Variant report

Variant	nsv1002928
Chromosome Location	chr1:95126536-95152838
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:148)
CpG islands
(count:183)
Chromatin interactive
region (count:9)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:148 , 50 per page) page: 1 2 3

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	chr1:95143325-95143609	K562	blood:	n/a	n/a
4	BHLHE40	chr1:95143320-95143564	K562	blood:	n/a	n/a
5	CEBPB	chr1:95143729-95144065	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:95148401-95148713	IMR90	lung:	n/a	chr1:95148548-95148559
7	CEBPB	chr1:95127192-95127290	K562	blood:	n/a	n/a
8	CEBPB	chr1:95148526-95148547	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:95138437-95138965	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:95127135-95127409	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:95140890-95141377	IMR90	lung:	n/a	chr1:95141176-95141189
12	CEBPB	chr1:95126571-95127497	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:95148455-95148686	Hela-S3	cervix:	n/a	chr1:95148548-95148559
14	CEBPB	chr1:95132331-95132574	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:95152451-95152699	HepG2	liver:	n/a	n/a
16	CTCF	chr1:95149995-95150037	MCF-7	breast:	n/a	chr1:95150025-95150033
17	CTCF	chr1:95150040-95150106	Fibrobl	skin:	n/a	n/a
18	CTCF	chr1:95134240-95134390	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr1:95149960-95150110	HCT-116	colon:	n/a	chr1:95150025-95150033
20	CTCF	chr1:95149920-95150070	HepG2	liver:	n/a	chr1:95150025-95150033
21	CTCF	chr1:95149983-95150055	MCF-7	breast:	n/a	chr1:95150025-95150033
22	CTCF	chr1:95148280-95148430	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr1:95149973-95150081	MCF-7	breast:	n/a	chr1:95150025-95150033
24	CTCF	chr1:95149955-95150077	H1-hESC	embryonic stem cell:	n/a	chr1:95150025-95150033
25	CTCF	chr1:95149940-95150090	MCF-7	breast:	n/a	chr1:95150025-95150033
26	CTCF	chr1:95149991-95149994	MCF-7	breast:	n/a	n/a
27	CTCF	chr1:95127052-95127160	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr1:95149960-95150110	HEK293	kidney:	n/a	chr1:95150025-95150033
29	E2F4	chr1:95137227-95137374	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F6	chr1:95149871-95150217	H1-hESC	embryonic stem cell:	n/a	n/a
31	EP300	chr1:95130100-95130300	Hela-S3	cervix:	n/a	n/a
32	EP300	chr1:95134844-95134975	K562	blood:	n/a	n/a
33	ESR1	chr1:95142321-95142714	ECC-1	luminal epithelium:	n/a	n/a
34	ESR1	chr1:95142127-95142755	ECC-1	luminal epithelium:	n/a	n/a
35	ESR1	chr1:95142263-95142651	ECC-1	luminal epithelium:	n/a	n/a
36	ESR1	chr1:95142164-95142730	ECC-1	luminal epithelium:	n/a	n/a
37	FOS	chr1:95143316-95143639	K562	blood:	n/a	n/a
38	FOXA1	chr1:95131200-95131489	HepG2	liver:	n/a	chr1:95131350-95131365
39	GATA1	chr1:95134491-95135353	PBDE	blood:	n/a	n/a
40	GATA3	chr1:95134665-95135267	SK-N-SH	brain:	n/a	n/a
41	GATA3	chr1:95143908-95144255	MCF-7	breast:	n/a	chr1:95144037-95144046
42	GATA3	chr1:95134647-95135287	SK-N-SH	brain:	n/a	n/a
43	GATA3	chr1:95143898-95144143	T-47D	breast:	n/a	chr1:95144037-95144046
44	GTF2F1	chr1:95126707-95126950	H1-hESC	embryonic stem cell:	n/a	n/a
45	HDAC2	chr1:95126394-95126878	H1-hESC	embryonic stem cell:	n/a	n/a
46	HDAC2	chr1:95132354-95132585	H1-hESC	embryonic stem cell:	n/a	n/a
47	JUND	chr1:95126541-95126955	H1-hESC	embryonic stem cell:	n/a	n/a
48	JUND	chr1:95148676-95148985	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
49	JUND	chr1:95148728-95148893	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
50	MAFF	chr1:95134814-95135118	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95149580-95149630	A549	lung:	n/a
2	chr1:95149580-95149630	AG04450	lung:	fetal
3	chr1:95149580-95149630	HRCEpiC	kidney:	n/a
4	chr1:95141800-95141850	SK-N-SH	brain:	n/a
5	chr1:95149580-95149630	SAEC	small airway:	n/a
6	chr1:95141800-95141850	NHDF-neo	bronchial:	n/a
7	chr1:95149580-95149630	HNPCEpiC	eye:	n/a
8	chr1:95141800-95141850	AoSMC	blood vessel:	n/a
9	chr1:95133907-95133957	LNCaP	prostate:	n/a
10	chr1:95149580-95149630	ovcar-3	ovarian:	n/a
11	chr1:95149580-95149630	IMR90	lung:	fetal
12	chr1:95141800-95141850	HPAEpiC	pulmonary alveolar:	n/a
13	chr1:95133907-95133957	PANC-1	pancreas:	n/a
14	chr1:95149580-95149630	SK-N-SH	brain:	n/a
15	chr1:95141800-95141850	K562	blood:	n/a
16	chr1:95149580-95149630	SK-N-MC	brain:	n/a
17	chr1:95133907-95133957	GM12878	blood:	n/a
18	chr1:95133907-95133957	ECC-1	luminal epithelium:	n/a
19	chr1:95133907-95133957	BE2_C	brain:	n/a
20	chr1:95149580-95149630	MCF-7	breast:	n/a
21	chr1:95133907-95133957	HCPEpiC	choroid plexus:	n/a
22	chr1:95133907-95133957	CMK	blood:	n/a
23	chr1:95133907-95133957	GM06990	blood:	n/a
24	chr1:95133907-95133957	HCF	heart:	n/a
25	chr1:95149580-95149630	HepG2	liver:	n/a
26	chr1:95141800-95141850	CMK	blood:	n/a
27	chr1:95133907-95133957	HAEpiC	amniotic membrane:	n/a
