Variant report

Variant	nsv1001391
Chromosome Location	chr1:175448870-175728998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2382)
CpG islands
(count:1592)
Chromatin interactive
region (count:79)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2382 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:175450223-175450578	K562	blood:	n/a	n/a
2	ARID3A	chr1:175712067-175712270	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:175677993-175678220	K562	blood:	n/a	n/a
4	ATF1	chr1:175567614-175567771	K562	blood:	n/a	n/a
5	ATF1	chr1:175560566-175560845	K562	blood:	n/a	n/a
6	ATF1	chr1:175702938-175703247	K562	blood:	n/a	n/a
7	ATF1	chr1:175694946-175695151	K562	blood:	n/a	n/a
8	ATF1	chr1:175530746-175530820	K562	blood:	n/a	n/a
9	ATF2	chr1:175567113-175567630	GM12878	blood:	n/a	n/a
10	ATF2	chr1:175546050-175546351	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr1:175569870-175570603	GM12878	blood:	n/a	n/a
12	ATF2	chr1:175567111-175567613	GM12878	blood:	n/a	n/a
13	BACH1	chr1:175712123-175712541	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr1:175570278-175570496	GM12878	blood:	n/a	n/a
15	BATF	chr1:175567105-175567461	GM12878	blood:	n/a	n/a
16	BATF	chr1:175601806-175602145	GM12878	blood:	n/a	chr1:175601977-175601988
17	BATF	chr1:175567143-175567484	GM12878	blood:	n/a	n/a
18	BATF	chr1:175601811-175602154	GM12878	blood:	n/a	chr1:175601977-175601988
19	BATF	chr1:175659425-175659778	GM12878	blood:	n/a	chr1:175659590-175659601
20	BATF	chr1:175570238-175570573	GM12878	blood:	n/a	n/a
21	BATF	chr1:175659507-175659689	GM12878	blood:	n/a	chr1:175659590-175659601
22	BCL11A	chr1:175545989-175546282	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCLAF1	chr1:175569764-175570602	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:175568409-175568632	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:175570039-175570625	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:175702931-175703343	K562	blood:	n/a	n/a
27	BHLHE40	chr1:175560446-175560858	K562	blood:	n/a	n/a
28	CBX3	chr1:175702890-175703263	K562	blood:	n/a	n/a
29	CBX3	chr1:175560458-175560815	K562	blood:	n/a	n/a
30	CCNT2	chr1:175702945-175703389	K562	blood:	n/a	n/a
31	CCNT2	chr1:175726668-175726976	K562	blood:	n/a	n/a
32	CCNT2	chr1:175560540-175560861	K562	blood:	n/a	n/a
33	CEBPB	chr1:175702905-175703334	K562	blood:	n/a	n/a
34	CEBPB	chr1:175501291-175501501	A549	lung:	n/a	chr1:175501354-175501365 chr1:175501354-175501367 chr1:175501356-175501367
35	CEBPB	chr1:175456167-175456194	HepG2	liver:	n/a	chr1:175456177-175456188
36	CEBPB	chr1:175570730-175570860	K562	blood:	n/a	chr1:175570824-175570835
37	CEBPB	chr1:175704612-175704898	K562	blood:	n/a	chr1:175704758-175704771 chr1:175704760-175704769 chr1:175704758-175704771 chr1:175704760-175704769 chr1:175704760-175704771 chr1:175704760-175704769 chr1:175704760-175704769
38	CEBPB	chr1:175570697-175570866	HepG2	liver:	n/a	chr1:175570824-175570835
39	CEBPB	chr1:175542571-175543002	MCF-7	breast:	n/a	chr1:175542813-175542826
40	CEBPB	chr1:175450243-175450597	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:175501279-175501481	K562	blood:	n/a	chr1:175501354-175501365 chr1:175501354-175501367 chr1:175501356-175501367
42	CEBPB	chr1:175702884-175703276	K562	blood:	n/a	n/a
43	CEBPB	chr1:175542728-175542915	K562	blood:	n/a	chr1:175542813-175542826
44	CEBPB	chr1:175450262-175450610	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr1:175716502-175716663	HepG2	liver:	n/a	chr1:175716563-175716574
46	CEBPB	chr1:175480154-175480188	K562	blood:	n/a	n/a
47	CEBPB	chr1:175505552-175505689	K562	blood:	n/a	n/a
48	CEBPB	chr1:175467148-175467554	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr1:175501194-175501532	HepG2	liver:	n/a	chr1:175501354-175501365 chr1:175501354-175501367 chr1:175501356-175501367
50	CEBPB	chr1:175450290-175450581	A549	lung:	n/a	n/a

