Variant report

Variant	nsv1004338
Chromosome Location	chr1:194143315-194381135
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:935)
CpG islands
(count:61)
Chromatin interactive
region (count:54)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:935 , 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	chr1:194264954-194265127	HepG2	liver:	n/a	n/a
2	ATF1	chr1:194264272-194264437	K562	blood:	n/a	n/a
3	ATF1	chr1:194193801-194193807	K562	blood:	n/a	n/a
4	ATF1	chr1:194343865-194344032	K562	blood:	n/a	n/a
5	ATF1	chr1:194267197-194267479	K562	blood:	n/a	n/a
6	ATF2	chr1:194258660-194259165	GM12878	blood:	n/a	n/a
7	ATF2	chr1:194258580-194259085	GM12878	blood:	n/a	n/a
8	ATF2	chr1:194249054-194249438	GM12878	blood:	n/a	n/a
9	ATF3	chr1:194312059-194312295	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr1:194311963-194312358	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr1:194249125-194249361	GM12878	blood:	n/a	n/a
12	BATF	chr1:194258679-194259064	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:194258667-194259124	GM12878	blood:	n/a	n/a
14	BCL3	chr1:194258709-194259079	GM12878	blood:	n/a	n/a
15	BCL3	chr1:194258639-194259038	GM12878	blood:	n/a	n/a
16	BCLAF1	chr1:194248979-194249416	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:194258602-194259073	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:194195031-194195231	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:194258729-194258996	GM12878	blood:	n/a	n/a
20	CEBPB	chr1:194158508-194158697	HepG2	liver:	n/a	chr1:194158594-194158605
21	CEBPB	chr1:194330573-194330832	K562	blood:	n/a	chr1:194330728-194330739
22	CEBPB	chr1:194380325-194380663	IMR90	lung:	n/a	chr1:194380492-194380501 chr1:194380490-194380501 chr1:194380490-194380503
23	CEBPB	chr1:194330514-194330873	Hela-S3	cervix:	n/a	chr1:194330728-194330739
24	CEBPB	chr1:194143968-194144293	IMR90	lung:	n/a	chr1:194144108-194144117 chr1:194144108-194144117 chr1:194144108-194144117 chr1:194144108-194144119 chr1:194144108-194144117
25	CEBPB	chr1:194143944-194144294	A549	lung:	n/a	chr1:194144108-194144117 chr1:194144108-194144117 chr1:194144108-194144117 chr1:194144108-194144119 chr1:194144108-194144117
26	CEBPB	chr1:194267151-194267568	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:194237780-194238333	IMR90	lung:	n/a	chr1:194238139-194238150
28	CEBPB	chr1:194368814-194369097	A549	lung:	n/a	chr1:194368953-194368964 chr1:194368954-194368965 chr1:194368953-194368966 chr1:194368953-194368966 chr1:194368953-194368966
29	CEBPB	chr1:194380423-194380607	K562	blood:	n/a	chr1:194380492-194380501 chr1:194380490-194380501 chr1:194380490-194380503
30	CEBPB	chr1:194153682-194153783	A549	lung:	n/a	n/a
31	CEBPB	chr1:194368912-194369048	K562	blood:	n/a	chr1:194368953-194368964 chr1:194368954-194368965 chr1:194368953-194368966 chr1:194368953-194368966 chr1:194368953-194368966
32	CEBPB	chr1:194267201-194267460	A549	lung:	n/a	n/a
33	CEBPB	chr1:194267192-194267549	IMR90	lung:	n/a	n/a
34	CEBPB	chr1:194267220-194267531	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr1:194264851-194265147	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr1:194368800-194369138	IMR90	lung:	n/a	chr1:194368953-194368964 chr1:194368954-194368965 chr1:194368953-194368966 chr1:194368953-194368966 chr1:194368953-194368966
37	CEBPB	chr1:194267210-194267527	K562	blood:	n/a	n/a
38	CEBPB	chr1:194380328-194380670	HepG2	liver:	n/a	chr1:194380492-194380501 chr1:194380490-194380501 chr1:194380490-194380503
39	CEBPB	chr1:194368769-194369099	Hela-S3	cervix:	n/a	chr1:194368953-194368964 chr1:194368954-194368965 chr1:194368953-194368966 chr1:194368953-194368966 chr1:194368953-194368966
40	CEBPB	chr1:194330550-194330806	A549	lung:	n/a	chr1:194330728-194330739
41	CEBPB	chr1:194267201-194267495	K562	blood:	n/a	n/a
42	CEBPB	chr1:194237983-194238329	Hela-S3	cervix:	n/a	chr1:194238139-194238150
43	CEBPB	chr1:194330473-194330868	IMR90	lung:	n/a	chr1:194330728-194330739
44	CEBPB	chr1:194267110-194267655	HCT-116	colon:	n/a	n/a
45	CEBPB	chr1:194264750-194265141	MCF-7	breast:	n/a	n/a
46	CEBPB	chr1:194143936-194144216	HepG2	liver:	n/a	chr1:194144108-194144117 chr1:194144108-194144117 chr1:194144108-194144117 chr1:194144108-194144119 chr1:194144108-194144117
47	CEBPB	chr1:194273767-194273838	A549	lung:	n/a	n/a
48	CEBPB	chr1:194267170-194267552	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:194143955-194144186	H1-hESC	embryonic stem cell:	n/a	chr1:194144108-194144117 chr1:194144108-194144117 chr1:194144108-194144117 chr1:194144108-194144119 chr1:194144108-194144117
50	CEBPB	chr1:194355353-194355553	HepG2	liver:	n/a	chr1:194355445-194355456 chr1:194355444-194355457