28	chr1:95133907-95133957	IMR90	lung:	fetal
29	chr1:95141800-95141850	ECC-1	luminal epithelium:	n/a
30	chr1:95141800-95141850	LNCaP	prostate:	n/a
31	chr1:95141800-95141850	HCT-116	colon:	n/a
32	chr1:95149580-95149630	HEEpiC	esophagus:	n/a
33	chr1:95141800-95141850	HNPCEpiC	eye:	n/a
34	chr1:95133907-95133957	HEK293	kidney:	embryo
35	chr1:95149580-95149630	K562	blood:	n/a
36	chr1:95133907-95133957	RPTEC	kidney:	n/a
37	chr1:95133907-95133957	GM12892	blood:	n/a
38	chr1:95133907-95133957	NT2-D1	testis:	n/a
39	chr1:95133907-95133957	HRPEpiC	eye:	n/a
40	chr1:95141800-95141850	AG04449	skin:	fetal
41	chr1:95141800-95141850	RPTEC	kidney:	n/a
42	chr1:95133907-95133957	U87	brain:	n/a
43	chr1:95141800-95141850	HCM	heart:	n/a
44	chr1:95141800-95141850	GM12878	blood:	n/a
45	chr1:95141800-95141850	GM12891	blood:	n/a
46	chr1:95149580-95149630	GM12892	blood:	n/a
47	chr1:95133907-95133957	SK-N-MC	brain:	n/a
48	chr1:95141800-95141850	HepG2	liver:	n/a
49	chr1:95149580-95149630	HEK293	kidney:	embryo
50	chr1:95133907-95133957	HEEpiC	esophagus:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:95143459..95146021-chr1:95146335..95147850,2	K562	blood:
2	chr1:95134967..95137782-chr1:95144953..95147356,2	K562	blood:
3	chr1:95145448..95146125-chr1:113615023..113615898,2	K562	blood:
4	chr1:95134967..95137782-chr1:95144953..95147356,2	K562	blood:
5	chr1:95135759..95138517-chr1:95142176..95146453,3	K562	blood:
6	chr1:95135759..95138517-chr1:95142176..95146453,3	K562	blood:
7	chr1:95130856..95133124-chr1:95137358..95139966,2	K562	blood:
8	chr1:95147936..95149911-chr1:95157813..95160581,2	K562	blood:
9	chr1:95143459..95146021-chr1:95146335..95147850,2	K562	blood:

(count:20 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 948 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:948 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182862518	chr1:95126552-95126553	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs368608700	chr1:95126612-95126613	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs548509623	chr1:95126630-95126631	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs374935330	chr1:95126638-95126639	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs568004973	chr1:95126655-95126656	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs537056915	chr1:95126664-95126665	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs77417331	chr1:95126674-95126675	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs576947981	chr1:95126692-95126693	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs375472235	chr1:95126716-95126717	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs6670296	chr1:95126729-95126730	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs372541432	chr1:95126802-95126803	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs80128488	chr1:95126836-95126837	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs376445810	chr1:95126882-95126883	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs575959399	chr1:95126889-95126890	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs564594038	chr1:95126895-95126896	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs543461328	chr1:95126929-95126930	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs371243419	chr1:95126944-95126945	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs532128633	chr1:95127002-95127003	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs552276475	chr1:95127003-95127004	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs559179646	chr1:95127004-95127005	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs528328966	chr1:95127005-95127006	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs548039265	chr1:95127020-95127021	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs568017479	chr1:95127023-95127024	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs146107530	chr1:95127039-95127040	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs550577645	chr1:95127056-95127057	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs572128621	chr1:95127073-95127074	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs570547383	chr1:95127100-95127101	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs377728173	chr1:95127153-95127154	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs140140400	chr1:95127187-95127188	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs2971941	chr1:95127212-95127213	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs112736534	chr1:95127236-95127237	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs150740853	chr1:95127240-95127241	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs374916951	chr1:95127248-95127249	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs192891568	chr1:95127268-95127269	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs549078623	