Variant report

Variant	nsv871764
Chromosome Location	chr1:94917402-95004084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1334)
CpG islands
(count:307)
Chromatin interactive
region (count:21)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:1334 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:94979757-94979966	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:94929310-94929611	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:94980945-94981143	K562	blood:	n/a	n/a
4	BHLHE40	chr1:94981123-94981297	K562	blood:	n/a	n/a
5	BHLHE40	chr1:94979694-94979963	K562	blood:	n/a	n/a
6	BRCA1	chr1:94985616-94985642	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:94979723-94980021	K562	blood:	n/a	n/a
8	CEBPB	chr1:94979764-94979998	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:94986346-94986444	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:94979701-94980026	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:94993012-94993538	Hela-S3	cervix:	n/a	chr1:94993111-94993123
12	CEBPB	chr1:94993057-94993213	H1-hESC	embryonic stem cell:	n/a	chr1:94993111-94993123
13	CEBPB	chr1:94999331-94999531	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:94993779-94994114	Hela-S3	cervix:	n/a	chr1:94993925-94993936
15	CEBPB	chr1:94979729-94980040	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr1:94979787-94979988	MCF-7	breast:	n/a	n/a
17	CEBPB	chr1:94986257-94986544	IMR90	lung:	n/a	n/a
18	CEBPB	chr1:94937794-94938064	IMR90	lung:	n/a	chr1:94937930-94937943
19	CHD1	chr1:94994939-95011321	IMR90	lung:	n/a	n/a
20	CHD2	chr1:95003902-95004179	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr1:94993009-94994191	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr1:94947100-94947250	HL-60	blood:	n/a	n/a
23	CTCF	chr1:94929380-94929530	RPTEC	kidney:	n/a	n/a
24	CTCF	chr1:94929400-94929550	GM12872	blood:	n/a	n/a
25	CTCF	chr1:94979800-94979950	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr1:94987952-94988152	HepG2	liver:	n/a	chr1:94988043-94988064 chr1:94988041-94988059 chr1:94988042-94988058
27	CTCF	chr1:94929271-94929653	K562	blood:	n/a	n/a
28	CTCF	chr1:95003900-95004050	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr1:94929330-94929609	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr1:95003880-95004030	AG04449	skin:	n/a	n/a
31	CTCF	chr1:94979780-94979930	HMF	breast:	n/a	n/a
32	CTCF	chr1:94987574-94988418	SK-N-SH	brain:	n/a	chr1:94988043-94988064 chr1:94988041-94988059 chr1:94988042-94988058
33	CTCF	chr1:94947014-94947327	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr1:94993000-94993150	HCFaa	heart:	n/a	chr1:94993070-94993088 chr1:94993072-94993093
35	CTCF	chr1:95002470-95002477	IMR90	lung:	n/a	n/a
36	CTCF	chr1:94929400-94929550	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr1:94947140-94947290	HMF	breast:	n/a	n/a
38	CTCF	chr1:94993020-94993170	HCPEpiC	choroid plexus:	n/a	chr1:94993070-94993088 chr1:94993072-94993093
39	CTCF	chr1:94987940-94988090	HL-60	blood:	n/a	chr1:94988043-94988064 chr1:94988041-94988059 chr1:94988042-94988058
40	CTCF	chr1:94987967-94988131	Medullo	brain:	n/a	chr1:94988043-94988064 chr1:94988041-94988059 chr1:94988042-94988058
41	CTCF	chr1:94946976-94947357	K562	blood:	n/a	n/a
42	CTCF	chr1:94979760-94979910	HPF	lung:	n/a	n/a
43	CTCF	chr1:94979380-94979530	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr1:94987940-94988090	HMEC	breast:	n/a	chr1:94988043-94988064 chr1:94988041-94988059 chr1:94988042-94988058
45	CTCF	chr1:94979721-94979966	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr1:94979760-94979910	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:94929360-94929510	AG04450	lung:	n/a	n/a
48	CTCF	chr1:94947140-94947290	HepG2	liver:	n/a	n/a
49	CTCF	chr1:94929360-94929510	A549	lung:	n/a	n/a
50	CTCF	chr1:94947140-94947290	GM12867	blood:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95001236-95001286	IMR90	lung:	fetal
2	chr1:95003968-95004018	HCT-116	colon:	n/a
3	chr1:95001236-95001286	IMR90	lung:	fetal
4	chr1:95003968-95004018	HCT-116	colon:	n/a
5	chr1:94929484-94929534	LNCaP	prostate:	n/a
6	chr1:94995935-94995985	CMK	blood:	n/a
7	chr1:94983186-94983236	AG04449	skin:	fetal
