Variant report

Variant	nsv436535
Chromosome Location	chr1:95128791-95155240
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:137)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:137 , 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	chr1:95154249-95154715	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr1:95154094-95154593	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr1:95143325-95143609	K562	blood:	n/a	n/a
5	BHLHE40	chr1:95143320-95143564	K562	blood:	n/a	n/a
6	CEBPB	chr1:95143729-95144065	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:95152451-95152699	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:95148455-95148686	Hela-S3	cervix:	n/a	chr1:95148548-95148559
9	CEBPB	chr1:95140890-95141377	IMR90	lung:	n/a	chr1:95141176-95141189
10	CEBPB	chr1:95148526-95148547	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:95132331-95132574	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr1:95138437-95138965	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:95148401-95148713	IMR90	lung:	n/a	chr1:95148548-95148559
14	CHD2	chr1:95154200-95154634	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr1:95154170-95154639	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:95149995-95150037	MCF-7	breast:	n/a	chr1:95150025-95150033
17	CTCF	chr1:95149991-95149994	MCF-7	breast:	n/a	n/a
18	CTCF	chr1:95134240-95134390	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr1:95150040-95150106	Fibrobl	skin:	n/a	n/a
20	CTCF	chr1:95149960-95150110	HEK293	kidney:	n/a	chr1:95150025-95150033
21	CTCF	chr1:95149940-95150090	MCF-7	breast:	n/a	chr1:95150025-95150033
22	CTCF	chr1:95149920-95150070	HepG2	liver:	n/a	chr1:95150025-95150033
23	CTCF	chr1:95148280-95148430	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr1:95149983-95150055	MCF-7	breast:	n/a	chr1:95150025-95150033
25	CTCF	chr1:95154620-95154770	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr1:95149973-95150081	MCF-7	breast:	n/a	chr1:95150025-95150033
27	CTCF	chr1:95149960-95150110	HCT-116	colon:	n/a	chr1:95150025-95150033
28	CTCF	chr1:95149955-95150077	H1-hESC	embryonic stem cell:	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	chr1:95154046-95154617	H1-hESC	embryonic stem cell:	n/a	n/a
33	EP300	chr1:95134844-95134975	K562	blood:	n/a	n/a
34	ESR1	chr1:95142321-95142714	ECC-1	luminal epithelium:	n/a	n/a
35	ESR1	chr1:95142164-95142730	ECC-1	luminal epithelium:	n/a	n/a
36	ESR1	chr1:95142127-95142755	ECC-1	luminal epithelium:	n/a	n/a
37	ESR1	chr1:95142263-95142651	ECC-1	luminal epithelium:	n/a	n/a
38	FOS	chr1:95143316-95143639	K562	blood:	n/a	n/a
39	FOXA1	chr1:95131200-95131489	HepG2	liver:	n/a	chr1:95131350-95131365
40	GATA1	chr1:95134491-95135353	PBDE	blood:	n/a	n/a
41	GATA3	chr1:95143898-95144143	T-47D	breast:	n/a	chr1:95144037-95144046
42	GATA3	chr1:95134647-95135287	SK-N-SH	brain:	n/a	n/a
43	GATA3	chr1:95143908-95144255	MCF-7	breast:	n/a	chr1:95144037-95144046
44	GATA3	chr1:95134665-95135267	SK-N-SH	brain:	n/a	n/a
45	GTF2F1	chr1:95154288-95154524	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	chr1:95148728-95148893	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
48	JUND	chr1:95148676-95148985	H1-hESC	embryonic stem cell:	n/a	chr1:95148807-95148815
49	JUND	chr1:95154310-95154479	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAFF	chr1:95142674-95143010	HepG2	liver:	n/a	chr1:95142838-95142856

