Variant report

Variant	esv2755232
Chromosome Location	chr1:95119790-95151813
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:260)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:95134884-95134905	K562	blood:	n/a	n/a
2	ATF2	chr1:95126491-95127014	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr1:95123440-95123857	HCT-116	colon:	n/a	n/a
4	ATF3	chr1:95123472-95123678	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr1:95143325-95143609	K562	blood:	n/a	n/a
6	BHLHE40	chr1:95143320-95143564	K562	blood:	n/a	n/a
7	BRCA1	chr1:95123460-95124186	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr1:95119505-95119959	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:95119504-95120465	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:95127192-95127290	K562	blood:	n/a	n/a
11	CEBPB	chr1:95120162-95120392	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:95140890-95141377	IMR90	lung:	n/a	chr1:95141176-95141189
13	CEBPB	chr1:95123481-95123658	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:95148455-95148686	Hela-S3	cervix:	n/a	chr1:95148548-95148559
15	CEBPB	chr1:95123420-95123775	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr1:95132331-95132574	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:95123438-95124284	IMR90	lung:	n/a	n/a
18	CEBPB	chr1:95148401-95148713	IMR90	lung:	n/a	chr1:95148548-95148559
19	CEBPB	chr1:95148526-95148547	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:95123360-95123910	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr1:95123371-95123906	HCT-116	colon:	n/a	n/a
22	CEBPB	chr1:95127135-95127409	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr1:95126571-95127497	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:95143729-95144065	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:95123365-95124075	HCT-116	colon:	n/a	n/a
26	CEBPB	chr1:95138437-95138965	IMR90	lung:	n/a	n/a
27	CHD2	chr1:95123362-95124002	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr1:95119344-95119986	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr1:95123457-95123663	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:95127052-95127160	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr1:95149973-95150081	MCF-7	breast:	n/a	chr1:95150025-95150033
32	CTCF	chr1:95149983-95150055	MCF-7	breast:	n/a	chr1:95150025-95150033
33	CTCF	chr1:95149955-95150077	H1-hESC	embryonic stem cell:	n/a	chr1:95150025-95150033
34	CTCF	chr1:95149995-95150037	MCF-7	breast:	n/a	chr1:95150025-95150033
35	CTCF	chr1:95126260-95126410	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr1:95123720-95123870	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr1:95123800-95123950	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr1:95149920-95150070	HepG2	liver:	n/a	chr1:95150025-95150033
39	CTCF	chr1:95148280-95148430	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr1:95149960-95150110	HEK293	kidney:	n/a	chr1:95150025-95150033
41	CTCF	chr1:95120119-95120213	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr1:95149991-95149994	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:95149940-95150090	MCF-7	breast:	n/a	chr1:95150025-95150033
44	CTCF	chr1:95134240-95134390	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr1:95150040-95150106	Fibrobl	skin:	n/a	n/a
46	CTCF	chr1:95149960-95150110	HCT-116	colon:	n/a	chr1:95150025-95150033
47	E2F4	chr1:95137227-95137374	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F6	chr1:95123421-95123759	H1-hESC	embryonic stem cell:	n/a	n/a
49	E2F6	chr1:95149871-95150217	H1-hESC	embryonic stem cell:	n/a	n/a
50	EGR1	chr1:95122613-95122811	K562	blood:	n/a	chr1:95122617-95122630