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:194327715-194327765	HRCEpiC	kidney:	n/a
2	chr1:194327715-194327765	GM12878	blood:	n/a
3	chr1:194327715-194327765	AG09309	skin:	n/a
4	chr1:194327715-194327765	CMK	blood:	n/a
5	chr1:194327715-194327765	SK-N-SH_RA	brain:	n/a
6	chr1:194327715-194327765	NHDF-neo	bronchial:	n/a
7	chr1:194327715-194327765	HRE	kidney:	n/a
8	chr1:194327715-194327765	RPTEC	kidney:	n/a
9	chr1:194327715-194327765	HMEC	breast:	n/a
10	chr1:194327715-194327765	HUVEC	blood vessel:	n/a
11	chr1:194327715-194327765	SKMC	muscle:	n/a
12	chr1:194327715-194327765	HPAEpiC	pulmonary alveolar:	n/a
13	chr1:194327715-194327765	PFSK-1	brain:	n/a
14	chr1:194327715-194327765	K562	blood:	n/a
15	chr1:194327715-194327765	PrEC	prostate:	n/a
16	chr1:194327715-194327765	HNPCEpiC	eye:	n/a
17	chr1:194327715-194327765	HCF	heart:	n/a
18	chr1:194327715-194327765	Jurkat	blood:	n/a
19	chr1:194327715-194327765	AG10803	skin:	n/a
20	chr1:194327715-194327765	PANC-1	pancreas:	n/a
21	chr1:194327715-194327765	AoSMC	blood vessel:	n/a
22	chr1:194327715-194327765	Caco-2	colon:	n/a
23	chr1:194327715-194327765	HCM	heart:	n/a
24	chr1:194327715-194327765	IMR90	lung:	fetal
25	chr1:194327715-194327765	GM12892	blood:	n/a
26	chr1:194327715-194327765	MCF-7	breast:	n/a
27	chr1:194327715-194327765	HEEpiC	esophagus:	n/a
28	chr1:194327715-194327765	AG04449	skin:	fetal
29	chr1:194327715-194327765	U87	brain:	n/a
30	chr1:194327715-194327765	SAEC	small airway:	n/a
31	chr1:194327715-194327765	NH-A	brain:	n/a
32	chr1:194327715-194327765	SK-N-SH	brain:	n/a
33	chr1:194327715-194327765	ovcar-3	ovarian:	n/a
34	chr1:194327715-194327765	HEK293	kidney:	embryo
35	chr1:194327715-194327765	MCF10A-Er-Src	breast:	n/a
36	chr1:194327715-194327765	T-47D	breast:	n/a
37	chr1:194327715-194327765	ProgFib	skin:	n/a
38	chr1:194327715-194327765	HepG2	liver:	n/a
39	chr1:194327715-194327765	HIPEpiC	eye:	n/a
40	chr1:194327715-194327765	GM06990	blood:	n/a
41	chr1:194327715-194327765	NB4	blood:	n/a
42	chr1:194327715-194327765	LNCaP	prostate:	n/a
43	chr1:194327715-194327765	GM19239	blood:	n/a
44	chr1:194327715-194327765	AG04450	lung:	fetal
45	chr1:194327715-194327765	HAEpiC	amniotic membrane:	n/a
46	chr1:194327715-194327765	HCT-116	colon:	n/a
47	chr1:194327715-194327765	A549	lung:	n/a
48	chr1:194327715-194327765	SK-N-MC	brain:	n/a
49	chr1:194327715-194327765	HCPEpiC	choroid plexus:	n/a
50	chr1:194327715-194327765	H1-hESC	embryonic stem cell:	embryo