8	chr1:95003968-95004018	MCF10A-Er-Src	breast:	n/a
9	chr1:94983186-94983236	AG09309	skin:	n/a
10	chr1:94983186-94983236	Hepatocyte	liver:	n/a
11	chr1:95001236-95001286	HRCEpiC	kidney:	n/a
12	chr1:94929484-94929534	HEK293	kidney:	embryo
13	chr1:95003968-95004018	RPTEC	kidney:	n/a
14	chr1:95001236-95001286	AG10803	skin:	n/a
15	chr1:94983186-94983236	HMEC	breast:	n/a
16	chr1:95003968-95004018	Hepatocyte	liver:	n/a
17	chr1:94995935-94995985	AoSMC	blood vessel:	n/a
18	chr1:95001236-95001286	SK-N-SH_RA	brain:	n/a
19	chr1:94929484-94929534	HUVEC	blood vessel:	n/a
20	chr1:94929484-94929534	NH-A	brain:	n/a
21	chr1:94995935-94995985	RPTEC	kidney:	n/a
22	chr1:95001236-95001286	GM19239	blood:	n/a
23	chr1:94995935-94995985	ProgFib	skin:	n/a
24	chr1:94995935-94995985	HRE	kidney:	n/a
25	chr1:95001236-95001286	AG09319	gingival:	n/a
26	chr1:94983186-94983236	AG09319	gingival:	n/a
27	chr1:95003968-95004018	HRPEpiC	eye:	n/a
28	chr1:94929484-94929534	GM12878	blood:	n/a
29	chr1:95001236-95001286	HEK293	kidney:	embryo
30	chr1:95003968-95004018	HL-60	blood:	n/a
31	chr1:95003968-95004018	GM12878	blood:	n/a
32	chr1:95003968-95004018	ovcar-3	ovarian:	n/a
33	chr1:95003968-95004018	HCF	heart:	n/a
34	chr1:95001236-95001286	AG04450	lung:	fetal
35	chr1:95003968-95004018	HIPEpiC	eye:	n/a
36	chr1:94995935-94995985	HEK293	kidney:	embryo
37	chr1:94929484-94929534	AG10803	skin:	n/a
38	chr1:94929484-94929534	HRE	kidney:	n/a
39	chr1:94995935-94995985	GM12891	blood:	n/a
40	chr1:94995935-94995985	LNCaP	prostate:	n/a
41	chr1:95003968-95004018	AG04450	lung:	fetal
42	chr1:95003968-95004018	BJ	skin:	n/a
43	chr1:94995935-94995985	T-47D	breast:	n/a
44	chr1:95001236-95001286	GM12891	blood:	n/a
45	chr1:95001236-95001286	SKMC	muscle:	n/a
46	chr1:95003968-95004018	HNPCEpiC	eye:	n/a
47	chr1:95003968-95004018	AG09309	skin:	n/a
48	chr1:94929484-94929534	HRCEpiC	kidney:	n/a
49	chr1:95001236-95001286	RPTEC	kidney:	n/a
50	chr1:95001236-95001286	Jurkat	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:94526680..94527603-chr1:94928967..94929584,2	K562	blood:
2	chr1:94997172..94998108-chr1:95064305..95065624,5	MCF-7	breast:
3	chr1:94997312..94997997-chr1:95271190..95272030,3	MCF-7	breast:
4	chr1:94992707..94993493-chr1:95064769..95065395,2	MCF-7	breast:
5	chr1:95002334..95004389-chr1:95062847..95065293,3	MCF-7	breast:
6	chr1:94510948..94511922-chr1:94929239..94929819,2	K562	blood:
7	chr1:94941332..94943153-chr1:94956990..94959761,2	MCF-7	breast:
8	chr1:94883768..94885488-chr1:94926929..94929559,2	MCF-7	breast:
9	chr1:94987992..94988549-chr1:95064767..95065433,2	MCF-7	breast:
10	chr1:94987984..94988512-chr1:95267242..95268185,2	MCF-7	breast:
11	chr1:94946963..94948709-chr1:95581027..95583387,2	K562	blood:
12	chr1:94901652..94904489-chr1:94917080..94919308,2	MCF-7	breast:
13	chr1:94923038..94925155-chr1:94932732..94934568,2	K562	blood:
14	chr1:94965266..94968110-chr1:94970843..94972625,2	MCF-7	breast:
15	chr1:94923038..94925155-chr1:94932732..94934568,2	K562	blood:
16	chr1:94965266..94968110-chr1:94970843..94972625,2	MCF-7	breast:
17	chr1:94816155..94817816-chr1:94928944..94931018,2	MCF-7	breast:
18	chr1:94883223..94885583-chr1:94928116..94929855,2	MCF-7	breast:
19	chr1:94941332..94943153-chr1:94956990..94959761,2	MCF-7	breast:
20	chr1:94947212..94947799-chr1:95319643..95320515,2	K562	blood:
21	chr1:95001173..95003691-chr1:95006398..95009153,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F3-3	chr1:94970402-94970548	l_89_chr1:94917575-94970548_76bGuttman_hLF
2	lnc-F3-3	chr1:94917576-94917751	l_89_chr1:94917575-94970548_76bGuttman_hLF
3	lnc-F3-3	chr1:94943583-94943687	l_89_chr1:94917575-94970548_76bGuttman_hLF

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	F3	hsa-miR-130b-3p	chr1:94995114-94995135
2	F3	hsa-miR-93-5p	chr1:94995112-94995134
3	ABCD3	hsa-miR-21-5p	chr1:94983826-94983845
4	F3	hsa-miR-93-5p	chr1:94995118-94995111
5	F3	hsa-miR-130b-3p	chr1:94995974-94995995
6	F3	hsa-miR-26b-5p	chr1:94994895-94994916

Variant related genes	Relation type
ABCD3	TF binding region
F3	TF binding region
ABCD3	CpG island
F3	CpG island
ENSG00000117525	chromatin interactions
ENSG00000152078	chromatin interactions