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95133907-95133957	HEK293	kidney:	embryo
2	chr1:95141800-95141850	BJ	skin:	n/a
3	chr1:95149580-95149630	HCM	heart:	n/a
4	chr1:95133907-95133957	HUVEC	blood vessel:	n/a
5	chr1:95133907-95133957	HRE	kidney:	n/a
6	chr1:95133907-95133957	HepG2	liver:	n/a
7	chr1:95149580-95149630	Hepatocyte	liver:	n/a
8	chr1:95133907-95133957	SK-N-MC	brain:	n/a
9	chr1:95141800-95141850	Jurkat	blood:	n/a
10	chr1:95149580-95149630	NHBE	bronchial:	n/a
11	chr1:95149580-95149630	PrEC	prostate:	n/a
12	chr1:95141800-95141850	GM12878	blood:	n/a
13	chr1:95141800-95141850	HCF	heart:	n/a
14	chr1:95133907-95133957	Hepatocyte	liver:	n/a
15	chr1:95149580-95149630	NB4	blood:	n/a
16	chr1:95133907-95133957	Hela-S3	cervix:	n/a
17	chr1:95141800-95141850	HRPEpiC	eye:	n/a
18	chr1:95141800-95141850	SK-N-SH	brain:	n/a
19	chr1:95141800-95141850	A549	lung:	n/a
20	chr1:95149580-95149630	HMEC	breast:	n/a
21	chr1:95133907-95133957	BE2_C	brain:	n/a
22	chr1:95141800-95141850	PANC-1	pancreas:	n/a
23	chr1:95141800-95141850	CMK	blood:	n/a
24	chr1:95149580-95149630	K562	blood:	n/a
25	chr1:95149580-95149630	HRCEpiC	kidney:	n/a
26	chr1:95141800-95141850	U87	brain:	n/a
27	chr1:95133907-95133957	NHDF-neo	bronchial:	n/a
28	chr1:95133907-95133957	AG09309	skin:	n/a
29	chr1:95149580-95149630	H1-hESC	embryonic stem cell:	embryo
30	chr1:95149580-95149630	HCT-116	colon:	n/a
31	chr1:95133907-95133957	GM12892	blood:	n/a
32	chr1:95149580-95149630	NH-A	brain:	n/a
33	chr1:95149580-95149630	AG10803	skin:	n/a
34	chr1:95141800-95141850	NHBE	bronchial:	n/a
35	chr1:95141800-95141850	HNPCEpiC	eye:	n/a
36	chr1:95133907-95133957	CMK	blood:	n/a
37	chr1:95149580-95149630	HIPEpiC	eye:	n/a
38	chr1:95149580-95149630	HNPCEpiC	eye:	n/a
39	chr1:95133907-95133957	HCT-116	colon:	n/a
40	chr1:95133907-95133957	AG10803	skin:	n/a
41	chr1:95149580-95149630	HAEpiC	amniotic membrane:	n/a
42	chr1:95133907-95133957	GM12891	blood:	n/a
43	chr1:95141800-95141850	ECC-1	luminal epithelium:	n/a
44	chr1:95149580-95149630	GM12892	blood:	n/a
45	chr1:95149580-95149630	BJ	skin:	n/a
46	chr1:95149580-95149630	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:95149580-95149630	GM12878	blood:	n/a
48	chr1:95141800-95141850	AG04450	lung:	fetal
49	chr1:95133907-95133957	AG04450	lung:	fetal
50	chr1:95141800-95141850	BE2_C	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:95116283..95118037-chr1:95153158..95155389,2	K562	blood:
2	chr1:95147936..95149911-chr1:95157813..95160581,2	K562	blood:
3	chr1:95134967..95137782-chr1:95144953..95147356,2	K562	blood:
4	chr1:95135759..95138517-chr1:95142176..95146453,3	K562	blood:
5	chr1:95143459..95146021-chr1:95146335..95147850,2	K562	blood:
6	chr1:95134967..95137782-chr1:95144953..95147356,2	K562	blood:
7	chr1:95135759..95138517-chr1:95142176..95146453,3	K562	blood:
8	chr1:95145448..95146125-chr1:113615023..113615898,2	K562	blood:
9	chr1:95143459..95146021-chr1:95146335..95147850,2	K562	blood:
10	chr1:95130856..95133124-chr1:95137358..95139966,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNN3-3	chr1:95138453-95138827	ENSG00000224081.2
2	lnc-CNN3-3	chr1:95138685-95138827	ENSG00000224081.2
3	lnc-SLC44A3-2	chr1:95143531-95144178	NONHSAT004611
4	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
5	lnc-F3-2	chr1:95138492-95138827	NONHSAT004608
6	lnc-F3-2	chr1:95144981-95145163	NONHSAT004613
7	lnc-F3-2	chr1:95144981-95145163	NONHSAT004608
8	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
9	lnc-F3-2	chr1:95144981-95145163	NONHSAT004609
10	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
11	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
12	lnc-CNN3-3	chr1:95144981-95145163	ENSG00000224081.2
13	lnc-SLC44A3-2	chr1:95153449-95153875	XLOC_000303
14	lnc-SLC44A3-2	chr1:95144981-95145163	NONHSAT004611
15	lnc-SLC44A3-2	chr1:95153449-95155440	XLOC_000303
16	lnc-F3-2	chr1:95145136-95145163	ENSG00000224081.3
17	lnc-SLC44A3-2	chr1:95149856-95150619	XLOC_000303
18	lnc-SLC44A3-2	chr1:95149016-95149176	XLOC_000303
19	lnc-SLC44A3-2	chr1:95148857-95149176	XLOC_000303
20	lnc-F3-2	chr1:95144981-95145163	NONHSAT004607
21	lnc-SLC44A3-2	chr1:95143554-95143579	XLOC_000303
22	lnc-F3-2	chr1:95138492-95138827	NONHSAT004609
23	lnc-SLC44A3-2	chr1:95153449-95153875	XLOC_000303