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:194259902..194262813-chr1:194263543..194265808,3	K562	blood:
2	chr1:194137184..194139202-chr1:194141999..194143832,2	K562	blood:
3	chr1:194272409..194275339-chr1:194275984..194279040,4	K562	blood:
4	chr1:194326093..194330986-chr1:194331715..194336171,7	K562	blood:
5	chr1:194070430..194072677-chr1:194322592..194324190,2	K562	blood:
6	chr1:194146413..194149000-chr1:194719547..194721730,2	K562	blood:
7	chr1:194328262..194330986-chr1:194334081..194336171,2	K562	blood:
8	chr1:194286927..194289015-chr1:194296923..194299296,2	K562	blood:
9	chr1:194277312..194279906-chr1:194286603..194288414,2	K562	blood:
10	chr1:194325391..194328027-chr1:194331850..194333464,2	K562	blood:
11	chr1:194307530..194310929-chr1:194324369..194327548,3	K562	blood:
12	chr1:194317795..194320009-chr1:194323102..194324851,2	K562	blood:
13	chr1:194326093..194330986-chr1:194331715..194336171,7	K562	blood:
14	chr1:194307530..194310929-chr1:194324369..194327548,3	K562	blood:
15	chr1:194237234..194239650-chr1:194241367..194244055,3	K562	blood:
16	chr1:194259902..194262813-chr1:194263543..194265808,3	K562	blood:
17	chr1:194315164..194317998-chr1:194319254..194321893,3	K562	blood:
18	chr1:194210426..194212793-chr1:194215119..194216699,2	K562	blood:
19	chr1:194290793..194293350-chr1:194303671..194305841,2	K562	blood:
20	chr1:194308962..194311330-chr4:127715408..127718280,2	MCF-7	breast:
21	chr1:194162785..194164571-chr1:194166368..194168944,2	MCF-7	breast:
22	chr1:194306516..194309030-chr1:194325392..194327548,2	K562	blood:
23	chr1:194128967..194129865-chr1:194264643..194265551,3	MCF-7	breast:
24	chr1:194325391..194328027-chr1:194331850..194333464,2	K562	blood:
25	chr1:194256252..194258027-chr1:194260432..194262987,2	K562	blood:
26	chr1:194237234..194239650-chr1:194241367..194244055,3	K562	blood:
27	chr1:194315945..194318461-chr1:194337918..194339837,2	K562	blood:
28	chr1:194272409..194275339-chr1:194275984..194279040,4	K562	blood:
29	chr1:194249167..194252027-chr1:194255378..194258049,2	MCF-7	breast:
30	chr1:194266672..194269041-chr1:194271611..194273227,2	K562	blood:
31	chr1:194071422..194072384-chr1:194264231..194265518,7	MCF-7	breast:
32	chr1:194315945..194318461-chr1:194337918..194339837,2	K562	blood:
33	chr1:194128824..194129656-chr1:194264555..194265184,3	MCF-7	breast:
34	chr1:194306516..194309030-chr1:194325392..194327548,2	K562	blood:
35	chr1:193576702..193577442-chr1:194264619..194265502,2	MCF-7	breast:
36	chr1:194320848..194323111-chr1:194332698..194335480,2	K562	blood:
37	chr1:194266672..194269041-chr1:194271611..194273227,2	K562	blood:
38	chr1:193587120..193589760-chr1:194326578..194328851,2	K562	blood:
39	chr1:194290793..194293350-chr1:194303671..194305841,2	K562	blood:
40	chr1:193151512..193152776-chr1:194264703..194265563,3	MCF-7	breast:
41	chr1:194286927..194289015-chr1:194296923..194299296,2	K562	blood:
42	chr1:194320848..194323111-chr1:194332698..194335480,2	K562	blood:
43	chr1:193375639..193376499-chr1:194264953..194265474,2	MCF-7	breast:
44	chr1:194317795..194320009-chr1:194323102..194324851,2	K562	blood:
45	chr1:194277312..194279906-chr1:194286603..194288414,2	K562	blood:
46	chr1:194162785..194164571-chr1:194166368..194168944,2	MCF-7	breast:
47	chr1:194146588..194147088-chr15:62042094..62042595,2	MCF-7	breast:
48	chr1:194328262..194330986-chr1:194334081..194336171,2	K562	blood:
49	chr1:194256252..194258027-chr1:194260432..194262987,2	K562	blood:
50	chr1:194202325..194204844-chr1:194209712..194211273,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B3GALT2-5	chr1:194280749-194281292	NONHSAT008580
2	lnc-CDC73-3	chr1:194166653-194166716	ENSG00000227240.1
3	lnc-B3GALT2-5	chr1:194296750-194296826	NONHSAT008580
4	lnc-CDC73-3	chr1:194167441-194167824	ENSG00000227240.1
5	lnc-CDC73-4	chr1:194321413-194321556	XLOC_000510
6	lnc-CDC73-4	chr1:194320073-194320368	XLOC_000510
7	lnc-CDC73-4	chr1:194320009-194320481	NONHSAT008581
8	lnc-CDC73-4	chr1:194320593-194321556	NONHSAT008581