ENSG00000117528	chromatin interactions
ENSG00000198691	chromatin interactions

Extended variants
information (count: 3036 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3036 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4148057	chr1:94917402-94917403	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563361968	chr1:94917432-94917433	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531941706	chr1:94917479-94917480	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560889699	chr1:94917499-94917500	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570758423	chr1:94917550-94917551	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373751316	chr1:94917598-94917599	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs72727492	chr1:94917600-94917601	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs182773825	chr1:94917611-94917612	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs77461205	chr1:94917633-94917634	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs536084499	chr1:94917639-94917640	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs556092333	chr1:94917663-94917664	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs370661377	chr1:94917683-94917684	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs374562189	chr1:94917687-94917688	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs78294493	chr1:94917729-94917730	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs188443579	chr1:94917738-94917739	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs543051909	chr1:94917788-94917789	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374567691	chr1:94917795-94917796	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556870994	chr1:94917799-94917800	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576788396	chr1:94917815-94917816	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562935011	chr1:94917874-94917875	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192272247	chr1:94918015-94918016	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552687773	chr1:94918019-94918020	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183917242	chr1:94918098-94918099	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112177576	chr1:94918109-94918110	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368540646	chr1:94918120-94918121	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371811693	chr1:94918124-94918125	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530568682	chr1:94918132-94918133	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541660077	chr1:94918141-94918142	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187806146	chr1:94918156-94918157	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141611986	chr1:94918174-94918175	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs367646807	chr1:94918184-94918185	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548445997	chr1:94918201-94918202	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564469589	chr1:94918214-94918215	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531864043	chr1:94918222-94918223	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551879401	chr1:94918227-94918228	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201578949	chr1:94918278-94918279	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564912654	chr1:94918284-94918285	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376897175	chr1:94918285-94918286	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200255610	chr1:94918288-94918289	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376768403	chr1:94918293-94918294	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539437385	chr1:94918342-94918343	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567017903	chr1:94918367-94918368	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192429083	chr1:94918379-94918380	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547369957	chr1:94918388-94918389	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113874094	chr1:94918410-94918411	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs373888060	chr1:94918469-94918470	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs549559949	chr1:94918536-94918537	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs569355982	chr1:94918540-94918541	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs61772850	chr1:94918541-94918542	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs370948110	chr1:94918573-94918574	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1955 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94908600-94918800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:94910600-94928600	Weak transcription	A549	lung
