1:184559200-184580400	Weak transcription	Adipose Nuclei	Adipose
7	chr1:184559400-184580400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr1:184559600-184578000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr1:184560600-184571400	Weak transcription	Fetal Intestine Large	intestine
10	chr1:184560600-184591000	Weak transcription	Fetal Intestine Small	intestine
11	chr1:184562400-184580000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr1:184562800-184579600	Weak transcription	Stomach Smooth Muscle	stomach
13	chr1:184563000-184573200	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr1:184563800-184573600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr1:184564200-184580200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:184564200-184580200	Weak transcription	Ovary	ovary
17	chr1:184564400-184574200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:184564400-184578200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr1:184565000-184578200	Weak transcription	Esophagus	oesophagus
20	chr1:184565200-184573400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:184565400-184569400	Weak transcription	Brain Germinal Matrix	brain
22	chr1:184565400-184578200	Weak transcription	NH-A	brain
23	chr1:184566400-184573400	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr1:184566600-184569800	Strong transcription	Liver	Liver
25	chr1:184566600-184578000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr1:184566800-184568200	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr1:184566800-184588600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:184567000-184570200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr1:184567000-184571200	Weak transcription	Small Intestine	intestine
30	chr1:184567000-184572400	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr1:184567000-184573400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:184567000-184573800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr1:184567000-184577600	Weak transcription	Right Ventricle	heart
34	chr1:184567000-184580000	Weak transcription	Fetal Kidney	kidney
35	chr1:184567000-184580400	Weak transcription	Psoas Muscle	Psoas
36	chr1:184567200-184569800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr1:184567200-184571200	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr1:184567200-184573000	Weak transcription	Left Ventricle	heart
39	chr1:184567200-184573400	Weak transcription	Fetal Muscle Leg	muscle
40	chr1:184567200-184580400	Weak transcription	Colonic Mucosa	Colon
41	chr1:184567200-184580400	Weak transcription	Right Atrium	heart
42	chr1:184567200-184580400	Weak transcription	NHEK	skin
43	chr1:184567200-184590200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr1:184567400-184573400	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr1:184567400-184573800	Weak transcription	Stomach Mucosa	stomach
46	chr1:184567400-184575600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:184567600-184577400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr1:184567800-184568200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr1:184567800-184568200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr1:184567800-184573400	Weak transcription	Duodenum Mucosa	Duodenum

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