Variant report

Variant	nsv997689
Chromosome Location	chr1:72746521-72812440
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:675)
CpG islands
(count:1098)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:72750319-72750713	GM12878	blood:	n/a	n/a
2	ATF2	chr1:72750376-72750736	GM12878	blood:	n/a	n/a
3	BACH1	chr1:72748894-72749768	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:72748062-72748227	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:72750317-72750778	GM12878	blood:	n/a	n/a
6	BATF	chr1:72750337-72750724	GM12878	blood:	n/a	n/a
7	BRCA1	chr1:72748195-72748394	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr1:72750323-72751066	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:72746375-72746702	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:72812157-72812489	Hela-S3	cervix:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
11	CEBPB	chr1:72748554-72748740	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:72748420-72750957	Hela-S3	cervix:	n/a	chr1:72750584-72750595 chr1:72748863-72748876 chr1:72750585-72750596 chr1:72750147-72750158
13	CEBPB	chr1:72812174-72812494	HepG2	liver:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
14	CEBPB	chr1:72762099-72762426	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:72749367-72749678	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr1:72750011-72750992	IMR90	lung:	n/a	chr1:72750584-72750595 chr1:72750585-72750596 chr1:72750147-72750158
17	CEBPB	chr1:72755092-72755159	HepG2	liver:	n/a	chr1:72755122-72755131 chr1:72755120-72755131
18	CEBPB	chr1:72748450-72748905	IMR90	lung:	n/a	chr1:72748863-72748876
19	CEBPB	chr1:72750450-72750705	HepG2	liver:	n/a	chr1:72750584-72750595 chr1:72750585-72750596
20	CEBPB	chr1:72746375-72746718	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr1:72812260-72812424	H1-hESC	embryonic stem cell:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
22	CEBPB	chr1:72749276-72749833	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr1:72748537-72748783	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr1:72811065-72811328	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:72812222-72812489	A549	lung:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
26	CHD1	chr1:72748624-72750228	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr1:72748366-72748381	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr1:72748405-72750930	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr1:72749095-72750447	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr1:72748543-72748846	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr1:72748399-72748786	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr1:72750306-72750765	GM12878	blood:	n/a	n/a
33	CREB1	chr1:72748477-72748773	A549	lung:	n/a	n/a
34	CTBP2	chr1:72747565-72750445	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr1:72748300-72748450	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr1:72748180-72748330	BJ	skin:	n/a	chr1:72748229-72748238 chr1:72748226-72748236 chr1:72748257-72748267
37	CTCF	chr1:72748180-72748330	HRE	kidney:	n/a	chr1:72748229-72748238 chr1:72748226-72748236 chr1:72748257-72748267
38	CTCF	chr1:72748080-72748230	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr1:72748400-72748550	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr1:72748580-72748730	GM12873	blood:	n/a	n/a
41	CTCF	chr1:72748380-72748530	AG04450	lung:	n/a	n/a
42	CTCF	chr1:72788280-72788430	SAEC	small airway:	n/a	n/a
43	CTCF	chr1:72748380-72748530	HCM	heart:	n/a	n/a
44	CTCF	chr1:72750073-72750244	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr1:72749637-72749730	Fibrobl	skin:	n/a	n/a
46	CTCF	chr1:72750040-72750190	AG09319	gingival:	n/a	n/a
47	CTCF	chr1:72750119-72750219	GM12878	blood:	n/a	n/a
48	CTCF	chr1:72748340-72748490	GM06990	blood:	n/a	n/a
49	CTCF	chr1:72750180-72750330	WI-38	lung:	n/a	n/a
50	CTCF	chr1:72748380-72748530	Caco-2	colon:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72748607-72748657	MCF10A-Er-Src	breast:	n/a
2	chr1:72749880-72749930	AG04449	skin:	fetal
3	chr1:72748601-72748651	HEEpiC	esophagus:	n/a
4	chr1:72750502-72750552	HCM	heart:	n/a
5	chr1:72748601-72748651	SAEC	small airway:	n/a
6	chr1:72749581-72749631	HCT-116	colon:	n/a
7	chr1:72748389-72748439	H1-hESC	embryonic stem cell:	embryo
8	chr1:72748607-72748657	PFSK-1	brain:	n/a
9	chr1:72749880-72749930	HCM	heart:	n/a
10	chr1:72750671-72750721	HAEpiC	amniotic membrane:	n/a
11	chr1:72749275-72749325	HEK293	kidney:	embryo
12	chr1:72748610-72748660	SK-N-SH	brain:	n/a
13	chr1:72749735-72749785	HCM	heart:	n/a
14	chr1:72747802-72747852	NHDF-neo	bronchial:	n/a
15	chr1:72749735-72749785	ECC-1	luminal epithelium:	n/a
16	chr1:72750124-72750174	HCPEpiC	choroid plexus:	n/a
17	chr1:72750124-72750174	RPTEC	kidney:	n/a
18	chr1:72750502-72750552	GM12878	blood:	n/a
19	chr1:72750241-72750291	GM12891	blood:	n/a