(count:1592 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:175653121-175653171	MCF-7	breast:	n/a
2	chr1:175713248-175713298	T-47D	breast:	n/a
3	chr1:175568559-175568609	Hepatocyte	liver:	n/a
4	chr1:175525106-175525156	HEK293	kidney:	embryo
5	chr1:175568559-175568609	NHDF-neo	bronchial:	n/a
6	chr1:175533566-175533616	PFSK-1	brain:	n/a
7	chr1:175653121-175653171	MCF-7	breast:	n/a
8	chr1:175713248-175713298	T-47D	breast:	n/a
9	chr1:175568559-175568609	Hepatocyte	liver:	n/a
10	chr1:175525106-175525156	HEK293	kidney:	embryo
11	chr1:175568559-175568609	NHDF-neo	bronchial:	n/a
12	chr1:175533566-175533616	PFSK-1	brain:	n/a
13	chr1:175490611-175490661	AoSMC	blood vessel:	n/a
14	chr1:175653121-175653171	K562	blood:	n/a
15	chr1:175568377-175568427	HCF	heart:	n/a
16	chr1:175683971-175684021	AG09319	gingival:	n/a
17	chr1:175642761-175642811	GM12892	blood:	n/a
18	chr1:175568559-175568609	SK-N-MC	brain:	n/a
19	chr1:175474471-175474521	MCF-7	breast:	n/a
20	chr1:175511259-175511309	AoSMC	blood vessel:	n/a
21	chr1:175712382-175712432	ECC-1	luminal epithelium:	n/a
22	chr1:175712382-175712432	ProgFib	skin:	n/a
23	chr1:175568216-175568266	BE2_C	brain:	n/a
24	chr1:175525986-175526036	HRCEpiC	kidney:	n/a
25	chr1:175570022-175570072	HEK293	kidney:	embryo
26	chr1:175565371-175565421	AG04450	lung:	fetal
27	chr1:175570022-175570072	ovcar-3	ovarian:	n/a
28	chr1:175642761-175642811	GM06990	blood:	n/a
29	chr1:175713248-175713298	ProgFib	skin:	n/a
30	chr1:175533566-175533616	HepG2	liver:	n/a
31	chr1:175712871-175712921	Jurkat	blood:	n/a
32	chr1:175571970-175572020	Hepatocyte	liver:	n/a
33	chr1:175525106-175525156	IMR90	lung:	fetal
34	chr1:175713219-175713269	ECC-1	luminal epithelium:	n/a
35	chr1:175642761-175642811	HMEC	breast:	n/a
36	chr1:175712871-175712921	NHBE	bronchial:	n/a
37	chr1:175671657-175671707	HCM	heart:	n/a
38	chr1:175525986-175526036	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:175565371-175565421	Caco-2	colon:	n/a
40	chr1:175568216-175568266	SK-N-SH	brain:	n/a
41	chr1:175568216-175568266	AG10803	skin:	n/a
42	chr1:175713248-175713298	HIPEpiC	eye:	n/a
43	chr1:175568377-175568427	HCM	heart:	n/a
44	chr1:175683971-175684021	T-47D	breast:	n/a
45	chr1:175712552-175712602	RPTEC	kidney:	n/a
46	chr1:175549030-175549080	SK-N-MC	brain:	n/a
47	chr1:175533566-175533616	HCM	heart:	n/a
48	chr1:175571970-175572020	MCF10A-Er-Src	breast:	n/a
49	chr1:175490611-175490661	GM19239	blood:	n/a
50	chr1:175642761-175642811	HEK293	kidney:	embryo

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:175515953..175518588-chr1:175527952..175530742,2	MCF-7	breast:
2	chr1:175709353..175712316-chr1:175718100..175722074,3	MCF-7	breast:
3	chr1:175623612..175625312-chr1:175626921..175628780,2	K562	blood:
4	chr1:175345040..175345574-chr1:175450603..175451457,2	MCF-7	breast:
5	chr1:175342681..175343454-chr1:175450088..175451392,6	MCF-7	breast:
6	chr1:175703408..175708282-chr1:175710356..175712842,4	K562	blood:
7	chr1:175623253..175625914-chr1:175631373..175633913,2	K562	blood:
8	chr1:175596398..175599153-chr1:175609947..175612782,2	K562	blood:
9	chr1:175725153..175728054-chr6:53947666..53950173,2	MCF-7	breast:
10	chr1:175709353..175712316-chr1:175718100..175722074,3	MCF-7	breast:
11	chr1:175474623..175477393-chr1:175480380..175482566,2	MCF-7	breast:
12	chr1:175616387..175618880-chr1:175622177..175624894,2	MCF-7	breast:
13	chr1:175712269..175713164-chr1:175726366..175727326,3	MCF-7	breast:
14	chr1:175695673..175698499-chr1:175710964..175712851,2	MCF-7	breast:
15	chr1:175623612..175626086-chr1:175627280..175629192,2	K562	blood:
16	chr1:175450058..175450683-chr1:175793398..175794082,2	MCF-7	breast:
17	chr1:175619703..175621428-chr1:175631712..175633665,2	K562	blood:
18	chr1:175449652..175450434-chr1:175792990..175793754,2	K562	blood:
19	chr1:175677536..175679863-chr1:175684649..175686890,2	K562	blood:
20	chr1:175502104..175504991-chr1:175505616..175508224,2	MCF-7	breast:
21	chr1:175555708..175557465-chr1:175560630..175563099,2	MCF-7	breast:
22	chr1:175518429..175521323-chr1:175522798..175524454,2	K562	blood:
23	chr1:175619703..175621428-chr1:175631712..175633665,2	K562	blood:
24	chr1:175120874..175121520-chr1:175449995..175450848,2	MCF-7	breast:
25	chr1:175515953..175518588-chr1:175527952..175530742,2	MCF-7	breast:
26	chr1:175120985..175121765-chr1:175450538..175451369,3	MCF-7	breast:
27	chr1:175586743..175589262-chr1:175590428..175592846,2	MCF-7	breast:
28	chr1:175474623..175477393-chr1:175480380..175482566,2	MCF-7	breast:
29	chr1:175630324..175632456-chr1:175632718..175635511,2	MCF-7	breast:
30	chr1:175514377..175516679-chr1:175519088..175521360,2	K562	blood:
31	chr1:175619488..175620053-chr2:29991948..29992448,2	NB4	blood:
32	chr1:175555708..175557465-chr1:175560630..175563099,2	MCF-7	breast:
33	chr1:175636404..175638015-chr1:175641711..175644234,2	MCF-7	breast:
34	chr1:175450085..175451047-chr1:175712257..175712999,4	MCF-7	breast:
35	chr1:175638168..175641161-chr1:175648590..175650196,2	MCF-7	breast:
36	chr1:175592287..175594796-chr1:175597956..175600571,2	K562	blood:
37	chr1:175450451..175451287-chr1:175647331..175647999,2	MCF-7	breast:
38	chr1:175713728..175714591-chr1:175856822..175857663,2	MCF-7	breast:
39	chr1:175714332..175717213-chr1:175717860..175720283,2	K562	blood:
40	chr1:175528817..175531396-chr1:175532065..175533684,2	MCF-7	breast:
41	chr1:175623612..175625312-chr1:175626921..175628780,2	K562	blood:
42	chr1:175528817..175531396-chr1:175532065..175533684,2	MCF-7	breast:
43	chr1:175548057..175550584-chr1:175551957..175553666,2	K562	blood:
44	chr1:175684925..175686685-chr1:175703553..175705621,2	K562	blood:
45	chr1:175450451..175451287-chr1:175647331..175647999,2	MCF-7	breast:
46	chr1:175684925..175686685-chr1:175703553..175705621,2	K562	blood:
47	chr1:175479902..175482193-chr1:175482223..175485139,2	K562	blood:
48	chr1:175512204..175514383-chr1:175514961..175517684,2	K562	blood:
49	chr1:175521179..175523999-chr1:175667216..175668901,2	K562	blood:
50	chr1:175638168..175641161-chr1:175648590..175650196,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNN-3	chr1:175526124-175526435	NONHSAT007758
2	lnc-TNR-3	chr1:175712773-175712906	NONHSAT007755
3	lnc-TNN-4	chr1:175592606-175592824	NONHSAT007759
4	lnc-TNR-5	chr1:175629438-175629547	NONHSAT007760
5	lnc-TNR-3	chr1:175497405-175497505	NONHSAT007755
6	lnc-RFWD2-2	chr1:175507911-175508312	ENSG00000235628.1
7	lnc-TNN-4	chr1:175599198-175599300	NONHSAT007759
8	lnc-TNN-4	chr1:175587345-175587409	NONHSAT007759
9	lnc-TNN-4	chr1:175601928-175602031	NONHSAT007759
10	lnc-TNN-3	chr1:175535772-175537384	NONHSAT007758
11	lnc-RFWD2-2	chr1:175525727-175525954	ENSG00000235628.1
12	lnc-TNN-3	chr1:175526124-175526435	NONHSAT007757
13	lnc-TNR-3	chr1:175712362-175712766	NONHSAT007755
14	lnc-TNN-3	chr1:175531373-175533005	NONHSAT007757

No data

Variant related genes	Relation type
TNR-IT1	TF binding region
TNR	TF binding region
TNR-IT1	CpG island
TNR	CpG island
ENSG00000116147	chromatin interactions
ENSG00000146147	chromatin interactions

Extended variants
information (count: 10412 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:10412 , 50 per page) page: 1 2 3 4 5 6 7 ... 209