3	chr1:94913800-94974200	Weak transcription	Psoas Muscle	Psoas
4	chr1:94914200-94917600	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr1:94914200-94917800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr1:94914200-94917800	ZNF genes & repeats	Primary B cells from peripheral blood	blood
7	chr1:94914200-94917800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
8	chr1:94914200-94918000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
9	chr1:94914200-94918000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
10	chr1:94914200-94918800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:94914200-94951800	Weak transcription	Brain Angular Gyrus	brain
12	chr1:94914400-94917600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
13	chr1:94914400-94918000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr1:94914400-94918000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr1:94914400-94918000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
16	chr1:94914400-94918200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
17	chr1:94914400-94918200	ZNF genes & repeats	Primary T cells from cord blood	blood
18	chr1:94914400-94918800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:94914400-94918800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
20	chr1:94914400-94918800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr1:94914600-94917600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
22	chr1:94914600-94918000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:94914600-94918000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
24	chr1:94914600-94918000	ZNF genes & repeats	Dnd41	blood
25	chr1:94914600-94918800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
26	chr1:94914600-94918800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
27	chr1:94914600-94918800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
28	chr1:94914600-94920000	ZNF genes & repeats	Fetal Intestine Large	intestine
29	chr1:94914800-94917600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:94914800-94917600	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
31	chr1:94914800-94917800	ZNF genes & repeats	Primary B cells from cord blood	blood
32	chr1:94914800-94918000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:94914800-94985800	Weak transcription	NHLF	lung
34	chr1:94915400-94929800	Weak transcription	Hela-S3	cervix
35	chr1:94915400-94930400	Weak transcription	Brain Anterior Caudate	brain
36	chr1:94915400-94934000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:94915400-94993200	Weak transcription	HSMMtube	muscle
38	chr1:94915800-94918200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:94915800-94924600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:94915800-94925400	Weak transcription	Fetal Kidney	kidney
41	chr1:94915800-94925400	Weak transcription	HMEC	breast
42	chr1:94915800-94929400	Weak transcription	Stomach Smooth Muscle	stomach
43	chr1:94915800-94930600	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr1:94915800-94935000	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr1:94915800-94955400	Weak transcription	NHDF-Ad	bronchial
46	chr1:94915800-94956600	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr1:94916000-94917600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr1:94916000-94918400	Strong transcription	Fetal Thymus	thymus
49	chr1:94916000-94921600	Weak transcription	Left Ventricle	heart
50	chr1:94916000-94923200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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