20	chr1:72749064-72749114	GM12892	blood:	n/a
21	chr1:72748607-72748657	NT2-D1	testis:	n/a
22	chr1:72748124-72748174	MCF-7	breast:	n/a
23	chr1:72748607-72748657	AG10803	skin:	n/a
24	chr1:72747802-72747852	PANC-1	pancreas:	n/a
25	chr1:72748139-72748189	ovcar-3	ovarian:	n/a
26	chr1:72750502-72750552	SK-N-SH	brain:	n/a
27	chr1:72748601-72748651	HL-60	blood:	n/a
28	chr1:72750502-72750552	SK-N-MC	brain:	n/a
29	chr1:72749015-72749065	MCF-7	breast:	n/a
30	chr1:72748124-72748174	ovcar-3	ovarian:	n/a
31	chr1:72753076-72753126	U87	brain:	n/a
32	chr1:72749880-72749930	AoSMC	blood vessel:	n/a
33	chr1:72749880-72749930	GM12878	blood:	n/a
34	chr1:72749275-72749325	HCT-116	colon:	n/a
35	chr1:72748139-72748189	MCF-7	breast:	n/a
36	chr1:72750502-72750552	Hela-S3	cervix:	n/a
37	chr1:72749735-72749785	Hepatocyte	liver:	n/a
38	chr1:72750241-72750291	AG09319	gingival:	n/a
39	chr1:72749064-72749114	HCF	heart:	n/a
40	chr1:72749015-72749065	AG04450	lung:	fetal
41	chr1:72749064-72749114	HEEpiC	esophagus:	n/a
42	chr1:72749880-72749930	AG09309	skin:	n/a
43	chr1:72749275-72749325	SK-N-SH_RA	brain:	n/a
44	chr1:72748610-72748660	HRPEpiC	eye:	n/a
45	chr1:72753076-72753126	NHBE	bronchial:	n/a
46	chr1:72748139-72748189	HAEpiC	amniotic membrane:	n/a
47	chr1:72748610-72748660	HUVEC	blood vessel:	n/a
48	chr1:72750502-72750552	NHBE	bronchial:	n/a
49	chr1:72750124-72750174	HEEpiC	esophagus:	n/a
50	chr1:72750124-72750174	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:72748841..72749750-chr13:47370740..47371446,2	NB4	blood:
2	chr1:72748974..72749649-chr17:56420933..56421808,2	NB4	blood:
3	chr1:72752065..72752600-chr8:87527466..87528155,2	MCF-7	breast:

No data

Variant related genes	Relation type
RPL31P12	TF binding region
NEGR1	TF binding region
RPL31P12	CpG island
NEGR1	CpG island
ENSG00000139684	chromatin interactions

Extended variants
information (count: 530 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185294949	chr1:72746627-72746628	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552961126	chr1:72746632-72746633	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77709389	chr1:72746633-72746634	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541773826	chr1:72746671-72746672	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555180616	chr1:72746732-72746733	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191185587	chr1:72746742-72746743	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543656289	chr1:72746780-72746781	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576404725	chr1:72746785-72746786	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377536499	chr1:72746789-72746790	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532704086	chr1:72746848-72746849	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs546068024	chr1:72746862-72746863	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs559969745	chr1:72746872-72746873	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs528483953	chr1:72746893-72746894	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs114612999	chr1:72746914-72746915	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs562085576	chr1:72746916-72746917	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs545284973	chr1:72746919-72746920	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs183805357	chr1:72746930-72746931	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs143520431	chr1:72746937-72746938	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs560212949	chr1:72746951-72746952	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs371147316	chr1:72747037-72747038	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs570637849	chr1:72747040-72747041	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs138260922	chr1:72747062-72747063	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs201784475	chr1:72747079-72747080	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs372537839	chr1:72747080-72747081	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs546591819	chr1:72747082-72747083	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs566719595	chr1:72747097-72747098	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs527797783	chr1:72747102-72747103	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs535109322	chr1:72747156-72747157	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs35633925	chr1:72747173-72747174	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