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95149580-95149630	HCF	heart:	n/a
2	chr1:95149580-95149630	AG04450	lung:	fetal
3	chr1:95149580-95149630	SK-N-MC	brain:	n/a
4	chr1:95133907-95133957	HRCEpiC	kidney:	n/a
5	chr1:95141800-95141850	Hela-S3	cervix:	n/a
6	chr1:95141800-95141850	GM19239	blood:	n/a
7	chr1:95141800-95141850	AG09309	skin:	n/a
8	chr1:95141800-95141850	SK-N-MC	brain:	n/a
9	chr1:95149580-95149630	MCF10A-Er-Src	breast:	n/a
10	chr1:95149580-95149630	GM12892	blood:	n/a
11	chr1:95141800-95141850	NHDF-neo	bronchial:	n/a
12	chr1:95149580-95149630	CMK	blood:	n/a
13	chr1:95133907-95133957	SK-N-SH	brain:	n/a
14	chr1:95133907-95133957	Jurkat	blood:	n/a
15	chr1:95141800-95141850	IMR90	lung:	fetal
16	chr1:95133907-95133957	GM12891	blood:	n/a
17	chr1:95141800-95141850	GM06990	blood:	n/a
18	chr1:95141800-95141850	HPAEpiC	pulmonary alveolar:	n/a
19	chr1:95133907-95133957	HRPEpiC	eye:	n/a
20	chr1:95149580-95149630	HMEC	breast:	n/a
21	chr1:95133907-95133957	GM12878	blood:	n/a
22	chr1:95141800-95141850	MCF-7	breast:	n/a
23	chr1:95141800-95141850	AG10803	skin:	n/a
24	chr1:95149580-95149630	GM12878	blood:	n/a
25	chr1:95141800-95141850	SK-N-SH	brain:	n/a
26	chr1:95141800-95141850	AG04449	skin:	fetal
27	chr1:95133907-95133957	BJ	skin:	n/a
28	chr1:95149580-95149630	T-47D	breast:	n/a
29	chr1:95149580-95149630	NT2-D1	testis:	n/a
30	chr1:95141800-95141850	MCF10A-Er-Src	breast:	n/a
31	chr1:95149580-95149630	AG09319	gingival:	n/a
32	chr1:95149580-95149630	HCT-116	colon:	n/a
33	chr1:95149580-95149630	BJ	skin:	n/a
34	chr1:95141800-95141850	Jurkat	blood:	n/a
35	chr1:95133907-95133957	AG04449	skin:	fetal
36	chr1:95141800-95141850	RPTEC	kidney:	n/a
37	chr1:95149580-95149630	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:95149580-95149630	PrEC	prostate:	n/a
39	chr1:95133907-95133957	NHDF-neo	bronchial:	n/a
40	chr1:95149580-95149630	RPTEC	kidney:	n/a
41	chr1:95149580-95149630	HRE	kidney:	n/a
42	chr1:95141800-95141850	GM12892	blood:	n/a
43	chr1:95133907-95133957	HIPEpiC	eye:	n/a
44	chr1:95149580-95149630	BE2_C	brain:	n/a
45	chr1:95149580-95149630	HCPEpiC	choroid plexus:	n/a
46	chr1:95149580-95149630	A549	lung:	n/a
47	chr1:95149580-95149630	SAEC	small airway:	n/a
48	chr1:95141800-95141850	HRCEpiC	kidney:	n/a
49	chr1:95133907-95133957	IMR90	lung:	fetal
50	chr1:95149580-95149630	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:95135759..95138517-chr1:95142176..95146453,3	K562	blood:
2	chr1:95006986..95007963-chr1:95119179..95120118,2	Hela-S3	cervix:
3	chr1:95143459..95146021-chr1:95146335..95147850,2	K562	blood:
4	chr1:95135759..95138517-chr1:95142176..95146453,3	K562	blood:
5	chr1:95134967..95137782-chr1:95144953..95147356,2	K562	blood:
6	chr1:95130856..95133124-chr1:95137358..95139966,2	K562	blood:
7	chr1:95134967..95137782-chr1:95144953..95147356,2	K562	blood:
8	chr1:95143459..95146021-chr1:95146335..95147850,2	K562	blood:
9	chr1:95115535..95119175-chr1:95123580..95126438,3	K562	blood:
10	chr1:95147936..95149911-chr1:95157813..95160581,2	K562	blood:
11	chr1:95145448..95146125-chr1:113615023..113615898,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F3-2	chr1:95144981-95145163	NONHSAT004609
2	lnc-CNN3-3	chr1:95123481-95123611	ENSG00000224081.2
3	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
4	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
5	lnc-F3-2	chr1:95138492-95138827	NONHSAT004609
6	lnc-SLC44A3-2	chr1:95149016-95149176	XLOC_000303
7	lnc-SLC44A3-2	chr1:95143531-95144178	NONHSAT004611
8	lnc-F3-2	chr1:95145136-95145163	ENSG00000224081.3
9	lnc-F3-2	chr1:95123530-95123608	NONHSAT004607
10	lnc-F3-2	chr1:95144981-95145163	NONHSAT004613
11	lnc-F3-2	chr1:95144981-95145163	NONHSAT004607
12	lnc-SLC44A3-2	chr1:95149856-95150619	XLOC_000303
13	lnc-F3-2	chr1:95138492-95138827	NONHSAT004608
14	lnc-CNN3-3	chr1:95138453-95138827	ENSG00000224081.2
15	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
16	lnc-CNN3-3	chr1:95123089-95123611	ENSG00000224081.2
17	lnc-SLC44A3-2	chr1:95143554-95143579	XLOC_000303
18	lnc-CNN3-3	chr1:95123762-95123806	ENSG00000224081.2
19	lnc-SLC44A3-2	chr1:95144981-95145163	NONHSAT004611
20	lnc-CNN3-3	chr1:95138685-95138827	ENSG00000224081.2
21	lnc-SLC44A3-2	chr1:95148857-95149176	XLOC_000303
22	lnc-F3-2	chr1:95144981-95145163	NONHSAT004608
23	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
24	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2

No data

Variant related genes	Relation type
KATNBL1P2	TF binding region
LINC01057	TF binding region
PGBD4P7	TF binding region
KATNBL1P2	CpG island
LINC01057	CpG island
PGBD4P7	CpG island
ENSG00000117525	chromatin interactions
ENSG00000232857	chromatin interactions
ENSG00000238198	chromatin interactions
ENSG00000198799	chromatin interactions
ENSG00000244433	chromatin interactions
FUBP1	miRNA target sites
SPTLC1	miRNA target sites

