Variant report

Variant	nsv1009069
Chromosome Location	chr3:163787128-164323219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1415)
CpG islands
(count:611)
Chromatin interactive
region (count:63)
LncRNA
region (count:8)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:164241910-164242382	HepG2	liver:	n/a	n/a
2	BACH1	chr3:164321025-164321070	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:164133548-164133563	K562	blood:	n/a	n/a
4	BACH1	chr3:163946376-163946549	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr3:164178610-164178800	GM12878	blood:	n/a	n/a
6	BATF	chr3:164244057-164244370	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:164244047-164244303	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:164242057-164242298	HepG2	liver:	n/a	n/a
9	BHLHE40	chr3:164065590-164065659	K562	blood:	n/a	n/a
10	BHLHE40	chr3:164242007-164242375	HepG2	liver:	n/a	n/a
11	BRCA1	chr3:164315407-164315518	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr3:163881866-163881882	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr3:164169712-164169773	Hela-S3	cervix:	n/a	n/a
14	CCNT2	chr3:164177641-164177933	K562	blood:	n/a	n/a
15	CEBPB	chr3:164201888-164202124	HepG2	liver:	n/a	chr3:164201989-164202000
16	CEBPB	chr3:164107093-164107343	IMR90	lung:	n/a	chr3:164107227-164107236 chr3:164107225-164107238 chr3:164107227-164107236 chr3:164107227-164107236 chr3:164107226-164107237 chr3:164107225-164107238 chr3:164107225-164107236 chr3:164107227-164107236
17	CEBPB	chr3:164285753-164286114	Hela-S3	cervix:	n/a	chr3:164285965-164285978 chr3:164285946-164285959
18	CEBPB	chr3:163980067-163980373	HepG2	liver:	n/a	chr3:163980184-163980195
19	CEBPB	chr3:163937023-163937362	A549	lung:	n/a	chr3:163937193-163937204
20	CEBPB	chr3:163937094-163937307	K562	blood:	n/a	chr3:163937193-163937204
21	CEBPB	chr3:163980083-163980289	Hela-S3	cervix:	n/a	chr3:163980184-163980195
22	CEBPB	chr3:164270273-164270503	HepG2	liver:	n/a	n/a
23	CEBPB	chr3:164177551-164177860	K562	blood:	n/a	n/a
24	CEBPB	chr3:164121426-164121694	K562	blood:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
25	CEBPB	chr3:164212217-164212575	A549	lung:	n/a	chr3:164212397-164212410
26	CEBPB	chr3:164317755-164317980	HepG2	liver:	n/a	chr3:164317849-164317860
27	CEBPB	chr3:164093320-164093640	HepG2	liver:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
28	CEBPB	chr3:163800790-163801049	HepG2	liver:	n/a	chr3:163800890-163800901
29	CEBPB	chr3:164241668-164242478	MCF-7	breast:	n/a	chr3:164241831-164241842
30	CEBPB	chr3:163811663-163811965	MCF-7	breast:	n/a	chr3:163811787-163811796 chr3:163811785-163811796
31	CEBPB	chr3:163980107-163980307	H1-hESC	embryonic stem cell:	n/a	chr3:163980184-163980195
32	CEBPB	chr3:163890801-163890962	H1-hESC	embryonic stem cell:	n/a	chr3:163890911-163890922
33	CEBPB	chr3:164121369-164121693	A549	lung:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
34	CEBPB	chr3:163811615-163811972	Hela-S3	cervix:	n/a	chr3:163811787-163811796 chr3:163811785-163811796
35	CEBPB	chr3:164143715-164143729	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr3:164164587-164164921	HepG2	liver:	n/a	chr3:164164746-164164757
37	CEBPB	chr3:164132486-164132757	A549	lung:	n/a	chr3:164132597-164132608
38	CEBPB	chr3:164216794-164216934	HepG2	liver:	n/a	n/a
39	CEBPB	chr3:164085608-164085831	IMR90	lung:	n/a	chr3:164085753-164085766
40	CEBPB	chr3:164093408-164093523	K562	blood:	n/a	chr3:164093476-164093487
41	CEBPB	chr3:164085628-164085750	K562	blood:	n/a	n/a
42	CEBPB	chr3:163917760-163918155	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr3:164093357-164093663	A549	lung:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
44	CEBPB	chr3:163885974-163886233	A549	lung:	n/a	chr3:163886110-163886119 chr3:163886110-163886119 chr3:163886110-163886119 chr3:163886109-163886120 chr3:163886108-163886121 chr3:163886108-163886119 chr3:163886110-163886119
45	CEBPB	chr3:163886053-163886253	HepG2	liver:	n/a	chr3:163886110-163886119 chr3:163886110-163886119 chr3:163886110-163886119 chr3:163886109-163886120 chr3:163886108-163886121 chr3:163886108-163886119 chr3:163886110-163886119
46	CEBPB	chr3:163937048-163937294	Hela-S3	cervix:	n/a	chr3:163937193-163937204
47	CEBPB	chr3:164078081-164078324	MCF-7	breast:	n/a	chr3:164078134-164078145
48	CEBPB	chr3:163925893-163926208	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr3:164077996-164078260	A549	lung:	n/a	chr3:164078134-164078145
50	CEBPB	chr3:163937041-163937366	HepG2	liver:	n/a	chr3:163937193-163937204