30	rs527464861	chr1:72747215-72747216	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549162575	chr1:72747218-72747219	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567810415	chr1:72747224-72747225	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555340304	chr1:72747249-72747250	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76129735	chr1:72747254-72747255	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537536006	chr1:72747257-72747258	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142008864	chr1:72747263-72747264	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577048012	chr1:72747277-72747278	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546346593	chr1:72747301-72747302	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531396308	chr1:72747334-72747335	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559797669	chr1:72747362-72747363	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150277706	chr1:72747415-72747416	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374299940	chr1:72747451-72747452	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549945151	chr1:72747478-72747479	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571221669	chr1:72747480-72747481	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562043901	chr1:72747510-72747511	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189167868	chr1:72747546-72747547	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191445633	chr1:72747574-72747575	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564537251	chr1:72747604-72747605	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182917331	chr1:72747664-72747665	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138882652	chr1:72747668-72747669	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:582 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72743800-72751600	Active TSS	Brain Inferior Temporal Lobe	brain
2	chr1:72745000-72746800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:72745000-72750800	Active TSS	Stomach Smooth Muscle	stomach
4	chr1:72745000-72751200	Active TSS	Brain Angular Gyrus	brain
5	chr1:72745000-72751600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr1:72745200-72751400	Active TSS	Right Atrium	heart
7	chr1:72745400-72747200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr1:72745400-72747800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:72745400-72747800	Flanking Active TSS	HUVEC	blood vessel
10	chr1:72745600-72747200	Flanking Active TSS	Osteobl	bone
11	chr1:72745800-72746800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:72745800-72746800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:72745800-72746800	Active TSS	Brain Cingulate Gyrus	brain
14	chr1:72745800-72747000	Active TSS	Rectal Mucosa Donor 29	rectum
15	chr1:72745800-72747600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr1:72745800-72747600	Active TSS	Adipose Nuclei	Adipose
17	chr1:72745800-72747600	Active TSS	Fetal Muscle Leg	muscle
18	chr1:72745800-72748200	Flanking Active TSS	Dnd41	blood
19	chr1:72745800-72750800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr1:72745800-72750800	Active TSS	Brain Substantia Nigra	brain
21	chr1:72745800-72751200	Active TSS	Colon Smooth Muscle	Colon
22	chr1:72745800-72751400	Active TSS	Duodenum Smooth Muscle	Duodenum
23	chr1:72745800-72751400	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr1:72746000-72746600	Enhancers	Brain Hippocampus Middle	brain
25	chr1:72746000-72746600	Weak transcription	Fetal Stomach	stomach
26	chr1:72746000-72746600	Weak transcription	HSMM	muscle
27	chr1:72746000-72746800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr1:72746000-72747000	Weak transcription	Ovary	ovary
29	chr1:72746000-72751400	Active TSS	Brain Anterior Caudate	brain
30	chr1:72746000-72751400	Active TSS	NHLF	lung
31	chr1:72746200-72746600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr1:72746200-72746600	Active TSS	Primary hematopoietic stem cells short term culture	blood
33	chr1:72746200-72746800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:72746200-72746800	Active TSS	NH-A	brain
35	chr1:72746400-72746600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr1:72746400-72746600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
37	chr1:72746400-72746600	Active TSS	Fetal Brain Female	brain
38	chr1:72746400-72746800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:72746400-72746800	Enhancers	Fetal Brain Male	brain
40	chr1:72746400-72746800	Flanking Active TSS	NHDF-Ad	bronchial
41	chr1:72746400-72747000	Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr1:72746400-72747400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr1:72746400-72748000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr1:72746400-72750800	Active TSS	Rectal Smooth Muscle	rectum
45	chr1:72746400-72751000	Active TSS	HSMMtube	muscle
46	chr1:72746600-72746800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr1:72746600-72746800	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr1:72746600-72746800	Active TSS	Muscle Satellite Cultured Cells	--
49	chr1:72746600-72746800	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr1:72746600-72747000	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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