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539723388	chr1:175448892-175448893	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs149210933	chr1:175448894-175448895	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs542654342	chr1:175448919-175448920	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs562229603	chr1:175448929-175448930	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs113300061	chr1:175448936-175448937	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs545168818	chr1:175448956-175448957	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs565150813	chr1:175448959-175448960	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs527943410	chr1:175449048-175449049	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs142466066	chr1:175449143-175449144	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs567993348	chr1:175449159-175449160	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs12068222	chr1:175449237-175449238	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs577168319	chr1:175449243-175449244	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs550236445	chr1:175449244-175449245	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs570145251	chr1:175449281-175449282	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs151335306	chr1:175449335-175449336	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs140684308	chr1:175449355-175449356	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs145817745	chr1:175449361-175449362	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs34031344	chr1:175449431-175449432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571477415	chr1:175449451-175449452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12068323	chr1:175449459-175449460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200426775	chr1:175449523-175449524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542868278	chr1:175449529-175449530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs367653117	chr1:175449540-175449541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139099386	chr1:175449545-175449546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4989524	chr1:175449552-175449553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373622666	chr1:175449555-175449556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200828309	chr1:175449556-175449557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs145801335	chr1:175449559-175449560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs199763120	chr1:175449579-175449580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534047491	chr1:175449581-175449582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553779440	chr1:175449583-175449584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573913572	chr1:175449585-175449586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542237142	chr1:175449587-175449588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555760702	chr1:175449589-175449590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs199546891	chr1:175449599-175449600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575695847	chr1:175449620-175449621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368440613	chr1:175449652-175449653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73044466	chr1:175449682-175449683	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs184876684	chr1:175449683-175449684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546049685	chr1:175449712-175449713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76999950	chr1:175449731-175449732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562586709	chr1:175449739-175449740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370306098	chr1:175449760-175449761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs859416	chr1:175449781-175449782	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs531602493	chr1:175449815-175449816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76357826	chr1:175449838-175449839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs76911993	chr1:175449858-175449859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563690634	chr1:175449879-175449880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532612266	chr1:175449883-175449884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs56405804	chr1:175449891-175449892	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	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