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:164119959-164120009	K562	blood:	n/a
2	chr3:164119959-164120009	K562	blood:	n/a
3	chr3:164059255-164059305	HIPEpiC	eye:	n/a
4	chr3:164009569-164009619	HL-60	blood:	n/a
5	chr3:164050953-164051003	HEK293	kidney:	embryo
6	chr3:164050953-164051003	Caco-2	colon:	n/a
7	chr3:164119959-164120009	NHBE	bronchial:	n/a
8	chr3:164009569-164009619	ovcar-3	ovarian:	n/a
9	chr3:164009569-164009619	BE2_C	brain:	n/a
10	chr3:164009569-164009619	GM12892	blood:	n/a
11	chr3:164119020-164119070	HUVEC	blood vessel:	n/a
12	chr3:164056753-164056803	HCPEpiC	choroid plexus:	n/a
13	chr3:164050953-164051003	IMR90	lung:	fetal
14	chr3:164059011-164059061	K562	blood:	n/a
15	chr3:164009569-164009619	ProgFib	skin:	n/a
16	chr3:164119737-164119787	HL-60	blood:	n/a
17	chr3:164119959-164120009	HEEpiC	esophagus:	n/a
18	chr3:164059011-164059061	Jurkat	blood:	n/a
19	chr3:164056463-164056513	Caco-2	colon:	n/a
20	chr3:164050953-164051003	SK-N-SH	brain:	n/a
21	chr3:164056463-164056513	HCPEpiC	choroid plexus:	n/a
22	chr3:164050953-164051003	HAEpiC	amniotic membrane:	n/a
23	chr3:164119737-164119787	RPTEC	kidney:	n/a
24	chr3:164119959-164120009	RPTEC	kidney:	n/a
25	chr3:164059011-164059061	HL-60	blood:	n/a
26	chr3:164119020-164119070	HCM	heart:	n/a
27	chr3:164050953-164051003	AG10803	skin:	n/a
28	chr3:164009569-164009619	Hela-S3	cervix:	n/a
29	chr3:164059011-164059061	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:164056753-164056803	HRE	kidney:	n/a
31	chr3:164119959-164120009	HepG2	liver:	n/a
32	chr3:164059124-164059174	ovcar-3	ovarian:	n/a
33	chr3:164059255-164059305	A549	lung:	n/a
34	chr3:164059255-164059305	SKMC	muscle:	n/a
35	chr3:164059255-164059305	SK-N-SH_RA	brain:	n/a
36	chr3:164119020-164119070	H1-hESC	embryonic stem cell:	embryo
37	chr3:164119020-164119070	GM12891	blood:	n/a
38	chr3:164119959-164120009	NT2-D1	testis:	n/a
39	chr3:164056753-164056803	BJ	skin:	n/a
40	chr3:164056753-164056803	HCT-116	colon:	n/a
41	chr3:164059011-164059061	SK-N-SH_RA	brain:	n/a
42	chr3:164119020-164119070	CMK	blood:	n/a
43	chr3:164059124-164059174	AG10803	skin:	n/a
44	chr3:164059255-164059305	BE2_C	brain:	n/a
45	chr3:164050953-164051003	GM12892	blood:	n/a
46	chr3:164119020-164119070	IMR90	lung:	fetal
47	chr3:164119020-164119070	HIPEpiC	eye:	n/a
48	chr3:164056463-164056513	IMR90	lung:	fetal
49	chr3:164009569-164009619	PrEC	prostate:	n/a
50	chr3:164059011-164059061	U87	brain:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:164097647..164098715-chr3:164154502..164155534,19	MCF-7	breast:
2	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
3	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
4	chr3:164240704..164243300-chr3:164249655..164252008,2	MCF-7	breast:
5	chr3:163916797..163919508-chr3:163924219..163927520,3	MCF-7	breast:
6	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
7	chr3:164097647..164098715-chr3:164154502..164155534,19	MCF-7	breast:
8	chr3:164154966..164155479-chr3:164352397..164353197,2	MCF-7	breast:
9	chr3:164240704..164243300-chr3:164249655..164252008,2	MCF-7	breast:
10	chr3:164145149..164147604-chr3:164148897..164151396,2	MCF-7	breast:
11	chr14:86195432..86196215-chr3:163793960..163794780,2	MCF-7	breast:
12	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:
13	chr3:163816031..163818067-chr3:163819325..163821288,2	MCF-7	breast:
14	chr17:57914661..57917089-chr3:163901184..163903192,2	MCF-7	breast:
15	chr3:164097731..164098551-chr3:164154660..164155422,4	MCF-7	breast:
16	chr3:164256176..164258649-chr3:164263680..164265313,2	MCF-7	breast:
17	chr3:164050649..164051226-chr3:164523700..164524566,2	MCF-7	breast:
18	chr3:164241644..164242499-chr3:164352238..164353178,5	MCF-7	breast:
19	chr3:163831824..163833454-chr3:163836559..163838959,2	K562	blood:
20	chr3:164097647..164098678-chr3:164154502..164155534,10	MCF-7	breast:
21	chr3:164097708..164098703-chr3:164352353..164353241,9	MCF-7	breast:
22	chr3:164212016..164212593-chr6:120624651..120625343,2	MCF-7	breast:
23	chr3:164097731..164098551-chr3:164154660..164155422,4	MCF-7	breast:
24	chr3:164097711..164099012-chr3:164352332..164353250,14	MCF-7	breast:
25	chr3:164172109..164174038-chr3:164174239..164176085,2	MCF-7	breast:
26	chr3:164097647..164098678-chr3:164154502..164155534,10	MCF-7	breast:
27	chr3:164097711..164098324-chr3:164241488..164242187,2	MCF-7	breast:
28	chr3:164190398..164192515-chr3:164196627..164199488,2	K562	blood:
29	chr3:163919977..163922257-chr3:163923536..163925910,2	MCF-7	breast:
30	chr3:164155004..164155575-chr3:164352325..164352831,2	MCF-7	breast:
31	chr3:164190398..164192515-chr3:164196627..164199488,2	K562	blood:
32	chr3:164097659..164099012-chr3:164352282..164353331,34	MCF-7	breast:
33	chr3:164172109..164174038-chr3:164174239..164176085,2	MCF-7	breast:
34	chr3:164097711..164098324-chr3:164241488..164242482,3	MCF-7	breast:
35	chr15:52587462..52588981-chr3:163831086..163833177,2	MCF-7	breast:
36	chr3:164097709..164098424-chr3:164241494..164242452,3	MCF-7	breast:
37	chr3:164241773..164244042-chr3:164244735..164247521,2	MCF-7	breast:
38	chr3:164097711..164098324-chr3:164241488..164242187,2	MCF-7	breast:
39	chr3:163816031..163818067-chr3:163819325..163821288,2	MCF-7	breast:
40	chr3:163919977..163922257-chr3:163923536..163925910,2	MCF-7	breast:
41	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:
42	chr3:164256176..164258649-chr3:164263680..164265313,2	MCF-7	breast:
43	chr19:15442848..15443641-chr3:164192625..164193437,2	Hela-S3	cervix:
44	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
45	chr3:163831824..163833454-chr3:163836559..163838959,2	K562	blood:
46	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:
47	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
48	chr3:164145149..164147604-chr3:164148897..164151396,2	MCF-7	breast:
49	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:
50	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SERPINI1-9	chr3:164280960-164281013	XLOC_002900
2	lnc-OTOL1-4	chr3:164137191-164137295	XLOC_002899
3	lnc-SERPINI1-9	chr3:164280960-164281013	XLOC_002900
4	lnc-SERPINI1-9	chr3:164169033-164169323	XLOC_002900
5	lnc-SERPINI1-9	chr3:164169033-164169323	XLOC_002900
6	lnc-OTOL1-4	chr3:164078868-164078917	XLOC_002899
7	lnc-OTOL1-4	chr3:164136236-164136391	XLOC_002899
8	lnc-OTOL1-4	chr3:164088402-164088464	XLOC_002899