Extended variants
information (count: 1167 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1167 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10782987	chr1:95119790-95119791	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565777103	chr1:95119799-95119800	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146446343	chr1:95119896-95119897	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs554707705	chr1:95119977-95119978	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs10874873	chr1:95119988-95119989	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs537324757	chr1:95120039-95120040	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs181105250	chr1:95120051-95120052	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs370155407	chr1:95120058-95120059	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs556953932	chr1:95120062-95120063	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs539580176	chr1:95120084-95120085	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs6658715	chr1:95120151-95120152	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs17411907	chr1:95120174-95120175	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs61661539	chr1:95120202-95120203	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs11586466	chr1:95120211-95120212	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
15	rs201422551	chr1:95120224-95120225	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs11165191	chr1:95120228-95120229	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs574921455	chr1:95120231-95120232	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs186699423	chr1:95120353-95120354	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs544920370	chr1:95120368-95120369	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs4847207	chr1:95120399-95120400	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs564746235	chr1:95120426-95120427	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs532191900	chr1:95120446-95120447	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs201001219	chr1:95120556-95120557	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs140949506	chr1:95120566-95120567	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs528140423	chr1:95120594-95120595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191236789	chr1:95120603-95120604	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557796986	chr1:95120613-95120614	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142055077	chr1:95120643-95120644	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568213970	chr1:95120704-95120705	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536838537	chr1:95120717-95120718	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556866151	chr1:95120718-95120719	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151145167	chr1:95120726-95120727	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182630782	chr1:95120730-95120731	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552910660	chr1:95120745-95120746	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573262263	chr1:95120762-95120763	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187636414	chr1:95120874-95120875	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371986919	chr1:95120883-95120884	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376079140	chr1:95120916-95120917	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192260282	chr1:95120988-95120989	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541176329	chr1:95121040-95121041	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555562203	chr1:95121058-95121059	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575820631	chr1:95121072-95121073	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1624081	chr1:95121103-95121104	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs564809925	chr1:95121118-95121119	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140351933	chr1:95121125-95121126	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150381824	chr1:95121147-95121148	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559362932	chr1:95121222-95121223	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74101831	chr1:95121239-95121240	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548302260	chr1:95121243-95121244	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1778198	chr1:95121248-95121249	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
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
Medulloblastoma	21979893	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
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95114600-95123400	Weak transcription	NHDF-Ad	bronchial
2	chr1:95114600-95124000	Weak transcription	Small Intestine	intestine
3	chr1:95114600-95126600	Weak transcription	Esophagus	oesophagus
4	chr1:95114800-95123800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr1:95118800-95120200	Enhancers	Ovary	ovary
6	chr1:95118800-95120800	Enhancers	Fetal Intestine Large	intestine
7	chr1:95118800-95120800	Enhancers	NHEK	skin
8	chr1:95118800-95121200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:95118800-95121200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:95118800-95121200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:95119000-95119800	Enhancers	Aorta	Aorta
12	chr1:95119000-95119800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr1:95119000-95119800	Enhancers	Right Atrium	heart
14	chr1:95119000-95120000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:95119000-95120000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:95119000-95120000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr1:95119000-95120000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:95119000-95120000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr1:95119000-95120000	Enhancers	Gastric	stomach
20	chr1:95119000-95120000	Enhancers	Stomach Mucosa	stomach
21	chr1:95119000-95120000	Enhancers	HSMM	muscle
22	chr1:95119000-95120000	Enhancers	HUVEC	blood vessel
23	chr1:95119000-95120000	Enhancers	NH-A	brain
24	chr1:95119000-95120000	Enhancers	NHLF	lung
25	chr1:95119000-95120400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr1:95119000-95120400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:95119000-95120400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:95119000-95120400	Enhancers	Colon Smooth Muscle	Colon
29	chr1:95119000-95120600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr1:95119000-95120600	Enhancers	Duodenum Mucosa	Duodenum
31	chr1:95119000-95120600	Enhancers	Fetal Intestine Small	intestine
32	chr1:95119000-95120800	Enhancers	Pancreas	Pancrea
33	chr1:95119000-95120800	Enhancers	HepG2	liver
34	chr1:95119000-95121000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr1:95119000-95121000	Enhancers	HMEC	breast
36	chr1:95119000-95125000	Enhancers	Fetal Heart	heart
37	chr1:95119200-95119800	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr1:95119200-95120000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:95119200-95120000	Enhancers	Muscle Satellite Cultured Cells	--
40	chr1:95119200-95120000	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr1:95119200-95120000	Enhancers	Placenta Amnion	Placenta Amnion
42	chr1:95119200-95120200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr1:95119400-95119800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:95119400-95119800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:95119400-95119800	Enhancers	Osteobl	bone
46	chr1:95119400-95120000	Enhancers	Rectal Smooth Muscle	rectum
47	chr1:95119400-95120600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr1:95119400-95123400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr1:95119400-95123400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr1:95119400-95123400	Weak transcription	Lung	lung

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