chr1:95127373-95127374	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs565703737	chr1:95127430-95127431	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs544953887	chr1:95127434-95127435	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs558465953	chr1:95127443-95127444	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs13374946	chr1:95127456-95127457	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs11165192	chr1:95127463-95127464	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs577819480	chr1:95127509-95127510	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs34038557	chr1:95127535-95127536	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs397864109	chr1:95127544-95127545	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs562182444	chr1:95127545-95127546	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs536936935	chr1:95127559-95127560	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs75190550	chr1:95127566-95127567	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs528127352	chr1:95127579-95127580	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs139107844	chr1:95127645-95127646	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs183211929	chr1:95127763-95127764	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs530605089	chr1:95127786-95127787	Enhancers Weak transcription Flanking Active TSS	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:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95114600-95126600	Weak transcription	Esophagus	oesophagus
2	chr1:95120000-95126600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:95120000-95126600	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr1:95124000-95126800	Weak transcription	HepG2	liver
5	chr1:95124200-95126600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr1:95124200-95126600	Weak transcription	Stomach Mucosa	stomach
7	chr1:95124200-95127000	Weak transcription	Duodenum Mucosa	Duodenum
8	chr1:95124200-95131800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr1:95125000-95133200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:95125400-95128400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:95125600-95128400	Enhancers	Hela-S3	cervix
12	chr1:95125800-95128800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:95125800-95128800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr1:95126000-95126800	Enhancers	H9 Cell Line	embryonic stem cell
15	chr1:95126000-95127400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:95126000-95127400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr1:95126000-95127400	Enhancers	Fetal Heart	heart
18	chr1:95126000-95127600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr1:95126000-95128400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr1:95126000-95128600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:95126000-95128800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:95126000-95128800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:95126200-95126800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr1:95126200-95127000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr1:95126200-95127000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr1:95126200-95127000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:95126200-95127000	Enhancers	Placenta Amnion	Placenta Amnion
28	chr1:95126200-95127200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:95126200-95127800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr1:95126400-95126800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:95126400-95126800	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr1:95126400-95126800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:95126400-95126800	Enhancers	Gastric	stomach
34	chr1:95126400-95126800	Enhancers	Left Ventricle	heart
35	chr1:95126400-95126800	Enhancers	Pancreas	Pancrea
36	chr1:95126400-95126800	Enhancers	Right Atrium	heart
37	chr1:95126400-95126800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr1:95126400-95126800	Enhancers	HMEC	breast
39	chr1:95126400-95126800	Enhancers	HSMM	muscle
40	chr1:95126400-95126800	Enhancers	HSMMtube	muscle
41	chr1:95126400-95126800	Enhancers	NH-A	brain
42	chr1:95126400-95126800	Enhancers	NHLF	lung
43	chr1:95126400-95127000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:95126400-95127000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:95126400-95127000	Enhancers	NHEK	skin
46	chr1:95126400-95127200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:95126400-95127400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr1:95126400-95127400	Enhancers	NHDF-Ad	bronchial
49	chr1:95126400-95127600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:95126400-95127600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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