No data

Variant related genes	Relation type
EEF1A1P14	TF binding region
ENSG00000231714	TF binding region
EEF1A1P14	CpG island
ENSG00000231714	CpG island
ENSG00000231714	chromatin interactions

Extended variants
information (count: 5770 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5770 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376142828	chr1:194143359-194143360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76461695	chr1:194143506-194143507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184395730	chr1:194143531-194143532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189109890	chr1:194143556-194143557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555357013	chr1:194143603-194143604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566369593	chr1:194143690-194143691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533507236	chr1:194143737-194143738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555426585	chr1:194143754-194143755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573745801	chr1:194143803-194143804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374069214	chr1:194143808-194143809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544311102	chr1:194143899-194143900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535122238	chr1:194143931-194143932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556324743	chr1:194143934-194143935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148798852	chr1:194143948-194143949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143857560	chr1:194144024-194144025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72747335	chr1:194144038-194144039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527603607	chr1:194144193-194144194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369697876	chr1:194144224-194144225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542620285	chr1:194144242-194144243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560931207	chr1:194144285-194144286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531623531	chr1:194144292-194144293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115748489	chr1:194144296-194144297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1487530	chr1:194144303-194144304	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs73070733	chr1:194144322-194144323	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs547970531	chr1:194144342-194144343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566215274	chr1:194144353-194144354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536970484	chr1:194144447-194144448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548935821	chr1:194144463-194144464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146874440	chr1:194144530-194144531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537888167	chr1:194144549-194144550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567245154	chr1:194144577-194144578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560211463	chr1:194144590-194144591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs603248	chr1:194144602-194144603	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs77824613	chr1:194144640-194144641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4657909	chr1:194144643-194144644	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs561112631	chr1:194144644-194144645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72747337	chr1:194144692-194144693	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs542491750	chr1:194144711-194144712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560896311	chr1:194144784-194144785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576016522	chr1:194144859-194144860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112760047	chr1:194144906-194144907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543419611	chr1:194145008-194145009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181085808	chr1:194145014-194145015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373996316	chr1:194145120-194145121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140688452	chr1:194145124-194145125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12097590	chr1:194145131-194145132	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs116568597	chr1:194145175-194145176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548898934	chr1:194145187-194145188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570403997	chr1:194145221-194145222	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs111589723	chr1:194145247-194145248	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:194142600-194145800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr1:194142800-194146000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr1:194143400-194145800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr1:194143400-194145800	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr1:194143600-194144000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr1:194143600-194144200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr1:194143600-194145200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr1:194143600-194145400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr1:194143800-194144200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:194144000-194144800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:194144000-194145200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr1:194144200-194145200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr1:194144200-194145200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:194144400-194144800	Enhancers	Placenta Amnion	Placenta Amnion
15	chr1:194144600-194145400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:194144600-194145800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:194145200-194145400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr1:194145200-194145600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr1:194145200-194145800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:194145200-194145800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:194145200-194145800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr1:194145200-194146000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr1:194145200-194146000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:194145400-194145800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr1:194145800-194146000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr1:194148400-194148800	Active TSS	Primary T helper naive cells from peripheral blood	blood
27	chr1:194148600-194152200	Weak transcription	Primary T cells from cord blood	blood
28	chr1:194150400-194151200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr1:194150400-194151400	ZNF genes & repeats	Thymus	Thymus
30	chr1:194150600-194151400	ZNF genes & repeats	Fetal Thymus	thymus
31	chr1:194151400-194158600	Weak transcription	Thymus	Thymus
32	chr1:194158600-194159400	Strong transcription	Thymus	Thymus
33	chr1:194159400-194195200	Weak transcription	Thymus	Thymus
34	chr1:194176000-194189200	Weak transcription	Primary T cells from cord blood	blood
35	chr1:194184000-194195400	Weak transcription	Fetal Thymus	thymus
36	chr1:194187000-194194600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr1:194187800-194188200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr1:194188000-194188400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:194188200-194188400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr1:194188400-194188800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:194193000-194193400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr1:194193400-194194600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr1:194193600-194196200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr1:194194400-194196000	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr1:194194400-194196200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr1:194194400-194196400	Enhancers	Primary T cells from cord blood	blood
47	chr1:194194400-194196400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr1:194194600-194195600	Bivalent Enhancer	Primary B cells from cord blood	blood
49	chr1:194194600-194195600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:194194600-194195800	Enhancers	Primary hematopoietic stem cells	blood

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