No data

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

Extended variants
information (count: 985 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:985 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147817313	chr1:95128798-95128799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs4847329	chr1:95128806-95128807	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs558343423	chr1:95128848-95128849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4847330	chr1:95128861-95128862	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs377195905	chr1:95128894-95128895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115867836	chr1:95128914-95128915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529495798	chr1:95128926-95128927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4847331	chr1:95128927-95128928	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs143570253	chr1:95128957-95128958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535071646	chr1:95128958-95128959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1098615	chr1:95128960-95128961	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs555979703	chr1:95128965-95128966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1098616	chr1:95128970-95128971	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs544007977	chr1:95128971-95128972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538452074	chr1:95128986-95128987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200549200	chr1:95128988-95128989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551130738	chr1:95129006-95129007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540194455	chr1:95129026-95129027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560387764	chr1:95129028-95129029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529354492	chr1:95129029-95129030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549352392	chr1:95129038-95129039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562980067	chr1:95129067-95129068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531806176	chr1:95129068-95129069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552025496	chr1:95129069-95129070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571775236	chr1:95129070-95129071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs58981969	chr1:95129096-95129097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558130529	chr1:95129103-95129104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567944114	chr1:95129124-95129125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140737067	chr1:95129202-95129203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs59566212	chr1:95129222-95129223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373332395	chr1:95129260-95129261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554899538	chr1:95129339-95129340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs60897247	chr1:95129365-95129366	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs189209125	chr1:95129368-95129369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs34573410	chr1:95129531-95129532	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs557821254	chr1:95129546-95129547	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs540215343	chr1:95129554-95129555	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs6680518	chr1:95129556-95129557	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs11165193	chr1:95129585-95129586	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs192546678	chr1:95129594-95129595	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs536008631	chr1:95129626-95129627	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543059946	chr1:95129641-95129642	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185258220	chr1:95129642-95129643	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374332038	chr1:95129661-95129662	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573785472	chr1:95129697-95129698	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs61302933	chr1:95129761-95129762	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs11165194	chr1:95129763-95129764	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs12129812	chr1:95129807-95129808	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs143031405	chr1:95129827-95129828	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372036873	chr1:95129859-95129860	ZNF genes & repeats Weak transcription Enhancers	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:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95124200-95131800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:95125000-95133200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:95125800-95128800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:95125800-95128800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr1:95126000-95128800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:95126000-95128800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:95126800-95133000	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr1:95126800-95137800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr1:95126800-95141600	Weak transcription	Pancreas	Pancrea
10	chr1:95126800-95164200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:95127000-95130000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr1:95127400-95128800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr1:95127400-95129400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr1:95127400-95130000	Weak transcription	Fetal Heart	heart
15	chr1:95127400-95130000	Weak transcription	Stomach Mucosa	stomach
16	chr1:95127600-95128800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr1:95127600-95128800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr1:95127600-95133200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr1:95127600-95133400	Weak transcription	Fetal Intestine Small	intestine
20	chr1:95127600-95134600	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr1:95127800-95128800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr1:95128400-95129600	Weak transcription	Hela-S3	cervix
23	chr1:95128400-95131800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:95128400-95134200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr1:95128400-95134400	Weak transcription	Fetal Intestine Large	intestine
26	chr1:95128400-95154600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:95128800-95129400	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr1:95128800-95129600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr1:95128800-95130000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:95128800-95130000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr1:95128800-95130400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr1:95128800-95131800	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr1:95128800-95134200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:95129400-95131000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
35	chr1:95129600-95130600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
36	chr1:95129600-95130600	Enhancers	Rectal Smooth Muscle	rectum
37	chr1:95130000-95130400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:95130000-95130400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr1:95130000-95130400	Enhancers	Fetal Heart	heart
40	chr1:95130000-95130400	Enhancers	Stomach Mucosa	stomach
41	chr1:95130000-95131000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
42	chr1:95130400-95130600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr1:95130400-95133200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:95130400-95133200	Weak transcription	Stomach Mucosa	stomach
45	chr1:95130600-95131400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr1:95130600-95131800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr1:95131000-95131400	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr1:95131000-95131800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr1:95131400-95131800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr1:95131400-95132000	Enhancers	Primary neutrophils fromperipheralblood	blood

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