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1263	chr3:163889311-163889332	MIMAT0005915

No data

Variant related genes	Relation type
MIR1263	TF binding region
MIR720	TF binding region
MIR1263	CpG island
MIR720	CpG island
ENSG00000141867	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000128833	chromatin interactions
AKAP12	miRNA target sites
QKI	miRNA target sites

Extended variants
information (count: 14442 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:14442 , 50 per page) page: 1 2 3 4 5 6 7 ... 289

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535471002	chr3:163787171-163787172	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs35543488	chr3:163787179-163787180	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555775793	chr3:163787184-163787185	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13069803	chr3:163787307-163787308	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs140743747	chr3:163787356-163787357	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564315529	chr3:163787368-163787369	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181068050	chr3:163787370-163787371	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs13070113	chr3:163787372-163787373	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs371123620	chr3:163787375-163787376	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560404642	chr3:163787393-163787394	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574317720	chr3:163787440-163787441	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368689743	chr3:163787455-163787456	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12493528	chr3:163787459-163787460	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs185385285	chr3:163787484-163787485	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562514646	chr3:163787501-163787502	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531273492	chr3:163787503-163787504	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12487050	chr3:163787542-163787543	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs545908264	chr3:163787546-163787547	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562474077	chr3:163787568-163787569	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190636614	chr3:163787580-163787581	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77222219	chr3:163787595-163787596	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527572320	chr3:163787628-163787629	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114793858	chr3:163787655-163787656	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150112684	chr3:163787656-163787657	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545832606	chr3:163787685-163787686	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370062591	chr3:163787727-163787728	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73170705	chr3:163787728-163787729	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs138562136	chr3:163787741-163787742	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182858442	chr3:163787793-163787794	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569257756	chr3:163787812-163787813	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537883621	chr3:163787813-163787814	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35297573	chr3:163787824-163787825	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs577758125	chr3:163787829-163787830	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540425418	chr3:163787834-163787835	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553949370	chr3:163787861-163787862	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140298619	chr3:163787897-163787898	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145423800	chr3:163787898-163787899	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562316709	chr3:163787904-163787905	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531313244	chr3:163787928-163787929	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115702357	chr3:163787963-163787964	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189246332	chr3:163787981-163787982	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530324856	chr3:163788009-163788010	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527428160	chr3:163788010-163788011	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547565594	chr3:163788021-163788022	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138059392	chr3:163788022-163788023	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114312375	chr3:163788023-163788024	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377082915	chr3:163788060-163788061	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550031421	chr3:163788078-163788079	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569888424	chr3:163788128-163788129	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71315996	chr3:163788141-163788142	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Bladder cancer	21909424	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Alcoholism	21790672	CNVD
Schizophrenia	20967226	CNVD
Acute myeloid leukemia	19651600	CNVD
Autism	19287141	CNVD
Incontinentia Pigmenti	22033527	CNVD
Rett syndrome	21593744	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Recurrent pregnancy loss	19789632	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163771800-163795600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:163795600-163796000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:163796000-163797400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:163797400-163798800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:163798800-163803400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:163803400-163804400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:163804400-163805400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:163805400-163806800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:163806800-163811400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:163811400-163814400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:163811800-163814400	Enhancers	Dnd41	blood
12	chr3:163814400-163832200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:163831200-163831600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr3:163831200-163831600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr3:163831200-163832000	Enhancers	Dnd41	blood
16	chr3:163832200-163833000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:163833000-163837800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:163837800-163839200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:163839200-163852000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:163841400-163841800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr3:163841400-163841800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:163841400-163841800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr3:163841800-163842200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr3:163848600-163849800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:163852000-163854600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:163854600-163862000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:163860000-163861400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr3:163862000-163870200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:163863200-163866400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
30	chr3:163865800-163867600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
31	chr3:163868200-163870200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr3:163870200-163874600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:163873400-163873800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr3:163874600-163879600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:163875800-163876200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr3:163879600-163898800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:163881400-163881600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr3:163883600-163885200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr3:163885200-163886000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr3:163886000-163886200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr3:163890800-163892800	Enhancers	Dnd41	blood
42	chr3:163892600-163892800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr3:163896800-163897400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr3:163898800-163904200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:163904200-163912800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr3:163911000-163911600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr3:163912400-163912800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr3:163912800-163913000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:163912800-163918400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr3:163913000-163914000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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