Retinoblastoma	19183342	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
Chordoma	18071362	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
Burkitt''s lymphoma	19759907	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
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1500 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175446400-175451000	Enhancers	Fetal Intestine Large	intestine
2	chr1:175447200-175454200	Weak transcription	Brain Germinal Matrix	brain
3	chr1:175447600-175449200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:175447800-175462000	Weak transcription	Fetal Brain Female	brain
5	chr1:175448000-175452800	Weak transcription	Fetal Brain Male	brain
6	chr1:175448200-175449400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr1:175448400-175449400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:175448400-175449400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:175448400-175449400	Flanking Active TSS	Hela-S3	cervix
10	chr1:175448400-175449400	Enhancers	HSMMtube	muscle
11	chr1:175448600-175449200	Enhancers	NH-A	brain
12	chr1:175448800-175449400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
13	chr1:175448800-175450400	Weak transcription	Fetal Intestine Small	intestine
14	chr1:175449000-175449200	Enhancers	HSMM	muscle
15	chr1:175449400-175450800	Enhancers	Hela-S3	cervix
16	chr1:175450400-175452200	Enhancers	HUVEC	blood vessel
17	chr1:175450600-175450800	Enhancers	Fetal Intestine Small	intestine
18	chr1:175450600-175451200	Enhancers	Lung	lung
19	chr1:175450600-175451200	Enhancers	Spleen	Spleen
20	chr1:175451200-175452200	Weak transcription	Lung	lung
21	chr1:175451200-175452400	Enhancers	Stomach Smooth Muscle	stomach
22	chr1:175452200-175452400	Enhancers	Lung	lung
23	chr1:175452400-175452800	Weak transcription	Lung	lung
24	chr1:175452400-175453200	Enhancers	Brain Cingulate Gyrus	brain
25	chr1:175452800-175453000	Enhancers	Fetal Brain Male	brain
26	chr1:175452800-175453200	Enhancers	Lung	lung
27	chr1:175454200-175454800	Enhancers	Brain Germinal Matrix	brain
28	chr1:175456400-175457400	Enhancers	Duodenum Mucosa	Duodenum
29	chr1:175456400-175458400	Enhancers	Fetal Brain Male	brain
30	chr1:175456600-175457200	Enhancers	Fetal Intestine Large	intestine
31	chr1:175458400-175458800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:175458400-175462800	Weak transcription	Fetal Brain Male	brain
33	chr1:175458800-175477600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:175461400-175461600	Enhancers	Brain Cingulate Gyrus	brain
35	chr1:175461400-175461600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr1:175461600-175461800	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr1:175461600-175462400	Weak transcription	Brain Cingulate Gyrus	brain
38	chr1:175462000-175462200	Enhancers	Fetal Brain Female	brain
39	chr1:175462000-175464000	Enhancers	Brain Germinal Matrix	brain
40	chr1:175462200-175462400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr1:175462200-175462600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
42	chr1:175462200-175462600	Weak transcription	Fetal Brain Female	brain
43	chr1:175462400-175462600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
44	chr1:175462400-175462600	Enhancers	Brain Cingulate Gyrus	brain
45	chr1:175462600-175462800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
46	chr1:175462600-175462800	Bivalent Enhancer	Placenta	Placenta
47	chr1:175462600-175463000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr1:175462600-175463200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
49	chr1:175462600-175463200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr1:175462600-175463200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell

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